Ga. Young et al., INCREASED PLASMA LEPTIN FAT RATIO IN PATIENTS WITH CHRONIC-RENAL-FAILURE - A CAUSE OF MALNUTRITION/, Nephrology, dialysis, transplantation, 12(11), 1997, pp. 2318-2323
Background. Protein-energy malnutrition occurs in patients with chroni
c renal failure primarily due to loss of appetite. The ob gene protein
, leptin, which is secreted by adipocytes, regulates body composition
by lowering food intake. We have measured plasma leptin in undialysed
and dialysed patients and in controls and the concentrations have been
related to body composition, dietary intake, and biochemistry. Method
s. Plasma leptin was measured by radioimmunoassay in 93 individuals in
groups of undialysed, peritoneal dialysed, and haemodialysed patients
and controls. Body composition was determined by DEXA. Results. Prote
in-energy malnutrition was evident in non-dialysed and dialysed patien
ts from low lean or fat tissues, plasma albumin and transferrin. A thi
rd of the dialysis patients were eating less than prescribed intakes.
Leptin relative to total fat mass (ng/ml/kg) was significantly greater
for patients than for controls, particularly the dialysed patients. L
eptin was highly correlated with total, arm, leg, and all other fat me
asurements, e.g. r for leptin vs% total fat was: undialysed 0.88, PD 0
.81, HD 0.93, and controls 0.83 (P < 0.0001 for all). Dialysis patient
s with the highest leptin/fat mass ratio had low protein intakes and s
ignificantly lower lean tissue mass. Leptin/fat ratio correlated inver
sely with dietary intake e.g, with protein intake in g/day and margina
lly in g/kg of ideal weight/day. Leptin concentration was unrelated to
plasma creatinine or residual renal function or to the protein 'nutri
tional indices', albumin and transferrin. Conclusions. Our data sugges
ts that leptin is markedly increased in some patients with chronic ren
al failure. The association of increased leptin with low protein intak
e and loss of lean tissue is consistent with leptin contributing to ma
lnutrition but a definitive role cannot be substantiated by this study
.