EFFECT OF LOW-DOSE OXANDROLONE AND TESTOSTERONE TREATMENT ON THE PITUITARY-TESTICULAR AND GH AXES IN BOYS WITH CONSTITUTIONAL DELAY OF GROWTH AND PUBERTY
Ec. Crowne et al., EFFECT OF LOW-DOSE OXANDROLONE AND TESTOSTERONE TREATMENT ON THE PITUITARY-TESTICULAR AND GH AXES IN BOYS WITH CONSTITUTIONAL DELAY OF GROWTH AND PUBERTY, Clinical endocrinology, 46(2), 1997, pp. 209-216
OBJECTIVE To investigate the effect of low dose oxandrolone and testos
terone on the pituitary-testicular and GH-IGF-I axes. DESIGN Prospecti
ve double-blind placebo-controlled trial. PATIENTS Sixteen boys with c
onstitutional delay of growth and puberty (CDGP) with testicular volum
es 4-6 ml were randomized to 3 months treatment: Group 1 (n=5), daily
placebo: Group 2 (n=5), 2.5 mg oxandrolone daily or Group 3 (n=6), 50
mg testosterone monthly intramuscular injections with assessment (grow
th, pubertal development and overnight hormone profiles) at 0, 3, 6 an
d 12 months.MAIN OUTCOME MEASURES LH and GH profiles (15-minute sample
s) were analysed by peak detection (Pulsar), Fourier transformation an
d autocorrelation. Testosterone levels were measured hourly and insuli
n, SHBG, IGF-I, and IGFBP-3 levels at 0800 h. Statistical analysis was
by multivariate analysis of variance for repeated measures. RESULTS L
H and testosterone parameters increased significantly with time in all
16 (LH AUG, P < 0.001; peak amplitude, P = 0.02; number of peaks, P =
0.02; testosterone AUC, P = 0.02; morning testosterone, P = 0.002). I
n Group 2, however, LH and testosterone parameters decreased at 3 mont
hs followed by a rebound increase at 6 and 12 months. SHBG levels were
markedly reduced at 3 months (P = 0.006) and a wider range of dominan
t GH frequencies was present although GH AUC was not increased until 6
months, with an increase in GH pulse frequency but not amplitude. IGF
-I levels were increased at both 3 and 12 months. In Group 3, pituitar
y-testicular suppression was not apparent, but GH levels increased wit
h an increase in GH amplitude at 3 and 12 months. CONCLUSION Oxandrolo
ne transiently suppressed the pituitary-testicular axis and altered GH
pulsatility. Testosterone increased GH via amplitude modulation.