Wj. Canovatchel et al., LUTEINIZING-HORMONE PULSATILITY IN SUBJECTS WITH 5-ALPHA-REDUCTASE DEFICIENCY AND DECREASED DIHYDROTESTOSTERONE PRODUCTION, The Journal of clinical endocrinology and metabolism, 78(4), 1994, pp. 916-921
The pattern of LH pulsatility in male pseudohermaphrodites with inheri
ted 5 alpha-reductase-2 deficiency (5 alpha RD) and decreased levels o
f plasma dihydrotestosterone was compared to that in normal males. Ana
lysis of 10-min plasma LH sampling during either a 10- or 24-h period
demonstrated that the subjects with 5 alpha RD had 1) a mean plasma LH
level, mean LH pulse amplitude, and mean plasma LH nadir that were ap
proximately twice normal; and 2) a mean LH pulse frequency similar to
that in normal males, whether described as pulses per h or pulses per
study period. An increased plasma LH response to GnRH administration w
as also noted. The findings suggest that a deficiency of DHT results i
n decreased negative feedback at the level of the hypothalamus and/or
pituitary, resulting in an increase in mean plasma LH, LH pulse amplit
ude, and LH responsiveness to GnRH. In response to increased LH, mean
plasma testosterone (T), free T, and plasma estradiol (E(2)) are incre
ased. The pulse amplitude is increased despite elevated plasma T and E
(2) levels; this underscores the importance of DHT in pulse amplitude
regulation. LH pulse frequency is not decreased despite elevated plasm
a T and E(2), raising the possibility that DHT deficiency increased pu
lse frequency that was normalized by increased T and/or E(2) In conclu
sion, studies of LH pulsatility in subjects with 5 alpha RD suggest a
role for DHT in the modulation of LH.