Effects of continuous combined hormone replacement therapy and clodronate on bone mineral density in osteoporotic postmenopausal women: A 5-year follow-up

被引:11
作者
Tuppurainen, Marjo [1 ,2 ]
Harma, Kirsi [3 ]
Komulainen, Marja [1 ]
Kiviniemi, Vesa [4 ]
Kroger, Heikki [2 ,5 ,6 ]
Honkanen, Risto [2 ]
Alhava, Esko [7 ]
Jurvelin, Jukka [8 ]
Saarikoski, Seppo [1 ]
机构
[1] Kuopio Univ Hosp, Dept Obstet & Gynecol, FIN-70211 Kuopio, Finland
[2] Univ Eastern Finland, Bone & Cartilage Res Unit, Clin Res Ctr, Kuopio, Finland
[3] Cent Hosp S Karelia, Lappeenranta, Finland
[4] Univ Eastern Finland, IT Ctr, Kuopio, Finland
[5] Kuopio Univ Hosp, Dept Orthoped, FIN-70211 Kuopio, Finland
[6] Kuopio Univ Hosp, Dept Traumatol & Handsurg, FIN-70211 Kuopio, Finland
[7] Univ Eastern Finland, Inst Clin Med, Kuopio, Finland
[8] Kuopio Univ Hosp, Dept Clin Physiol & Nucl Med, FIN-70211 Kuopio, Finland
关键词
HRT; Clodronate; Menopause; BMD; Osteoporosis; RANDOMIZED CONTROLLED-TRIAL; ELDERLY-WOMEN; FRACTURE RISK; DOUBLE-BLIND; ALENDRONATE; ESTROGEN; METAANALYSIS; COMBINATION; PREVENTION; TURNOVER;
D O I
10.1016/j.maturitas.2010.04.013
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
030301 [社会学]; 100201 [内科学];
摘要
Objective: To determine the effects of HRT with or without clodronate on bone mineral density (BMD) change and bone turnover markers. Design: Prospective, partly randomized trial. Setting: Kuopio University Hospital, Finland. Population: 167 osteoporotic women (61 +/- 2.7 years; T-score <= -2.5 SD). Methods: Estradiol 2 mg + NETA 1 mg, randomization to additional 800 mg clodronate (n = 55, HT + C-group) or placebo (n = 55, HT-group); if contraindications to HRT, clodronate (n = 57, C-group). Main outcome measures: BMD by DXA after 1,3 and 5 years, serum osteocalcin (OC) and bone-specific alkaline phosphatase (BAP) at the baseline and after 3 years. Results: After 5 years, adjusted lumbar BMD increased by 4.2% in the HT-group and 3.7% in the HT + C-group. The C-group showed a decrease of -1.1%, the total difference being 5.3% and 4.8% between HT, HT + C vs. C-group, respectively (p < 0.001). In the femoral neck, the adjusted 5-year BMD benefit was 1.3% and 2.4% in the HT- and HT + C-groups, respectively, the net loss of BMD in the C-group was -3.3% (p < 0.05 between HT + C vs. C). By 3 years, DC decreased by 55.0%, 70.3% and 53.8% in the HT-, HT + C and C-groups, respectively (p < 0.001 vs. baseline). The significant decreases of BAP were 39.4% in the HT-group, 42.1% in the HT + C-group and 30.2% in the C-group with no significant differences between the groups after adjustments. Conclusions: In postmenopausal women with osteoporosis, HRT increased spinal and femoral BMD, but the combination of HRT and clodronate did not offer an extra gain of bone mass. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:423 / 430
页数:8
相关论文
共 36 条
[1]
Effects of conjugated, equine estrogen in postmenopausal women with hysterectomy - The women's health initiative randomized controlled trial [J].
