Headache associated with hormonal fluctuations …

Marianna Vinokur DO

General Neurology

Updated 05.23.2024
Released 11.23.1993
Expires For CME 05.23.2027

Headache associated with hormonal fluctuations

Author: Marianna Vinokur DO

See Contributor Disclosures

Editor: Stephen D Silberstein MD

Headache associated with hormonal fluctuations

In This Article

Quick Link

Introduction

Overview

In this article, the author reviews the complex relations between headache and ovarian sex hormones. The author discusses the changes in headache patterns during major hormonal events (such as menarche, pregnancy, menopause) in the woman's life cycle and the effects of hormonal contraception and hormone replacement therapy on headache. Advances in elucidating the association between hormonal milieu and headache and new data on the possible mechanisms through which sex hormones affect migraine and pain perception are discussed. Therapeutic approaches and evidence-based practice regarding the management of menstrual migraine, migraine during pregnancy, and migraine in the perimenopausal and postmenopausal periods are analyzed. The potential complications and benefits of the use of hormonal contraceptives and hormone replacement therapy in people with migraine are also discussed based on evidence from clinical studies.

Historical note and terminology

For the purposes of this article:

	Cisgender: A person whose gender identity is consistent with the sex assigned at birth based on traditional social constructs.
	Transgender: A person whose gender identity does not correspond with the sex assigned at birth based on traditional social constructs.
	Trans man/transgender man: A person assigned female at birth whose gender identity aligns with being a man. This person may use the words boy/man to identify themselves and use he/his pronouns.
	Trans woman/transgender woman: A person who was assigned male at birth whose gender identity aligns with being a woman. This person may use the words girl/woman to identify themselves and use she/her pronouns.
	Gender nonconforming/nonbinary: a person who does not identify with either gender and are neither cis nor trans-gender. This person may use terms such as genderqueer, genderfluid, agender, bigender to identify themselves and use they/them pronouns, ze/zir, ey/em pronouns.
	Gender-affirming hormone therapy (GAHT): feminizing or masculinizing hormone treatment to align secondary sex characteristics with gender identity
	Female: person with biologically female reproductive organs
	Male: person with biologically male reproductive organs
Adapted from (148)

Clinical manifestations

Presentation and course

Migraine prevalence. The global burden of migraine is invariably high at 618.4 (95% UI 392.5-898.8) years lived with disability (YLDs) per 100,000 people, and accounts for 6.6% (95% UI 4.6–8.7) of years lived with disability in women and 4.4% (95% UI 3.0-6.1) in men (67). Changes in sex-hormone levels during menarche, menstruation, pregnancy, and menopause may affect the prevalence and character of migraine and other types of headaches (09). There is no gender difference in the incidence of migraine before puberty. In adults, however, the prevalence of migraine is in the United States has been remarkably stable over approximately 20 years, affecting roughly one of every six Americans, 9.7% of males and 20.7% of females (25). According to the 2017 data, migraine prevalence peaks for both sexes between ages 35 to 39 reaching 34.5% in cisgender women (95% UI 29.9-39.3) and 20.3% in cisgender men (95% UI 17.5-27.2) (67). Migraine without aura is more common in both cisgender men and women (141).

The frequency, duration, and disability of attacks tend to be higher in cisgender women (03). There is no consensus on the likelihood that female sex is a risk of factor for transition from episodic to chronic migraine; some studies have reported that the transition is more likely in women (OR 2.9, 95% CI 1.2-6.9) (141), whereas others show a nearly indistinguishable transition rate within 1 year (5.4% in cisgender men and 4.4% in cisgender women) (99). Multiple studies across different countries have demonstrated the same findings that heritability of migraine was essentially equal between cisgender men and cisgender women (65; 52; 51). These findings suggest the prominent sex difference in migraine prevalence cannot be entirely explained by genetic factors or heritability. Furthermore, there is a significant increase in migraine risk for females with a male, co-twin as compared to females with a female co-twin, suggesting that masculinization of the prenatal environment may actually increase migraine risk for females (51). Headache and migraine prevalence are increased in adolescents with early menarche, which seems to increase headache susceptibility (01). These data further suggest that cisgender women’s increased migraine risk results from exposure to endogenous or exogenous factors rather than from a genetic predisposition. The epidemiology of headache in transgender individuals is complicated by a lack of population-based studies.

Menstrual and menstrually-related migraine. The diagnostic criteria for menstrual migraine have been included in the appendix, a section reserved for proposed diagnoses pending further scientific evidence rather than formal diagnoses, of the International Classification of Headache Disorders (ICHD) since its second edition (ICHD-2). In the International Classification of Headache Disorders- 3 (ICHD-3), published in 2018, pure menstrual migraine is defined as migraine attacks that occur exclusively between days -2 and +3 of the menstrual cycle (where day 1 is defined as the first day of menstruation) in at least two of three menstrual cycles (61; 62). Menstrually-related migraine is defined as migraine attacks that occur between days -2 and +3 of the menstrual cycle in at least two of three menstrual cycles and additionally at other times of the cycle. Both pure menstrual migraine as well as menstrually-related migraine can be with or without aura (see Table 1).

Table 1. International Headache Society Definitions of Pure Menstrual Migraine and of Menstrually-Related Migraine

Pure menstrual migraine with or without aura
	Diagnostic criteria:
		• Attacks in a menstruating woman, fulfilling criteria for 1.1 Migraine without aura • Attacks occur exclusively on days 1±2 (ie, days -2 to +3) of menstruation in at least two of three menstrual cycles and at no other times of the cycle
Menstrually-related migraine with or without aura
	Diagnostic criteria:
		• Attacks in a menstruating woman, fulfilling criteria for 1.1 Migraine without aura • Attacks occur on days 1±2 (ie, days -2 to +3) of menstruation in at least two of three menstrual cycles and additionally at other times of the cycle
Notes: 1. The first day of menstruation is day 1 and the preceding day is day -1, there is no day 0. 2. For the purposes of ICHD-3, menstruation is considered to be endometrial bleeding resulting either from the normal menstrual cycle or from the withdrawal of exogenous progestogens, as in the use of combined oral contraceptives or cyclical hormone replacement therapy. 3. For research purposes a prospective diary is recommended, but this is not mandatory for clinical diagnosis of pure menstrual migraine without aura or menstrually-related migraine without aura.

Many people report that their migraine headaches are more frequent or severe during their menses than at other times. However, increased probability of headache during menses does not always mean a patient has menstrual-migraine. A potential point of confusion is that headache in the perimenstrual period, which might occur by chance in all people who menstruate affected by migraines, can be mistaken for menstrual migraine, in which attacks occur reliably around menstruation. There is a large variation in prevalence of menstrually-related migraine among studies, which is likely explained by changing diagnostic criteria, differences in study design such as headache calendars versus questionnaires, retrospective versus prospective, and populations studied (general population vs. headache clinic patients).

A study of 237 people based on the ICHD3-beta appendix criteria revealed prevalence among people who menstruate as follows: any type of menstrual migraine, 7.6%; menstrual migraine without aura, 6.1%; menstrual migraine with aura, 0.6%; probable menstrual migraine without aura, 0.6%; and probable menstrual migraine with aura, 0.3% (142). The corresponding figures among patients with migraine: any type of menstrual migraine, 22.0%; menstrual migraine without aura, 17.6%; menstrual migraine with aura, 1.7%; probable menstrual migraine without aura, 1.6%; and probable menstrual migraine with aura, 1.0% (142). A 2015 study by Pavlovic and colleagues evaluated 1697 subjects who met modified ICHD-2 criteria for migraine and found prevalence of pure menstrual migraine to be 5.5%, menstrually-associated migraine at 53.8%, and menstrually-unassociated migraine to be 40.7% (104). Patients with pure menstrual migraine had an older age of migraine onset and had fewer headache days but appeared to be more impaired by attacks based on HIT-6 and MIDAS scores. When headache diaries were used, only 7% of people with migraine were found to have menstrual migraine (80; 82). In a population-based study, the rate of menstrual migraine was significantly lower (0.85%) than that of menstrually-related, which was 8% (36). However, most studies as well as the ICHD-3 agree that the most predominant subtype of menstrual migraine is migraine without aura. In comparison, migraine that occurs for the first time during pregnancy (an uncommon occurrence) or is induced by oral (exogenous estrogen) is often migraine with aura.

Estrogen, progesterone, and testosterone are lipophilic molecules that are able to cross the blood brain barrier into the central nervous system (CNS), where they serve as precursors for further steroid production in the CNS (02). Generally, current data suggest that estrogen receptors are expressed in the trigeminovascular system and cyclical changes in estrogen levels can influence cytokine release, including CGRP and receptor signaling (29). Headaches associated with menses may occur alone or as part of premenstrual syndrome (late luteal phase dysphoric disorder). In a Swedish study of 266 menstruating, those who had premenstrual syndrome were found to have a significantly increased risk for migraine without aura (93).

Higher levels of estrogen are associated with increased frequency of migraine aura. Conversely, in low estrogen states, as occurs in menstrually-related migraine, the onset of menses occurs as a result of a drop in estrogen. Thus, menstrually-related migraines are predominantly without aura. Another general consensus is that steady or rising levels of estrogen are not associated with migraine; however, a rapid decline in estrogen levels, for example, those that occur before menstruation, perimenopausally, etc., can precipitate individual migraine attacks, as may occur with menstrually-related migraines, or worsening intensity or frequency of attacks over a longer period. However, this is a general guideline with many exceptions. For example, some experience new headaches or worsening of their migraine attacks during the first trimester of pregnancy, although estrogen levels are generally rising.

It has been postulated that oxytocin may play a role in menstrually-related migraine. Oxytocin is a hypothalamic hormone and neurotransmitter, which is postulated to inhibit trigeminal neuronal excitability. During menstruation, levels of estrogen and oxytocin decrease, and furthermore, it is a state of decreased oxytocin affinity for its receptor, and decreased expression of the trigeminal oxytocin receptor, resulting in decreased inhibition, thereby promoting lower thresholds for activation of meningeal trigeminal nociceptors and increasing the likelihood of an menstrually-related migraine attack (15).

An important distinction to be made is whether menstrually-related migraine occurs in setting of exogenous hormone use versus as a result of an unimpeded hypothalamic-pituitary-ovarian (HPO) axis. Sixty four point nine percent of 72.2 million females aged 15 to 49 in the United States use a form of contraception (38). The most common contraceptive methods currently used were female sterilization (18.6%), oral contraceptive pill (12.6%), long-acting reversible contraceptives (LARCs) (10.3%), and male condom (8.7%) (38). The reported incidence of headache with hormonal contraception use is variable and related to the agent’s composition and the estrogen dose (92). Migraine is more likely to worsen or remain the same, rather than improve, following oral contraception initiation; however, the effects that an individual woman may experience are largely unpredictable (12). In a study of people taking high-dose oral contraceptives (50 or greater µg of ethinyl estradiol), 10% of those who had not had headaches before oral contraceptive use reported headaches after starting oral contraceptives (75). In a double-blind study of 704 females, the use of low-dose combined oral contraceptives (20 µg ethinyl estradiol/100 µg levonorgestrel) was not associated with a higher headache incidence than placebo (35). The use of progestin implantable contraceptives is associated with a higher headache rate (10% to 30%) compared with combined oral contraceptives (22). In a literature review, Loder and colleagues concluded that in most contraceptive trials there was no statistically significant difference in overall headache complaints between treatment and control subjects (77). There is also evidence that migraine with aura is more likely to be exacerbated with oral contraceptive pill intake compared with migraine without aura (88; 89).

