Change in Bone Density and Reduction in Fracture Risk: A Meta-Regression of Published Trials

被引:139
作者
Bouxsein, Mary L. [1 ,2 ]
Eastell, Richard [3 ]
Lui, Li-Yung [4 ]
Wu, Lucy A. [5 ]
de Papp, Anne E. [6 ]
Grauer, Andreas [7 ]
Marin, Fernando [8 ]
Cauley, Jane A. [9 ]
Bauer, Douglas C. [5 ,10 ]
Black, Dennis M. [5 ]
机构
[1] Beth Israel Deaconess Med Ctr, Dept Orthoped Surg, Ctr Adv Orthoped Studies, Boston, MA 02215 USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Univ Sheffield, Acad Unit Bone Metab, Sheffield, S Yorkshire, England
[4] Calif Pacific Med Ctr, San Francisco, CA USA
[5] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[6] Merck & Co Inc, Kenilworth, NJ USA
[7] Amgen Inc, Thousand Oaks, CA 91320 USA
[8] Eli Lilly & Co, Lilly Res Ctr, Windlesham, Surrey, England
[9] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Epidemiol, Pittsburgh, PA 15260 USA
[10] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
关键词
BONE MINERAL DENSITY; CLINICAL TRIAL; META-REGRESSION; OSTEOPOROSIS; SURROGATE; JAPANESE POSTMENOPAUSAL WOMEN; CONJUGATED EQUINE ESTROGEN; MINERAL DENSITY; VERTEBRAL FRACTURES; ZOLEDRONIC ACID; RANDOMIZED-TRIAL; DOUBLE-BLIND; ELDERLY-WOMEN; NONVERTEBRAL FRACTURES; ANTIFRACTURE EFFICACY;
D O I
10.1002/jbmr.3641
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Meta-analyses conducted >15 years ago reported that improvements in bone mineral density (BMD) were associated with reduction in vertebral and nonvertebral fractures in osteoporosis trials. Numerous studies have been conducted since then, incorporating new therapies with different mechanisms of action and enrolling many more subjects. To extend these prior analyses, we conducted a meta-regression of 38 placebo-controlled trials of 19 therapeutic agents to determine the association between improvements in BMD and reductions in fracture risk. We used a linear model to examine the relationship between mean percent difference in BMD change between treatment and placebo groups and the logarithm of the relative risk. We found that greater improvements in BMD were strongly associated with greater reductions in vertebral and hip fractures but not nonvertebral fractures. For vertebral fracture, the r(2) values for total hip, femoral neck, and lumbar spine BMD change were 0.56, 0.54, and 0.63, respectively (p <= 0.0002). For a 2% or 6% improvement in total hip BMD, we might expect a 28% or 66% reduction, respectively, in vertebral fracture risk. For hip fracture, the r(2) values for total hip, femoral neck, and lumbar spine BMD change were 0.48 (p = 0.01), 0.42 (p = 0.02), and 0.22 (ns), respectively. For a 2% or 6% improvement in total hip BMD, we might expect a 16% or 40% reduction in hip fracture risk. In conclusion, our results extend prior observations that larger improvements in dual-energy X-ray absorptiometry (DXA)-based BMD are associated with greater reductions in fracture risk, particularly for vertebral and hip fractures. Although these results cannot be directly applied to predict the treatment benefit in an individual patient, they provide compelling evidence that improvements in BMD with osteoporosis therapies may be useful surrogate endpoints for fracture in trials of new therapeutic agents. (c) 2019 American Society for Bone and Mineral Research.
引用
收藏
页码:632 / 642
页数:11
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