TY - JOUR
T1 - Preserving adult height potential in girls with idiopathic true precocious puberty
AU - Kreiter, Mary
AU - Burstein, Stephen
AU - Rosenfield, Robert L.
AU - Moll, George W.
AU - Cara, José F.
AU - Yousefzadeh, David K.
AU - Cuttler, Leona
AU - Levitsky, Lynne L.
N1 - Funding Information:
True precocious puberty appears to be caused by premature maturation of the normal hypothalamic-pituitary-gonadal axis. As a consequence, secondary sexual characteristics develop early and skeletal maturation and linear growth accelerate. The only permanent physical sequela of preco- Supported in part by U.S. Public Health Service grants RR-00055 (General Clinical Research Center), NIADDK 07011-15 (M.K.), and HD-06308 (R.L.R.) and in part by Syntex Corporation. Submitted for publication May 23, 1989; accepted April 11, 1990. Reprint requests: Robert L. Rosenfield, MD, Wyler Children's Hospital, Section of Pediatric Endocrinology, 5841 S. Maryland, Box 118, Chicago, IL 60637. 9/20/21523 cious puberty is attenuation of adult stature, and this effect is variable. 1-3 Recently, long-acting gonadotropin releasing hormone agonists have been reported to be effective in ar-
PY - 1990/9
Y1 - 1990/9
N2 - We designed a prospective study of height potential in giris with idiopathic precocious puberty, comparing the presenting features of giris with and without evidence of reduced adult height potential. The 14 giris with impaired adult helght prognoses (group 1) were reexamined after treatment with a gonadotropin releasing hormone agonist, nafarelin. The seven giris with the prognosis of unimpaired height (group 2) were followed without therapy. We found that the group could be distinguished at initial examination by the greater bone age/height age ratio of group 1 (mean ± SEM: 1.4 ± 0.06 vs 1.0 ± 0.05; p <0.005) and by the greater difference between predicted height and target height in group 1. The mean predicted height in group 1 was significantly less than the mean target height (150.7 ± 2.1 vs 165.4 ± 3.0 cm; p<0.005), whereas the mean predicted and target heights in group 2 were similar (165.4 ± 3.0 vs 164.3 ± 2.1 cm). Initial estradiol levels were also greater in group 1 than in group 2 (21.6 vs 10.6 pg/ml; p<0.05), although this difference was not sustained during follow-up. In group 1, nafarelin therapy suppressed the pltuitary-gonadal axis, and although there was a transient reduction in height potential in giris with the youngest bone ages during the first 6 months of therapy, 2 years of treatment slightly improved predicted heights from 150.7 ± 2.1 to 152.7 ± 2.0 cm (p<0.05). Height predictions also increased without therapy during the 2-year observation period in group 2, from 165.4 ± 3.0 to 168.7 ± 4.1 cm (p<0.05). Our data indicate that gonadotropin releasing hormone agonist therapy preserves height potential in giris with an initially impaired height prognosis, and that height potential is preserved without therapy in those with a good initial height prognosis.
AB - We designed a prospective study of height potential in giris with idiopathic precocious puberty, comparing the presenting features of giris with and without evidence of reduced adult height potential. The 14 giris with impaired adult helght prognoses (group 1) were reexamined after treatment with a gonadotropin releasing hormone agonist, nafarelin. The seven giris with the prognosis of unimpaired height (group 2) were followed without therapy. We found that the group could be distinguished at initial examination by the greater bone age/height age ratio of group 1 (mean ± SEM: 1.4 ± 0.06 vs 1.0 ± 0.05; p <0.005) and by the greater difference between predicted height and target height in group 1. The mean predicted height in group 1 was significantly less than the mean target height (150.7 ± 2.1 vs 165.4 ± 3.0 cm; p<0.005), whereas the mean predicted and target heights in group 2 were similar (165.4 ± 3.0 vs 164.3 ± 2.1 cm). Initial estradiol levels were also greater in group 1 than in group 2 (21.6 vs 10.6 pg/ml; p<0.05), although this difference was not sustained during follow-up. In group 1, nafarelin therapy suppressed the pltuitary-gonadal axis, and although there was a transient reduction in height potential in giris with the youngest bone ages during the first 6 months of therapy, 2 years of treatment slightly improved predicted heights from 150.7 ± 2.1 to 152.7 ± 2.0 cm (p<0.05). Height predictions also increased without therapy during the 2-year observation period in group 2, from 165.4 ± 3.0 to 168.7 ± 4.1 cm (p<0.05). Our data indicate that gonadotropin releasing hormone agonist therapy preserves height potential in giris with an initially impaired height prognosis, and that height potential is preserved without therapy in those with a good initial height prognosis.
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U2 - 10.1016/S0022-3476(05)81074-1
DO - 10.1016/S0022-3476(05)81074-1
M3 - Article
C2 - 2144020
AN - SCOPUS:0025143814
SN - 0022-3476
VL - 117
SP - 364
EP - 370
JO - The Journal of pediatrics
JF - The Journal of pediatrics
IS - 3
ER -