In contrast to migraine, cluster headache is rarely related to menses, although exceptions exist. A report described a woman with episodic cluster headache whose attacks were temporally linked to her menstrual cycle and occurred regularly on days 4 to 9 of her menstrual cycle. Suppressing menstruation with oral contraceptives resulted in cessation of her cluster headache attacks. However, a study of 224 cisgender women with cluster headache showed that menstruation, pregnancy, menopause, and the use of oral contraceptives had little effect on their headache attacks (140).

Tension-type headache is less likely to be exacerbated during menstruation as well (69). In a large, prospective, questionnaire-based study, patients with migraine were 3.12 times more likely to experience a headache attack during menstruation compared to patients with tension-type headache. However, pure menstrual headaches were experienced by 4.4% of menstruating migraine patients and 8.2% of people experiencing menstruating tension-type headache (p = 0.032). In the same study, the odds ratio for disappearance of headache in migraineurs during pregnancy compared to tension-type headache patients was 2.56 (69). Oral contraceptives worsened migraine significantly more than tension-type headache, whereas menopause had a slight improving effect on migraine compared to tension-type headache (p = 0.046).

Chronic paroxysmal hemicrania (a cluster-like headache characterized by daily, short duration, high-frequency headaches responsive to indomethacin) is more common in women than men. Pregnancy seems to have an ameliorating effect on attack frequency and severity. Headache onset sometimes occurs immediately after delivery (132).

Migraine in gender diverse people. The study of headache disorders in gender minorities is critical for improving access to care for a historically underserved population. Additionally, it is crucial for a comprehensive scientific understanding of the field. Most available information about the effects of hormones on headache originate from studies on cisgender individuals, most commonly the effect of estrogen on cisgender women. However, the influence of gender as a social construct as well as the use of exogenous hormones on headache disorders are both areas requiring further research and attention. In a report from 2016 to 2017, it was estimated that collectively greater than 1.6 million people identify as transgender in the United States (63). This makes up roughly 0.5% of American adults, 1.3 million, and 1.4% of American teens aged 13 to 17, or 300,000. Of the 1.3 million adults who identify as transgender, 38.5% (515,200) are transgender women, 35.9% (480,000) are transgender men, and 25.6% (341,800) reported they are gender nonconforming. However, the exact numbers are difficult to estimate in part because this is a stigmatized and medically underserved population (63).

Gender-affirming hormone therapy (GAHT) is an umbrella term that encapsulates a variety of treatments, including puberty blockade and use of exogenous hormones to alter secondary sex characteristics to better match a person’s gender identity. It is important to note, not all people who identify as gender-diverse choose to undergo hormonal and surgical gender-affirming therapies, and those who do, choose from a wide spectrum of options ranging from noninvasive, such as clothing and hair choices, to feminizing or masculinizing hormone administration and puberty blockade, to surgical treatments. Puberty blockade therapy is often started during puberty, Tanner stages 2 and 3 to pause and delay development of secondary sex characteristics. Masculinizing hormone therapies typically involve administration of testosterone via nasal, subcutaneous, and transdermal gel or patch routes (109; 110). Feminizing hormone therapies typically include estrogen treatment, usually given in the form of 17-beta-estradiol via parenteral, oral, or transdermal routes. This form of estrogen has a lower risk of thromboembolic events than unconjugated estrogens or ethinyl estradiol. Androgen blockade is often given concurrently to reduce endogenous testosterone production (110).

Clinical studies have shown that exogenous estrogen use in transgender women generally causes worsening of pain, including headache (83). Gender diverse people who have used exogenous estrogen have a similar migraine prevalence to cisgender women (83). The use of exogenous estrogen, like oral hormonal contraception and pregnancy, is considered to be a high estrogen state. This translates into real world examples where transgender women reported higher rates of aura with higher corresponding therapeutic estrogen levels, similar to observations of increased migraine aura in cisgender women using estrogen replacement therapy (109). A study of 17 cisgender men with episodic migraine without aura showed that compared to 22 cisgender male controls, those with migraine had significantly higher inter-ictal estrogen levels (139).

Progesterone is thought to have a neuroprotective effect in the CNS in a variety of neurologic conditions including traumatic brain injury, catamenial epilepsy, and migraine by reducing nociception in the trigeminovascular system (130; 112; 02).

Generally, it is thought that testosterone is protective against pain. In a pilot study of 27 cisgender women treated with subcutaneous testosterone, 92% experienced improved headache severity by 3.3 points on a 5-point scale, (p< 0.001) (55). Testosterone is thought to be antinociceptive through various mechanisms including suppression of cortical spreading depolarization and anti-inflammatory effects (26; 43). Testosterone use is proposed in the treatment of migraine, although its effect is still poorly understood.

Therapies for gender affirming care are an important topic with many nuances, variation in treatment, and treatment related adverse effects far exceeding the scope of this article. Generally, providers should approach a gender diverse patient’s treatment like any other person’s, while keeping in mind that certain medications may interact with gender-affirming hormone therapy. As gender-affirming hormone therapy medications are titrated, it is helpful to keep a headache diary to track what changes if any, in gender-affirming hormone therapy cause an increase in headache frequency or severity and at what doses or hormone levels. However, transgender people should not be taken off of gender-affirming hormone therapy in order to treat migraine unless all other avenues of treatment have been explored, as this may cause worsening of gender dysphoria, distress, depression, and it may increase risk of suicidality and worsen migraine burden.

Prognosis and complications

The relationship between estrogen containing contraceptives, stroke, and migraine has been a widely investigated and debated subject, dating almost to the initial launch of continuous hormonal contraceptives in the 1960s. However, it is important to note that the first generations of continual hormonal contraceptives used in trials dating back to the 1970s and 1980s generally used products that were almost uniformly high-dose estrogen containing pills, defined as 50 µg or more of ethinyl estradiol. In subsequent decades, the dose of estrogen was successively reduced, so much so that some pills on the market today contain only 10 µg of ethinyl estradiol.

The relationships among oral contraceptives, migraine, and stroke are complex. American College of Obstetrics and Gynecology in 2010 noted that extended-cycle or continuous hormonal contraceptives, including oral and parenteral products, might provide relief of migraines by eliminating the drops in estrogen levels that precipitate them (08). Conversely, a 2016 update from the U.S. Centers for Disease Control and Prevention on hormonal contraceptive use in various conditions, deemed combined hormonal contraceptives safe in those with migraine without aura (37). However, in the case of migraine with aura, the consensus was that the risk of stroke outweighs the benefit of continuous hormonal contraceptives in patients with migraine with aura. Current guidelines restrict the use of combined hormonal contraceptives in the setting of migraine with aura; migraine without aura is not a contraindication to oral contraceptive use.

Several studies suggest migraine alone is a risk factor for ischemic stroke in young cisgender women, with odds ratio ranging from 1.9 to 4.3 (137; 12; 32; 41; 120). In a case control study, ischemic stroke was strongly associated with migraine, both migraine without aura (OR 3.0, 95% CI: 1.5 to 5.8), and migraine with aura (OR 6.2, 95% CI: 2.1 to 18.0). The risk of ischemic stroke was substantially increased for cisgender women with migraine that were using oral contraceptives (OR 13.9) or who were heavy smokers (≥ 20 cigarettes/day) (OR 10.2) (138). However, a metaanalysis identified a relative risk of 8.72 for an ischemic stroke in patients with migraine taking oral contraceptive pills. This risk rises disproportionately in cisgender women who smoke.

Stroke risk is higher for migraine with aura compared to migraine without aura. In one study, migraine was associated with an increased risk of ischemic stroke (OR, 3.54 for all migraines; 3.81 for migraine with aura, 2.97 for migraine without aura) but not of hemorrhagic stroke (OR, 1.1). A landmark Women’s Health Study, including data from 27,798 cisgender women with a follow-up period of 9 years, found patients who had migraine with aura between ages of 45 and 55 years had the highest relative risk for cardio and cerebrovascular disease, including stroke, which correlated directly with aura frequency (74). Aura frequency less than once a month conferred two times higher risk than in cisgender women without migraine, and more than four times higher risk when aura frequency exceeded once a week. By contrast, migraine without aura was not a risk factor for stroke (70).

Because the prevalence of stroke in young cisgender women is low, the absolute stroke risk in young female patient who experiences migraine is still low (17/100,000 to 19/100,000 women per year) in the absence of other risk factors. However, a World Health Organization study of stroke in young cisgender women found that the adjusted risk of ischemic stroke was significantly and directly associated with aura frequency (41). A large-scale epidemiologic study from the Netherlands showed that migraine patients, especially those with migraine with aura, had a less favorable cardiovascular risk profile compared with nonmigraine controls (119). There is some evidence that levels of platelet activating factor as well as von Willebrand factor increase during migraine attacks (30; 117). The increase in the platelet activating factor may be mediated through release of the CGRP from the trigeminovascular system.

The results of these clinical studies have been supported by neuroimaging findings. In a population-based MRI study from the Netherlands, patients with migraine had a higher prevalence of silent cerebellar infarcts compared with age- and sex-matched controls (73). Migraine was also associated with an increase in deep white matter lesions in cisgender women but not in cisgender men.

A 1996 World Health Organization study reported an increased risk of stroke among Europeans taking high-dose combined oral contraceptives (OR 5.30, 95% CI 2.56–11.0). However, the risk of stroke was not statistically significant in studying preparations containing less than 50 μg of ethinyl estradiol (OR 1.53, 95% CI 0.71–3.31) (07). By comparison, the average relative risk, compared with nonusers, is 4.1. With the use of low-dose oral contraceptives, the risk for stroke is lower and, in some studies, not significantly different from that of nonusers (131). Oral contraceptive use is a strong risk factor for cerebral venous thrombosis (19). An increased risk for stroke among patients who use triptans has not been found thus far, although triptans should be used in setting of an appropriate cardiovascular risk evaluation (60).

The decision to prescribe oral contraceptives to a patient with migraine should be individualized, and the risk/benefit ratio considered. Most young females with migraine without aura can take low-dose (35 µg or less of ethinyl estradiol daily) combined oral contraceptives safely unless they have other vascular risk factors. Patients should be strongly advised to refrain from or stop smoking. Any modifiable risk factor (eg, hypertension) should be controlled. For females with migraine with aura, the decision should be made on a case-to-case basis and should consider the woman’s age and other risk factors.

It is also important to note current guidelines note that progestin-only pills can be safely offered to females with migraine with aura. However, progestin-only pills must be taken consistently and exactly on time to ensure contraceptive efficacy and are often difficult for patient compliance and, therefore, may increase risk of unintended pregnancy. Additionally, a progestin-only arm implant is considered safe to use in women with migraine with aura. Females with a family history of thromboembolic events should undergo screening for prothrombotic states and, if confirmed, should not use oral contraceptives.

