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Submitted on November 9, 2005
Accepted on May 16, 2006
Children's Hospital of Pittsburgh, Pennsylvania, Weight Management & Wellness Center and Division of Pediatric Endocrinology, Metabolism and Diabetes Mellitus
* To whom correspondence should be addressed. E-mail: Silva.Arslanian{at}chp.edu.
Objective: Obesity prevalence is higher in African American (AA) vs. American White (AW) youth. Ghrelin is a "hunger" peptide high preprandially and decreases postprandially, and peptide YY (PYY) is a "satiety" hormone increasing after meals. Impaired regulation of ghrelin/PYY may be conducive to obesity. We hypothesized that racial differences in childhood obesity could partly be explained by differences in ghrelin/PYY dynamics.
Research Design and Methods: We investigated: 1) ghrelin suppression/ PYY elevation in response to an oral glucose tolerance test (OGTT) in AA vs. AW, and 2) the relationship of ghrelin and PYY dynamics to insulin sensitivity (IS).
Thirty-three AA and 54 AW prepubertal children underwent an OGTT measuring ghrelin, PYY, glucose, and insulin. Fasting glucose to insulin ratio (GF/IF) was used to assess the relationship of IS to fasting and post OGTT ghrelin and PYY levels.
Results: OGTT-induced suppression in ghrelin (
ghrelin) was lower in AA youth.
ghrelin correlated with GF/IF (r=0.47, P < 0.001) and with
insulin at 30 min (r0.47, P < 0.001). In multiple regression analysis, race (P = 0.013) and GF/IF (P = 0.004) contributed independently to the variance in
ghrelin (R2=0.28, P < 0.001). Fasting and post OGTT PYY levels were lower in AAs and were not related to insulin sensitivity.
Conclusion: The lower suppression of ghrelin in AA, but not the lower PYY levels, correlates with insulinemia and insulin resistance. Less ghrelin suppression and PYY elevation after a meal in black youth could be a potential mechanism of race related differences in hunger/satiety predisposing to risk of obesity.
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