Skip to main content
Download PDF
Download ePub
  • Research article
  • Open access
  • Published:

Risk for ischemic stroke and coronary heart disease associated with migraine and migraine medication among older adults

The Journal of Headache and Pain volume 22, Article number: 124 (2021) Cite this article

Abstract

Background

Migraine has been associated with cardiovascular disease (CVD) events among middle-aged adults. The objective of this study was to determine the risk for ischemic stroke and coronary heart disease (CHD) events among older adults with versus without migraine.

Methods

This retrospective cohort study was conducted using data from US adults ≥66 years of age with Medicare health insurance between 2008 and 2017. After stratification by history of CVD, patients with a history of migraine were matched 1:4 to those without a history of migraine, based on calendar year, age, and sex. Patients were followed through December 31, 2017 for ischemic stroke and CHD events including myocardial infarction or coronary revascularization. All analyses were done separately for patients with and without a history of CVD.

Results

Among patients without a history of CVD (n = 109,950 including n = 21,990 with migraine and n = 87,960 without migraine), 1789 had an ischemic stroke and 3552 had a CHD event. The adjusted hazard ratio (HR) among patients with versus without migraine was 1.20 (95% confidence interval [95%CI], 1.07–1.35) for ischemic stroke and 1.02 (95%CI, 0.93–1.11) for CHD events. Compared to patients without migraine, those with migraine who were taking an opioid medication had a higher risk for ischemic stroke (adjusted HR 1.43 [95%CI, 1.20–1.69]), while those taking a triptan had a lower risk for CHD events (adjusted HR 0.79 [95%CI, 0.67–0.93]). Among patients with a history of CVD (n = 79,515 including n = 15,903 with migraine and n = 63,612 without migraine), 2960 had an ischemic stroke and 7981 had a CHD event. The adjusted HRs (95%CI) for ischemic stroke and CHD events associated with migraine were 1.27 (1.17–1.39) and 0.99 (0.93–1.05), respectively. Patients with migraine taking an opioid medication had a higher risk for ischemic stroke (adjusted HR 1.21 [95%CI, 1.07–1.36]), while those taking a triptan had a lower risk for CHD events (adjusted HR 0.83 [95%CI, 0.72–0.95]), each versus those without migraine.

Conclusions

Older adults with migraine are at increased risk for ischemic stroke. The risk for ischemic stroke among older adults with migraine may differ by migraine medication classes.

Introduction

Studies of middle-aged adults have shown migraine to be associated with an increased risk for cardiovascular disease (CVD) events, including ischemic stroke and coronary heart disease (CHD) events [1]. The mechanisms linking migraine to CVD events are unclear, but have been speculated to include cortical spreading depression, hypercoagulation, endothelial dysfunction, shared genetic risk, vasospasm, or a higher prevalence of cardiovascular risk factors among patients with migraine [2, 3]. The risk for CVD events is higher among older versus middle-aged adults [4]. However, many risk factors for CVD events in middle-aged adults, including serum cholesterol and blood pressure, are not associated with increased CVD risk in older adults [5]. Little is known about the risk for CVD events associated with migraine in older adults [1, 6].

It has been suggested that certain classes of medications used to treat migraine, including triptans and ergotamines, are associated with an increased risk for CVD events [6, 7]. Also, specific migraine medications, including triptans, are contra-indicated for some patients with a history of CVD or high CVD risk [8, 9]. Few data are available on the risk for CVD events among older adults taking different classes of migraine medication [10]. A better understanding of the CVD risk associated with migraine and the use of migraine medications in older adults may advance knowledge of, and inform appropriate use of, migraine therapies in this population.

The primary objective of the current study was to compare the risk for ischemic stroke and CHD events among older US adults with versus without migraine. Since an association between some migraine medications and an increased risk for CVD events has been reported, we also analyzed the risk for ischemic stroke and CHD events among older adults with migraine taking different migraine medication classes [11,12,13,14]. As the risk for CVD events is higher among adults with versus without a history of CVD [15], all analyses were conducted for patients with and without a history of CVD, separately.

Methods

We conducted a retrospective cohort study using data from a 5 % random sample of Medicare beneficiaries. Medicare is a government health insurance program for US adults aged 65 years and older, and adults younger than 65 years with end-stage renal disease or who are disabled. Medicare data were obtained from the Centers for Medicare and Medicaid Services (CMS) Chronic Condition Data Warehouse. The institutional review board at the University of Alabama at Birmingham approved the study and waived the requirement to obtain informed consent.