A new-onset aura or a dramatic change in an established aura requires discontinuing estrogen-containing oral contraceptives (12). Females with additional risk factors should be offered nonestrogen methods of contraception.

Interestingly, estrogen is likely to play a role in the pathogenesis of migraines and breast cancer, and studies have shown an association between them. However, a 2022 metaanalysis revealed that there was statistically significant inverse relationship between migraine and breast cancer in case-control studies 0.68 (95% CI: 0.56, 0.82), but no significant relationship was found in cohort studies 0.98 (95% CI: 0.91, 1.06) (64).

Migraine in pregnancy. Pregnancy can change the pattern of established migraine. Migraine improves during pregnancy in 50% to 90% of cisgender women, mostly in the second and third trimesters (84; Silberstein 1997a; 116; 18). The course of migraine during pregnancy was assessed in a prospective Italian study of 49 pregnant patients with migraine (116). Of the 47 people who had migraine without aura, migraine improved in 46.8%, 83%, and 87.2% in the first, second, and third trimester, respectively. Improvement during pregnancy was more likely when the migraine was menstrually related (94). Migraine attacks may even cease during pregnancy, especially in the second and third trimesters. The improvement in migraine that most people experience during pregnancy has been attributed to the rising or sustained high levels of estrogen that occur at that time. Only 4% to 8% of people experienced migraine worsening during pregnancy. Increased migraine burden during pregnancy is more common in people with migraine with aura. Breast-feeding seems to exert a prophylactic effect in the postpartum period (144), whereas bottle-feeding is associated with an accelerated return of migraines (116). It has been posited that oxytocin may play a role in the protective effect of breast-feeding against migraine attacks.

Migraine alone does not increase the risk of birth defects or pregnancy and labor complications (143; 10). Patients with migraine do not differ from the general population in the prevalence of miscarriages, toxemia, congenital anomalies, or stillbirths (125). However, in an Italian case-control study, pregnant people who had preeclampsia were more likely to report a history of migraine without aura than controls with uneventful pregnancies (44). Cisgender women who have migraine may also bear infants of lower birth weight.

Several studies have shown that approximately 70% of people who experience migraine have improvement in migraine symptoms during the second and third trimester of pregnancy, but 20% have no change in headache pattern, and 10% have their first attack of migraine during pregnancy (79; 84). Improvement is more common in cisgender women with menstrual migraine than in women with non-menstrually-related migraine. Cisgender women whose migraine began at menarche have a higher remission rate than women whose headaches began at other times.

Migraine improves during pregnancy in 50% to 90% of cisgender women, mostly in the second and third trimesters, but remains unchanged in 5% to 30% of cases (84; Silberstein 1997a; 116).

Migraine that develops for the first time during pregnancy usually appears during the first trimester. Approximately 10% of patients with migraine report that symptoms began during pregnancy (10). Migraine with aura is more common than migraine without aura when onset occurs during pregnancy. As noted above, approximately 70% of women with migraine improve during pregnancy, usually during the second and third trimesters.

Forty percent of women will have migraine attacks during the week following childbirth (134). As mentioned above, breastfeeding may have a protective effect towards migraine recurrence.

Migraine in menopause. Clinical observations and epidemiologic studies suggest that migraine generally worsens during the perimenopausal transition, presumed to correlate with fluctuation of sex hormones, and improves postmenopause, presumed to correlate with stabilization of sex hormone levels (49; 103). In an observational study of 100 postmenopausal women, headache (38%) was the most frequent pain complaint (95). This is probably due to erratic estrogen secretion at these times (49). The prevalence of new onset migraine during menopause may vary between 8% and 13% (54; 72). Some evidence suggests that women with premenstrual syndrome and migraine without aura might be more prone to headache exacerbation in the perimenopausal period (146).

Neri and colleagues, in a sample of 556 postmenopausal people, found a 13.7% prevalence of primary headaches (101). Migraine improved in almost two thirds of postmenopausal patients with migraine, but tension-type headache worsened or did not change in 70%. None of the study patients reported migraine with aura or cluster headache. Two thirds of patients with migraine who underwent surgical menopause reported a worsening of their headache. Ten percent of cisgender women may continue to experience migraine in the seventh and eighth decades of life (101).

After menopause, most cisgender women have improvement in their migraine. Women who have a physiologic menopause experience a more favorable course of migraine than those who have surgical menopause (79). In a study of 112 women taking hormone replacement therapy, 50 cisgender women reported improvement, 52 felt that their migraine worsened, and 10 noted no change. If hormone replacement is used, there is debate as to whether oral versus transdermal replacement is favored. The use of oral hormonal replacement therapy may exacerbate migraine (98), likely due to unpredictable absorption and plasma levels, but there is evidence to the contrary as well (57). However, in a multivariate analysis of 18,221 postmenopausal women treated with hormone therapy, an intermediate dose of estrogen of 0.625 mg/d was associated with reduced headache frequency compared with higher or lower doses (96). In contrast to oral therapy, transdermal hormonal replacement therapy does not seem to exacerbate migraine and can even have preventive effects (88; 89), again possibly due to more stable absorption and less fluctuation in hormonal plasma levels. When the types of hormone replacement therapy were analyzed, significantly more improved using transdermal estrogen than oral estrogen (78).

Clinical vignette

Vignette 1. A 30-year-old woman presented to the clinic complaining of headache attacks associated with her menses. The attacks consisted of unilateral, severe, throbbing headache associated with photophobia, phonophobia, and nausea. The headaches would start about 2 days prior to the onset of the menstrual flow, occur daily for 5 days and then disappear. The attacks were rather disabling. In mid-cycle, around the expected ovulation day, she would also develop an attack of lesser severity, typically lasting for 1 day and resolving. The duration of the cycles was quite steady. She had a past history of similar attacks, which for several years were not so tightly associated with menses, although the attacks were more frequent perimenstrually.

She was given treatment with frovatriptan, a long-acting triptan, at 2.5 mg daily, starting with the onset of the first headache and continuing daily for 5 days. This resulted in excellent and consistent control of the migraine attacks. She later became pregnant. During the first trimester, she experienced erratic migraine attacks, but early in the second trimester, the attacks disappeared completely for the duration of the pregnancy.

Vignette 2. A 33-year-old woman came to the clinic complaining of a headache that began at work. She was sitting at her desk and noticed zig-zag lines in her left visual field. This lasted for 30 minutes and was followed by a severe, throbbing headache in her right temporal area. The headache was associated with nausea and vomiting. She had no past history of headaches. She missed her last menstrual period but did not believe she was pregnant. Her neurologic examination was normal.

A urine beta-HCG test was positive. An MRI of the head without gadolinium was normal. A diagnosis of migraine with aura was made. She was educated on the benign nature of her disease and told that her migraine would probably improve during the later stages of pregnancy. A nonpharmacologic treatment plan (including advice on avoiding triggers, getting regular sleep, maintaining a regular meal schedule, and doing relaxation exercises) was initiated. With this treatment plan, she continued to have infrequent, mild to moderate migraine attacks (one to two per month) that responded to oral ibuprofen. She became headache-free during the last trimester of her pregnancy. She delivered a healthy baby at 38 weeks of gestation. Four weeks after delivery, she had a typical migraine with aura attack that responded again to nonsteroidal anti-inflammatory drugs (NSAIDs). Over the following months, despite optimal nonpharmacologic treatment, her attack frequency increased to four headaches per month. A typical attack lasted 12 to 24 hours, and she had significant disability during the attack. She was, therefore, put on amitriptyline 25 mg/day as a preventive medication. When the dose was increased to 50 mg/day, she had a good response, with decreased migraine attack severity and frequency. Acute attacks were managed with almotriptan 12.5 mg with good results.

Biological basis

Etiology and pathogenesis

Neuroimaging. Brain MRI studies support both structural and functional sex differences in patients with migraine. Maleki and colleagues used high-field MRI to compare male and female patients with migraine to healthy controls (86). Women with migraine were found to have thicker posterior insula and precuneus cortices as compared to male patients and healthy controls. Using functional MRI, noxious thermal stimuli produced stronger responses in the amygdala and parahippocampus in female as compared with male participants with migraine. This study was of particular interest because the anatomical differences found in the females who experience migraine are attributable neither to the female sex nor the migraine disease state alone. One can, thus, hypothesize that a combination of being female and having migraine may lead to changes in brain anatomy and sensory responsiveness and result in differences in migraine characteristics (31).

Neurophysiology. Cortical spreading depression has been implicated in the pathogenesis of migrainous aura. Effects of sex hormones on cortical spreading depression might be another explanation of the variability of headache syndrome during a woman’s lifetime. Both estrogens and, more surprisingly, progesterone increase cortical spreading depression susceptibility. Furthermore, L-kynurenine is more efficient in suppressing cortical spreading depression when progesterone levels are high. This might be relevant for the aggravation/appearance of migraine with aura during pregnancy or intake of a combined contraceptive pill (34).

In a pilot study of 11 cisgender women receiving combined hormonal contraceptives who were developing migraine attacks occurring exclusively during the estrogen-withdrawal period, the investigators evaluated the nociceptive reflex, a neurophysiological assessment of pain control systems, during the third week of active treatment and during the hormone-free interval (39). During the hormone-free interval, the nociceptive withdrawal reflex threshold was significantly lower than that of the third week of hormonal treatment. These results indicate that estrogen withdrawal may mediate increased sensitivity to somatosensory stimuli in women with migraine attacks occurring during the hormone-free interval.

Cell biology. A role for intracranial mast cell activation in migraine pathophysiology has been proposed (136). Fluctuations in dural mast cell density during the estrous cycle were demonstrated. This effect was abolished by splenectomy, which suggests estrogen-related recruitment of mast cells from the spleen. This might, at least in part, explain the higher frequency of migraine in women as well as the fluctuations in headache during the menstrual cycle (16).

In one study, nitroglycerin, a well-known nitric oxide donor that provokes spontaneous-like migraine attacks, administration in male and female rats induced a significant Fos expression in the paraventricular and supraoptic nucleus of the hypothalamus, central nucleus of the amygdala, nucleus of tractus solitaries, area postrema and nucleus trigeminalis caudalis. Sex, however, influenced the Fos expression, with higher expression in the specific nuclei in the female rats. Ovariectomy significantly reduced nitroglycerin-induced Fos immunoreactivity in all the nuclei that were activated in the intact females, suggesting that at least partially the vascular effect of estrogens may be mediated through nitric oxide and that these effects are associated with an increased production of nitric oxide (56). An alternative mechanism of action of estrogens could be linked with calcitonin-gene related peptide (CGRP), a vasodilator agent that plays a role in determining migraine attacks.

Neurochemistry and endocrinology. The high estrogen levels sustained during pregnancy are thought to protective against migraine attacks. It has also been suggested that the improvement might be related to changes in serotonin metabolism during pregnancy and increased endorphin concentrations during the last two trimesters (124). The rapidly falling concentrations of estrogen that follow childbirth are thought to be responsible for postpartum headaches.

Serotonergic pathways are certainly involved. A PET study showed that migraine patients had lower brain serotonin levels between attacks compared with controls and that those levels increased to the normal range during an attack (115). The study suggested that migraine may be associated with a low-serotonin state between attacks. Furthermore, there is evidence that serotonin synthesis is influenced by ovarian hormones (13). Data from primate experiments support the notion that the serotonergic tone is enhanced by estrogen (88; 89).

