Questionnaire-Based Polyexposure Assessment Outperforms Polygenic Scores for Classification of Type 2 Diabetes in a Multiancestry Cohort

Author:

Akhtari Farida S.12,Lloyd Dillon1,Burkholder Adam3,Tong Xiaoran1,House John S.1,Lee Eunice Y.1,Buse John4,Schurman Shepherd H.2,Fargo David C.3,Schmitt Charles P.5,Hall Janet2,Motsinger-Reif Alison A.1ORCID

Affiliation:

1. 1Biostatistics & Computational Biology Branch, National Institute of Environmental Health Sciences, Durham, NC

2. 2Clinical Research Branch, National Institute of Environmental Health Sciences, Durham, NC

3. 3Office of the Director, National Institute of Environmental Health Sciences, Durham, NC

4. 4Department of Medicine, University of North Carolina, Chapel Hill, NC

5. 5Office of Data Science, National Institute of Environmental Health Science, Durham, NC

Abstract

OBJECTIVE 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 multiancestry Personalized Environment and Genes Study to assess the effects of environmental factors on type 2 diabetes. RESEARCH DESIGN AND METHODS Using logistic regression for single-exposure analysis, we identified exposures associated with type 2 diabetes, adjusting for age, 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 status and a polyexposure score (PXS) as a weighted sum of 13 environmental variables. Using UK Biobank data, we developed a multiancestry PGS and calculated it for participants. RESULTS 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. CONCLUSIONS Our findings in a multiancestry 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.

Funder

National Institute of Environmental Health Sciences

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

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