Anderson, GL ;
Limacher, M ;
Assaf, AR ;
Bassford, T ;
Beresford, SAA ;
Black, H ;
Bonds, D ;
Brunner, R ;
Brzyski, R ;
Caan, B ;
Chlebowski, R ;
Curb, D ;
Gass, M ;
Hays, J ;
Heiss, G ;
Hendrix, S ;
Howard, BV ;
Hsia, J ;
Hubbell, A ;
Jackson, R ;
Johnson, KC ;
Judd, H ;
Kotchen, JM ;
Kuller, L ;
LaCroix, AZ ;
Lane, D ;
Langer, RD ;
Lasser, N ;
Lewis, CE ;
Manson, J ;
Margolis, K ;
Ockene, J ;
O'Sullivan, MJ ;
Phillips, L ;
Prentice, RL ;
Ritenbaugh, C ;
Robbins, J ;
Rossouw, JE ;
Sarto, G ;
Stefanick, ML ;
Van Horn, L ;
Wactawski-Wende, J ;
Wallace, R ;
Wassertheil-Smoller, S .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2004, 291 (14) :1701-1712
[2]
Two to three years of hormone replacement treatment in healthy women have long-term preventive effects on bone mass and osteoporotic fractures:: the PERF study [J].
Bagger, YZ ;
Tankó, LB ;
Alexandersen, P ;
Hansen, HB ;
Mollgaard, A ;
Ravn, P ;
Qvist, P ;
Kanis, JA ;
Christiansen, C .
BONE, 2004, 34 (04) :728-735
[3]
Fracture incidence in relation to the pattern of use of hormone therapy in postmenopausal women [J].
Banks, E ;
Beral, V ;
Reeves, G ;
Balkwill, A ;
Barnes, I .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2004, 291 (18) :2212-2220
[4]
Alendronate and estrogen effects in postmenopausal women with low bone mineral density [J].
Bone, HG ;
Greenspan, SL ;
McKeever, C ;
Bell, N ;
Davidson, M ;
Downs, RW ;
Emkey, R ;
Meunier, PJ ;
Miller, SS ;
Mulloy, AL ;
Recker, RR ;
Weiss, SR ;
Heyden, N ;
Musliner, T ;
Suryawanshi, S ;
Yates, AJ ;
Lombardi, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (02) :720-726
[5]
CAMBAGGIANI M, 2008, MATURITAS, V59, P2
[6]
Hormone replacement therapy and risk of venous thromboembolism in postmenopausal women: systematic review and meta-analysis [J].
Canonico, Marianne ;
Plu-Bureau, Genevieve ;
Lowe, Gordon D. O. ;
Scarabin, Pierre-Yves .
BMJ-BRITISH MEDICAL JOURNAL, 2008, 336 (7655) :1227-+
[7]
The impact of compliance with osteoporosis therapy on fracture rates in actual practice [J].
Caro, JJ ;
Ishak, KJ ;
Huybrechts, KF ;
Raggio, G ;
Naujoks, C .
OSTEOPOROSIS INTERNATIONAL, 2004, 15 (12) :1003-1008
[8]
Effects of estrogen plus progestin on risk of fracture and bone mineral density - The Women's Health Initiative randomized trial [J].
Cauley, JA ;
Robbins, J ;
Chen, Z ;
Cummings, SR ;
Jackson, RD ;
LaCroix, AZ ;
LeBoff, M ;
Lewis, CE ;
McGowan, J ;
Neuner, J ;
Pettinger, M ;
Stefanick, ML ;
Wactawski-Wende, J ;
Watts, NB .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2003, 290 (13) :1729-1738
[9]
Comparison of the effects of raloxifene and low-dose hormone replacement therapy on bone mineral density and bone turnover in the treatment of postmenopausal osteoporosis [J].
Dane, Cem ;
Dane, Banu ;
Cetin, Ahmet ;
Erginbas, Murat .
GYNECOLOGICAL ENDOCRINOLOGY, 2007, 23 (07) :398-403
[10]
Effects of alendronate and hormone replacement therapy, alone and in combination, on bone mass and markers of bone turnover in elderly women with osteoporosis [J].
Eviö, S ;
Tiitinen, A ;
Laitinen, K ;
Ylikorkala, O ;
Välimäki, MJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (02) :626-631