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Parathyroid hormone changes following denosumab treatment in postmenopausal osteoporosis.

Authors :
Makras P
Polyzos SA
Papatheodorou A
Kokkoris P
Chatzifotiadis D
Anastasilakis AD
Source :
Clinical endocrinology [Clin Endocrinol (Oxf)] 2013 Oct; Vol. 79 (4), pp. 499-503. Date of Electronic Publication: 2013 Apr 01.
Publication Year :
2013

Abstract

Objective: Denosumab is a new potent antiresorptive treatment of osteoporosis that can potentially induce a compensatory increase in parathyroid hormone (PTH) levels. We aimed to evaluate the alteration of PTH 1 and 6 months after denosumab's administration with different regimens of calcium and vitamin D (Ca/D) supplementation.<br />Design: Prospective, multicenter, study in a relatively small, heterogeneous sample of postmenopausal women followed for 6 months.<br />Patients: Forty seven postmenopausal women followed in 2 outpatient clinics, requiring onset or continuation of osteoporosis treatment. We administered 1 g calcium carbonate and 800 IU cholecalciferol daily for 6 months (Group A) or the double dose for the first month followed by the 1 g/800 IU Ca/D regimen for the next 5 months (Group B).<br />Measurements: Parathyroid hormone (PTH) alterations between and within groups, and their associations with serum Ca and bone markers.<br />Results: Parathyroid hormone (PTH) levels were significantly higher at month 1 and 6 only in Group A; Ca levels were significantly decreased at month 1 and returned to baseline values at month 6 within the same Group. The mean per cent change between month 1 and baseline for PTH [Δ(PTH1-0 )] was significantly higher in Group A than B (63·5% ± 28·2% vs -3·0% ± 4·7%, P = 0·029). Δ(PTH1-0 ) was correlated with the reciprocal Δ-changes of Ca (rs  = -0·610; P = 0·002) and collagen type I C-terminal telopeptide (rs  = -0·697; P = 0·003) only in Group A.<br />Conclusions: An increase in PTH should be expected, at least following the first administration of denosumab in common clinical practice. The effect of this compensatory onsequence in bone metabolism warrants further investigation.<br /> (© 2013 John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1365-2265
Volume :
79
Issue :
4
Database :
MEDLINE
Journal :
Clinical endocrinology
Publication Type :
Academic Journal
Accession number :
23452098
Full Text :
https://doi.org/10.1111/cen.12188