Key result
Oral contraceptive use linked to ~140% higher ischemic stroke risk, exacerbated by high genetic risk.
Why the study?
Vascular risk factors increase oral contraceptive-associated ischemic stroke risk, but whether a genomic risk score for ischemic stroke modifies this risk remains to be evaluated.
Does a genomic risk score modify the risk of ischemic stroke associated with oral contraceptive use in premenopausal women?
Case-Control (n=340)
No
Does a genomic risk score modify the risk of ischemic stroke associated with oral contraceptive use in premenopausal women?
A high genomic risk score may amplify the risk of ischemic stroke associated with oral contraceptive use in premenopausal women, suggesting a potential role for genetic profiling in risk stratification.
May indicate genomic risk modifies OC-stroke association; hypothesis-generating and requires prospective validation before any clinical use.
Background Oral contraceptives (OCs) are generally safe but vascular risk factors increase OC-associated ischemic stroke risk. We performed a case-control study to evaluate whether a genomic risk score for ischemic stroke modifies OC-associated ischemic stroke risk. Methods The Genetics of Early-Onset Stroke (GEOS) study includes 340 premenopausal women (143 ischemic stroke cases and 197 controls) with data on OC use within 30 days before the index event (for cases) or interview (for controls). Using a previously validated genetic risk score (metaGRS) for ischemic stroke based on 19 polygenic risk scores of vascular events and risk factors, we stratified our sample into tertiles of genomic risk. We evaluated the association between OC use and ischemic stroke within each tertile. We tested if the association between OC use and ischemic stroke depended on the genomic risk of stroke using logistic regression with an OC use × metaGRS interaction term. Results Among all women, OC use was significantly associated with ischemic stroke (odds ratio = 2.4, p = 0.002). The odds ratio for ischemic stroke associated with OC use increased from 1.5 in the tertile with the lowest genomic risk to 3.9 in the tertile with the highest genomic risk of ischemic stroke. The formal test of interaction was consistent with our hypothesis (p = 0.07) that the genomic risk score modifies the association of OC use with ischemic stroke. Conclusions Our results suggest that genomic profile modifies the OC-associated ischemic stroke risk. Larger studies are warranted to determine whether a genomic risk score could be clinically useful in reducing OC-associated ischemic stroke.
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Lin et al. (2022) conducted a case-control in Ischemic stroke (n=340). Oral contraceptives vs. No oral contraceptive use was evaluated on Ischemic stroke (OR 2.4, 95% CI 1.4-4.3, p=0.002).
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