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Hyperinsulinemia in African-American Adolescents Compared With Their American White Peers Despite Similar Insulin Sensitivity

A reflection of upregulated β-cell function?

  1. Tamara S. Hannon, MD1,
  2. Fida Bacha, MD1,
  3. Yan Lin, PHD2 and
  4. Silva A. Arslanian, MD1
  1. 1Division of Pediatric Endocrinology, Metabolism, and Diabetes, Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania
  2. 2Center for Research on Health Care, University of Pittsburgh, Pittsburgh, Pennsylvania
  1. Corresponding author: Tamara S. Hannon, tamara.hannon{at}chp.edu

Abstract

OBJECTIVE—African-American (AA) children are hyperinsulinemic and insulin resistant compared with American white (AW) children. Previously, we demonstrated that insulin secretion relative to insulin sensitivity was ∼75% higher in AA compared with AW children, suggesting that hyperinsulinemia in AA children is not merely a compensatory response to lower insulin sensitivity. The aim of the present investigation was to assess whether glucose-stimulated insulin response is higher in AA versus AW adolescents who have comparable in vivo insulin sensitivity.

RESEARCH DESIGN AND METHODS—The hyperinsulinemic-euglycemic and hyperglycemic clamp techniques were utilized to assess first- and second-phase insulin secretion. Insulin secretion relative to insulin sensitivity was calculated as the glucose disposition index.

RESULTS—AA adolescents compared with their AW peers with comparable insulin sensitivity and body composition had higher first-phase insulin concentrations.

CONCLUSIONS—The quantitative relationship between insulin sensitivity and first-phase insulin appears to differ among AA and AW adolescents.

Footnotes

  • Published ahead of print at http://care.diabetesjournals.org on 16 April 2008.

    Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.

    The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C Section 1734 solely to indicate this fact.

    • Accepted April 9, 2008.
    • Received January 22, 2008.
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This Article

  1. Diabetes Care July 2008 vol. 31 no. 7 1445-1447
  1. All Versions of this Article:
    1. dc08-0116v1
    2. 31/7/1445 most recent
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