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Utility of Diabetes Type-Specific Genetic Risk Scores for the Classification of Diabetes Type Among Multiethnic Youth.

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posted on 2025-08-01, 14:31 authored by RA Oram, SA Sharp, C Pihoker, L Ferrat, G Imperatore, A Williams, MJ Redondo, L Wagenknecht, LM Dolan, JM Lawrence, MN Weedon, R D'Agostino, WA Hagopian, J Divers, D Dabelea
OBJECTIVE: Genetic risk scores (GRSs) aid classification of diabetes type in White European adult populations. We aimed to assess the utility of GRS in the classification of diabetes type among racially/ethnically diverse youth in the U.S. RESEARCH DESIGN AND METHODS: We generated type 1 diabetes (T1D)- and type 2 diabetes (T2D)-specific GRSs in 2,045 individuals from the SEARCH for Diabetes in Youth study. We assessed the distribution of genetic risk stratified by diabetes autoantibody positive or negative (DAA+/-) and insulin sensitivity (IS) or insulin resistance (IR) and self-reported race/ethnicity (White, Black, Hispanic, and other). RESULTS: T1D and T2D GRSs were strong independent predictors of etiologic type. The T1D GRS was highest in the DAA+/IS group and lowest in the DAA-/IR group, with the inverse relationship observed with the T2D GRS. Discrimination was similar across all racial/ethnic groups but showed differences in score distribution. Clustering by combined genetic risk showed DAA+/IR and DAA-/IS individuals had a greater probability of T1D than T2D. In DAA- individuals, genetic probability of T1D identified individuals most likely to progress to absolute insulin deficiency. CONCLUSIONS: Diabetes type-specific GRS are consistent predictors of diabetes type across racial/ethnic groups in a U.S. youth cohort, but future work needs to account for differences in GRS distribution by ancestry. T1D and T2D GRS may have particular utility for classification of DAA- children.

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© 2022 by the American Diabetes Association

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This is the author accepted manuscript. The final version is available from the American Diabetes Association via the DOI in this record

Journal

Diabetes Care

Pagination

dc202872-

Publisher

American Diabetes Association

Place published

United States

Version

  • Accepted Manuscript

Language

en

FCD date

2022-07-04T06:52:40Z

FOA date

2022-07-04T06:54:27Z

Citation

Vol. 45(5), pp. 1124–1131

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