Study population

We identified Medicare beneficiaries with a history of migraine between January 1, 2008 and December 31, 2017, using inpatient and outpatient healthcare utilization claims for migraine and pharmacy fills for acute migraine medications as defined in Supplemental Table 1. To provide adequate time to identify patient characteristics including the presence of comorbidities, we restricted the study population to Medicare beneficiaries who were living in the US and had continuous inpatient, outpatient, and pharmacy coverage for the 365 days prior to meeting the definition of history of migraine. As we were interested in studying history of migraine in older adults, we further restricted the study population to Medicare beneficiaries ≥66 years of age on the date they met the definition of history of migraine which means they were ≥ 65 years of age 365 days prior to meeting the definition of history of migraine (i.e., at the start of the look-back period). We required each beneficiary to be alive on the date they met the criteria for having a history of migraine. For each beneficiary, the earliest date they met all of the inclusion criteria described above was defined as their index date.

To serve as a control group, we identified beneficiaries who did not have a history of migraine, as defined above, using all available Medicare claims on or before December 31, 2017. For each beneficiary without a history of migraine, we randomly selected a day between January 1, 2008 and December 31, 2017 to serve as their index date. We applied identical inclusion/exclusion criteria for beneficiaries without a history of migraine as for those with a history of migraine. Specifically, we restricted the analysis to patients without a history of migraine who lived in the US and had continuous inpatient, outpatient, and pharmacy coverage for the 365 days before their index date. We further restricted the analysis to beneficiaries ≥66 years of age who were alive on their index date. For patients with and without a history of CVD, separately, beneficiaries without a history of migraine were frequency matched to those with a history of migraine four to one based on the calendar year of their index date, age in years on their index date, and sex.

Patient characteristics

We used Medicare beneficiary and claims data between January 1, 2007 and each patient’s index date to define characteristics (Supplemental Table 2). In addition to age on their index date, sex, and history of CVD, patient characteristics analyzed included race/ethnicity, receiving a low-income subsidy to pay for their health insurance, smoking status, history of diabetes, hypertension, chronic kidney disease (CKD), heart failure, dementia, depression, an anxiety disorder, insomnia, cancer, epilepsy, and hospitalization within the past year. Among beneficiaries with migraine, we further identified those with a history of migraine with aura. Beneficiaries who did not meet the definition for comorbidities listed above were assumed not to have those conditions. Area-level income was defined by the median income level within the patient’s zip code of residence according to data from the 2017 American Community Survey [16]. We also used Medicare pharmacy claims within 90 days prior to each patient’s index date to identify the use of antihypertensive medication, glucose-lowering medication, statins, non-statin lipid-lowering medications, medications for insomnia, and, among women, hormone replacement therapy. A list of these medications is provided in Supplemental Table 3.

Migraine medication use

For patients with a history of migraine, we used Medicare pharmacy claims within 90 days prior to each patient’s index date to identify use of acute migraine medications (i.e., triptans, ergotamine, nonsteroidal anti-inflammatory drugs [NSAID], and opioids) and preventive migraine medications (i.e., select antiepileptic agents, select antihypertensive agents, select antidepressants, botulinum toxin, and other agents). A list of the medications in each of these classes is provided in Supplemental Table 4.

Cardiovascular outcomes

Patients were followed from their index date through December 31, 2017 for ischemic stroke events and CHD events (i.e., myocardial infarction hospitalization or coronary revascularization), separately, with censoring occurring if they lost Medicare fee-for-service inpatient or outpatient coverage or died. The definitions of ischemic stroke and CHD events are provided in Supplemental Table 5. As a secondary outcome, we analyzed the risk for CVD events, defined as the composite of an ischemic stroke or CHD event.

Statistical analysis

All statistical analyses described below were conducted among Medicare beneficiaries with and without a history of CVD, separately. We calculated summary statistics of patient characteristics for those with and without a history of migraine. We calculated the cumulative incidence and incidence rates of ischemic stroke, CHD and CVD events for patients with and without a history of migraine accounting for the competing risk of all-cause mortality as described by Fine and Gray [17]. We used Cox proportional hazard models with the Breslow method for tie handling to estimate hazard ratios (HR) and 95% confidence intervals (CI) for the risk of ischemic stroke, CHD events, and composite CVD events among patients with versus without a history of migraine. Four models with progressive adjustment for covariates were used. Model 1 was unadjusted. Model 2 included adjustment for age, sex, and race/ethnicity. Model 3 included adjustment for age, sex, race/ethnicity, low-income subsidy, area-level income, smoking status, diabetes, hypertension, CKD, heart failure, dementia, depression, insomnia, cancer, epilepsy, and hospitalization within the past year. Model 4 included adjustment for the variables in the third model and use of antihypertensive medication, glucose-lowering medication, statins, non-statin lipid-lowering therapy, medication for insomnia, and among women, hormone replacement therapy. As prior studies have shown an association between migraine with aura and increased risk of ischemic stroke [18, 19], we also estimated incidence rates and HRs for ischemic stroke associated with a history of migraine with and without aura, separately.

