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, hyperten-sion, 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 at-tributed 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. EmR2TaFJ.
Original language | English |
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Pages (from-to) | 929-937 |
Number of pages | 9 |
Journal | Diabetes Care |
Volume | 46 |
Issue number | 5 |
DOIs | |
State | Published - May 2023 |
Bibliographical note
Publisher Copyright:© 2023 by the American Diabetes Association.
Funding
Acknowledgments. The authors would like to thank the PEGS participants for their contributions to this work. The authors would also like to thank the staff at DLH Corporation, namely Samantha Shuptrine, Rebecca Ritter, Nathaniel MacNell, Jamie Glover, Jennifer Emerson, and Nicole Edwards, for their support in creating and maintaining the PEGS cohort and data. Additionally, the authors would like to thank Hannah Collins, National Institute of Environmental Health Sciences, for help with manuscript preparation. Funding. Financial support was received from intramural funds from the National Institutes of Health, National Institute of Environmental Health Sciences.
Funders | Funder number |
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National Institutes of Health (NIH) | |
National Institutes of Health/National Institute of Environmental Health Sciences |
ASJC Scopus subject areas
- Internal Medicine
- Endocrinology, Diabetes and Metabolism
- Advanced and Specialized Nursing