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Variation in maturity-onset diabetes of the young genes influence response to interventions for diabetes prevention

Billings, Liana K. (author)
Harvard Medical School,Massachusetts General Hospital,NorthShore University HealthSystem
Jablonski, Kathleen A (author)
George Washington University
Warner, A. Sofia (author)
Massachusetts General Hospital
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Cheng, Yu Chien (author)
NorthShore University HealthSystem,University of Chicago
McAteer, Jarred B. (author)
Massachusetts General Hospital
Tipton, Laura (author)
George Washington University
Shuldiner, Alan R. (author)
Ehrmann, David A (author)
University of Chicago
Manning, Alisa K. (author)
Broad Institute,Harvard Medical School,Massachusetts General Hospital
Dabelea, Dana (author)
Colorado School of Public Health
Franks, Paul W. (author)
Lund University,Lunds universitet,Genetisk och molekylär epidemiologi,Forskargrupper vid Lunds universitet,Genetic and Molecular Epidemiology,Lund University Research Groups
Kahn, Steven E (author)
University of Washington
Pollin, Toni I (author)
University of Maryland, Baltimore
Knowler, William C (author)
National Institute of Diabetes and Digestive and Kidney Diseases
Altshuler, David (author)
Harvard Medical School,Broad Institute
Florez, Jose C. (author)
Massachusetts General Hospital,Harvard Medical School,George Washington University,Broad Institute
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 (creator_code:org_t)
 
2017-04-27
2017
English 12 s.
In: Journal of Clinical Endocrinology and Metabolism. - : The Endocrine Society. - 0021-972X .- 1945-7197. ; 102:8, s. 2678-2689
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Context: Variation in genes that cause maturity-onset diabetes of the young (MODY) has been associated with diabetes incidence and glycemic traits. Objectives: This study aimed to determine whether genetic variation in MODY genes leads to differential responses to insulin-sensitizing interventions. Design and Setting: This was a secondary analysis of a multicenter, randomized clinical trial, the Diabetes Prevention Program (DPP), involving 27 US academic institutions. We genotyped 22 missense and 221 common variants in the MODY-causing genes in the participants in the DPP. Participants and Interventions: The study included 2806 genotyped DPP participants randomized to receive intensive lifestyle intervention (n = 935), metformin (n = 927), or placebo (n = 944). Main Outcome Measures: Association of MODY genetic variants with diabetes incidence at a median of 3 years and measures of 1-year β-Cell function, insulinogenic index, and oral disposition index. Analyses were stratified by treatment group for significant single-nucleotide polymorphism 3 treatment interaction (Pint, 0.05). Sequence kernel association tests examined the association between an aggregate of rare missense variants and insulinogenic traits. Results: After 1 year, the minor allele of rs3212185 (HNF4A) was associated with improved β-Cell function in the metformin and lifestyle groups but not the placebo group; the minor allele of rs6719578 (NEUROD1) was associated with an increase in insulin secretion in the metformin group but not in the placebo and lifestyle groups. Conclusions: These results provide evidence that genetic variation among MODY genes may influence response to insulin-sensitizing interventions.

Subject headings

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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