Journal
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
Volume 98, Issue 5, Pages 2062-2069Publisher
ENDOCRINE SOC
DOI: 10.1210/jc.2012-3492
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Funding
- U.S. Public Health Service [RO1-HD-27503, K24-HD-01357]
- University of Pittsburgh Medical Center
- Clinical and Translational Science Award, National Institutes of Health T32 scholar [UL1-RR-024153, T32-DK-07729]
- Department of Defense [FA7014-09-2-0008]
- Italian Ministry of University and Research [PRIN 2008CJ7CTW_002]
- University of Verona
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Objective: Overweight/obese (OW/OB) African American (AA) adolescents have a more diabetogenic insulin secretion/sensitivity pattern compared with their American white (AW) peers. The present study investigated beta-cell lipotoxicity to test whether increased free fatty acid (FFA) levels result in greater beta-cell dysfunction in AA vs AW OW/OB adolescents. Research Design and Methods: Glucose-stimulated insulin secretion was modeled, from glucose and C-peptide concentrations during a 2-hour hyperglycemic (225 mg/dL) clamp in 22 AA and 24 AW OW/OB adolescents, on 2 occasions after a 12-hour overnight infusion of either normal saline or intralipid (IL) in a random sequence. beta-Cell function relative to insulin sensitivity, the disposition index (DI), was examined during normal saline and IL conditions. Substrate oxidation was evaluated with indirect calorimetry and body composition and abdominal adiposity with dual-energy X-ray absorptiometry and magnetic resonance imaging at L4-L5, respectively. Results: Age, sex, body mass index, total and sc adiposity were similar between racial groups, but visceral adiposity was significantly lower in AAs. During IL infusion, FFAs and fat oxidation increased and insulin sensitivity decreased similarly in AAs and AWs. beta-Cell glucose sensitivity of first and second-phase insulin secretion did not change significantly during IL infusion in either group, but DI in each phase decreased significantly and similarly in AAs and AWs. Conclusions: Overweight/obese AA and AW adolescents respond to an overnight fat infusion with significant declines in insulin sensitivity, DI, and beta-cell function relative to insulin sensitivity, suggestive of beta-cell lipotoxicity. However, contrary to our hypothesis, there does not seem to be a race differential in beta-cell lipotoxicity. Longer durations of FFA elevation may unravel such race-related contrasts.
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