In general, ovarian steroid hormones regulate nociceptive pathways at multiple levels. The trigeminal vascular system is significantly modulated by estrogens and is probably the major determinant of sexual dimorphism observed in migraine (59). This relationship is well exemplified by the interaction between CGRP-ergic and serotoninergic pathways with estrogens (59).

In a case-control study of patients with menstrually-related migraine, the investigators confirmed that the premenstrual withdrawal of estradiol influences the function of the trigeminovascular system (66). In the same study, the investigators also found that there is disturbed systemic as well as trigeminovascular vasodilator system cyclicity in patients with menstrually related migraine, which may augment their susceptibility to migraine around the time of menstruation.

Prostaglandins intensify nociception. This might provide a partial explanation for the commonly held view that menstrual migraine is generally more severe and less responsive to treatment compared with migraine not related to the menstrual cycle. However, there is little support for prostaglandins as primary mediators in migraine. Nattero and colleagues found that controls and migraine sufferers had similar prostaglandin levels during the cycle. However, migraine patients had significantly higher levels during a migraine attack than on any other day of their menstrual cycle (100). These results do not lend support to the idea that elevated prostaglandin levels per se trigger menstrual migraine. Because dysmenorrhea is clearly related to elevated prostaglandin levels (which intensify uterine contractions), one would expect that migraine and dysmenorrhea would correlate if prostaglandin levels played a primary role in menstrual migraine pathophysiology.

In a study in rats, deficiency of female sex hormones was found to influence prostaglandin E2 (PGE2) and CGRP levels in the midbrain periaqueductal gray. More specifically, the authors found that circulating 17β-estradiol and/or progesterone influence the levels of PGE2 and CGRP in the periaqueductal gray, a lower level of 17β-estradiol and/or progesterone augments PGE2 and its EP3 receptor, and that PGE2 plays a role in regulating expression of CGRP in the periaqueductal gray (145).

Mechanisms relating to dopamine and opioids have also been proposed for menstrual migraine, including reduction in serum dopamine beta-hydroxylase concentrations (85), dysfunction of opioid control of the hypothalamic-pituitary-adrenal axis (46), reduced levels of magnesium (48), and platelet dysfunction.

Estradiol and progesterone seem to have opposite effects on neuronal excitability, with estradiol being excitatory and progesterone inhibitory. Estradiol augments N-methyl-D-aspartate-mediated glutamate receptor activity, whereas progesterone enhances gamma-aminobutyric acid-mediated chloride conductance. Sex steroid regulation of the balance of neuroexcitatory and neuroinhibitory activities may also have a role in modulating clinical susceptibility to migraine (50).

Other hormonal systems also have been implicated in the pathophysiology of migraine. Insulin resistance has been found in migraine patients compared with control subjects (28), raising the question of whether diabetes could be linked to migraine. Bosco and colleagues detected an increase in plasma prolactin levels during migraine attacks in migraine and tension-type headache patients with microprolactinoma--although the sample was small and did not include control subjects (17). Chronic migraine and chronic tension-type headache could be associated with abnormal sleep melatonin secretion (24). Whether this is the cause or the effect of chronic headache remains to be clarified. The orexin system has also been linked to migraine and medication overuse headache. In a study by Sarchielli and colleagues, CSF levels of corticotrophin releasing factor (CRF) and orexin-A were elevated in patients with chronic migraine and medication overuse headache (118).

Differential diagnosis

Headaches that are exclusively linked to the menstrual cycle are almost always benign, and diagnostic studies are rarely indicated.

Headaches that begin during pregnancy can raise concerns about serious underlying illness, such as eclampsia or preeclampsia, idiopathic intracranial hypertension, subarachnoid hemorrhage from aneurysm or arteriovenous malformation, cortical vein thrombosis, pituitary tumor, and choriocarcinoma (125). Pregnancy can also unmask an intracranial neoplasm. The diagnosis of a serious disorder can easily be missed, as the symptoms of headache, vomiting, and visual disturbance can be encountered in pregnant women with or without preeclampsia (33). The history of the headache onset and a careful neurologic examination, including blood pressure measurement, ophthalmoscopy, and a thorough check for signs of meningeal irritation, are usually sufficient to rule out these problems. Migraine usually can be diagnosed on clinical grounds alone, but uncertainty may result when the patient is seen during the initial attack, particularly if the migraine is associated with aura. In such cases, neuroimaging should be considered.

Headache in the postpartum period is common and usually caused by migraine (134; 116). Sances and colleagues found that migraine recurred during the first week after delivery in 34% of women and after the first month in 55% (116). Other causes of headache, such as venous sinus thrombosis, should be considered if the headache is not typically migrainous in nature, even if it is not accompanied by fever, convulsions, altered consciousness, hemiplegia, or papilledema (11). Postpartum headache may also result from low intracranial pressure due to a CSF leak caused by an inadvertent dural puncture during epidural anesthesia (106).

In rare instances, hormone replacement therapy triggers benign intracranial hypertension (123). Transient visual obscurations and tinnitus commonly accompany benign intracranial hypertension. These features should prompt lumbar puncture (after CT) to exclude this important cause of headache.

Management

The treatment of acute migraine attacks caused by hormonal fluctuations is similar to that of migraine attacks unrelated to hormonal fluctuations. Patients with typical episodic migraine without aura are less likely to be referred to neurologists than are patients with unusual features, comorbid disorders (medical and psychiatric), severe clinical disability, or refractoriness to standard therapy. Menstrual migraine is said to be more difficult to treat than migraine not associated with the menses. Clinical evidence supports this notion. In a study of 64 cisgender women with migraine, perimenstrual attacks were found to be significantly longer, less responsive to acute treatment, and cause greater work-related disability compared with attacks not associated with the menses (53). In general, treatment options that can be considered include acute attack treatment, preemptive treatment or short-term prophylaxis, standard migraine prophylaxis, hormonal treatment, and others.

Treatment of acute attack. The drugs of choice for acute attacks include NSAIDs, acetaminophen, triptans, gepants, and dihydroergotamine. Second-line abortive agents include narcotics, corticosteroids, neuroleptics, and intravenous dihydroergotamine alone or in combination with other intravenous medications in a “migraine cocktail.” Antiemetics are important adjuncts for those who experience severe nausea or vomiting. In a randomized placebo controlled trial, a single dose of naratriptan 2.5 mg was superior to placebo in alleviating pain and associated symptoms of menstrually-related migraine attacks (91). Another placebo-controlled study of 93 people with menstrually-related migraine showed that sumatriptan 100 mg was effective in acute treatment of migraine for both perimenstrual attacks and nonmenstrually-related attacks (42). Rapoport and colleagues reported that migraine attacks occurring during the menstrual period responded better to zolmitriptan (a 2-hour response rate of 72%) than attacks that occur outside the menstrual period (a 2-hour response rate of 67%) (111). However, there were no comparisons of patients with migraine attacks confined to the menses versus patients with attacks unrelated to the menstrual cycle. However, Bhambri and associates reported that when comparing treatment of migraine attacks during menstrual and nonmenstrual time periods with eletriptan, there were higher recurrence rates and lower sustained response rates at 2 to 24 hours in the group treated during the menstrual time period (62; 14). In a pooled analysis of three double-blind, randomized, crossover, multicenter clinical trials, frovatriptan was found to be more suitable for the management of menstrual migraine occurring during the hormone withdrawal phase, producing pain free and pain relief state in 25% and 51% of patients respectively (nonsignificant difference against rizatriptan, almotriptan, or zolmitriptan), but produced more sustained relief, with 71% and 83% of patients being pain free or having pain relief at 24 hours (05).

Preemptive treatment or short-term prophylaxis. Several drugs have been used as short-term prophylaxis for menstrual migraine, including NSAIDs, ergotamine, dihydroergotamine, magnesium, and the triptans (21; 126). Three triptans have been shown to be effective in menstrual migraine prevention. These include sumatriptan 25 mg three times a day, beginning 2 to 3 days before the expected day of headache onset and continued for a total of 5 days; naratriptan 1 mg twice daily for 5 days, beginning 2 days before the expected onset of menses; and frovatriptan 2.5 mg once or twice daily, starting 2 days before the anticipated start of the headache and continuing for 6 days (125; 97). The combination of a triptan with an NSAID (such as sumatriptan and naproxen sodium) can be an effective way of managing menstrual migraine while also addressing other prominent menstrual symptoms (04; 87).

Menstrual migraine can also be treated by the premenstrual use of standard prophylactic medication (antidepressants, beta-blockers, valproate, or calcium channel blockers). The following medications may be used: amitriptyline, 25 mg to 50 mg at bedtime; nadolol, 40 mg to 160 mg every day; verapamil, 80 mg to 160 mg three times a day; or valproate, 250 mg three times a day. People who already use prophylactic medication for nonmenstrual migraine can increase the dose prior to their menses.

Hormonal treatment. Hormonal manipulation was once posited as a short-term prophylaxis for menstrual migraine. For the sake of completeness, we will include these studies although the general consensus is to avoid estrogen replacement during menses for the purpose of migraine treatment.

Percutaneous estradiol gel (1.5 mg in 2.5 gr gel), started 2 days before the menses and continued for 7 days, was associated with reduced frequency, severity, and duration of menstrual migraine (40). The transdermal formulation of estradiol (100 µg) is the most convenient. In their study, Pradalier and colleagues found that a perimenstrually applied 100 mcg estradiol patch was effective in preventing menstrual migraines, whereas a 50 mcg patch was not (107). It is, thus, reasonable to believe that estrogen levels need to be kept above a certain cutoff to prevent an attack. In a placebo-controlled study, MacGregor and colleagues examined the efficacy of estradiol gel (1.5 mg) in menstrual migraine prevention (81). Women treated six cycles in a cross-over design. Gel was applied daily from the 10th day after ovulation to the second day of menses. During the time of gel application, estradiol treatment was associated with a 22% reduction in migraine days compared with placebo. However, migraine increased in the estradiol group during the 5 days following cessation of gel application compared with the placebo group. Patch administration of estrogen was evaluated in two small studies and seems to be much less effective, although they may have been underpowered (107; 133). In a retrospective review of 229 patients with menstrually-related migraine, Calhoun and Ford found that hormonal manipulation reduced chronification of headache and analgesic use (27). NSAIDs (eg, naproxen sodium 250 mg three times daily or indomethacin 25 mg three times daily) may also be used perimenstrually for migraine prophylaxis. The drug is started 2 days before menses and continued for 5 days. Dihydroergotamine mesylate given intranasally to 40 women with menstrual-related migraine for 6 days, starting 2 days before the expected onset of the migraine attack, was shown to reduce the severity of headache (127). Frovatriptan 2.5 mg a day was more efficacious than transdermal estrogen and naproxen sodium for the management of menstrual migraine in a small, open-label, nonrandomized trial (58). Based on a systematic review of 19 prospective, double-blind, randomized trials, Pringsheim and colleagues concluded that grade B recommendations could be made for sumatriptan 50 and 100 mg daily, mefenamic acid 500 mg and rizatriptan 10 mg for the acute treatment of menstrual related migraine (108). For prevention, the same authors made grade B recommendations for transcutaneous estrogen 1.5 mg daily, frovatriptan 2.5 mg twice daily, and naratriptan 1 mg twice daily. The choice of agent should be based on patient profile, drug side effects, and physician experience.

