AIM: To evaluate whether fat distribution plays a role in determining serum
leptin concentrations.
PATIENTS AND METHODS: One-hundred and forty-seven obese patients, 77 males
and 70 females, aged 45.1 +/- 13.2 y (mean +/- s.d.; range 21 - 73 y), with
body mass index (BMI) ranging from 30 to 55 kg/m(2) (mean 42.3 +/- 5.9). U
ltrasound assessment of the thickness of subcutaneous and preperitoneal far
was carried out and calculation of their ratio as abdominal fat index (AFI
), waist-hip ratio (WHR), body composition by bioelectrical impedance to ev
aluate the percentage of fat mass (FM%) and total amount of fat (FMKg) were
also determined. Plasma leptin was measured by radio immune assay (RIA).
RESULTS: In the whole group of patients, serum leptin concentrations were 3
7.2 +/- 18.4 ng/ml (range 6-101.3 ng/ml); in spite of BMI values not being
significantly different, women had leptin values significantly higher (47.4
+/- 17.4 ng/ml) (P < 0.01) than males (28.1 +/- 15.1 ng/ml), also after co
rrection for fat mass. The mean thickness of abdominal subcutaneous fat was
33.7 +/- 12.9 mm and it was significantly (P < 0.001) higher in female (40
.9 +/- 10.6 mm) than in male (27.1 +/- 11.2 mm) patients; preperitoneal thi
ckness was 22.9 +/- 7.1 mm, with significantly (P < 0.05) higher values in
males (24.2 +/- 6.8 mm) than in females (21.7 +/- 7.3 mm). Accordingly, AFI
tin all patients 0.84 +/- 0.6) was significantly higher in males (1.09 +/-
0.6) than in females (0.56 +/- 0.2). In the overall population, leptin con
centrations were directly and significantly related to subcutaneous but not
preperitoneal fat; they showed a strong inverse relationship with AFI and
WHR, When the results were evaluated dividing the patients according to gen
der, subcutaneous fat thickness showed a stronger association with leptin l
evels in males than in females, whereas no association was found with prepe
ritoneal fat thickness. Leptin and AFI values were significantly related on
ly in men. WHR values were not correlated with leptin concentrations in eit
her sex. When fat mass was added to the model, subcutaneous fat thickness,
AFI and WHR remained independently associated with leptin concentrations. A
ge and diabetes did not influence these measures.
CONCLUSIONS: Fat distribution contributes to the variability in serum lepti
n in obese patients. In particular, subcutaneous abdominal fat is a determi
nant of leptin concentration, also independently of the amount of fat mass,
whereas the contribution of preperitoneal visceral fat is not significant.