The calculation of rates and HRs for ischemic stroke, CHD events, and CVD events described above was repeated comparing patients with migraine but not taking migraine medications, those with migraine taking each migraine medication class and taking two or more migraine medication classes, each versus their counterparts without migraine. Few patients with migraine with and without a history of CVD were using ergotamines or botulinum toxin and the number of outcome events during follow-up in these subgroups was low. Therefore, we did not analyze the risk for outcome events among patients with migraine taking ergotamines or botulinum toxin. All analyses were conducted using SAS 9.4 (SAS Institute) with a two-sided level of statistical significance of 0.05.

Results

Overall, 37,893 Medicare beneficiaries with a history of migraine met the inclusion criteria for the current study, including 21,990 without a history of CVD and 15,903 with a history of CVD (Fig. 1). The 21,990 patients with a history of migraine who did not have a history of CVD were matched to 87,960 patients without a history of migraine or CVD. Also, the 15,903 patients with a history of migraine who had a history of CVD were matched to 63,612 patients without a history of migraine with a history of CVD.

Fig. 1
figure 1

Consort diagram of Medicare beneficiaries with a history of migraine included and not included in the current analysis. CVD: cardiovascular disease

Full size image

Patients without a history of CVD

Compared to their counterparts without a history of migraine, patients with a history of migraine were more likely to have depression, an anxiety disorder, and insomnia, and to have been hospitalized in the prior year (Table 1). Patients with a history of migraine were also more likely to take medications for insomnia and, among women, hormone replacement therapy.

Table 1 Characteristics of patients without a history of cardiovascular disease who had and did not have a history of migraine
Full size table

Over a median follow-up time of 3.4 years (maximum of 10 years), among patients with and without a history of migraine, there were 406 and 1383 ischemic stroke events, respectively, 720 and 2832 CHD events, respectively, and 1084 and 4050 CVD events, respectively. The cumulative incidence of ischemic stroke was higher among patients with versus without a history of migraine (Fig. 2). There was no evidence of a difference in the cumulative incidence of CHD or CVD between patients with versus without a history of migraine. After multivariable adjustment, history of migraine was associated with a higher risk for ischemic stroke (HR 1.20 [95% CI, 1.07–1.35]) and CVD events (HR 1.08 [95% CI, 1.01–1.16]) but not CHD events (HR 1.02 [95% CI, 0.93–1.11]) (Table 2). Compared to those without a history of migraine, the multivariable-adjusted HR for ischemic stroke events was 1.21 (95% CI, 1.07–1.37) for patients with a history of migraine without aura and 1.18 (95% CI, 0.88–1.57) for patients with a history of migraine with aura (Supplemental Table 6).

Fig. 2
figure 2

Cumulative incidence ischemic stroke, coronary heart disease and cardiovascular events among patients with and without a history of migraine, restricted to those without a history of cardiovascular disease. CHD: coronary heart disease; CVD: cardiovascular disease. The cumulative incidence was calculated accounting for the competing risk of all-cause mortality using the method of Fine and Gray [17].

Full size image
Table 2 Incidence rates and hazard ratios for ischemic stroke, coronary heart disease and cardiovascular disease events associated with a history of migraine among patients without a history of cardiovascular disease
Full size table

Among patients with a history of migraine, opioids and triptans were the acute migraine medications most commonly used, being taken by 36% of patients for both therapies, while antihypertensive medications were the most commonly used migraine-preventive therapy (Supplemental Table 7). After multivariable adjustment, patients with a history of migraine taking an opioid medication had a higher risk for ischemic stroke and CHD events versus their counterparts without a history of migraine. Patients with a history of migraine taking a triptan had a lower risk for CHD events versus those without a history of migraine, but there was no evidence of a difference in the risk for ischemic stroke.

Patients with a history of CVD

Among patients with a history of CVD, those who had a history of migraine were more likely to have depression, an anxiety disorder, and insomnia, and to have been hospitalized in the prior year compared to their counterparts without a history of migraine (Table 3). Patients with a history of migraine were also more likely to be taking medication for insomnia.

Table 3 Characteristics of patients with a history of cardiovascular disease who had and did not have a history of migraine
Full size table

Over a median follow-up time of 3.1 years (maximum of 10 years), among patients with and without a history of migraine, there were 765 and 2195 ischemic stroke events, respectively, 1677 and 6304 CHD events, respectively and 2301 and 8062 CVD events, respectively. The cumulative incidence of ischemic stroke and CVD events but not CHD events was higher among patients with a history of migraine versus without a history of migraine (Fig. 3). After multivariable adjustment, a history of migraine was associated with a higher risk for ischemic stroke (HR 1.27 [95% CI, 1.17–1.39]) and CVD events (HR 1.06 [95% CI, 1.01–1.12]) but not for CHD events (HR 0.99 [95% CI, 0.93–1.05]) (Table 4). After multivariable adjustment and compared to patients without a history of migraine, the HR for ischemic stroke events was 1.27 (95% CI, 1.16–1.39) and 1.29 (95% CI, 1.06–1.57) for patients with a history of migraine without and with aura, respectively (Supplemental Table 8).

