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维得利珠单抗治疗与炎症性肠病患者关节炎/关节痛的关联:系统评价和荟萃分析。

Association Between Vedolizumab Treatment and Arthritis/Arthralgia in Patients with Inflammatory Bowel Disease: A Systematic Review and Meta-analysis.

机构信息

Deparment of Medicine, University Center of Volta Redonda, Volta Redonda, Rio de Janeiro (RJ), Brazil.

Department of Medicine, Federal University of Santa Maria, Brazil.

出版信息

J Gastrointestin Liver Dis. 2024 Sep 29;33(3):379-385. doi: 10.15403/jgld-5546.

Abstract

BACKGROUND AND AIMS

Vedolizumab is a humanized gut selective drug that targets α4β7 integrin and has been used successfully in the treatment of inflammatory bowel disease (IBD). Pivotal studies have already demonstrated the drug's safety, but some real-life cohorts have shown an increase in arthralgia and arthritis in patients using vedolizumab. These findings raised the question of whether these joint symptoms are extraintestinal manifestations of IBD (since the drug acts only in the gut) or if they are associated with the use of vedolizumab. This systematic review and meta-analysis aimed to assess the incidence of arthralgia/arthritis in patients receiving vedolizumab and to investigate whether these events are indeed drug related.

METHODS

Pubmed, Cochrane, and Scopus were searched for randomized clinical trials reporting the incidence of joint manifestations in patients with Crohn's disease (CD) or ulcerative colitis (UC) who were treated with vedolizumab. The considered outcomes were arthritis and arthralgia. We used RevMan to calculate the pooled incidence of the reported outcomes and their corresponding 95% confidence intervals (95% CI).

RESULTS

The search strategy yielded 4,206 articles. After removal of duplicates and screening of results, 6 randomized studies met the inclusion criteria. A total of 3,134 patients with moderately to severe IBD were included. Of those, 2,119 were randomized to receive vedolizumab and 1,015 to placebo. In the intervention group, 210 patients developed arthritis or arthralgia of any kind while 84 patients developed those symptoms in the placebo group (RR=1.09; 95%CI: 0.86-1.38; p=0.49, I2=0%), showing no significant association. Results also showed no significant association between exposure and the studied outcome after comparing CD (RR=1.02; 95%CI: 0.76-1.37, p=0.89, I2=0%) and UC (RR=1.24; 95%CI: 0.81-1.89, p=0.32, I2=43%) separately.

CONCLUSIONS

The meta-analysis showed no association of these symptoms to the treatment with vedolizumab. Therefore, the new onset of worsening arthritis and arthralgia may be associated with the course of the disease itself, with the body's response to the drugs or with the exclusion of corticosteroids or anti-TNF from concomitant treatment with vedolizumab. Further studies with larger sample sizes are required, especially randomized clinical trials comparing anti-TNF, corticosteroid and immunomodulators to evaluate the incidence of joint manifestations in patients with IBD and even other rheumatological manifestations that may be associated as well.

摘要

背景与目的

Vedolizumab 是一种人源化肠道选择性药物,靶向 α4β7 整合素,已成功用于治疗炎症性肠病 (IBD)。关键性研究已经证明了该药的安全性,但一些真实世界的队列研究表明,使用 vedolizumab 的患者关节痛和关节炎的发生率增加。这些发现提出了一个问题,即这些关节症状是否是 IBD 的肠外表现(因为药物仅在肠道中起作用),或者是否与 vedolizumab 的使用有关。本系统评价和荟萃分析旨在评估接受 vedolizumab 治疗的克罗恩病 (CD) 或溃疡性结肠炎 (UC) 患者关节痛/关节炎的发生率,并探讨这些事件是否确实与药物有关。

方法

检索 Pubmed、Cochrane 和 Scopus 以获取报告 vedolizumab 治疗的 CD 或 UC 患者关节表现发生率的随机临床试验。考虑的结局是关节炎和关节痛。我们使用 RevMan 计算报告结局及其相应的 95%置信区间 (95%CI) 的汇总发生率。

结果

搜索策略产生了 4206 篇文章。在去除重复项和筛选结果后,符合纳入标准的 6 项随机研究。共有 3134 名中重度 IBD 患者入组。其中,2119 名患者随机接受 vedolizumab 治疗,1015 名患者接受安慰剂治疗。在干预组中,210 名患者出现任何类型的关节炎或关节痛,而安慰剂组中 84 名患者出现这些症状(RR=1.09;95%CI:0.86-1.38;p=0.49,I2=0%),无显著相关性。结果还表明,在比较 CD(RR=1.02;95%CI:0.76-1.37,p=0.89,I2=0%)和 UC(RR=1.24;95%CI:0.81-1.89,p=0.32,I2=43%)后,暴露与研究结局之间无显著相关性。

结论

荟萃分析显示这些症状与 vedolizumab 治疗无关联。因此,新发的关节炎和关节痛加重可能与疾病本身的进程、机体对药物的反应或排除 vedolizumab 联合治疗中的皮质类固醇或抗 TNF 有关。需要进一步开展样本量更大的研究,特别是随机临床试验,以比较抗 TNF、皮质类固醇和免疫调节剂,评估 IBD 患者甚至其他可能相关的风湿表现的关节表现发生率。

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