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Fat oxidation in Black and white youth: A metabolic phenotype potentially predisposing Black girls to obesity

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15 Citations (Scopus)

Abstract

Introduction: The prevalence of obesity is higher in Blacks with racial divergence in adiposity in girls starting during adolescence. Our hypothesis is that in Black children, puberty associated increase in fat oxidation is diminished and could play a role in predisposing to fat accretion triggered during puberty. Thus, we examined the relationships between race, pubertal development, and postabsorptive fat oxidation in youth. Subjects and Methods: This was a cross-sectional design of healthy Black (n = 50) and white (n = 51) youth. Resting metabolic rate (RMR) and substrate oxidation rate were measured after an overnight fast with indirect calorimetry. Body composition was measured by dual-energy x-ray absorptiometry. Results and Discussion: Within each race, RMR (kcal/kg fat free mass·min) was lower (puberty effect; P < 0.05) in the pubertal vs. prepubertal group independent of gender. In girls, RMR was lower (race effect; P < 0.05) in Blacks vs. whites. In girls but not boys, Blacks had lower (race effect; P = 0.033) fat oxidation (μmol/kg fat free mass·min) compared with whites independent of pubertal status. Furthermore, the difference in fat oxidation between the prepubertal vs. pubertal groups tended to be greater (puberty x race interaction; P = 0.089) in white girls (3.7 ± 0.5 vs. 6.5 ± 0.5) than in Black girls (3.4 ± 0.6 vs. 4.5 ± 0.5). These data suggest that the lower fat oxidation and RMR during puberty in Black girls could be a risk factor predisposing to obesity. This metabolic phenotype could potentially explain the divergence in adiposity in Black girls during adolescence against the backdrop of an obesogenic environment.

Original languageEnglish
Pages (from-to)4547-4551
Number of pages5
JournalJournal of Clinical Endocrinology and Metabolism
Volume93
Issue number11
DOIs
Publication statusPublished - Nov 2008

Bibliographical note

Funding Information:
This research was funded by Grants R01-HD-27503, K24-HD-01357, and UL1 RR024153 CTSA (previously M01-RR-00084) (to S.A.A.). S.L. is supported by a Junior Faculty Award from the American Diabetes Association.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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