Other. A short course of a neuroleptic or corticosteroids may be used. These include: prednisone, 80 mg/day for 7 days to 10 days with a rapid taper; dexamethasone, 20 mg/day for 4 days to 7 days with a rapid taper; or chlorpromazine 10-s 50 mg twice a day for 4 days to 7 days.

A placebo-controlled, double-blind study of 24 women with premenstrual syndrome and migraine has shown that oral magnesium (360 mg of magnesium pyrrolidone carboxylic acid) decreases the severity of the premenstrual symptoms and the duration and intensity of menstrual migraine occurring prior to the onset of menstruation (47; 48; 45).

Table 2. Current Acute Headache Treatments and Prescription Directions for Adults

Migraine abortive agents	Directions (adults)
Simple analgesics, aspirin, acetaminophen	One to two orally, three times daily as necessary; limit use to 3 days per week (exception: migraine confined to menstrual period).
Combination analgesics, butalbital-containing agents	One to two orally, three times daily as necessary; limit use to 2 days per week; avoid activities requiring full alertness and motor coordination.
Oral nonsteroidal anti-inflammatory agents Naproxen 375 mg Ibuprofen 400 mg	One to two orally at onset of migraine; may repeat in 1 hour; limit to four per day; limit use to 3 days per week; take with food.
Injectable ketorolac	30 to 60 mg intramuscularly; may repeat in 1 hour; limit daily dose to 120 mg; limit use to 5 days per month.
Indomethacin	Oral: 25 to 75 mg at onset of attack (with food). May repeat in 2 hours. Suppositories (50 mg): one rectally at onset of migraine; may repeat in 1 hour; limit three per day; limit use to 4 days per week.
Dihydroergotamine	1 mg intramuscularly at onset of migraine; may repeat at 1-hour intervals to a total dose of 3 mg. Total weekly dosage should not exceed 6 mg. (Exception: repetitive dihydroergotamine for severe rebound headache or status migrainosus). DHE nasal spray (0.5 mg/spray): one spray in each nostril; may repeat q 15 minutes up to a total dose of 2 mg/attack. Do not exceed 4 mg/week.
Frovatriptan	2.5 mg orally. May repeat in 2 hours as needed. Maximum of 7.5 mg per day.
Rizatriptan benzoate (5 mg and 10 mg)	5 mg, one orally for migraine attack; may repeat in 2 hours; limit 30 mg per day. Limit use to 2 days per week; 10 mg, one orally for migraine attack. May repeat in 2 hours; limit 30 mg per day. Limit use to 2 days per week.
Sumatriptan succinate oral (25, 50 and 100 mg)	25 mg to 100 mg at onset of migraine. If headache recurs, an additional dose may be taken in 2 hours. Limit use to 2 days per week.
Sumatriptan succinate injectable (6 mg)	6 mg subcutaneously at onset of migraine; can repeat after 2 hours; limit use to 12 mg per 24 hours; limit use to 2 days per week.
Zolmitriptan (2.5 mg and 5.0 mg)	2.5 mg, one orally at onset of headache; may repeat in 2 hours; limit use to 10 mg (4) per day; 5 mg one orally at onset of headache; may repeat in 2 hours; limit dose to 10 mg per day. Limit use to 2 days per week.
Zolmitriptan nasal spray (5 mg)	One spray intranasally at headache onset, may repeat in 2 hours. Limit dose to 10 mg per day. Limit use to 2 days per week.
Naratriptan hydrochloride (2.5 mg)	One orally at onset of headache; may repeat in 4 hours if headache recurs; limit to 5 mg per day. Limit use to 2 days per week.
Almotriptan	Oral 12.5 mg at attack onset, may repeat after 2 hours; maximum dose 25 mg per day. Limit use to 2 days per week.
Eletriptan	Oral 40 mg at attack onset, may repeat after 2 hours. Maximum dose is 80 mg per day. Limit use to 2 days per week.

Treatment of migraine during pregnancy. Treatment for young, healthy women with menstrual migraine includes NSAIDs administered 2 days to 3 days before menses and continuing through menstruation.

Popular, but ineffective, therapies include diuretics and vitamins.

There is no place for hysterectomy in the management of menstrual migraine (79).

Because migraine usually improves after the first trimester of pregnancy, many patients can manage their headaches with reassurance and nonpharmacologic means of coping, such as ice, massage, and biofeedback. Riboflavin is safe at physiological doses, but safety has not been proven at the high doses used for migraine prevention. Despite the fact that 67% of cisgender women take medications during pregnancy and 50% take them during the first trimester, insufficient knowledge exists about the risks of birth defects from drug exposure. Acetaminophen (alone or with codeine), codeine, or other narcotics can be used during pregnancy. Narcotics should be avoided in the late third trimester because of possible neonatal withdrawal symptoms. Indiscriminate codeine use may present a risk to the fetus during the first or second trimester. Cleft lip, cleft palate, inguinal hernia, hip dislocation, and cardiac and respiratory system defects have been reported (125). However, migraine per se does not constitute a risk factor for congenital malformations (23).

NSAIDs should be avoided in the late third trimester because they can lead to premature closure of the ductus arteriosus. Aspirin can also increase intrapartum blood loss and impair neonatal hemostasis. NSAIDs in the third trimester also increase the risk of preeclampsia, prolonged labor, and neonatal pulmonary hypertension (10).

The effect of sumatriptan on pregnancy outcome has been evaluated (76). In a review of pregnancy registries, Reiff-Eldridge and colleagues found a 3.8% rate of birth defects in cisgender women who were exposed to sumatriptan during the first trimester. This is comparable to the risk in the general population (3% to 5%). No defect pattern was observed (113). Olesen and colleagues identified 34 patients who were exposed to sumatriptan during pregnancy and compared their pregnancy outcomes with general population controls and migraine controls (102). The risk of preterm delivery was elevated among those exposed to sumatriptan during pregnancy compared with both migraine controls (OR, 6.3; CI, 1.2-32.0) and general population controls (OR, 3.3; CI,1.3-8.5). The risk of having a low birthweight newborn was elevated for all patients with migraine compared with healthy controls (OR, 3.0; CI, 1.3-7.0). Kallen and colleagues identified 912 infants who had been exposed to antimigraine drugs prenatally, mostly sumatriptan (68). There was an insignificant increase in the rate of preterm deliveries and low birthweight infants. No increase in the rate of congenital malformations was seen. Current data show no evidence for teratogenicity from sumatriptan use in pregnancy; however, the drug should be used with caution, weighing potential risks against benefit.

Pharmacologic migraine prophylaxis is rarely indicated in pregnancy and should be used only as a last resort and after the risks have been explained to the patient. Beta-blockers have been used in these circumstances. Propranolol has been used safely during pregnancy to treat hypertension, and there is no evidence that it is teratogenic (20). Metoprolol is also considered relatively acceptable during pregnancy (105).

Valproate may cause neural tube defects and is contraindicated during pregnancy. Amitriptyline must be stopped at least 2 weeks before the due date because respiratory distress and feeding difficulties have been described in infants born of women taking tricyclics up to the time of birth. None of the preventive agents are classified as category A (controlled studies show no risk).

CGRP antagonists, erenumab, galcanezumab, fremenumab, eptinezumab, as well as “gepants,” such as ubrogepant, atogepant, and rimegepant should be avoided in pregnancy as there are no long-term safety data. However, if a patient chooses to continue on these medications, their outcomes may be reported and prospectively followed. Wash out period of at least five half-lives should be completed during pregnancy planning in order to clear the antibodies prior to conception as they have long, multi-month half-lives.

Although there are limited high powered safety studies on pregnant patients receiving onabotulinumtoxinA, it is generally considered safe in pregnancy by experts. In a study of 32 patients who remained on treatment with onabotulinumtoxinA through pregnancy, many showed a good response, whereas 11 out of 13 who withdrew from treatment experienced a relapse (147). In a retrospective review of nine subjects who received onabotulinumtoxinA injections for migraine during pregnancy, none of the 10 pregnancies reported any organ malformations at delivery (135).

Nerve blocks with lidocaine, targeting branches of the trigeminal and occipital nerves in the face and scalp, performed as often as every 2 weeks or as a cycle breaker for status migrainosus is considered safe during pregnancy, although the procedure itself may be uncomfortable.

Although the medical risks of pregnancy have declined significantly over the past 50 years, the medicolegal risk of caring for the pregnant patient has increased dramatically. Many experts fear that any malformation (which occurs spontaneously in 2% to 3% of births) will be blamed on medication (105). The current medicolegal environment makes it difficult to recommend any preventive therapy as safe for all headache patients. Full disclosure of potential risks and documentation of informed consent is advisable. For those patients who require specific antimigraine acute or preventive therapy, consultation with a medical geneticist or perinatologist can be helpful.

When migraine is first diagnosed or worsens during pregnancy, a secondary cause of headache (eg, subarachnoid hemorrhage, cerebral sinus venous thrombosis, benign intracranial hypertension) must be carefully excluded.

Migraine treatment and menopause. For the perimenopausal woman with migraine, the same preventive and abortive options used for the general migraine patient population should be the first step in treatment. However, for those who need hormone replacement, care should be taken to avoid associated risks of estrogen replacement. Continuous combined estrogen and progesterone (or estrogen alone, if the uterus has been removed) replacement is the preferred therapy. This can be achieved with a 50 µg/day estrogen skin patch or an oral estrogen, with half the daily dose given every 12 hours to maintain optimal stability. When the uterus is present, progesterone should be added, either as low-dose medroxyprogesterone acetate 2.5 mg every evening or micronized progesterone 100 mg every evening (49).

In cisgender women who develop headaches as a result of hormone replacement therapy, reducing the dose of estrogen or changing the estrogen type may reduce headache (128). When headaches are associated with estrogen withdrawal, changing from interrupted to continuous administration may be effective. Changing the route of administration may also reduce headache occurrence. Raloxifene, a selective estrogen receptor modulator, can be used if a woman requires, but cannot tolerate, estrogen. Another approach is to use targeted drug delivery, such as a progesterone-containing vaginal gel. This maximizes progesterone’s effect on the uterus while minimizing its potential adverse effects, including headaches.

Estrogen and selective estrogen receptor modulators increase the risk of venous thromboembolism 3-fold. The risk for breast cancer increases after 5 years of hormone replacement therapy. The excess risk of estrogen use is 2/1000 users over 20 years in women aged 50 years to 70 years if hormone replacement therapy has been used for 5 years.

The Women’s Health Initiative trial included 27,500 postmenopausal cisgender women. The active treatment in this trial was conjugated estrogen for women without a uterus and estrogen with medroxyprogesterone acetate for women with an intact uterus. The study was terminated early because of increased risk of breast cancer, and evidence for greater overall risk than benefit in the active treatment group. More surprisingly, the risk of myocardial infarction (and of stroke) was higher in the hormone replacement therapy group; however, the absolute risk was small. There was no difference in mortality between the active treatment and the control groups (114; 06). Migraine has not been shown to be a risk factor for stroke in postmenopausal women (71). Therefore, in considering symptomatic hormone replacement therapy for postmenopausal patients with migraine, the usual indications and contraindications should be applied.

