Key result
Higher T2D polygenic risk score linked to ~4% greater ischemic stroke risk across diverse populations.
Why the study?
A higher T2D polygenic risk score has been linked to higher stroke risk, but this relationship had not been comprehensively evaluated in diverse populations.
Does a higher genetic predisposition to Type 2 Diabetes (measured by polygenic risk score) increase the risk of incident stroke in a diverse multiethnic population?
Cohort (n=33,385)
Yes
Does a higher genetic predisposition to Type 2 Diabetes (measured by polygenic risk score) increase the risk of incident stroke in a diverse multiethnic population?
Genetic predisposition to type 2 diabetes, measured by a polygenic risk score, is significantly associated with an increased risk of incident ischemic stroke across diverse racial and ethnic groups, a risk that may be attenuated by diet quality.
Supports T2D PRS in multiethnic stroke risk models; extends prior associations but remains hypothesis-generating.
Introduction: Type 2 diabetes (T2D) is a risk factor for stroke, with large-scale studies suggesting shared genetic susceptibility. A higher T2D polygenic risk score (PRS) has been linked to higher stroke risk, but this relationship has not been comprehensively evaluated in diverse populations. We investigated whether genetic predisposition to T2D is associated with incident stroke in the Multiethnic Cohort Study (MEC) and explored potential effect modification by race/ethnicity, known T2D, smoking status, and diet quality. Methods: We performed a nested cohort study of MEC participants recruited from Hawaii and Los Angeles identifying as Native Hawaiian, Japanese, Hispanic/Latino, Black, and White. Eligible participants were Medicare beneficiaries with hospital discharge data, no baseline history of stroke, and available genotyping data. Genetic predisposition to T2D was quantified using a validated multiethnic T2D PRS, analyzed both continuously and by quartiles. Associations between T2D PRS and incident stroke were assessed using Cox proportional hazards models, adjusting for age, sex, race/ethnicity, BMI, and the first genetic principal components to account for population stratification. Effect modification was evaluated via product terms. Results: Among 33,385 participants (mean age of 67.7±4.4 years; 52.6% female; 7.3% Native Hawaiian, 43.2% Japanese, 16.8% Hispanic/Latino, 10.7% Black, and 22.0% White), 8,502 incident strokes occurred during follow-up (25.5%; mean age of 78.6±7.2 years). Higher T2D PRS was associated with higher risk of ischemic stroke, both continuously (HR 1.04, 95% CI 1.02—1.07, p=0.001) and by quartiles (Q3 HR 1.12, 95% CI 1.05—1.20, p<0.001; Q4 HR 1.13, 95% CI 1.06—1.21, p<0.001; referent category: Q1). Race/ethnicity, smoking status, and diagnosed T2D did not significantly modify this association. Diet quality, measured by the Healthy Eating Index, appeared to attenuate stroke risk among those in intermediate PRS categories (product term p-value=0.02). Conclusions: In a large multiethnic cohort, genetic predisposition to T2D was associated with higher incident stroke risk, regardless of race/ethnicity or clinical diabetes status. Diet quality may mitigate this risk among individuals with intermediate genetic susceptibility. These findings suggest that integrating genetic risk assessment with lifestyle interventions may enhance stroke prevention strategies in diverse populations.
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Brown et al. (2026) conducted a cohort in Incident stroke (n=33,385). Type 2 diabetes polygenic risk score (T2D PRS) vs. Lower T2D PRS was evaluated on Incident ischemic stroke (HR 1.04, 95% CI 1.02-1.07, p=0.001). A higher type 2 diabetes polygenic risk score was continuously associated with an increased risk of ischemic stroke (HR 1.04; 95% CI 1.02-1.07; p=0.001) across diverse populations.
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