4.7 Article

Metabolic Risk Factors and Type 2 Diabetes Incidence in American Indian Children

期刊

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
卷 101, 期 4, 页码 1437-1444

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ENDOCRINE SOC
DOI: 10.1210/jc.2015-4309

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  1. Intramural Research Program of the National Institute of Diabetes and Digestive and Kidney Diseases

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Context: Data are lacking on how metabolic risk factors during childhood affect the long-term risk of type 2 diabetes. Objectives: Assess four metabolic risk factors as predictors of type 2 diabetes and determine whether the risk differs between younger and older children. Design: In a prospective cohort study conducted between 1965 and 2007, participants were followed for development of diabetes. Baseline measurements included body mass index (BMI), blood pressure, serum cholesterol, and 2-hour plasma glucose after an oral glucose tolerance test. Additional analyses divided subjects into two groups according to baseline age, 5-11 and 12-19 years. Setting: Gila River Indian Community in Arizona. Participants: A total of 5532 nondiabetic Pima Indian children 5-19 years old. Results: A total of 1281 children developed diabetes (median follow-up, 12.4 years). Diabetes incidence was higher in overweight children (BMI >= 85th percentile) than in nonoverweight children. Nonoverweight children had the lowest risk of diabetes (20-year cumulative incidence, 9.5%), whereas overweight children with impaired glucose tolerance (2-hour glucose >= 140 mg/dL) had the highest (79.0%). The relative risk for children with metabolic abnormalities compared with their healthy counterparts was higher in younger children than in older children early in follow-up. BMI and 2-hour glucose were related to incident diabetes in multivariable models (predicted 15-year cumulative incidence for the highest vs lowest quartile was 3.9 and 1.8 times as high for BMI and 2-hour glucose, respectively; P < .001), whereas blood pressure and cholesterol were not. Conclusions: BMI and impaired glucose tolerance in children are strong predictors of type 2 diabetes. Other components of the metabolic syndrome are not.

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