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地舒单抗与双膦酸盐类药物治疗原发性骨质疏松症的比较:随机对照试验中安全性的荟萃分析。

Denosumab vs. bisphosphonates in primary osteoporosis: a meta-analysis of comparative safety in randomized controlled trials.

机构信息

Department of Orthopaedic Surgery, Taku City Hospital, Saga, Japan.

Department of Orthopaedic Surgery, Faculty of Medicine, Saga University, Saga, Japan.

出版信息

Osteoporos Int. 2024 Aug;35(8):1377-1393. doi: 10.1007/s00198-024-07118-0. Epub 2024 May 11.

Abstract

Denosumab and bisphosphonates for primary osteoporosis are generally well-tolerated, but their comparative safety remains unclear. We aimed to explore the comparative safety of denosumab and bisphosphonates in primary osteoporosis. Databases such as PubMed and Google Scholar were searched for relevant peer-reviewed randomized controlled trials published in English (as of December 2023). Trials comparing adverse events (AE) between denosumab and bisphosphonates in patients with primary osteoporosis were investigated. Data were pooled using a fixed- or random-effects model to determine the risk ratios (RR) and 95% confidence intervals (CIs) for various AEs in patients treated with denosumab in comparison to patients treated with bisphosphonates. Eleven trials (5,545 patients; follow-up period: 12-24 months) were included in this meta-analysis. All trials had a risk of bias (e.g., reporting bias linked to secondary endpoints and selection bias linked to random allocation). In comparison to bisphosphonates, denosumab was significantly associated with less withdrawal due to AEs (RR = 0.49; 95% CI 0.34-0.71), more five-point major adverse cardiovascular events (RR = 2.05; 95% CI 1.03-4.09), more cardiovascular AEs (RR = 1.61; 95% CI 1.07-2.41), more infections (RR = 1.14; 95% CI 1.02-1.27), more upper respiratory tract infections (RR = 1.56; 95% CI 1.08-2.25), less vertebral fractures (RR = 0.54; 95% CI 0.31-0.93), and less abdominal pain (RR = 0.44;95% CI 0.22-0.87). We explored the comparative safety of denosumab and bisphosphonates for primary osteoporosis, some of which could be attributed to their beneficial effects. However, all trials had a risk of bias. Further investigations are required to confirm our results.

摘要

地舒单抗和双磷酸盐类药物通常用于治疗原发性骨质疏松症,且耐受性良好,但它们的相对安全性尚不清楚。我们旨在探讨地舒单抗和双磷酸盐类药物治疗原发性骨质疏松症的相对安全性。检索了 PubMed 和 Google Scholar 等数据库,以获取截至 2023 年 12 月发表的英文同行评议随机对照试验。调查了比较地舒单抗和双磷酸盐类药物治疗原发性骨质疏松症患者不良事件(AE)的随机对照试验。使用固定或随机效应模型汇总数据,以确定与接受双磷酸盐类药物治疗的患者相比,接受地舒单抗治疗的患者发生各种 AE 的风险比(RR)和 95%置信区间(CI)。本 meta 分析纳入了 11 项试验(5545 例患者;随访时间:12-24 个月)。所有试验均存在偏倚风险(例如,与次要结局相关的报告偏倚和与随机分组相关的选择偏倚)。与双磷酸盐类药物相比,地舒单抗与因 AE 而停药的风险显著降低(RR=0.49;95%CI 0.34-0.71)、五点重大不良心血管事件(RR=2.05;95%CI 1.03-4.09)、心血管不良事件(RR=1.61;95%CI 1.07-2.41)、感染(RR=1.14;95%CI 1.02-1.27)、上呼吸道感染(RR=1.56;95%CI 1.08-2.25)、椎体骨折(RR=0.54;95%CI 0.31-0.93)和腹痛(RR=0.44;95%CI 0.22-0.87)的风险降低。我们探讨了地舒单抗和双磷酸盐类药物治疗原发性骨质疏松症的相对安全性,其中一些可能归因于它们的有益作用。然而,所有试验均存在偏倚风险。需要进一步的研究来证实我们的结果。

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