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. 2012 Nov;72(5):704-15.
doi: 10.1002/ana.23555. Epub 2012 Mar 1.

Trans fat, aspirin, and ischemic stroke in postmenopausal women

Sirin Yaemsiri  1 , Souvik Sen, Lesley Tinker, Wayne Rosamond, Sylvia Wassertheil-Smoller, Ka He
Affiliations

Trans fat, aspirin, and ischemic stroke in postmenopausal women

Sirin Yaemsiri et al. Ann Neurol. 2012 Nov.

Abstract

Objective: To examine the associations between dietary fat intake and ischemic stroke among postmenopausal women.

Methods: We conducted a prospective cohort study of 87,025 generally healthy postmenopausal women (age, 50-79 years) enrolled in the Women's Health Initiative Observational Study. Repeated and validated dietary assessments were done using a self-administered food frequency questionnaire. We used Cox proportional hazards models to estimate hazard ratios (HRs) of ischemic stroke based on quintiles of the cumulative average of fat intake.

Results: We documented 1,049 incident cases of ischemic stroke over 663,041 person-years of follow-up. Women in the highest quintile of trans fat intake had a significantly higher incidence of ischemic stroke (HR, 1.39; 95% confidence interval [CI], 1.08-1.79; p-trend = 0.048) compared with women in the lowest quintile, while controlling for multiple covariates. The observed association was modified by aspirin use (p-interaction = 0.02). The HR was 1.66 (95% CI, 1.21-2.36; p-trend < 0.01) among baseline non-aspirin users (n = 67,288) and 0.95 (95% CI, 0.60-1.48; p-trend = 0.43) among aspirin users (n = 19,736). No significant associations were found between intakes of saturated, monounsaturated, or polyunsaturated fat and ischemic stroke or any ischemic stroke subtypes.

Interpretation: In this large cohort of postmenopausal women, higher intake of trans fat was associated with incident ischemic stroke independent of major lifestyle/dietary factors. Aspirin use may attenuate the potential adverse effect of trans fat intake on ischemic stroke.

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Figures

Figure 1
Figure 1
Adjusted hazard ratios (HR) and 95% confidence intervals (CI) for ischemic stroke by quintiles (Q) of trans fat intake among non-aspirin users (A) and aspirin users (B). The P-value for interaction comparing the hazard ratios with interaction present vs. hazard ratios with interaction absent = 0.02. The HRs were adjusted for covariates listed in Table 2.
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