Tang Tao, Wan Bingwen, Zhang Alei, Zhang Xu, Wang Xuqing, Mao Shuiwei
Department of Orthopedics, The First People's Hospital of Jiashan, Jiaxing, Zhejiang Province, China.
BMC Musculoskelet Disord. 2025 May 7;26(1):450. doi: 10.1186/s12891-025-08688-8.
Rheumatoid arthritis (RA) can lead to significant bone destruction, which may occur locally near inflamed joints or systemically. As patients age, they often experience increased bone erosion around affected joints, heightened osteoclast activity, and systemic inflammation, which collectively result in bone loss. This condition is commonly referred to as osteopenia or osteoporosis.
A systematic search was conducted across multiple databases, including PubMed, Web of Science, Embase, and the Cochrane Library, to identify randomized controlled trials (RCTs) published on the use of denosumab in treating osteoporosis in patients with rheumatoid arthritis. The primary focus was to evaluate the impact of denosumab on various clinical measures, including bone mineral density (BMD), joint erosion scores, and overall joint maintenance. We performed a meta-analysis of six selected studies, all of which utilized these common metrics. The number of studies included in the analysis of each outcome varied depending on data availability in the original studies, with all included studies meeting our quality assessment criteria.
The results from these studies suggest that denosumab is effective in preventing further joint damage and bone loss in rheumatoid arthritis patients with osteoporosis. The data revealed a significant improvement in BMD, joint erosion scores, and joint narrowing scores in patients treated with denosumab compared to controls. These findings indicate the potential of denosumab as a preventive treatment for joint deterioration in RA patients with osteoporosis.
Denosumab demonstrates promising efficacy in maintaining bone health and preventing joint damage in rheumatoid arthritis patients with coexisting osteoporosis. However, further studies with larger sample sizes and long-term follow-up are necessary to confirm these findings and to comprehensively assess the long-term safety profile, including potential adverse events such as hypocalcemia, osteonecrosis of the jaw, and atypical femoral fractures.
类风湿关节炎(RA)可导致严重的骨质破坏,这种破坏可能发生在炎症关节附近的局部或全身性。随着患者年龄增长,他们通常会在受影响关节周围出现更多的骨质侵蚀、破骨细胞活性增强以及全身性炎症,这些共同导致骨质流失。这种情况通常被称为骨质减少或骨质疏松。
在多个数据库中进行了系统检索,包括PubMed、Web of Science、Embase和Cochrane图书馆,以识别关于地诺单抗用于治疗类风湿关节炎患者骨质疏松症的随机对照试验(RCT)。主要重点是评估地诺单抗对各种临床指标的影响,包括骨密度(BMD)、关节侵蚀评分和整体关节维持情况。我们对六项选定研究进行了荟萃分析,所有这些研究都使用了这些常见指标。分析每个结果所纳入的研究数量因原始研究中的数据可用性而异,所有纳入研究均符合我们的质量评估标准。
这些研究结果表明,地诺单抗在预防患有骨质疏松症的类风湿关节炎患者进一步的关节损伤和骨质流失方面是有效的。数据显示,与对照组相比,接受地诺单抗治疗的患者在骨密度、关节侵蚀评分和关节狭窄评分方面有显著改善。这些发现表明地诺单抗作为患有骨质疏松症的类风湿关节炎患者关节恶化的预防性治疗方法具有潜力。
地诺单抗在维持患有合并骨质疏松症的类风湿关节炎患者的骨骼健康和预防关节损伤方面显示出有前景的疗效。然而,需要进行更大样本量和长期随访的进一步研究来证实这些发现,并全面评估长期安全性,包括低钙血症、颌骨坏死和非典型股骨骨折等潜在不良事件。