Fig. 3
figure 3

Cumulative incidence of ischemic stroke, coronary heart disease and cardiovascular events among patients who had and did not have a history of migraine, restricted to those with a history of cardiovascular disease. CHD: coronary heart disease; CVD: cardiovascular disease. The cumulative incidence was calculated accounting for the competing risk of all-cause mortality using the method of Fine and Gray [17].

Full size image
Table 4 Incidence rates and hazard ratios for ischemic stroke, coronary heart disease and cardiovascular disease events associated with a history of migraine among patients with a history of cardiovascular disease
Full size table

Opioids (47%) and antihypertensive medications (54%) were the most commonly used acute and preventive migraine medications among patients with a history of migraine, respectively (Supplemental Table 9). Also, 15% of patients with a history of migraine were taking a triptan. After multivariable adjustment and compared to patients without a history of migraine, patients with a history of migraine who were taking an NSAID, opioid medication, antiepileptic agent, antihypertensive medication, antidepressant and two or more migraine agents had a higher risk for ischemic stroke. Patients with a history of migraine taking a triptan had a lower risk for CHD and CVD events versus those without a history of migraine.

Discussion

In the current analysis, the risk for ischemic stroke was higher among older adults with versus without a history of migraine. This association was present for patients with and without a history of CVD. Compared to patients without a history of migraine, the higher risk for ischemic stroke was present among patients with a history of migraine taking an opioid medication, but not among those taking a triptan. There was no evidence of a difference in the risk for CHD events for older adults with and without a history of migraine. However, patients with a history of migraine taking a triptan had lower risk for CHD events when compared to patients without migraine.

In previous studies of primarily middle-aged adults, migraine had been associated with an increased risk for stroke and CHD [1, 20,21,22]. In a meta-analysis of 16 cohort studies including more than one million participants, a history of migraine was associated with an increased risk for stroke (adjusted HR 1.41 [95% CI, 1.25–1.61]) and myocardial infarction (adjusted HR 1.23 [95% CI, 1.03–1.43]) [1]. However, substantial heterogeneity was present when comparing results across studies in this meta-analysis [1]. Few data are available examining the association of migraine with ischemic stroke and CHD events among older adults [1, 6]. In a study including 1919 adults ≥65 years of age, late-life non-migraine headache was associated with an increased risk for stroke [23]. There was no association between migraine and risk for stroke in this study. However, only 73 total stroke events, including two among those with migraine, occurred during follow up of this cohort. In another study that included 1292 adults (mean age 68 ± 9 years), migraine was associated with increased risk of stroke among smokers (adjusted HR 3.17; 95% CI 1.13, 8.85) but not in nonsmokers (adjusted HR 0.77; 95% CI 0.44, 1.35) [24]. In the current analysis, with a larger sample of older US adults with and without a history of migraine as well as thousands of stroke and CHD events that occurred during follow-up, a history of migraine was associated with a higher risk for ischemic stroke, but not with CHD events.

In a prior analysis of the Women’s Health Study, women who had migraine with aura had a higher risk for ischemic stroke compared to women without migraine [18]. However, women who had migraine without aura did not have an increased risk for ischemic stroke compared to those without migraine. The incidence rate of ischemic stroke in the current study was higher for individuals with a history of migraine, with and without aura, compared to those without a history of migraine. However, the current results need to be interpreted with caution as some patients with migraine with aura may have been misclassified as without aura if they did not have a specific diagnosis code for this condition.

Triptans are contraindicated for patients with a history of coronary artery disease, cerebrovascular disease or peripheral vascular disease, or with uncontrolled hypertension [8]. Consistent with prior studies, the use of triptans was lower among patients with a history of migraine included in the current analysis who had versus those who did not have a history of CVD [25, 26]. The use of triptans by patients with migraine was associated with a lower risk for CHD events compared to those without a history of migraine. This finding may be explained by physicians selectively prescribing triptans to those patients with a history of migraine perceived to be at a lower risk for future CVD events.

