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. 2023 Jun 13;20(6):e1004238.
doi: 10.1371/journal.pmed.1004238. eCollection 2023 Jun.

Migraine and risk of premature myocardial infarction and stroke among men and women: A Danish population-based cohort study

Affiliations

Migraine and risk of premature myocardial infarction and stroke among men and women: A Danish population-based cohort study

Cecilia Hvitfeldt Fuglsang et al. PLoS Med. .

Erratum in

Abstract

Background: Migraine carries risk of myocardial infarction (MI) and stroke. The risk of premature MI (i.e., among young adults) and stroke differs between men and women; previous studies indicate that migraine is mainly associated with an increased risk of stroke among young women. The aim of this study was to examine impact of migraine on the risk of premature (age ≤60 years) MI and ischemic/hemorrhagic stroke among men and women.

Methods and findings: Using Danish medical registries, we conducted a nationwide population-based cohort study (1996 to 2018). Redeemed prescriptions for migraine-specific medication were used to identify women with migraine (n = 179,680) and men with migraine (n = 40,757). These individuals were matched on sex, index year, and birth year 1:5 with a random sample of the general population who did not use migraine-specific medication. All individuals were required to be between 18 and 60 years old. Median age was 41.5 years for women and 40.3 years for men. The main outcome measures to assess impact of migraine were absolute risk differences (RDs) and hazard ratios (HRs) with 95% confidence intervals (CIs) of premature MI, ischemic, and hemorrhagic stroke, comparing individuals with migraine to migraine-free individuals of the same sex. HRs were adjusted for age, index year, and comorbidities. The RD of premature MI for those with migraine versus no migraine was 0.3% (95% CI [0.2%, 0.4%]; p < 0.001) for women and 0.3% (95% CI [-0.1%, 0.6%]; p = 0.061) for men. The adjusted HR was 1.22 (95% CI [1.14, 1.31]; p < 0.001) for women and 1.07 (95% CI [0.97, 1.17]; p = 0.164) for men. The RD of premature ischemic stroke for migraine versus no migraine was 0.3% (95% CI [0.2%, 0.4%]; p < 0.001) for women and 0.5% (95% CI [0.1%, 0.8%]; p < 0.001) for men. The adjusted HR was 1.21 (95% CI [1.13, 1.30]; p < 0.001) for women and 1.23 (95% CI [1.10, 1.38]; p < 0.001) for men. The RD of premature hemorrhagic stroke for migraine versus no migraine was 0.1% (95% CI [0.0%, 0.2%]; p = 0.011) for women and -0.1% (95% CI [-0.3%, 0.0%]; p = 0.176) for men. The adjusted HR was 1.13 (95% CI [1.02, 1.24]; p = 0.014) for women and 0.85 (95% CI [0.69, 1.05]; p = 0.131) for men. The main limitation of this study was the risk of misclassification of migraine, which could lead to underestimation of the impact of migraine on each outcome.

Conclusions: In this study, we observed that migraine was associated with similarly increased risk of premature ischemic stroke among men and women. For premature MI and hemorrhagic stroke, there may be an increased risk associated with migraine only among women.

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Conflict of interest statement

CHF owns stock in Novo Nordisk. MS is supported by the Novo Nordisk Foundation (grant NNF19OC0054908). The Department of Clinical Epidemiology, Aarhus University, receives funding for other studies in the form of institutional research grants to (and administered by) Aarhus University. None of these studies has any relation to the present study.

Figures

Fig 1
Fig 1. AR of premature MI, ischemic stroke, and hemorrhagic stroke among women with and without migraine and among men with and without migraine (migraine identified by prescriptions).
The 95% CIs illustrated by the shadowed areas. Difference in impact of migraine was evaluated for men and women separately using Gray’s test for the entire follow-up period. For MI and ischemic stroke, the p-value was <0.001 for both women and men. For hemorrhagic stroke, the p-value was 0.001 for women and 0.517 for men. AR, absolute risk; CI, confidence interval; MI, myocardial infarction.

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