Recent animal studies indicate that leptin is involved in the regulation of
blood pressure through the leptin receptor. Therefore, 51-yr-old men (N =
284) were selected; and anthropometric, endocrine, metabolic, and hemodynam
ic variables were examined in relation to polymorphisms of the leptin recep
tor gene (LEPR), by restriction fragment length polymorphism technique.
Three polymorphisms mere examined: Lys109Arg in exon 4, Gln223Arg in exon 6
, and Lys656Asn in exon 14. In comparison with Lys109 homozygotes, Arg109 h
omozygotes (9%) showed lower body mass index (BMI) and abdominal sagittal d
iameter, as well as lower systolic (10.0 mm Hg) and diastolic (7.8 mm Hg) b
lood pressure. Additionally, Arg223 homozygotes (26.8%) showed lower blood
pressure (7.6/5.7 mm Hg) than Gln223 homozygotes. These lower blood pressur
e levels were independent of other variables. No differences were found wit
h the Lys656Asn polymorphism.
Measurements of body fat mass correlated with leptin concentration in Lys10
9 homozygotes and in Lys109 heterozygotes but not in Arg109 homozygotes. Bl
ood pressure correlated with leptin only in men carrying the wild-type alle
le Lys109. With both elevated BMI and leptin, Lys109 homozygotes had higher
blood pressure than the Arg109 homozygous men (12.4/6.9 mm Hg). Men with b
lood pressure greater than or equal to 140/90 mm Hg had, in comparison with
normotensive men, increased BMI and leptin levels, and Lys109 homozygotes
were significantly more prevalent.
These results suggest that leptin is associated with blood pressure regulat
ion in men through the leptin receptor. When BMI and leptin are elevated, i
ncreased blood pressure is found only with the most prevalent LEPR genotype
at codons 109 and 223, whereas variants of this receptor seem to protect f
rom hypertension. This might explain why not all obese men are hypertensive
.