The use of opioids is not recommended by any migraine treatment guideline [27,28,29,30]. However, prior studies have shown that the use of opioids is high among middle-aged adults with migraine [31, 32]. In the current study, opioids were the acute migraine medications most commonly used by older adults with a history of migraine, both among those without and with a history of CVD. The use of opioids has been associated with an increased risk of CVD events [12,13,14]. This association may be mediated by opioid receptors in the cardiovascular system [33]. For example, it has been suggested that chronic use of opioid may increase the risk for ischemic stroke through an altered expression of tight junction proteins which could result in a disruption in the blood brain barrier [34]. In a study of Medicare beneficiaries from New Jersey and Pennsylvania, opioid use was associated with more than twice the risk of myocardial infarction compared with the use of NSAIDs [13]. Among patients with a history of CVD in the current study, those with history of migraine taking opioids had a higher risk of ischemic stroke and CHD events versus their counterparts without a history of migraine. However, we cannot rule out confounding by indication. This would occur, for example, if patients at high risk for CHD events were more likely to be treated with opioids versus other migraine medications.

In addition to the efficacy of a therapy, comorbid and coexisting conditions, potential adverse events, and patient preferences should be taken into consideration when developing a treatment plan for individuals with a history of migraine [28]. For many older individuals with a history of migraine, cardiovascular contraindications to migraine-specific therapies can pose substantial treatment challenges. Current treatment guidelines for episodic migraine do not provide specific recommendations for the management of older adults or those with increased CVD risk [27,28,29,30]. More specific recommendations for the treatment of older adults with migraine, particularly those with a history of CVD or high CVD risk, may lead to better migraine management by reducing the frequency, duration, and severity of migraine attacks and subsequently improving quality of life in this population.

The current study has several strengths. We included a large sample of adults ≥65 years with and without migraine. Since most older US adults have health insurance through Medicare, the current findings have a high degree of generalizability to older adults in the US [35]. Additionally, data on stroke, CHD, and CVD outcomes were available over 10 years of follow-up. We used a number of strategies to control for possible confounding and bias. We used the same inclusion/exclusion criteria and algorithms to identify outcome events among patients with and without migraine. We also used a matched design to control for differences in age, sex, and history of CVD. Lastly, we included numerous covariates in the statistical models to control potential residual confounding. However, the current study has several limitations. Patients with a history of migraine were identified using diagnosis codes and pharmacy claims data which may not capture individuals who are undiagnosed or who do not seek medical care for migraine. The current results may have been attenuated if patients with migraine were misclassified as not having migraine and still had CVD events. We were unable to assess time since migraine diagnosis, and attack frequency and severity for patient’s migraine attacks because these metrics are unavailable in claims data. We were unable to evaluate non-prescription treatment for alleviating migraine pain including over the counter medications, massage, hot or cold compresses, and nutraceuticals. Pharmacy claims can only identify that beneficiaries filled a prescription, but not that they actually took the medication. Additionally, many of these medications are taken as needed and we do not know how frequently patients used them. Finally, the preventive migraine medications and some acute migraine medications (e.g., opioids) included in this study have indications for other diseases. It is possible that patients with a history of migraine were taking these medications to treat other conditions.

Conclusion

In the current study of Medicare beneficiaries, rates of ischemic stroke were higher among those with versus without migraine, but migraine was not associated with a higher risk for CHD events. The risk for ischemic stroke among patients with migraine differed by migraine medication classes. The current findings have implications for clinicians treating older individuals with migraine. These results suggest the need for more specific clinical guidelines and recommendations to appropriately treat older adults with migraine.

Availability of data and materials

The datasets generated and/or analyzed during the current study will be made available from the corresponding author upon reasonable request.

Abbreviations

CHD:

Coronary heart disease

CI:

Confidence intervals

CKD:

Chronic kidney disease

CMS:

Centers for Medicare and Medicaid Services

CVD:

Cardiovascular disease

HR:

Hazard ratios

NSAID:

Nonsteroidal anti-inflammatory drug

References

  1. Mahmoud AN, Mentias A, Elgendy AY, Qazi A, Barakat AF, Saad M, Mohsen A, Abuzaid A, Mansoor H, Mojadidi MK, Elgendy IY (2018) Migraine and the risk of cardiovascular and cerebrovascular events: a meta-analysis of 16 cohort studies including 1 152 407 subjects. BMJ Open 8(3):e020498. https://doi.org/10.1136/bmjopen-2017-020498

    Article  Google Scholar 

  2. Bigal ME, Kurth T, Hu H, Santanello N, Lipton RB (2009) Migraine and cardiovascular disease: possible mechanisms of interaction. Neurology 72(21):1864–1871. https://doi.org/10.1212/WNL.0b013e3181a71220

    Article  CAS  Google Scholar 

  3. Agostoni EC, Longoni M (2018) Migraine and cerebrovascular disease: still a dangerous connection? Neurol Sci 39(S1):S33–S37. https://doi.org/10.1007/s10072-018-3429-8

    Article  Google Scholar 

  4. Dhingra R, Vasan RS (2012) Age as a risk factor. Med Clin North Am 96(1):87–91. https://doi.org/10.1016/j.mcna.2011.11.003