References

01: Aegidius KL, Zwart JA, Hagen K, Dyb G, Holmen TL, Stovner LJ. Increased headache prevalence in female adolescents and adult women with early menarche: the Head-HUNT studies. Europ J Neurol 2011;18:321-8. PMID 20636369
02: Ahmad SR, Rosendale N. Sex and gender considerations in episodic migraine. Curr Pain Headache Rep 2022;26(7):505-16. PMID 35679008
03: Allais G, Chiarle G, Sinigaglia S, Airola G, Schiapparelli P, Benedetto C. Gender-related differences in migraine. Neurol Sci 2020;41(Suppl 2):429-36. PMID 32845494
04: Allais G, Rolando S, Schiapparelli P, et al. Frovatriptan plus dexketoprofen in the treatment of menstrually related migraine: an open study. Neurol Sci 2013a;34(Suppl 1):S179-81. PMID 23695075
05: Allais G, Tullo V, Omboni S, et al. Frovatriptan vs. other triptans for the acute treatment of oral contraceptive-induced menstrual migraine: pooled analysis of three double-blind, randomized, crossover, multicenter studies. Neurol Sci 2013b;34 Suppl 1:S83-6. PMID 23695052
06: Anderson GL, Limacher M, Assaf AR, et al. Effects of conjugated equine estrogen in postmenopausal women with hysterectomy: the Women's Health Initiative randomized controlled trial. JAMA 2004;291(14):1701-12. PMID 15082697
07: Anonymous. Ischaemic stroke and combined oral contraceptives: results of an international, multicentre, case-control study. WHO Collaborative Study of Cardiovascular Disease and Steroid Hormone Contraception. Lancet 1996;348(9026):498-505. PMID 8757151
08: Anonymous. ACOG Practice Bulletin No. 110: noncontraceptive uses of hormonal contraceptives. Obstet Gynecol 2010;115(1):206-18. PMID 20027071
09: Ashkenazi A, Silberstein SD. Hormone related headache–pathophysiology and treatment. CNS Drugs 2006;20(2):125-41. PMID 16478288
10: Aube M. Migraine in pregnancy. Neurology 1999;53(Suppl 1):S26-8. PMID 10487510
11: Bansal BC, Gupta RR, Prakash C. Stroke during pregnancy and puerperium in young females below the age of 40 years as a result of cerebral venous/venous sinus thrombosis. Jpn Heart J 1980;21(2):171-83. PMID 7373858
12: Becker WJ. Use of oral contraceptives in patients with migraine. Neurology 1999;53(4 Suppl 1):S19-25. PMID 10487509
13: Bethea CL, Lu NZ, Gundlah C, Streicher JM. Diverse actions of ovarian steroids in the serotonin neural system. Front Neuroendocrinol 2002;23:41-100. PMID 11906203
14: Bhambri R, Martin VT, Abdulsattar Y, et al. Comparing the efficacy of eletriptan for migraine in women during menstrual and non-menstrual time periods: a pooled analysis of randomized controlled trials. Headache 2014;54(2):343-54. PMID 24256184
15: Bharadwaj VN, Porreca F, Cowan RP, Kori S, Silberstein SD, Yeomans DC. A new hypothesis linking oxytocin to menstrual migraine. Headache 2021;61(7):1051-9. PMID 34125955
16: Boes T, Levy D. Influence of sex, estrous cycle and estrogen on intracranial dural mast cells. Cephalalgia 2012;32(12)924-31. PMID 22833613
17: Bosco D, Belfiore A, Fava A, et al. Relationship between high prolactine levels and migraine attacks in patients with microprolactinoma. J Headache Pain 2008;9(2):103-7. PMID 18256782
18: Bousser MG. Estrogens, migraine, and stroke. Stroke 2004;35:2652-6. PMID 15459439
19: Bousser MG, Kittner SJ. Oral contraceptives and stroke. Cephalalgia 2000;20:183-9. PMID 10997765
20: Bousser MG, Massiou H. Migraine in the reproductive cycle. In: Olesen J, Tfelt-Hansen P, Welch KM, editors. The headaches. New York: Raven, 1993:413-9.
21: Boyle CA. Management of menstrual migraine. Neurology 1999;53(4 Suppl 1):S14-8. PMID 10487508
22: Brache V, Faundes A, Alvarez F, Cochon L. Nonmenstrual adverse events during use of implantable contraceptives for women: data from clinical trials. Contraception 2002;65(1):63-74. PMID 11861056
23: Brandes JL. The influence of estrogen on migraine: a systematic review. JAMA 2006;295(15)1824-30. PMID 16622144
24: Bruera O, Sances G, Leston J, et al. Plasma melatonin pattern in chronic and episodic headaches: evaluation during sleep and waking. Funct Neurol 2008;23(2):77-81. PMID 18671907
25: Burch R, Rizzoli P, Loder E. The prevalence and impact of migraine and severe headache in the United States: figures and trends from government health studies. Headache 2018;58(4):496-505. PMID 29527677
26: Cairns BE, Gazerani P. Sex-related differences in pain. Maturitas 2009;63(4):292-6. PMID 19595525
27: Calhoun A, Ford S. Elimination of menstrual-related migraine beneficially impacts chronification and medication overuse. Headache 2008;48(8):1186-93. PMID 18819179
28: Cavestro C, Rosatello A, Micca G, et al. Insulin metabolism is altered in migraineurs: a new pathogenic mechanism for migraine. Headache 2007;47(10):1436-42. PMID 18052953
29: Cetinkaya A, Kilinc E, Camsari C, Ogun MN. Effects of estrogen and progesterone on the neurogenic inflammatory neuropeptides: implications for gender differences in migraine. Exp Brain Res 2020;238(11):2625-39. PMID 32924075
30: Cesar JM, Garcia-Avello A, Vecino AM, et al. Increased levels of plasma von Willebrand factor in migraine crisis. Acta Neurol Scand 1995;91:412-3. PMID 7639074
31: Chai NC, Peterlin BL, Calhoun AH. Migraine and estrogen. Curr Opin Neurol 2014;27(3):315-24. PMID 24792340
32: Chang CL, Donaghy M, Poulter N. Migraine and stroke in young women: case-control study. The World Health Organization Collaborative Study of Cardiovascular Disease and Steroid Hormone Contraception. BMJ 1999;318:13-8. PMID 9872876
33: Chaudhuri P, Wallenburg HC. Brain tumors and pregnancy. Presentation of a case and a review of the literature. Eur J Obstet Gynecol Reprod Biol 1980;11(2):109-14. PMID 7192655
34: Chauvel V, Multon S, Schoenen J. Influence of ovarian hormones on occurrence of cortical spreading depression and its suppression of by L-kynurenine in rat. J Headache Pain 2013;1(Suppl 1):P84.
35: Coney P, Washenik K, Langley RG, DiGiovanna JJ, Harrison DD. Weight change and adverse event incidence with a low-dose oral contraceptive: two randomized, placebo-controlled trials. Contraception 2001;63(6):297-302. PMID 11672550
36: Couturier EG, Bomhof MA, Neven AK, van Duijn NP. Menstrual migraine in a representative Dutch population sample: prevalence, disability, and treatment. Cephalalgia 2003;23(4):302-8. PMID 12716349
37: Curtis KM, Tepper NK, Jatlaoui TC, et al. U.S. medical eligibility criteria for contraceptive use, 2016. MMWR Recomm Rep 2016;65(3):1-103. PMID 27467196
38: Daniels K, Abma JC. Current contraceptive status among women aged 15–49: United States, 2015–2017. NCHS Data Brief, no 327. Hyattsville, MD: National Center for Health Statistics. 2018.
39: De Icco R, Cucinella L, De Paoli I, et al. Modulation of nociceptive threshold by combined hormonal contraceptives in women with estrogen-withdrawal migraine attacks: a pilot study. J Headache Pain 2016;17(1):70. PMID 27488685
40: De Lignieres B, Vincens M, Mauvais-Jarvis P, Mas JL, Touboul PJ, Bousser MG. Prevention of menstrual migraine by percutaneous oestradiol. Br Med J 1986;293:1540. PMID 3099950
41: Donaghy M, Chang CL, Poulter N, et al. Duration, frequency, recency, and type of migraine and the risk of ischaemic stroke in women of childbearing age. J Neurol Neurosurg Psychiatr 2002;73(6):747-50. PMID 12438482
42: Dowson AJ, Massiou H, Aurora SK. Managing migraine headaches experienced by patients who self-report with menstrually related migraine: a prospective, placebo-controlled study with oral sumatriptan. J Headache Pain 2005;6(2):81-7. PMID 16362647
43: Eikermann-Haerter K, Baum MJ, Ferrari MD, van den Maagdenberg AM, Moskowitz MA, Ayata C. Androgenic suppression of spreading depression in familial hemiplegic migraine type 1 mutant mice. Ann Neurol 2009;66(4):564-8. PMID 19847904
44: Facchinetti F, Allais G, D’Amico R, Benedetto C, Volpe A. The relationship between headache and preeclampsia: a case-control study. Eur J Obstet Gynecol Reprod Biol 2005;121(2):143-8. PMID 16054953
45: Facchinetti F, Borella P, Sances G, Fioroni L, Nappi RE, Genazzani AR. Oral magnesium successfully relieves premenstrual mood changes. Obstet Gynecol 1991c;78:177-81. PMID 2067759
46: Facchinetti F, Martignoni E, Fioroni L, Sances G, Genazzani AR. Opioid control of the hypothalamus- pituitary adrenal axis cyclically fails in menstrual migraine. Cephalalgia 1990;10:51-6. PMID 2317851
47: Facchinetti F, Montorsi S, Borella P, et al. Magnesium prevention of premenstrual migraine: a placebo controlled study, In: Clifford Rose F, editor. New advances in headache research: 2. London: Smith-Gordon, 1991a:329-32.
48: Facchinetti F, Sances G, Borella P, et al. Magnesium prophylaxis of menstrual migraine: effects on intracellular magnesium. Headache 1991b;31:298-301. PMID 1860787
49: Fettes I. Migraine in the menopause. Neurology 1999;53(4 Suppl 1):S29-33. PMID 10487511
50: Finocchi C, Ferrari M. Female reproductive steroids and neuronal excitability. Neurol Sci 2011;32(suppl 1):S31-5. PMID 21533709
51: Fitzgerald MC, Saelzler UG, Panizzon MS. Sex differences in migraine: a twin study. Front Pain Res 2021;2:766718. PMID 35295437
52: Gervil M, Ulrich V, Kaprio J, Olesen J, Russell MB. The relative role of genetic and environmental factors in migraine without aura. Neurology 1999;53(5):995-9. PMID 10496258
53: Granella F, Sances G, Allais G, et al. Characteristics of menstrual and nonmenstrual attacks in women with menstrually related migraine referred to headache centres. Cephalalgia 2004;24:707-16. PMID 15315526
54: Granella F, Sances G, Zanferrari C, Costa A, Martignoni E, Manzoni GC. Migraine without aura and reproductive life events: a clinical epidemiological study in 1300 women. Headache 1993;33(7):385-9. PMID 8376100
55: Glaser R, Dimitrakakis C, Trimble N, Martin V. Testosterone pellet implants and migraine headaches: a pilot study. Maturitas 2012;71(4):385-8. PMID 22310106
56: Greco R, Tassorelli C, Mangione AS, et al. Effect of sex and estrogens on neuronal activation in an animal model of migraine. Headache 2013;53(2):288-96. PMID 22913654
57: Greendale GA, Reboussin BA, Hogan P, et al. Symptom relief and side effects of postmenopausal hormones: results from the Postmenopausal Estrogen/Progestin Interventions Trial. Obstet Gynecol 1998;92(6):982-8. PMID 9840563
58: Guidotti M, Mauri M, Barrila C, Guidotti F, Belloni C. Frovatriptan vs. transdermal oestrogens or naproxen sodium for the prophylaxis of menstrual migraine. J Headache Pain 2007;8(5):283-8. PMID 17955167
59: Gupta S, McCarson KE, Welch KM, Berman EJ. Mechanisms of pain modulation by sex hormones. Headache 2011;51:905-22. PMID 21631476
60: Hall GC, Brown MM, Mo J, et al. Triptans in migraine: the risks of stroke, cardiovascular disease, and death in practice. Neurology 2004;24(62):563-8. PMID 14981171
61: Headache Classification Committee. The International Classification of Headache Disorders. 2nd edition. Cephalalgia 2004;24:1-160.
62: Headache Classification Committee of the International Headache Society. The International Classification of Headache Disorders, 3rd edition (beta version). Cephalalgia 2013;33(9):629-808. PMID 23771276
63: Herman JL, Flores AR, O’Neill KK. How many adults and youth identify as transgender in the United States? The Williams Institute: UCLA School of Law, 2022.
64: Hesari E, Ahmadinezhad M, Arshadi M, Azizi H, Khodamoradi F. The association between migraine and breast cancer risk: a systematic review and meta-analysis. PLoS One 2022;17(2):e0263628. PMID 35143585
65: Honkasalo ML, Kaprio J, Winter T, Heikkilä K, Sillanpää M, Koskenvuo M. Migraine and concomitant symptoms among 8167 adult twin pairs. Headache 1995;35:70-8. PMID 7737864
66: Ibrahimi K, Van Ousterhout WP, Van Dorp W, et al. Reduced trigeminovascular cyclicity in patients with menstrually related migraine. Neurology 2015;84:125-31. PMID 25503623
67: Institute for Health Metrics and Evaluation GBD Results Tool. IHME. University of Washington Seattle: Washingtn, 2020. Available at:http://ghdx.healthdata.org/gbd-results-tool
68: Kallen B, Lygner PE. Delivery outcome in women who used drugs for migraine during pregnancy with special reference to sumatriptan. Headache 2001;41(4):351-6. PMID 11318881
69: Karli N, Baykan B, Ertas M, et al. Impact of sex hormonal changes on tension-type headache and migraine: a cross-sectional population based survey in 2,600 women. J Headache Pain 2012;13(7):557-65. PMID 22935969
70: Katsarava Z, Rabe K, Dienr H-C. From migraine to stroke. Intern Emerg Med 2008;3(1):9-16. PMID 18781406
71: Kittner SJ, Bousser MG. Postmenopausal hormone replacement therapy and stroke risk. Cephalalgia 2000;20:208-13. PMID 10997775
72: Koseoglu E, Nacar M, Talaslioglu A, Cetinkaya F. Epidemiological and clinical characteristics of migraine and tension type headache in 1146 females in Kayseri, Turkey. Cephalalgia 2003;23(5):381-8. PMID 12780769
