Questionnaire-based polyexposure assessment outperforms polygenic scores for classification of type 2 diabetes in a multi-ancestry cohort Article Swipe
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· 2022
· Open Access
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· DOI: https://doi.org/10.2337/figshare.21399177.v1
· OA: W4309150649
<p> </p> <p> </p> <p><em>Objective. </em>Environmental exposures may have greater predictive power for type 2 diabetes than polygenic scores (PGS). Studies examining environmental risk factors, however, have included only individuals with European ancestry, limiting the applicability of results. We conducted an exposome-wide association study in the multi-ancestry Personalized Environment and Genes Study to assess the effects of environmental factors on type 2 diabetes. </p> <p><em>Research Design and Methods. </em>Using logistic regression for single-exposure analysis, we identified exposures associated with type 2 diabetes, adjusting for age, body mass index (BMI), household income, and self-reported sex and race. To compare cumulative genetic and environmental effects, we computed an overall clinical score (OCS) as a weighted sum of BMI and prediabetes, hypertension, and high cholesterol and a polyexposure score (PXS) as a weighted sum of 13 environmental variables. Using UK Biobank data, we developed a multi-ancestry PGS and calculated it for participants. </p> <p><em>Results.</em> We found 76 significant associations with type 2 diabetes, including novel associations of asbestos and coal dust exposure. OCS, PXS, and PGS were significantly associated with type 2 diabetes. PXS had moderate power to determine associations, with larger effect size and greater power and reclassification improvement than PGS. For all scores, the results differed by race. </p> <p><em>Conclusions. </em>Our findings in a multi-ancestry cohort elucidate how type 2 diabetes odds can be attributed to clinical, genetic, and environmental factors and emphasize the need for exposome data in disease-risk association studies. Race-based differences in predictive scores highlight the need for genetic and exposome-wide studies in diverse populations. </p>