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Decreased β-Cell Function in Overweight Latino Children With Impaired Fasting Glucose

  1. Marc J. Weigensberg, MD1,
  2. Geoff D.C. Ball, PHD2,
  3. Gabriel Q. Shaibi, BA2,
  4. Martha L. Cruz, PHD2 and
  5. Michael I. Goran, PHD23
  1. 1Department of Pediatrics, Keck School of Medicine, University of Southern California, Los Angeles, California
  2. 2Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, California
  3. 3Department of Physiology and Biophysics, Keck School of Medicine, University of Southern California, Los Angeles, California
  1. Address correspondence and reprint requests to Michael I. Goran, PhD, 1540 Alcazar St., Room 208-D, Department of Preventive Medicine, University of Southern California, Los Angeles, California 90033. E-mail: goran{at}usc.edu

Abstract

OBJECTIVE—To determine whether overweight Latino children with impaired fasting glucose (IFG) (≥100 mg/dl) have increased insulin resistance or decreased β-cell function compared with those with normal fasting glucose (NFG).

RESEARCH DESIGN AND METHODS—We studied 207 healthy overweight Latino children, aged 8–13 years, with a family history of type 2 diabetes. Fasting and 2-h glucose and insulin were assessed by oral glucose tolerance test. Insulin sensitivity (Si), the acute insulin response to glucose (AIRg), and the disposition index (DI; an index of β-cell function) were determined using the insulin-modified intravenous glucose tolerance test and minimal modeling. Body composition was determined by dual-energy X-ray absorptiometry.

RESULTS—There were no differences in body composition between NFG (n = 182) and IFG (n = 25) children. Compared with children with NFG, children with IFG had higher fasting and 2-h glucose values and higher fasting insulin. After adjusting for covariates, children with IFG had no difference in Si but 15% lower DI than NFG children (2,224 ± 210 vs. 2,613 ± 76, P < 0.05). Multivariate linear regression showed that AIRg and DI, but not Si, were significant predictors of fasting blood glucose.

CONCLUSIONS—In overweight Latino adolescents with a family history of type 2 diabetes, IFG is associated with impaired β-cell function and therefore may identify children likely to be at risk for progression to type 2 diabetes. The actual risk of progression of IFG to type 2 diabetes remains to be determined by prospective longitudinal studies.

Footnotes

  • A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.

    • Accepted July 7, 2005.
    • Received April 13, 2005.
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