Kk. Miller et al., DECREASED LEPTIN LEVELS IN NORMAL-WEIGHT WOMEN WITH HYPOTHALAMIC AMENORRHEA - THE EFFECTS OF BODY-COMPOSITION AND NUTRITIONAL INTAKE, The Journal of clinical endocrinology and metabolism, 83(7), 1998, pp. 2309-2312
Leptin is a protein encoded by the ob gene and expressed in adipocytes
. A sensitive marker of nutritional status, leptin is known to correla
te with fat mass and to respond to changes in caloric intake. Leptin m
ay also be an important mediator of reproductive function, as suggeste
d by the effects of leptin infusions to restore ovulatory function in
an animal model of starvation. We hypothesized that leptin levels are
decreased in women with hypothalamic amenorrhea and that leptin may be
a sensitive marker of overall nutritional status in this population.
We, therefore, measured leptin levels and caloric intake in 21 women w
ith hypothalamic amenorrhea (HA) and 30 age-, weight-, and body fat-ma
tched eumenorrheic controls. Age (24 +/- 5 vs. 24 +/- 3 yr), body mass
index (20.6 +/- 1.3 vs. 21.1 +/- 1.5 kg/m(2)), percent ideal body wei
ght (94.9 +/- 5% vs. 96.3 +/- 6.3%), and fat mass (14.2 +/- 3.6 vs. 15
.5 +/- 2.9 kg, determined by dual energy x-ray absortiometry) did not
differ between the groups. Leptin levels were significantly lower in t
he HA subjects compared with those in the controls (7.1 +/- 3.0 vs. 10
.6 +/- 4.9 mu g/L; P = 0.005). Total caloric intake (1768 +/- 335 us.
2215 +/- 571 cal/day; P = 0.003), fat intake (333 +/- 144 vs. 639 +/-
261 cal/day; P < 0.0001), and insulin levels (5.6 +/- 1.2 vs. 7.4 +/-
3.2 mu U/mL; P = 0.015) were lower in the women with HA than in the eu
menorrheic controls. The difference in leptin levels remained signific
ant after controlling for insulin (P = 0.023). These data are the firs
t to demonstrate hypoleptinemia, independent of fat mass, in women wit
h HA. The hypoleptinemia may reflect inadequate calorie intake, fat in
take, and/or other subclinical nutritional disturbances in women with
HA. The mechanism and reproductive consequences of low leptin in this
large population of women remain unknown.