Hip and non-spine fracture risk reductions differ among antiresorptive agents: evidence from randomised controlled trials

被引:38
作者
Liberman, U. A. [1 ]
Hochberg, M. C.
Geusens, P.
Shah, A.
Lin, J.
Chattopadhyay, A.
Ross, P. D.
机构
[1] Tel Aviv Univ, Sackler Sch Med, Dept Physiol & Pharmacol, Felsenstein Med Res Ctr, IL-69978 Tel Aviv, Israel
[2] Univ Maryland, Sch Med, Dept Med, Div Clin Immunol & Rheumatol, Baltimore, MD 21201 USA
[3] Univ Hasselt, Biomed Res Inst, Diepenbeek, Belgium
[4] Univ Hosp, Maastricht, Netherlands
[5] Merck & Co Inc, Merck Res Labs, Rahway, NJ 07065 USA
关键词
osteoporosis; antiresorptive therapy; fracture; alendronate; risedronate; ibandronate; raloxifene; hormone therapy;
D O I
10.1111/j.1742-1241.2006.01148.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A number of antiresorptive agents reduce the risk of vertebral fractures, but few have shown consistent effects on hip and other non-spine fractures. Meta-analysis provides a more precise estimate than individual trials when results are consistent across pooled trials. Earlier meta-analyses summarised the results for vertebral and non-spine fractures. New data have emerged for hormone therapy (HT), alendronate (ALN), risedronate (RIS) and ibandronate (IBN). We surveyed recent reports of randomised, placebo-controlled trials with non-spine and/or hip fracture data, and used meta-analysis where appropriate to test for heterogeneity and derive pooled estimates. The magnitude of effect on hip fracture appears to be similar to that for non-spine fracture for each drug, but differs among drugs. Based on the current data, ALN reduces the risk of hip and non-spine fracture by 49-55%, HT by 25-36% and RIS by 26-27%. There is insufficient and/or inconsistent evidence of an effect on these fractures for IBN, calcitonin and raloxifene.
引用
收藏
页码:1394 / 1400
页数:7
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