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Hormone Replacement Therapy, Calcium and Vitamin D3 Versus Calcium and Vitamin D3 Alone Decreases Markers of Cartilage and Bone Metabolism in Rheumatoid Arthritis: a Randomized Controlled Trial [ISRCTN46523456]

Overview
Publisher Biomed Central
Specialty Rheumatology
Date 2004 Sep 24
PMID 15380045
Citations 3
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Abstract

This study aimed to evaluate the effects of hormone replacement therapy (HRT), known to prevent osteoporosis and fractures, on markers of bone and cartilage metabolism. Furthermore, we assessed whether changes in these markers corresponded to alterations in bone mineral density and radiographic joint destructions in postmenopausal women with rheumatoid arthritis. Eighty-eight women were randomized to receive HRT, calcium, and vitamin D3, or calcium and vitamin D3 alone, for 2 years. Bone turnover was studied by analyzing serum levels of C-terminal telopeptide fragments of type I collagen (CTX-I), C-terminal telopeptide of type I collagen (ICTP), bone sialoprotein, and C-terminal propeptide of type I procollagen (PICP) and cartilage turnover by urinary levels of collagen type II C-telopeptide degradation fragments (CTX-II) and cartilage oligomeric matrix protein (COMP) in serum. Treatment with HRT resulted in decrease in CTX-I (P < 0.001), ICTP (P < 0.001), PICP (P < 0.05), COMP (P < 0.01), and CTX-II (P < 0.05) at 2 years. Reductions in CTX-I, ICTP, and PICP were associated with improved bone mineral density. Of the markers tested, CTX-I reflected bone turnover most sensitively; it was reduced by 53 +/- 6% in the patients receiving HRT. Baseline ICTP (P < 0.001), CTX-II (P < 0.01), and COMP (P < 0.05) correlated with the Larsen score. We suggest that biochemical markers of bone and cartilage turnover may provide a useful tool for assessing novel treatment modalities in arthritis, concerning both joint protection and prevention of osteoporosis.

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References
1.
Larsen A . How to apply Larsen score in evaluating radiographs of rheumatoid arthritis in long-term studies. J Rheumatol. 1995; 22(10):1974-5. View

2.
Hall G, Spector T, Delmas P . Markers of bone metabolism in postmenopausal women with rheumatoid arthritis. Effects of corticosteroids and hormone replacement therapy. Arthritis Rheum. 1995; 38(7):902-6. DOI: 10.1002/art.1780380705. View

3.
Ravn P, Clemmesen B, Riis B, Christiansen C . The effect on bone mass and bone markers of different doses of ibandronate: a new bisphosphonate for prevention and treatment of postmenopausal osteoporosis: a 1-year, randomized, double-blind, placebo-controlled dose-finding study. Bone. 1996; 19(5):527-33. DOI: 10.1016/s8756-3282(96)00229-3. View

4.
Kameda T, Mano H, Yuasa T, Mori Y, Miyazawa K, Shiokawa M . Estrogen inhibits bone resorption by directly inducing apoptosis of the bone-resorbing osteoclasts. J Exp Med. 1997; 186(4):489-95. PMC: 2199029. DOI: 10.1084/jem.186.4.489. View

5.
Riggs B, Khosla S, Melton 3rd L . A unitary model for involutional osteoporosis: estrogen deficiency causes both type I and type II osteoporosis in postmenopausal women and contributes to bone loss in aging men. J Bone Miner Res. 1998; 13(5):763-73. DOI: 10.1359/jbmr.1998.13.5.763. View