73: Kruit MC, van Buchem MA, Hofman PA, et al. Migraine as a risk factor for subclinical brain lesions. JAMA 2004;291:427-34. PMID 14747499
74: Kurth T, Slomke MA, Kase CS, et al. Migraine, headache, and the risk of stroke in women: a prospective study. Neurology 2005;64:1020-6. PMID 15781820
75: Larsson-Cohn U, Lundberg PO. Headache and treatment with oral contraceptives. Acta Neurol Scand 1970;46:267-78. PMID 4918509
76: Loder E. Safety of sumatriptan in pregnancy: A review of the data so far. CNS Drugs 2003;17(1):1-7. PMID 12467489
77: Loder EW, Buse DC, Golub JR. Headache and combination estrogen-progestin oral contraceptives: Integrating evidence, guidelines, and clinical practice. Headache 2005;45(3):224-31. PMID 15836597
78: MacGregor EA. Is HRT giving you a headache. British Migraine Association Newsletter 1993:19-24.
79: MacGregor EA. Menstruation, sex hormones, and migraine. Neurol Clin 1997a;15:125-41. PMID 9058401
80: MacGregor EA, Chia H, Vohrah RC, Wilkinson M. Migraine and menstruation: a pilot study. Cephalalgia 1990;10:305-10. PMID 2289231
81: MacGregor EA, Frith A, Ellis J, Aspinall L, Hackshaw A. Incidence of migraine relative to menstrual cycle phases of rising and falling estrogen. Neurology 2006;67:2154-8. PMID 16971700
82: MacGregor EA, Igarashi H, Wilkinson M. Headaches and hormones: subjective versus objective assessment. Headache Q 1997b;8:126-36.
83: MacGregor EA, van den Brink AM. Transgender and migraine. In: van den Brink JM, MacGregor EA. Gender and migraine. Netherlands: Springer, 2019.
84: Maggioni F, Alessi C, Maggino T, Zanchin G. Headache during pregnancy. Cephalalgia 1997;17:765-9. PMID 9399007
85: Magos A, Brincat M, Zilkha KJ, Studd JW. Serum dopamine beta-hydroxylase activity in menstrual migraine. J Neurol Neurosurg Psychiatry 1985;48:328-31. PMID 4039748
86: Maleki N, Linnman C, Brawn J, Burstein R, Becerra L, Borsook D. Her versus his migraine: multiple sex differences in brain function and structure. Brain 2012;135(Pt 8):2546-59. PMID 22843414
87: Martin VT, Ballard J, Diamond MP, et al. Relief of menstrual symptoms and migraine with a single-tablet formulation of sumatriptan and naproxen sodium. J Womens Health (Larchmt) 2014;23(5):389-96. PMID 24579886
88: Martin VT, Behbehani M. Ovarian hormones and migraine headache: understanding mechanisms and pathogenesis. Part 1. Headache 2006a;46:3-23. PMID 16412147
89: Martin VT, Behbehani M. Ovarian hormones and migraine headache: understanding mechanisms and pathogenesis. Part 2. Headache 2006b;46:365-86. PMID 16618254
90: Martin VT, Lipton RB. Epidemiology and biology of menstrual migraine. Headache 2008;48(Suppl 3):S124-30. PMID 19076658
91: Massiou H, Jamin C, Hinzelin G, Bidaut-Mazel C. The French Naramig Collaborative Study Group. Efficacy of oral naratriptan in the treatment of menstrually related migraine. 2005;12(10):774-81. PMID 16190915
92: Massiou H, MacGregor EA. Evolution and treatment of migraine with oral contraceptives. Cephalalgia 2000;20(3):170-4. PMID 10997770
93: Mattsson P. Hormonal factors in migraine: a population-based study of women aged 40 to 74 years. Headache 2003;43(1):27-34. PMID 12864755
94: Melhado E, Maciel JA Jr, Guerreiro CA. Headaches during pregnancy in women with a prior history of menstrual headaches. Arq Neuropsiquiatr 2005;63(4):934-40. PMID 16400408
95: Meriggiola MC, Nanni M, Bachiocco V, Vodo S, Aloisi AM. Menopause affects pain depending on pain type and characteristics. Menopause 2012;19(5):517-23. PMID 22334057
96: Misakian AL, Langer RD, Bensenor IM, et al. Postmenopausal hormone therapy and migraine headache. Womens Health (Larchmt) 2003;12:1027-36. PMID 14709191
97: Moschiano F, Allais G, Grazzi L, et al. Naratriptan in the short-term prophylaxis of pure menstrual migraine. Neurol Sci 2005;Suppl 2:s162-6. PMID 15926020
98: Mueller L. Predictability of exogenous hormone effect on subgroups of migraineurs. Headache 2000;40:189-93. PMID 10759920
99: Munakata J, Hazard E, Serrano D, et al. Economic burden of transformed migraine: results from the American Migraine Prevalence and Prevention (AMPP) study. Headache 2009;49(4):498-508. PMID 19245386
100: Nattero G, Allais G, DeLorenzo C, et al. Relevance of prostaglandins in true menstrual migraine. Headache 1989;29:232-8. PMID 2714974
101: Neri I, Granella F, Nappi R, Manzoni GC, Facchinetti F, Genazzani AR. Characteristics of headache at menopause: a clinico-epidemiologic study. Maturitas 1993;17:31-7. PMID 8412841
102: Olesen C, Steffensen FH, Sorensen HT, Nielsen GL, Olsen J. Pregnancy outcome following prescription for sumatriptan. Headache 2000;40:20-4. PMID 10759898
103: Pavlovic JM. Evaluation and management of migraine in midlife women. Menopause 2018;25(8):927-9. PMID 29787480
104: Pavlovic JM, Stewart WF, Bruce CA, et al. Burden of migraine related to menses: results from the AMPP study. J Headache Pain 2015;16:24. PMID 25902814
105: Pfaffenrath V, Rehm M. Migraine in pregnancy: what are the safest treatment options. Drug Saf 1998;19:383-8. PMID 9825951
106: Ponder TM. Differential diagnosis of postdural puncture headache in the parturient. CRNA 1999;10(4):145-54. PMID 10723292
107: Pradalier A, Vincent D, Beaulieu P, Baudesson G, Launay J-M. Correlation between oestradiol plasma level and therapeutic effect on menstrual migraine. In: Rose FC, editor. New Advances in Headache Research. 4th ed. London: Smith-Gordon; 1994:129-32.
108: Pringsheim T, Davenport WJ, Dodick D. Acute treatment and prevention of menstrually related migraine headache: evidence-based review. Neurology 2008;70(17):1555-63. PMID 18427072
109: Pringsheim T, Gooren L. Migraine prevalence in male to female transsexuals on hormone therapy. Neurology 2004;63(3):593-4. PMID 15304612
110: Radix A. Hormone therapy for transgender adults. Urol Clin North Am 2019;46(4):467-473.
111: Rapoport AM, Ramadan NM, Adelman JU, et al. A multicenter, double-blind, placebo-controlled, dose range-finding study--optimizing the dose of zolmitriptan (Zomig, 311C90) for the acute treatment of migraine. Neurology 1997;49:1210-8. PMID 9371896
112: Reddy DS, Gangisetty O, Briyal S. Disease-modifying activity of progesterone in the hippocampus kindling model of epileptogenesis. Neuropharmacology 2010;59(7-8):573-81. PMID 20804775
113: Reiff-Eldridge R, Heffner CR, Ephross SA, Tennis PS, White AD, Andrews EB. Monitoring pregnancy outcomes after prenatal drug exposure through prospective pregnancy registries: a pharmaceutical company commitment. Am J Obstet Gynecol 2000;182(1 Pt 1):159-63. PMID 10649172
114: Rossouw JE, Anderson GL, Prentice RL, et al. Risks and benefits of estrogen plus progestin in healthy postmenopausal women: Principal results from the Women's Health Initiative randomized controlled trial. JAMA 2002;288:321-33. PMID 12117397
115: Sakai Y, Dobson C, Diksic M, Aube M, Hamel E. Sumatriptan normalizes the migraine attack-related increase in brain serotonin synthesis. Neurology 2008;70(6):431-9. PMID 18250288
116: Sances G, Granella F, Nappi RE, et al. Course of migraine during pregnancy and postpartum prospective study. Cephalalgia 2003;23(3):197-205. PMID 12662187
117: Sarchielli P, Alberti A, Coppola F, et al. Platelet-activating factor (PAF) in internal jugular venous blood of migraine without aura patients assessed during migraine attacks. Cephalalgia 2004;24:623-30. PMID 15265050
118: Sarchielli P, Rainero I, Coppola F, et al. Involvement of corticotrophin-releasing factor and orexin-A in chronic migraine and medication-overuse headache: findings from cerebrospinal fluid. Cephalalgia 2008;28(7):714-22. PMID 18479471
119: Scher AI, Terwindt GM, Picavet HS, Verschuren WM, Ferrari, MD, Launer LJ. Cardiovascular risk factors and migraine: the GEM population-based study. Neurology 2005;64(4):614-20. PMID 15728281
120: Schwaag S, Nabavi DG, Frese A, Husstedt IW, Evers S. The association between migraine and juvenile stroke: a case-control study. Headache 2003;43(2):90-5. PMID 12558760
121: Schwartz RB. Neurodiagnostic imaging of the pregnant patient. In: Devinsky O, Feldmann E, Hainline B, editors. Neurologic complications of pregnancy. New York: Raven Press, 1994:243.
122: Schwartz RB. Neuroradiographic imaging: techniques and safety considerations. In: Hainline B, Devinsky O, editors. Neurological complications of pregnancy, 2nd ed. Philadelphia: Lippincott Williams & Wilkins, 2002:1-8.
123: Sheehan JP. Hormone replacement treatment and benign intracranial hypertension. Br Med J 1982;284:1675-6. PMID 6805652
124: Sicuteri F. Opioids, pregnancy and the disappearance of headache. Headache 1980;20:220-1. PMID 7390806
125: Silberstein SD. Migraine in pregnancy. Neurol Clin 2004;22:727-56. PMID 15474764
126: Silberstein SD, Armellino JJ, Hoffman HD, et al. Treatment of menstruation-associated migraine with the nonprescription combination of acetaminophen, aspirin, and caffeine: results from three randomized, placebo-controlled studies. Clin Ther 1999;21(3):475-91. PMID 10321417
127: Silberstein SD, Bradley K. DHE-45® in the prophylaxis of menstrually related migraine. Cephalalgia 1996;16:371.
128: Silberstein SD, De Lignieres B. Migraine, menopause and hormonal replacement therapy. Cephalalgia 2000;20:214-221. PMID 10997776
129: Silberstein SD, Elkind AH, Schreiber C. Randomized trial of frovatriptan for the intermittent prevention of menstrual migraine. Neurology 2004;63:261-9. PMID 15277618
130: Singh M, Su C. Progesterone and neuroprotection. Horm Behav 2013;63(2):284-90. PMID 22732134
131: Siritho S, Thrift AG, McNeil JJ, et al. Risk of ischemic stroke among users of the oral contraceptive pill: The Melbourne Risk Factor Study (MERFS) Group. Stroke 2003;34:1575-80. PMID 12805499
132: Sjaastad O, Apfelbaum R, Caskey W. Chronic paroxysmal hemicrania. The clinical manifestations. A review. Ups J Med Sci 1980;85(Suppl):27-33. PMID 6935856
133: Smits MG, van der Meer YG, Pfeil JP, et al. Perimenstrual migraine: effect of Estraderm TTS and the value of contingent negative variation and exteroceptive temporalis muscle suppression test. Headache 1994;34:103-6. PMID 8163364
134: Stein GS. Headaches in the first post partum week and their relationship to migraine. Headache 1981;21:201-5. PMID 7287418
135: Summers JE, Bedrin KO, Ailani J, Dougherty CO. Safety of using onabotulinumtoxinA for the treatment of chronic migraine in pregnancy. Headache 2020;60(S1 Suppl):1-156.
136: Theoharides TC, Donelan J, Kandere-Grzybowska K, Konstantinidou A. The role of mast cells in migraine pathophysiology. Brain Res Brain Res Rev 2005;49(1):65-76. PMID 15960987
137: Tzourio C, Iglesias S, Hubert JB, et al. Migraine and risk of ischaemic stroke: a case-control study. BMJ 1993;307(6899):289-92. PMID 8374374
138: Tzourio C, Tehindrazanarivelo A, Iglésias S, et al. Case-control study of migraine and risk of ischaemic stroke in young women. BMJ 1995;310(6983): 830-3. PMID 7711619
139: van Oosterhout WPJ, Schoonman GG, van Zwet EW, et al. Female sex hormones in men with migraine. Neurology 2018;91(4):e374-81. PMID 29950439
140: van Vliet JA, Favier I, Helmerhorst FM, Haan J, Ferrari MD. Cluster headache in women: relation with menstruation, use of oral contraceptives, pregnancy and menopause. J Neurol Neurosurg Psychiatry 2006;77(5):690-2. PMID 16407458
141: Vetvik KG, MacGregor EA. Sex differences in the epidemiology, clinical features, and pathophysiology of migraine. Lancet Neurol 2017;16(1):76-87. PMID 27836433
142: Vetvik KG, Macgregor EA, Lundqvist C, Russell MB. Prevalence of menstrual migraine: a population-based study. Cephalalgia 2014;34(4):280-8. PMID 24101732
143: Wainscott G, Sullivan FM, Volans GN, Wilkinson M. The outcome of pregnancy in women suffering from migraine. Postgrad Med J 1978;54:98-102. PMID 634879
144: Wall VR. Breastfeeding and migraine headaches. J Hum Lact 1992;8:209-12. PMID 1288557
145: Wang D, Zhao J, Wang J, Li J, Yu S, Guo X. Deficiency of female sex hormones augments PGE2 and CGRP levels within midbrain periaqueductal gray. J Neurol Sci 2014;346(1-2):107-11. PMID 25175853
146: Wang SJ, Fuh JL, Lu SR, Juang KD, Wang PH. Migraine prevalence during menopausal transition. Headache 2003;43(5):470-8. PMID 12752752
147: Wong HT, Khalil M, Ahmad F. OnabotulinumtoxinA for chronic migraine during pregnancy: a real world experience on 45 patients. J Headache Pain 2020;21(1):129. PMID 33121432
148: The World Professional Association for Transgender Health. Standards of Care for the Health of Transsexual, Transgender, and Gender Nonconforming People, 7th Version. Dundee: IL, 2011. Available at:https://www.wpath.org/publications/soc.

