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首页> 外文期刊>Arthritis and Rheumatism >A randomized, double-blind, multicenter, controlled clinical trial of chicken type II collagen in patients with rheumatoid arthritis.
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A randomized, double-blind, multicenter, controlled clinical trial of chicken type II collagen in patients with rheumatoid arthritis.

机译:鸡II型胶原蛋白在类风湿关节炎患者中的随机,双盲,多中心,对照临床试验。

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摘要

OBJECTIVE: To assess the efficacy and safety of chicken type II collagen (CCII) in rheumatoid arthritis (RA) compared with methotrexate (MTX). METHODS: We conducted a prospective, 24-week, followup, multicenter, double-blind, controlled study of CCII (0.1 mg/day) versus MTX (10 mg/week) in patients with active RA. Clinical assessments were performed at screening and at 12, 18, and 24 weeks of treatment. RESULTS: A total of 236 RA patients were included; 211 patients (89.4%) completed the 24-week followup. In both groups there was a decrease in pain, morning stiffness, tender joint count, swollen joint count, Health Assessment Questionnaire score, and investigator and patient assessment of function; all differences were statistically significant. In the MTX group, erythrocyte sedimentation rate and C-reactive protein level decreased. Rheumatoid factor did not change in either group. At 24 weeks, 68.57% of patients in the CCII group and 83.02% in the MTX group met the American College of Rheumatology 20%improvement criteria (ACR20), and 40.95% and 57.54%, respectively, met the ACR50 criteria. The ACR20 and ACR50 response rates in the CCII group were lower than those in the MTX group, and this difference was statistically significant (P 0.05). Gastrointestinal symptoms were common in both groups. There were fewer and milder side effects in the CCII group than the MTX group. The difference in incidence of adverse events between the 2 groups was statistically significant (P 0.05). CONCLUSION: CCII is effective in the treatment of RA. CCII is well tolerated, and the incidence of adverse events of CCII is lower than that of MTX.
机译:目的:比较甲氨蝶呤(MTX)评估鸡II型胶原蛋白(CCII)在类风湿性关节炎(RA)中的疗效和安全性。方法:我们对活动性RA患者的CCII(0.1 mg /天)与MTX(10 mg /周)进行了一项为期24周,随访,多中心,双盲,对照的前瞻性研究。在筛查以及治疗的第12、18和24周进行临床评估。结果:总共纳入了236例RA患者; 211名患者(89.4%)完成了24周的随访。两组患者的疼痛,晨僵,关节痛,关节肿胀,健康评估问卷得分以及研究者和患者的功能评估均降低。所有差异均具有统计学意义。在MTX组中,红细胞沉降率和C反应蛋白水平降低。两组中类风湿因子均未改变。在第24周时,CCII组的68.57%的患者和MTX组的83.02%的患者达到了美国风湿病学院20%改善标准(ACR20),分别达到ACR50标准的40.95%和57.54%。 CCII组的ACR20和ACR50应答率低于MTX组,且差异具有统计学意义(P <0.05)。两组均出现胃肠道症状。与MTX组相比,CCII组的副作用更少且更温和。两组之间不良事件发生率的差异具有统计学意义(P <0.05)。结论:CCII治疗RA有效。 CCII具有良好的耐受性,并且CCII的不良事件发生率低于MTX。

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