Homik J, Cranney A, Shea B, Tugwell P, Wells G, Adachi R, Suarez-Almazor M
Medicine, 562 Heritage Medical Research Centre, University of Alberta, Edmonton, Alberta, Canada, T6G 2S2.
Cochrane Database Syst Rev. 2000(2):CD001347. doi: 10.1002/14651858.CD001347.
To assess the effects of bisphosphonates for the prevention and treatment of corticosteroid-induced osteoporosis.
We searched the Cochrane Musculoskeletal Group trials register, Medline up to 1997 and Embase1988-1997), and selected hand searching of reference lists was conducted. Hand searching of scientific abstracts from relevant meetings for the last five years was also done. An electronic search in Current Contents was done for the last six months. The Cochrane Controlled Trials Register (CCTR) will be searched for future updates. All languages were included in the search. For practical reasons only those in English were included, but all languages will be retrieved and translated for future updates.
All controlled clinical trials (CCTs) dealing with prevention or treatment of corticosteroid-induced osteoporosis with bisphosphonates of any type and reporting the outcomes of interest were assessed. Trials had to involve adults only, and subjects had to be taking a mean steroid dose of 7.5 mg/day or more.
All data extraction was performed by two independent reviewers. Outcomes of interest included change in bone mineral density (BMD) at the lumbar spine and femoral neck at six and 12 months. If present, data on number of new fractures and withdrawals due to adverse effects were also extracted. All data extraction was performed by two independent reviewers. Both continuous and dichotomous data were analyzed using fixed effects models. When significant heterogeneity was present, a random effects model was used.
A total of 13 trials, including 842 patients are included in this meta-analysis. Results are reported as a weighted mean difference of the percent change in BMD between the treatment and placebo groups, with trials being weighted by the inverse of their variance. The 95% confidence intervals (95% CI) are presented. At the lumbar spine, the weighted mean difference of BMD between the treatment and placebo groups was 4.3% (95% CI 2.7, 5.9). At the femoral neck, the weighted mean difference was 2.1% (95%CI 0. 01, 3.8). Although there was a 24% reduction in odds of spinal fractures [OR 0.76 (95%CI 0.37, 1.53)], this result was not statistically significant.
REVIEWER'S CONCLUSIONS: Bisphosphonates are effective at preventing and treating corticosteroid-induced bone loss at the lumbar spine and femoral neck. Efficacy regarding fracture prevention cannot be concluded from this analysis, although bone density changes are correlated with fracture risk.
评估双膦酸盐类药物预防和治疗糖皮质激素诱导的骨质疏松症的效果。
我们检索了Cochrane肌肉骨骼组试验注册库、截至1997年的Medline以及1988 - 1997年的Embase,并对手检参考文献列表进行了筛选。还对手检过去五年相关会议的科学摘要进行了检索。对最近六个月的《现刊目次》进行了电子检索。未来更新时将检索Cochrane对照试验注册库(CCTR)。检索纳入所有语言。出于实际原因,本次仅纳入英文文献,但未来更新时将检索并翻译所有语言的文献。
评估所有使用任何类型双膦酸盐类药物预防或治疗糖皮质激素诱导的骨质疏松症并报告相关感兴趣结局的对照临床试验(CCT)。试验必须仅纳入成年人,且受试者平均类固醇剂量必须达到或超过7.5毫克/天。
所有数据提取由两名独立的审阅者进行。感兴趣的结局包括腰椎和股骨颈在6个月和12个月时骨矿物质密度(BMD)的变化。如有相关数据,还提取新骨折数量以及因不良反应退出试验的数量。所有数据提取由两名独立的审阅者进行。连续数据和二分数据均使用固定效应模型进行分析。当存在显著异质性时,使用随机效应模型。
本荟萃分析共纳入13项试验,包括842例患者。结果以治疗组与安慰剂组BMD百分比变化的加权平均差表示,各试验权重为其方差的倒数。给出了95%置信区间(95%CI)。在腰椎,治疗组与安慰剂组BMD的加权平均差为4.3%(95%CI 2.7,5.9)。在股骨颈,加权平均差为2.1%(95%CI 0.01,3.8)。尽管脊柱骨折的比值比降低了24%[比值比0.76(95%CI 0.37,1.53)],但该结果无统计学意义。
双膦酸盐类药物在预防和治疗糖皮质激素诱导的腰椎和股骨颈骨质流失方面有效。尽管骨密度变化与骨折风险相关,但本次分析无法得出其预防骨折的疗效结论。