BIOCHEMICAL MARKERS OF BONE METABOLISM IN BENIGN HUMAN OSTEOPETROSIS - A STUDY OF 2 TYPES AT BASE-LINE AND DURING STIMULATION WITH TRIIODOTHYRONINE

Citation
J. Bollerslev et al., BIOCHEMICAL MARKERS OF BONE METABOLISM IN BENIGN HUMAN OSTEOPETROSIS - A STUDY OF 2 TYPES AT BASE-LINE AND DURING STIMULATION WITH TRIIODOTHYRONINE, European journal of endocrinology, 139(1), 1998, pp. 29-35
Citations number
27
Categorie Soggetti
Endocrynology & Metabolism
ISSN journal
08044643
Volume
139
Issue
1
Year of publication
1998
Pages
29 - 35
Database
ISI
SICI code
0804-4643(1998)139:1<29:BMOBMI>2.0.ZU;2-3
Abstract
Biochemical markers of bone remodelling were used to evaluate bone tur nover in two types of autosomal dominant osteopetrosis (ADO) at baseli ne and during stimulation with triiodothyronine (T-3) Eight patients w ith Type I (aged 23-61 years, mean 40.4 years) and nine patients with Type II ADO (aged 20-49 years, mean 32.8 years) were compared with 10 normal controls (aged 22-54 pears, mean 35.4 years), The participants were treated with 100 mu g T-3 daily for 7 days and followed for a tot al of 16 weeks. Serum concentrations of T-3 increased and correspondin g suppression of TSH was observed in all participants. Both formative and resorptive bone markers were normal at baseline. After stimulation with T-3 a significant increase was seen in all groups for the format ive markers used. Secondary increments were observed at the end of the observation period for all groups, indicating activation of bone remo delling. A variety of resorptive markers was assessed, but no differen ces between patients and controls were seen. After stimulation, highly significant responses were found in all parameters in all groups, in accordance with stimulation of existing resorptive cells, However, no secondary increments were seen at the end of the observation period. A more pronounced response was found in crosslinks-related assays. The study demonstrates that it is possible to stimulate bone resorptive an d formative cells with thyroid hormones in both types of ADO. Moreover , it indicates that the remodelling process is activated by a short co urse of T-3 treatment.