    Article  Google Scholar 

  5. Ahmadi S-F, Streja E, Zahmatkesh G, Streja D, Kashyap M, Moradi H, Molnar MZ, Reddy U, Amin AN, Kovesdy CP, Kalantar-Zadeh K (2015) Reverse epidemiology of traditional cardiovascular risk factors in the geriatric population. J Am Med Dir Assoc 16(11):933–939. https://doi.org/10.1016/j.jamda.2015.07.014

    Article  Google Scholar 

  6. Roberto G, Raschi E, Piccinni C, Conti V, Vignatelli L, D’Alessandro R, de Ponti F, Poluzzi E (2015) Adverse cardiovascular events associated with triptans and ergotamines for treatment of migraine: systematic review of observational studies. Cephalalgia 35(2):118–131. https://doi.org/10.1177/0333102414550416

    Article  CAS  Google Scholar 

  7. Albieri V, Olsen TS, Andersen KK (2016) Risk of stroke in Migraineurs using Triptans. Associations with age, sex, stroke severity and subtype. EBioMedicine 6:199–205 https://doi.org/10.1016/j.ebiom.2016.02.039

    Article  Google Scholar 

  8. Ferrari MD, Roon KI, Lipton RB, Goadsby PJ (2001) Oral triptans (serotonin 5-HT 1B/1D agonists) in acute migraine treatment: a meta-analysis of 53 trials. Lancet 358(9294):1668–1675. https://doi.org/10.1016/S0140-6736(01)06711-3

    Article  CAS  Google Scholar 

  9. Dodick DW, Shewale AS, Lipton RB, Baum SJ, Marcus SC, Silberstein SD, Pavlovic JM, Bennett NL, Young WB, Viswanathan HN, Doshi JA, Weintraub H (2020) Migraine patients with cardiovascular disease and contraindications: an analysis of real-world claims data. J Prim Care Community Health 11:. https://doi.org/10.1177/2150132720963680:215013272096368

    Article  Google Scholar 

  10. Li H, Vincent M, Zhang X, Dennehy EB, Goodloe R, Aurora SK, Smith TR (2020) Acute migraine prescription patterns vary by baseline cardiovascular risk and clinical characteristics: a real-world evidence study. Pain Ther 9(2):499–509. https://doi.org/10.1007/s40122-020-00167-3

    Article  Google Scholar 

  11. Welch K, Mathew N, Stone P, Rosamond W, Saiers J, Gutterman D (2000) Tolerability of sumatriptan: clinical trials and post-marketing experience. Cephalalgia 20(8):687–695. https://doi.org/10.1111/j.1468-2982.2000.00116.x

    Article  CAS  Google Scholar 

  12. Khodneva Y, Muntner P, Kertesz S, Kissela B, Safford MM (2015) Prescription opioid use and risk of coronary heart disease, stroke, and cardiovascular death among adults from a prospective cohort (REGARDS study). Pain Med 17:444–455 https://doi.org/10.1111/pme.12916

    Google Scholar 

  13. Solomon DH (2010) The comparative safety of analgesics in older adults with arthritis. Arch Intern Med 170(22):1968–1976. https://doi.org/10.1001/archinternmed.2010.391

    Article  Google Scholar 

  14. Li L, Setoguchi S, Cabral H, Jick S (2013) Opioid use for noncancer pain and risk of myocardial infarction amongst adults. J Intern Med 273(5):511–526. https://doi.org/10.1111/joim.12035

    Article  CAS  Google Scholar 

  15. D’Agostino RB, Russell MW, Huse DM et al (2000) Primary and subsequent coronary risk appraisal: new results from the Framingham study. Am Heart J 139(2):272–281. https://doi.org/10.1067/mhj.2000.96469

    Article  Google Scholar 

  16. US Census Bureau American Community Survey (ACS). https://www.census.gov/programs-surveys/acs. Accessed 13 Apr 2020

  17. Fine JP, Gray RJ (1999) A proportional hazards model for the subdistribution of a competing risk. J Am Stat Assoc 94(446):496–509. https://doi.org/10.1080/01621459.1999.10474144

    Article  Google Scholar 

  18. Kurth T, Gaziano JM, Cook NR, Logroscino G, Diener HC, Buring JE (2006) Migraine and risk of cardiovascular disease in women. JAMA 296(3):283–292. https://doi.org/10.1001/jama.296.3.283

    Article  CAS  Google Scholar 

  19. Lee SY, Lim JS, Oh DJ, Kong IG, Choi HG (2019) Risk of ischaemic stroke in patients with migraine: a longitudinal follow-up study using a national sample cohort in South Korea. BMJ Open 9(4):1–8. https://doi.org/10.1136/bmjopen-2018-027701

