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Increased Genetic Risk for b-Cell Failure Is Associated With b-Cell Function Decline in People With Prediabetes

Billings, Liana K. (författare)
NorthShore University HealthSystem
Jablonski, Kathleen A. (författare)
George Washington University
Pan, Qing (författare)
George Washington University
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Florez, Jose C. (författare)
Harvard Medical School,Massachusetts General Hospital,Broad Institute
Franks, Paul W. (författare)
Lund University,Lunds universitet,Genetisk och molekylär epidemiologi,Forskargrupper vid Lunds universitet,Genetic and Molecular Epidemiology,Lund University Research Groups,Harvard University
Goldberg, Ronald B. (författare)
University of Miami
Hivert, Marie France (författare)
Harvard Pilgrim Health Care Institute,Massachusetts General Hospital
Kahn, Steven E. (författare)
Washington University School of Medicine
Knowler, William C. (författare)
National Institute of Diabetes and Digestive and Kidney Diseases
Lee, Christine G. (författare)
National Institute of Diabetes and Digestive and Kidney Diseases
Merino, Jordi (författare)
Harvard Medical School,Novo Nordisk Foundation Centre for Basic Metabolic Research,Massachusetts General Hospital,Broad Institute
Huerta-Chagoya, Alicia (författare)
Massachusetts General Hospital,Broad Institute
Mercader, Josep M. (författare)
Harvard Medical School,Massachusetts General Hospital,Broad Institute
Raghavan, Sridharan (författare)
University of Colorado School of Medicine,U.S. Department of Veterans Affairs
Shi, Zhuqing (författare)
NorthShore University HealthSystem
Srinivasan, Shylaja (författare)
University of California, San Francisco
Xu, Jianfeng (författare)
NorthShore University HealthSystem
Udler, Miriam S. (författare)
Harvard Medical School,Broad Institute,Massachusetts General Hospital
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 (creator_code:org_t)
2024
2024
Engelska 9 s.
Ingår i: Diabetes. - 0012-1797. ; 73:8, s. 1352-1360
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Partitioned polygenic scores (pPS) have been developed to capture pathophysiologic processes underlying type 2 diabetes (T2D). We investigated the association of T2D pPS with diabetes-related traits and T2D incidence in the Diabetes Prevention Program. We generated five T2D pPS (b-cell, proinsulin, liver/lipid, obesity, lipodystrophy) in 2,647 participants randomized to intensive lifestyle, metformin, or placebo arms. Associations were tested with general linear models and Cox regression with adjustment for age, sex, and principal components. Sensitivity analyses included adjustment for BMI. Higher b-cell pPS was associated with lower insulinogenic index and corrected insulin response at 1-year follow-up with adjustment for baseline measures (effect per pPS SD 20.04, P = 9.6 × 1027, and 28.45 lU/mg, P = 5.6 × 1026, respec-tively) and with increased diabetes incidence with adjustment for BMI at nominal significance (hazard ratio 1.10 per SD, P = 0.035). The liver/lipid pPS was associated with reduced 1-year baseline-adjusted triglyceride levels (effect per SD 24.37, P = 0.001). There was no significant interaction between T2D pPS and randomized groups. The remaining pPS were associated with baseline measures only. We conclude that despite interventions for diabetes prevention, participants with a high genetic burden of the b-cell cluster pPS had worsening in measures of b-cell function.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

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