In adults, visceral fat accumulation is associated with insulin resistance
and dyslipidemia. The cause-and-effect nature of these relationships is not
clear. The objective of the present study was to determine if similar rela
tionships exist in prepubertal children. Specifically, we determined whethe
r visceral fat was associated with fasting insulin, insulin sensitivity (Si
), serum triglyceride (TG) concentration, or serum HDL cholesterol (HDL-C)
concentration; whether visceral fat or Si was independently related to lipi
ds; and whether ethnicity influenced the relationship between visceral fat
and risk factors. Subjects were 61 prepubertal African-American and Caucasi
an children. Total body fat was determined by dual-energy X-ray absorptiome
try, visceral fat by computed tomography, and insulin sensitivity by the to
lbutamide-modified, frequently sampled intravenous glucose tolerance test w
ith minimal modeling. In multiple linear regression analysis (adjusting for
total fat, sex, and ethnicity), visceral fat was independently related to
TG (P < 0.05) and fasting insulin (P < 0.001), but not S-i (P = 0.425). Tot
al body fat was independently related to Si (P < 0.001). Si was independent
ly related to fasting insulin (P < 0.001) but not to TG or HDL-C (P = 0.941
and 0.201, respectively). S-i in African-Americans was 42% lower than in C
aucasians (0.50 +/- 0.05 vs. 0.86 +/- 0.11 x 10(-5) min(-1).pmol(-1).l, mea
n +/- SE after adjusting for total fat, P < 0.001). Nonetheless, ethnicity
was not independently related to either TG or HDL-C (P = 0.075 and 0.619, r
espectively, after adjusting for total and visceral fat and sex). The slope
s of the relationships of total and visceral fat with risk factors did not
differ with ethnicity. In conclusion, visceral fat appears metabolically un
ique in children, being independently associated with elevated TG and insul
in but not Si. Obese children and African-American children were more insul
in resistant, independent of visceral fat accumulation. Lower Si was associ
ated with higher, faster insulin, but not dyslipidemia. Thus, obesity, visc
eral fat accumulation, and ethnicity in children may confer negative, but i
ndependent, health risks.