    Google Scholar 

  20. Buse DC, Reed ML, Fanning KM, Kurth T, Lipton RB (2017) Cardiovascular events, conditions, and procedures among people with episodic migraine in the US population: results from the American Migraine Prevalence and Prevention (AMPP) study. Headache J Head Face Pain 57(1):31–44. https://doi.org/10.1111/head.12962

    Article  Google Scholar 

  21. Becker C, Brobert GP, Almqvist PM, Johansson S, Jick SS, Meier CR (2007) Migraine and the risk of stroke, TIA, or death in the UK (CME). Headache J Head Face Pain 47(10):1374–1384. https://doi.org/10.1111/j.1526-4610.2007.00937.x

    Article  Google Scholar 

  22. Sacco S, Ornello R, Ripa P, Tiseo C, Degan D, Pistoia F, Carolei A (2015) Migraine and risk of ischaemic heart disease: a systematic review and meta-analysis of observational studies. Eur J Neurol 22(6):1001–1011. https://doi.org/10.1111/ene.12701

    Article  CAS  Google Scholar 

  23. Norton J, Portet F, Gabelle A, Debette S, Ritchie K, Touchon J, Berr C (2016) Are migraine and non-migrainous headache risk factors for stroke in the elderly? Findings from a 12-year cohort follow-up. Eur J Neurol 23(9):1463–1470. https://doi.org/10.1111/ene.13060

    Article  CAS  Google Scholar 

  24. Monteith TS, Gardener H, Rundek T, Elkind MSV, Sacco RL (2015) Migraine and risk of stroke in older adults. Neurology 85(8):715–721. https://doi.org/10.1212/WNL.0000000000001854

    Article  Google Scholar 

  25. Bigal ME, Golden W, Buse D, Chen YT, Lipton RB (2010) Triptan use as a function of cardiovascular risk. A population-based study. Headache J Head Face Pain 50(2):256–263. https://doi.org/10.1111/j.1526-4610.2009.01595.x

    Article  Google Scholar 

  26. Hall GC, Brown MM, Mo J, MacRae KD (2004) Triptans in migraine: the risks of stroke, cardiovascular disease, and death in practice. Neurology 62(4):563–568. https://doi.org/10.1212/01.WNL.0000110312.36809.7F. https://doi.org/10.1212/01.WNL.0000110312.36809.7F

    Article  CAS  PubMed  Google Scholar 

  27. Holland S, Silberstein SD, Freitag F, Dodick DW, Argoff C, Ashman E, Quality Standards Subcommittee of the American Academy of Neurology and the American Headache Society (2012) Evidence-based guideline update: NSAIDs and other complementary treatments for episodic migraine prevention in adults report of the quality standards subcommittee of the american academy of neurology and the American headache society. Neurology 78(17):1346–1353. https://doi.org/10.1212/WNL.0b013e3182535d0c

    Article  CAS  Google Scholar 

  28. Marmura MJ, Silberstein SD, Schwedt TJ (2015) The acute treatment of migraine in adults: the american headache society evidence assessment of migraine pharmacotherapies. Headache 55(1):3–20. https://doi.org/10.1111/head.12499

    Article  Google Scholar 

  29. Worthington I, Pringsheim T, Gawel MJ et al (2013) Canadian headache society guideline: acute drug therapy for migraine headache. Can J Neurol Sci 40(S2):S1–S80. https://doi.org/10.1017/s0317167100015109

    Article  Google Scholar 

  30. Silberstein SD, Holland S, Freitag F, Dodick DW, Argoff C, Ashman E, Quality Standards Subcommittee of the American Academy of Neurology and the American Headache Society (2012) Evidence-based guideline update: pharmacologic treatment for episodic migraine prevention in adults: report of the Quality Standards Subcommittee of the American Academy of Neurology and the American Headache Society. Neurology 78(17):1337–1345. https://doi.org/10.1212/WNL.0b013e3182535d20

    Article  CAS  Google Scholar 

  31. Buse DC, Pearlman SH, Reed ML, Serrano D, Ng-Mak DS, Lipton RB (2012) Opioid use and dependence among persons with migraine: results of the AMPP study. Headache 52(1):18–36. https://doi.org/10.1111/j.1526-4610.2011.02050.x

    Article  Google Scholar 

  32. Bonafede M, Wilson K, Xue F (2019) Long-term treatment patterns of prophylactic and acute migraine medications and incidence of opioid-related adverse events in patients with migraine. Cephalalgia 39(9):1086–1098. https://doi.org/10.1177/0333102419835465

    Article  Google Scholar 

  33. Feng Y, He X, Yang Y, Chao D, H. Lazarus L, Xia Y (2012) Current research on opioid receptor function. Curr Drug Targets 13(2):230–246. https://doi.org/10.2174/138945012799201612

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. Peyravian N, Dikici E, Deo S, Toborek M, Daunert S (2019) Opioid antagonists as potential therapeutics for ischemic stroke. Prog Neurobiol 182:101679 https://doi.org/10.1016/J.PNEUROBIO.2019.101679

    Article  CAS  Google Scholar 

  35. Administration on Aging, Administration for Community Living, US Department of Health and Human Services (2018) A profile of older Americans: 2017

    Google Scholar 

Download references

Funding

The design and conduct of the study, interpretation of the results, and preparation of the manuscript was supported through a research grant from Amgen, Inc. (Thousand Oaks, CA). The academic authors conducted all analyses and maintained the rights to publish this article.

