类风湿性关节炎的治疗与胃肠道微生物群的改变有关。

K. Andréasson, T. Olofsson, V. Lagishetty, Z. Alrawi, Eline Klaassens, S. Holster, R. Hesselstrand, Jonathan P Jacobs, J. Wallman, E. Volkmann
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引用次数: 0

摘要

目的新近的研究表明,类风湿性关节炎(RA)与肠道菌群失调有关。这项前瞻性试验研究评估了开始接受甲氨蝶呤(MTX)或肿瘤坏死因子抑制剂(TNFi)治疗的类风湿关节炎患者肠道微生物组成的变化。方法符合 2010 年美国风湿病学会/EULAR 类风湿关节炎分类标准、开始接受 MTX 或 TNFi 治疗的连续患者在开始接受免疫抑制治疗时和 3 个月后提供粪便样本。采用基于 16S 核糖体 RNA 基因的有效微生物群测试(GA-map Dysbiosis Index Score [DIS],Genetic Analysis,挪威奥斯陆)来评估是否存在菌群失调以及失调的程度。通过定制的定量聚合酶链式反应分析粪便中 copri Prevotella(P. copri)的含量。结果基线时,50 名参与者中有 33 人(66%)存在菌群失调,病程超过 2 年的参与者中菌群失调更为常见(P = 0.019)。在3个月的随访中,50名参与者中有27人(54%)对治疗反应良好,50名参与者中有14人(28%)的DIS有所改善。与开始使用MTX的患者相比,开始使用TNFi的患者的DIS通常会有所改善(P = 0.031)。基线时,50 人中有 32 人(64%)发现了 P. copri。基于 28 个关节计数和 C 反应蛋白的疾病活动性评分的改善与 P. copri 丰度的同时下降有关(rs = 0.30,P = 0.036)。虽然患者并未随机接受 MTX 或 TNFi 治疗,但研究结果表明,特定疗法可能会对 RA 患者的胃肠道微生物群产生不同程度的调节作用。P.copri与治疗反应之间的关系需要进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Treatment for Rheumatoid Arthritis Associated With Alterations in the Gastrointestinal Microbiota.
OBJECTIVE Emerging research suggests that rheumatoid arthritis (RA) is associated with intestinal dysbiosis. This prospective pilot study evaluates changes in intestinal microbial composition in patients with RA initiating treatment with either methotrexate (MTX) or a tumor necrosis factor inhibitor (TNFi). METHODS Consecutive patients, fulfilling the 2010 American College of Rheumatology/EULAR classification criteria for RA, who started treatment with either MTX or TNFi delivered a stool sample upon initiation of immunosuppression and 3 months later. A 16S ribosomal RNA gene-based validated microbiota test (GA-map Dysbiosis Index Score [DIS], Genetic Analysis, Oslo, Norway) was used to evaluate for the presence and degree of dysbiosis. Fecal levels of Prevotella copri (P. copri) were analyzed by custom-made quantitative polymerase chain reaction. Changes in microbial composition were analyzed in relation to changes in disease activity, as measured by the disease activity score based on 28-joint counts, using C-reactive protein. RESULTS At baseline, dysbiosis was present in 33 of 50 (66%) participants and more common in participants with more than 2 years of disease duration (P = 0.019). At the 3-month follow-up, 27 of 50 (54%) were good treatment responders and the DIS had improved in 14 of 50 (28%). Participants initiating TNFi more often exhibited improvement in the DIS compared with those initiating MTX (P = 0.031). P. copri was identified in 32 of 50 (64%) at baseline. An improvement in disease activity score based on 28-joint counts, using C-reactive protein was associated with a simultaneous decrease in P. copri abundance (rs = 0.30, P = 0.036). CONCLUSION This study affirms that dysbiosis is a feature of RA. Although patients were not randomized to MTX or TNFi, the findings suggest that specific therapies may differentially modulate the gastrointestinal microbiota in RA. The association between P. copri and treatment response requires further study.
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