Contributors

All contributors' financial relationships have been reviewed and mitigated to ensure that this and every other article is free from commercial bias.

Author

Marianna Vinokur DO

Dr. Vinokur of Icahn School of Medicine at Mount Sinai has no relevant financial relationships to disclose.
See Profile

Editor

Stephen D Silberstein MD

Dr. Silberstein, Director of the Jefferson Headache Center at Thomas Jefferson University has no relevant financial relationships to disclose.
See Profile

Former Authors

Kenneth L Moore MD
Christos Sidiropoulos MD
Vivek Rai MD
Panayiotis Mitsias MD PhD
Avi Ashkenazi MD

Patient Profile

Age range of presentation: 6 to -65+ years
Sex preponderance: female>male, 3:1
Heredity: heredity may be a factor
Population groups selectively affected: none selectively affected
Occupation groups selectively affected: none selectively affected

This is an article preview.
Start a Free Account
to access the full version.

Nearly 3,000 illustrations, including video clips of neurologic disorders.
Every article is reviewed by our esteemed Editorial Board for accuracy and currency.
Full spectrum of neurology in 1,200 comprehensive articles.
Listen to MedLink on the go with Audio versions of each article.

Questions or Comment?

MedLink®, LLC

3525 Del Mar Heights Rd, Ste 304
San Diego, CA 92130-2122

Toll Free (U.S. + Canada): 800-452-2400

US Number: +1-619-640-4660

Support: service@medlink.com

Editor: editor@medlink.com

ISSN: 2831-9125

Headache associated with hormonal fluctuations

Associated Disorders

Anxiety disorder
Depression
Insomnia
Gastric ulcers
Gastritis
- Fibromyalgia
- Cervicalgia
- Menopausal syndrome
- Gender dysphoria

Differential Diagnosis

eclampsia
preeclampsia
idiopathic intracranial hypertension
subarachnoid hemorrhage from aneurysm or arteriovenous malformation
cortical vein thrombosis
- pituitary tumor
- choriocarcinoma
- intracranial neoplasm
- migraine
- venous sinus thrombosis
- low intracranial pressure
- benign intracranial hypertension

Also Relevant

Headache guidelines
Migraine
Migrainous infarction
Neuroimaging of headache
Psychological factors and headache
- Sex hormones and the nervous system

Headache associated with hormonal fluctuations …

Headache associated with hormonal fluctuations

Introduction

Overview

Historical note and terminology

Clinical manifestations

Presentation and course

Table 1. International Headache Society Definitions of Pure Menstrual Migraine and of Menstrually-Related Migraine

Prognosis and complications

Clinical vignette

Biological basis

Etiology and pathogenesis

Epidemiology

Prevention

Differential diagnosis

Diagnostic workup

Management

Table 2. Current Acute Headache Treatments and Prescription Directions for Adults

References

Contributors

Author

Editor

Former Authors

Patient Profile

ICD & OMIM codes

This is an article preview.
Start a Free Account
to access the full version.

Questions or Comment?

Also in This Category

Third nerve palsy

Nystagmus

Brain death/death by neurologic criteria

Late-life migrainous accompaniments

Hepatic encephalopathy

Cervical spondylotic myelopathy

Bowel dysfunction in neurologic disorders

Coma due to primary brainstem and diencephalic lesions

Headache associated with hormonal fluctuations

Introduction

Overview

Historical note and terminology

Clinical manifestations

Presentation and course

Table 1. International Headache Society Definitions of Pure Menstrual Migraine and of Menstrually-Related Migraine

Prognosis and complications

Clinical vignette

Biological basis

Etiology and pathogenesis

Epidemiology

Prevention

Differential diagnosis

Diagnostic workup

Management

Table 2. Current Acute Headache Treatments and Prescription Directions for Adults

References

Contributors

Author

Editor

Former Authors

Patient Profile

ICD & OMIM codes

This is an article preview. Start a Free Account to access the full version.

Questions or Comment?

Also in This Category

Third nerve palsy

Nystagmus

Brain death/death by neurologic criteria

Late-life migrainous accompaniments

Hepatic encephalopathy

Cervical spondylotic myelopathy

Bowel dysfunction in neurologic disorders

Coma due to primary brainstem and diencephalic lesions

This is an article preview.
Start a Free Account
to access the full version.