This Article Full Text Full Text (PDF) Submit a related Letter to the Editor Alert me when this article is cited Alert me when eLetters are posted Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Request Copyright Permission Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Antoniazzi, F. Articles by Tatò, L. Search for Related Content PubMed PubMed Citation Articles by Antoniazzi, F. Articles by Tatò, L.

Bone Mass at Final Height in Precocious Puberty after Gonadotropin-Releasing Hormone Agonist with and without Calcium Supplementation

Pediatric Clinic (F.A., G.Z., S.L., F.M., A.P., L.T.) and Department of Internal Medicine (F.B.), University of Verona I-37134, Italy

Address all correspondence and requests for reprints to: Dr. Franco Antoniazzi, Pediatric Clinic, University of Verona, Policlinico "Giambattista Rossi," Piazza Ludovico Antonio Scuro, 10, I-37134 Verona, Italy. E-mail: franco.antoniazzi{at}univr.it.

The aim of our longitudinal study was to evaluate bone mass in girls affected by central precocious puberty (CPP) that have reached final height, treated with GnRH agonist triptorelin (GnRHa), with or without calcium supplementation. We studied 48 Caucasian females affected by CPP (age at diagnosis, 7.19 ± 0.96 yr), randomly assigned to two groups: group A (n = 21) treated with GnRHa and group B (n = 27) treated with GnRHa plus calcium gluconolactate and carbonate (1 g calcium/day in two doses) for at least 2 yr. Auxological parameters (standing height, weight, body mass index) and bone mineral density (BMD) at the lumbar spine [L2-L4, anteroposterior (AP)-BMD; lateral BMD; volumetric (v)BMD)] by dual-energy x-ray absorptiometry were evaluated at the beginning [chronological age (CA), 7.29 ± 0.91 yr; bone age (BA), 8.80 ± 1.24 yr] and end of treatment (CA, 11.27 ± 0.97 yr; BA, 12.35 ± 0.43 yr) and at final height (CA, 16.17 ± 1.9 yr; BA, 16.93 ± 0.98 yr, in each case >15 yr). Total bone mineral content, total BMD, and fat percentage were evaluated at the end of the study period using dual-energy x-ray absorptiometry. Final height was significantly higher than predicted height at diagnosis (159.9 ± 6.3 cm vs. 152.9 ± 9.6 cm; P < 0.05). Body mass index and fat percentage were not statistically different from control values. Densitometric values at final evaluation in groups A and B together were lower than in controls, but the differences were not statistically significant. The vBMD was significantly higher in group B than in group A at the end of treatment period (0.213 ± 0.022 g/cm³ vs. 0.192 ± 0.021 g/cm³; P < 0.01) and at final evaluation (0.246 ± 0.023 g/cm³ vs. 0.227 ± 0.024 g/cm³; P < 0.05). The percentage change (%) between the start and end of treatment period in AP-BMD and vBMD was significantly higher in group B than in group A (% AP-BMD: 20.36% ± 1.10% vs. 16.16% ± 1.90%, P < 0.01; % vBMD: 19.08% ± 3.52% vs. 9.26% ± 5.15%; P < 0.01) and also between the start of treatment and final evaluation (% AP-BMD: 61.23% ± 1.61% vs. 56.97% ± 1.45%, P < 0.01; % vBMD: 36.69% ± 5.01% vs. 28.01% ± 5.76%, P < 0.01). In all our females with CPP treated with GnRHa, bone densitometric parameters were in the normal range for age and sex. However, bone mass achievement seemed to be better preserved in the group of patients supplemented with calcium.

Abbreviations: AP-BMD, Anteroposterior bone mineral density; BA, bone age; BMD, bone mineral density; BMI, body mass index; CA, chronological age; CPP, central precocious puberty; %, percentage variation; DXA, dual-energy x-ray absorptiometry; GnRHa, GnRH agonist; L-BMD, lateral BMD; PAH, predicted adult height; PBM, peak bone mass; % FAT, fat percentage; TBMC, total body bone mineral content; TBMD, total BMD; TH, target height; vBMD, volumetric BMD.

This article has been cited by other articles:

				J.-C. Carel, E. A. Eugster, A. Rogol, L. Ghizzoni, M. R. Palmert, and on behalf of the members of the ESPE-LWPES GnRH An Consensus Statement on the Use of Gonadotropin-Releasing Hormone Analogs in Children Pediatrics, April 1, 2009; 123(4): e752 - e762. [Abstract] [Full Text] [PDF]