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首页> 外文期刊>The American Journal of the Medical Sciences >The association of alpha-blockers and 5-alpha reductase inhibitors in benign prostatic hyperplasia with fractures
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The association of alpha-blockers and 5-alpha reductase inhibitors in benign prostatic hyperplasia with fractures

机译:前列腺增生与骨折中α-受体阻滞剂和5-α-还原酶抑制剂的关系

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摘要

BACKGROUND: Alpha-blockers and 5-alpha reductase inhibitors are common drugs used to treat benign prostatic hyperplasia (BPH), a prevalent problem in older men associated with significant morbidity and cost. Data regarding how these medications affect skeletal health and fracture risk remain scarce. METHODS: Studies were identified by searching PubMed, EMBASE, the Cochrane library and Thomson Reuters Web of Knowledge. Studies involving BPH patients that reported odds ratio (OR) estimates with 95% confidence intervals (CIs) for the association between fractures and exposure to 5-alpha reductase inhibitors or alpha-blockers were included. Pooled ORs were calculated using the random-effects model. RESULTS: Three studies addressed fracture risk in patients exposed to 5-alpha reductase inhibitors (21,366 fracture cases). Four studies addressed fracture risk in patients exposed to alpha-blockers (22,051 fracture cases). The pooled OR for fractures with 5-alpha reductase inhibitor use was 0.9 (95% CI = 0.7-1.1). For hip/femur fractures with 5-alpha reductase inhibitor use, the pooled OR was 0.8 (95% CI = 0.7-1.0). The pooled OR for fractures with alpha-blockers was 1.1 (95% CI = 0.9-1.3). There was significant statistical heterogeneity among studies for alpha-blockers. CONCLUSIONS: In patients with BPH, exposure to 5-alpha reductase inhibitors was not associated with change in fracture risk. The 5-alpha reductase inhibitors may have a small protective effect against hip/femur fractures although this was not statistically significant. Although alpha-blockers were not associated with change in fracture risk, caution is required when interpreting the results as significant heterogeneity was present.
机译:背景:α受体阻滞剂和5-α还原酶抑制剂是用于治疗良性前列腺增生(BPH)的常见药物,BPH是老年男性中普遍存在的问题,与较高的发病率和成本相关。关于这些药物如何影响骨骼健康和骨折风险的数据仍然很少。方法:通过搜索PubMed,EMBASE,Cochrane库和Thomson Reuters Web of Knowledge来鉴定研究。涉及BPH患者的研究报告了骨折与暴露于5-α还原酶抑制剂或α阻滞剂之间的关联,其比值比(OR)估计为95%置信区间(CIs)。使用随机效应模型计算合并的OR。结果:三项研究探讨了暴露于5-α还原酶抑制剂的患者的骨折风险(21,366例骨折病例)。有四项研究解决了暴露于α-受体阻滞剂的患者(22,051例骨折病例)的骨折风险。使用5-α还原酶抑制剂的骨折的合并OR为0.9(95%CI = 0.7-1.1)。对于使用5-α还原酶抑制剂的髋/股骨骨折,合并OR为0.8(95%CI = 0.7-1.0)。使用α受体阻滞剂的骨折的合并OR为1.1(95%CI = 0.9-1.3)。在α-受体阻滞剂的研究之间存在显着的统计学异质性。结论:在BPH患者中,暴露于5-α还原酶抑制剂与骨折风险的改变无关。 5-α还原酶抑制剂对髋/股骨骨折的保护作用可能较小,尽管这在统计学上并不显着。尽管α受体阻滞剂与骨折风险的改变无关,但是在解释结果时,由于存在明显的异质性,因此需要谨慎。

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