OBJECTIVE This study explored leptin concentrations in Prader-Willi syndrom
e (PWS), a genetic disorder characterized by significant obesity and presum
ed hypothalamic dysfunction. The potential interaction of leptin metabolism
with the growth hormone (GH) axis was also studied.
STUDY DESIGN Plasma leptin concentrations and percent body fat were determi
ned by radioimmunoassay and dual energy x-ray absorptionmetry, respectively
, in 23 children with Prader-Willi syndrome and 23 children with exogenous
obesity.
RESULTS Log plasma leptin concentrations were positively correlated with pe
rcentage body fat in PWS (r = 0.844) and exogenous obesity (r = 0.869). Whe
n the regression lines for the two groups were compared, there were no diff
erences in their slopes (P = 0.737) or intercepts (P = 0.701). Administrati
on of recombinant human growth hormone to PWS children for 12 months signif
icantly reduced both percentage body fat and plasma leptin concentrations,
but the relationship of log plasma leptin to percentage body fat was unchan
ged.
CONCLUSIONS Prader-Willi syndrome is not accompanied by deranged leptin con
centrations and there was no evidence of an interaction of the GH axis with
leptin metabolism in these GH-deficient children.