Maturitas 27 (1997) 171 – 177
Changes in bone collagen markers and in bone density in
hormone treated and untreated postmenopausal women
M. Brincat *, R. Galea, Y. Muscat Baron, A. Xuereb
Department of Obstetrics and Gynaecology, St Luke’s Hospital Medical School, Uniersity of Malta, Gwarda Mangia, Malta
Received 17 October 1996; received in revised form 3 February 1997; accepted 10 February 1997
Abstract
Objectie: This study aims to compare bone mineral density measurements (BMD), pyridinium crosslink levels and
pyridinium crosslink levels in untreated and hormone treated postmenopausal women. Methods: A cross-sectional
study comparing biophysical (BMD) and biochemical (pyridinium crosslink and PCICP) parameters in a group of
untreated postmenopausal women (n =145) to a group of postmenopausal women on hormone replacement therapy
(HRT) (n =92). Results: Untreated postmenopausal women compared to postmenopausal women on HRT had
higher Osteoblastic and Osteoclastic activity. Procollagen I C-end terminal peptide (PCICP) was 11.3% lower in the
women on HRT compared to controls whilst crosslinks were 27.2% lower than in controls. This seems to indicate that
women on HRT had a bone balance that was higher compared to the control group (15.9%). The difference in bone
density of L2–L4 between the two groups was (16.1%). Conclusions: This study seems to indicate that post-
menopausal women receiving HRT readjust their bone remodelling so that although osteoblastic function is reduced,
there is a much greater deduction in osteoclastic function and this results in an overall higher bone mass observed in
the BMD of women on HRT. © 1997 Elsevier Science Ireland Ltd.
Keywords: Biochemical parameters; Biophysical parameters; Treated menopausal women; Untreated menopausal
women
1. Introduction
The menopause with its associated hypoestro-
genism is being seen as having multisystemic ef-
fects. The short term symptoms such as flushes,
sweats, anxiety and irritability are readily iden-
* Corresponding author. Tel.: +356 223035; fax: +356
235638.
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