Diabetes Care
29:51-56,
2006
DOI: 10.2337/diacare.29.01.06.dc05-0952
© 2006 by the American Diabetes Association
Pathophysiology/Complications Original Article |
Racial Differences in Adiponectin in Youth
Relationship to visceral fat and insulin sensitivityv
SoJung Lee, PHD,
Fida Bacha, MD,
Neslihan Gungor, MD and
Silva A. Arslanian, MD
From the Division of Pediatric Endocrinology, Metabolism and Diabetes Mellitus, Weight Management and Wellness Center, Childrens Hospital of Pittsburgh, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania
Address correspondence and reprint requests to Silva A. Arslanian, MD, Childrens Hospital of Pittsburgh, 3705 Fifth Avenue at DeSoto St., Pittsburgh, PA 15213. E-mail: silva.arslanian{at}chp.edu
OBJECTIVEThe purpose of this study was to investigate 1) whether adiponectin is associated with insulin sensitivity independent of visceral adipose tissue in African-American and Caucasian youth and 2) whether adiponectin is associated with racial differences in insulin sensitivity.
RESEARCH DESIGN AND METHODSTotal body fat was measured by dual-energy X-ray absorptiometry and abdominal adipose tissue with computed tomography. Insulin sensitivity was measured by a 3-h hyperinsulinemic-euglycemic clamp.
RESULTSAdiponectin was inversely associated (P < 0.01) with visceral adipose tissue, fasting insulin, and proinsulin and was positively related (P < 0.01) to insulin sensitivity after controlling for Tanner stage and sex independent of race. Stepwise multiple regression revealed that adiponectin was a strong independent predictor of insulin sensitivity, explaining 27% of the variance in insulin sensitivity. When subjects were categorized into tertiles of visceral adipose tissue and further low ( 50th) and high (>50th) adiponectin groups, insulin sensitivity was significantly different across the visceral adipose tissue groups (main effect, P < 0.01) in both races. However, within each visceral adipose tissue group, subjects with high adiponectin had higher insulin sensitivity (main effect, P < 0.05) than subjects with low adiponectin, independent of race. Racial differences in insulin sensitivity remained significant (P < 0.01) after controlling for leptin and visceral adipose tissue but not (P > 0.05) after additional adjustment for adiponectin.
CONCLUSIONSAdiponectin is associated with insulin sensitivity independent of visceral adipose tissue in both African-American and Caucasian youth. Low adiponectin in African-American youth may be a biological marker that predisposes them to a greater risk of insulin resistance.

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Copyright © 2006 by the American Diabetes Association.
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