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

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Osteoporosis International Pub Date : 2024-08-01 Epub Date: 2024-05-11 DOI:10.1007/s00198-024-07118-0
Takaomi Kobayashi, Tadatsugu Morimoto, Koji Ito, Masaaki Mawatari, Takafumi Shimazaki
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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.

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原发性骨质疏松症中的地诺单抗与双膦酸盐:随机对照试验的安全性比较荟萃分析。
地诺单抗和双膦酸盐治疗原发性骨质疏松症的耐受性普遍良好,但它们的安全性比较仍不明确。我们旨在探讨地诺单抗和双膦酸盐在原发性骨质疏松症中的安全性比较。我们在 PubMed 和 Google Scholar 等数据库中检索了以英语发表的相关同行评审随机对照试验(截至 2023 年 12 月)。调查了比较原发性骨质疏松症患者服用地诺单抗和双磷酸盐类药物的不良事件(AE)的试验。采用固定效应或随机效应模型对数据进行汇总,以确定与使用双膦酸盐治疗的患者相比,使用地诺单抗治疗的患者发生各种不良事件的风险比 (RR) 和 95% 置信区间 (CI)。本次荟萃分析共纳入了11项试验(5,545名患者;随访期:12-24个月)。所有试验都存在偏倚风险(如与次要终点相关的报告偏倚和与随机分配相关的选择偏倚)。与双膦酸盐类药物相比,地诺单抗与较少的因AEs而停药(RR = 0.49; 95% CI 0.34-0.71)、较多的五点主要不良心血管事件(RR = 2.05; 95% CI 1.03-4.09)、较多的心血管AEs(RR = 1.61;95% CI 1.07-2.41)、更多感染(RR = 1.14;95% CI 1.02-1.27)、更多上呼吸道感染(RR = 1.56;95% CI 1.08-2.25)、更少椎体骨折(RR = 0.54;95% CI 0.31-0.93)和更少腹痛(RR = 0.44;95% CI 0.22-0.87)。我们探讨了地诺单抗和双膦酸盐治疗原发性骨质疏松症的安全性比较,其中一些可能是由于它们的有益作用。然而,所有试验都存在偏倚风险。要确认我们的结果,还需要进一步的调查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Osteoporosis International
Osteoporosis International 医学-内分泌学与代谢
CiteScore
8.10
自引率
10.00%
发文量
224
审稿时长
3 months
期刊介绍: An international multi-disciplinary journal which is a joint initiative between the International Osteoporosis Foundation and the National Osteoporosis Foundation of the USA, Osteoporosis International provides a forum for the communication and exchange of current ideas concerning the diagnosis, prevention, treatment and management of osteoporosis and other metabolic bone diseases. It publishes: original papers - reporting progress and results in all areas of osteoporosis and its related fields; review articles - reflecting the present state of knowledge in special areas of summarizing limited themes in which discussion has led to clearly defined conclusions; educational articles - giving information on the progress of a topic of particular interest; case reports - of uncommon or interesting presentations of the condition. While focusing on clinical research, the Journal will also accept submissions on more basic aspects of research, where they are considered by the editors to be relevant to the human disease spectrum.
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