Effects of 3 years of lasofoxifene treatment on bone turnover markers in women with postmenopausal osteoporosis

被引:5
作者
Eastell, Richard [1 ]
Reid, David M. [2 ]
Vukicevic, Slobodan [3 ]
Ensrud, Kristine E. [4 ,5 ]
LaCroix, Andrea Z. [6 ]
Thompson, John R. [7 ]
Thompson, David D. [7 ]
Cummings, Steven R. [8 ,9 ]
机构
[1] No Gen Hosp, Ctr Biomed Res, Sheffield S5 7AU, S Yorkshire, England
[2] Univ Aberdeen, Div Appl Med, Aberdeen, Scotland
[3] Univ Zagreb, Sch Med, Ctr Translat & Clin Res, Lab Mineralized Tissue, Zagreb 41001, Croatia
[4] Univ Minnesota, Minneapolis, MN USA
[5] Vet Affairs Med Ctr, Minneapolis, MN USA
[6] Fred Hutchinson Canc Res Ctr, Seattle, WA 98104 USA
[7] Pfizer Global Res & Dev, Groton, CT 06340 USA
[8] Univ Calif San Francisco, San Francisco, CA 94143 USA
[9] Calif Pacific Med Ctr, Res Inst, San Francisco Coordinating Ctr, San Francisco, CA USA
关键词
Osteoporosis; Bone turnover marker; Clinical trial; Treatment; BIOCHEMICAL MARKERS; MINERAL DENSITY; RESORPTION MARKERS; VERTEBRAL FRACTURE; ALENDRONATE; THERAPY; REDUCTION; MG;
D O I
10.1016/j.bone.2012.02.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aims of this study were to describe the changes in bone turnover markers (BTMs) in response to lasofoxifene therapy; to describe the changes in BTMs in the individual; and to examine the relationships between BTM levels on treatment and treatment outcomes. Women (n = 1126) aged 59-80 years with femoral neck or spine bone mineral density T-scores <=-2.5 were randomized to lasofoxifene 0.25 mg/d, 0.5 mg/d, or placebo for 5 years. We measured serum C-telopeptide of type I collagen (CTX) and serum procollagen I N-propeptide (PINP), osteocalcin, and bone alkaline phosphatase (ALP) at baseline and at 1, 3, 6, 12, 24, and 36 months. Lasofoxifene therapy resulted in a decrease in the concentrations of bone resorption and bone formation markers compared with placebo; the decrease was maximal between 6 and 24 months. The effect of lasofoxifene 0.5 mg/d was similar to that of lasofoxifene 0.25 mg/d. The decrease in bone ALP was less than the decreases in CTX, osteocalcin, and PINP. Lasofoxifene therapy 0.5 mg/d resulted in BTM-defined response rates for CTX (decrease in concentration from baseline > 60%), PINP (> 50%), and bone ALP (> 30%) of 35%, 45%, and 43% of women at month 12, respectively, compared with placebo responses of 4%, 4%, and 7%. In contrast, the increase in BMD took longer (50% responded after 36 months of lasofoxifene 0.5 mg/d) and was not as specific (15% of placebo group responded). Bone density change was weakly inversely correlated with change in the concentrations of BTMs. BTMs may prove useful in the monitoring of the response to lasofoxifene treatment for women with postmenopausal osteoporosis early in the course of treatment. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:1135 / 1140
页数:6
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