Department of Orthopedics, Jincheng General Hospital, Jincheng, China.
Department of Gynecology, Gaoping People's Hospital, Jincheng, China.
Front Endocrinol (Lausanne). 2024 Sep 2;15:1431676. doi: 10.3389/fendo.2024.1431676. eCollection 2024.
A systematic review and Meta-analysis.
To compare the efficacy and safety of denosumab and teriparatide versus oral bisphosphonates to treat postmenopausal osteoporosis.
While bisphosphonates have historically been the cornerstone of pharmacological management for bone protection in patients, emerging evidence suggests that teriparatide and denosumab warrant further investigation as potential first-line treatments. The optimal choice among denosumab, teriparatide, and oral bisphosphonates for the treatment of postmenopausal osteoporosis remains a subject of ongoing debate and controversy within the scientific community.
This systematic review adhered meticulously to the rigorous standards outlined by the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analysis) guidelines as well as the Cochrane Collaboration recommendations. Additionally, it employed the AMSTAR (Assessing the methodological quality of systematic reviews) criteria to ensure methodological robustness and enhance the credibility of the findings. A systematic electronic search was conducted across Web of Science, PubMed, and the Cochrane Library databases from their inception dates up to February 2024.
In this meta-analysis of studies, our findings suggest that compared to bisphosphonates, both teriparatide and denosumab demonstrated notable increases in percentage changes in lumbar spine bone mineral density (BMD) among postmenopausal osteoporosis patients. Furthermore, denosumab exhibited superiority over teriparatide and oral bisphosphonates in enhancing percentage changes in both femoral neck and total hip BMD, indicating its potential as a more efficacious option. Regarding safety outcomes, no significant differences were observed in the incidence of serious adverse events among patients treated with teriparatide, denosumab, and bisphosphonates. However, teriparatide showed superiority over oral bisphosphonates in terms of a lower risk of general adverse events, suggesting a favorable safety profile.
In conclusion, our study suggests that teriparatide and denosumab demonstrate comparable or potentially superior efficacy and safety profiles compared to oral bisphosphonates for the treatment of postmenopausal osteoporosis.
PROSPERO, identifier CRD42024508382.
系统评价和荟萃分析。
比较地舒单抗和特立帕肽与口服双膦酸盐治疗绝经后骨质疏松症的疗效和安全性。
虽然双膦酸盐一直是患者骨骼保护药物治疗的基石,但新出现的证据表明,特立帕肽和地舒单抗值得进一步研究,作为潜在的一线治疗药物。地舒单抗、特立帕肽和口服双膦酸盐治疗绝经后骨质疏松症的最佳选择仍然是科学界持续争论和争议的主题。
本系统评价严格遵循 PRISMA(系统评价和荟萃分析的首选报告项目)指南和 Cochrane 协作组建议规定的严格标准。此外,它还采用了 AMSTAR(系统评价方法学质量评估)标准,以确保方法学的稳健性并提高研究结果的可信度。系统地对 Web of Science、PubMed 和 Cochrane 图书馆数据库进行了电子检索,检索时间从数据库建立到 2024 年 2 月。
在这项对研究的荟萃分析中,我们的研究结果表明,与双膦酸盐相比,特立帕肽和地舒单抗均能显著增加绝经后骨质疏松症患者腰椎骨密度(BMD)的百分比变化。此外,地舒单抗在增强股骨颈和全髋 BMD 的百分比变化方面优于特立帕肽和口服双膦酸盐,表明其作为更有效治疗选择的潜力。关于安全性结果,接受特立帕肽、地舒单抗和双膦酸盐治疗的患者中,严重不良事件的发生率没有显著差异。然而,特立帕肽在一般不良事件风险较低方面优于口服双膦酸盐,提示其具有良好的安全性特征。
综上所述,我们的研究表明,特立帕肽和地舒单抗在治疗绝经后骨质疏松症方面与口服双膦酸盐相比具有相当或潜在更优的疗效和安全性。
PROSPERO,标识符 CRD42024508382。