Publication

Evidence of Reduced -Cell Function in Asian Indians With Mild Dysglycemia

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Last modified
  • 02/20/2025
Type of Material
Authors
    Lisa Staimez, Emory UniversityMary Weber, Emory UniversityHarish Ranjani, Madras Diabetes Research FoundationMohammed Ali, Emory UniversityJustin B. Echouffo-Tcheugui, Emory UniversityLawrence Phillips, Emory UniversityViswanathan Mohan, Madras Diabetes Research FoundationKabayam Venkat Narayan, Emory University
Language
  • English
Date
  • 2013-09-01
Publisher
  • American Diabetes Association
Publication Version
Copyright Statement
  • © 2013 by the American Diabetes Association.
License
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 0149-5992
Volume
  • 36
Issue
  • 9
Start Page
  • 2772
End Page
  • 2778
Grant/Funding Information
  • This project also was supported by Emory Global Health Institute, Molecules to Humankind Program sponsored by the Burroughs Wellcome Fund (L.R.S), the National Institutes of Health T32 grant (5T32DK007298-33 to M.B.W), VA award HSR&D IIR 07-138 (L.S.P. and K.M.V.N.), and Cystic Fibrosis Foundation award PHILLI12A0 (L.S.P.).
  • The project is supported by a BRiDGES grant from the International Diabetes Federation. BRiDGES, an International Diabetes Federation project, is supported by an educational grant from Lilly Diabetes.
Abstract
  • OBJECTIVE-To examine β-cell function across a spectrum of glycemia among Asian Indians, a population experiencing type 2 diabetes development at young ages despite low BMI. RESEARCH DESIGN AND METHODS-One-thousand two-hundred sixty-four individuals without known diabetes in the Diabetes Community Lifestyle Improvement Program in Chennai, India, had a 75-g oral glucose tolerance test,with glucose and insulinmeasured at 0, 30, and 120 min. Type 2 diabetes, isolated impaired fasting glucose (iIFG), isolated impaired glucose tolerance (iIGT), combined impaired fasting glucose and impaired glucose tolerance, and normal glucose tolerance (NGT) were defined by American Diabetes Association guidelines. Measures included insulin resistance and sensitivity (homeostasis model assessment of insulin resistance [HOMA-IR], modified Matsuda Index, 1/fasting insulin) and β-cell function (oral disposition index = [Δinsulin0-30/Δglucose0-30] × [1/fasting insulin]). RESULTS-Mean age was 44.2 years (SD, 9.3) and BMI 27.4 kg/m 2 (SD, 3.8); 341 individuals had NGT, 672 had iIFG, IGT, or IFG plus IGT, and 251 had diabetes. Patterns of insulin resistance or sensitivity were similar across glycemic categories. With mild dysglycemia, the absolute differences in age- and sex-adjusted oral disposition index (NGT vs. iIFG, 38%; NGT vs. iIGT, 32%) were greater than the differences in HOMA-IR (NGT vs. iIFG, 25%; NGT vs. iIGT, 23%; each P < 0.0001). Compared with NGT and adjusted for age, sex, BMI, waist circumference, and family history, the odds of mild dysglycemia were more significant per SD of oral disposition index (iIFG: odds ratio [OR], 0.36; 95% CI, 0.23-0.55; iIGT: OR, 0.37; 95% CI, 0.24-0.56) than per SD of HOMA-IR (iIFG: OR, 1.69; 95% CI, 1.23-2.33; iIGT: OR, 1.53; 95% CI, 1.11-2.11). CONCLUSIONS-Asian Indians with mild dysglycemia have reduced β-cell function, regardless of age, adiposity, insulin sensitivity, or family history. Strategies in diabetes prevention should minimize loss of β-cell function.
Author Notes
  • L.R.S. analyzed data, wrote the manuscript, drafted tables and figures, and reviewed and revised the manuscript. M.B.W. and H.R. researched data and reviewed and revised the manuscript.
Keywords
Research Categories
  • Health Sciences, Public Health
  • Health Sciences, Epidemiology
  • Health Sciences, Immunology

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