Author information

Authors and Affiliations

  1. Department of Epidemiology, University of Alabama at Birmingham, 1665 University Blvd, RPHB 523B, Birmingham, AL, 35233-0013, USA

    Emily C. McKinley, Ligong Chen, Lisandro D. Colantonio & Paul Muntner

  2. Centre for Headache, University of Toronto, Toronto, ON, Canada

    Christine L. Lay

  3. Icahn School of Medicine at Mount Sinai, New York, NY, USA

    Robert S. Rosenson

  4. Amgen Inc, Thousand Oaks, CA, USA

    Victoria Chia & Robert Urman

  5. Peter Munk Cardiac Centre and Heart and Stroke Richard Lewar Centre, University of Toronto, Toronto, Canada

    Michael E. Farkouh

Authors
  1. Emily C. McKinley
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Christine L. Lay
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Robert S. Rosenson
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Ligong Chen
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Victoria Chia
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Lisandro D. Colantonio
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Paul Muntner
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. Robert Urman
    View author publications

    You can also search for this author in PubMed Google Scholar

  9. Michael E. Farkouh
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

ECM contributed to the interpretation of the results and manuscript content. CLL contributed to the study concept, study design, interpretation of results, and manuscript content. RSR contributed to the study concept, study design, interpretation of results, and manuscript content. LC conducted the data analysis. VC contributed to the study concept, study design, interpretation of results, and manuscript content. LDC contributed to the study concept, study design, interpretation of results, and manuscript content. PM contributed to the study concept, study design, interpretation of results, and manuscript content. RU contributed to the study concept, study design, developed the final report, and manuscript content. MEF contributed to the study concept, study design, interpretation of results, and manuscript content. The author(s) read and approved the final manuscript.

Corresponding author

Correspondence to Emily C. McKinley.

Ethics declarations

Ethics approval and consent to participate

The institutional review board at the University of Alabama at Birmingham approved the study and waived the requirement to obtain informed consent.

Consent for publication

Not applicable

Competing interests

ECM receives research support from Amgen, Inc.

CLL receives research support from Amgen, Inc., Aralez, Eli Lilly; honoraria from Abbvie/Allergan; serves on the advisory board for Novartis.

RSR receives research support from Amgen, Inc., Astra Zeneca, Novartis and Regeneron; consulting fees from Amgen, Inc., Amryt, C5, CVS Caremark, Novartis, Regeneron and 89 Bio; honoraria from Amgen, Inc., Kowa and Regeneron; royalties from Wolters Kluwer (UpToDate, Inc.); and has stock in MediMergent, LLC.

VC is an employee and shareholder in Amgen, Inc.

LDC receives research support from Amgen, Inc.

PM receives research support and consulting fees from Amgen, Inc.

RU is an employee and shareholder in Amgen, Inc.

MEF receives research support from Amgen, Inc., Novo Nordisk, and Novartis.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Table S1.

Definition of a history of migraine. Table S2. Definition of patient characteristics. Table S3. Antihypertensive medications, glucose lowering medications, statins, non-statin lipid-lowering medication, medications for insomnia and hormone replacement therapy. Table S4. Migraine medications. Table S5. Definitions of ischemic stroke and coronary heart disease events. Table S6. Incidence rates and hazard ratios for ischemic stroke associated with a history of migraine with and without aura among patients without a history of cardiovascular disease. Table S7. Incidence rates and hazard ratios for ischemic stroke, coronary heart disease and cardiovascular disease associated with a history of migraine and migraine medication drug classes among patients without a history of cardiovascular disease. Table S8. Incidence rates and hazard ratios for risk of ischemic stroke associated with a history of migraine without and with aura among patients with a history of cardiovascular disease. Table S9. Incidence rates and hazard ratios for ischemic stroke, coronary heart disease and cardiovascular disease associated with a history of migraine and migraine medications among patients with a history of cardiovascular disease.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

McKinley, E.C., Lay, C.L., Rosenson, R.S. et al. Risk for ischemic stroke and coronary heart disease associated with migraine and migraine medication among older adults. J Headache Pain 22, 124 (2021). https://doi.org/10.1186/s10194-021-01338-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s10194-021-01338-z

Keywords

The Journal of Headache and Pain

ISSN: 1129-2377

Contact us