Literature DB >> 22174423

Insulin resistance and excess risk of diabetes in Mexican-Americans: the San Antonio Heart Study.

Carlos Lorenzo1, Helen P Hazuda, Steven M Haffner.   

Abstract

CONTEXT: Mexican-Americans have more diabetes than non-Hispanic whites, but the extent to which insulin resistance and insulin secretion explain the ethnic difference is unknown.
OBJECTIVE: We analyzed selected indices of insulin resistance and secretion for both the ethnic difference and predictive discrimination. DESIGN AND
SETTING: The San Antonio Heart Study is a longitudinal population-based study with a follow-up period of 7.5 yr. PARTICIPANTS: A total of 1540 nondiabetic individuals aged 25-64 yr were enrolled from January 1984 to December 1988.
INTERVENTIONS: Homeostasis model assessment (HOMA) of insulin resistance and secretion were estimated by available formulas (HOMA-IR and HOMA β-cell) and computer program (HOMA2S and HOMA2B). Matsuda index and insulinogenic index from 0 to 30 and 0 to 120 min (ΔI0-30/ΔG0-30 and ΔI0-120/ΔG0-120) were also calculated. MAIN OUTCOME MEASURE: Incident diabetes was defined by the 2003 American Diabetes Association criteria.
RESULTS: Incident diabetes was in excess in Mexican-Americans [odds ratio 2.26 (95% confidence interval, 1.53-3.34)]. Matsuda index explained a larger proportion of the ethnic difference than did HOMA-IR (49.2 vs. 31.0%; P<0.001). The ethnic difference was not explained by measures of insulin secretion. Matsuda index and ΔI0-30/ΔG0-30 had a better predictive discrimination than their HOMA equivalents and ΔI0-120/ΔG0-120. HOMA estimates by the computer program offered no advantage over simple formulas for HOMA.
CONCLUSIONS: Insulin resistance accounts for a large and significant proportion of the excess risk of diabetes in Mexican-Americans. Matsuda index is better than HOMA-IR for both explaining the ethnic difference and predicting diabetes.

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Year:  2011        PMID: 22174423      PMCID: PMC3319206          DOI: 10.1210/jc.2011-2272

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


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