Department of Clinical Pharmacology, College of Medicine, Mustansiriyah University , Baghdad, Iraq.
Department of Medicine, College of Medicine, University of Baghdad, Baghdad, Iraq.
Clin Rheumatol. 2018 Oct;37(10):2633-2641. doi: 10.1007/s10067-018-4164-5. Epub 2018 Jun 7.
This study designed to identify the therapeutic efficacy of niclosamide (NCL) in Iraqi patients suffering from active rheumatoid arthritis (RA) who were using etanercept (ETN) for more than 3 months and still had high or moderate active RA. One hundred ten patients suffering from active rheumatoid arthritis (RA) who were using etanercept (ETN) for more than 3 months and still had high or moderate active RA were allocated randomly into two equal groups: one of them treated with 1000 mg/day NCL and the other treated with 1000 mg/day lactose in capsule dosage form. The study duration was 8 weeks. Clinical efficacy of the NCL was measured depending on scoring of the 28-joint Disease Activity Score (DAS28), simple disease activity index (SDAI), clinical disease activity index (CDAI), and Health Assessment Questionnaire Disability Index (HAQ-DI) at the baseline and at the end of the 8-week treatment period. Moreover, blood sample were taken from the patients at baseline and at after 8 weeks of treatment for measurement of the erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), interleukin 1β (IL-1 β), interleukin-6, tumor necrosis factor (TNF-α), intercellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), and E-selectin. At the end of the clinical study, patients had good response to NCL when added to the ETN with a high significant improvement in the SJC, TJC, DAS-28, CDAI, SDAI, and HAQ-DI compared to patients who were received placebo drug. In addition to that, 33% of patients achieved an ACR 20% response (ACR20) on NCL and ETN. Of these, 4% achieved ACR50 and another 4% achieved ACR70 response. While those group treated by placebo + ETN, 5% achieved ACR20 response and no one reached to ACR50 or ACR70 response. Twenty-seven percent of RA patients who have taken the NCL achieved moderate EULAR score while only 17% from the group that taken placebo with ETN achieved moderate response. On the other hand, no significant reduction was found in CRP, ESR, TNF-α, and IL-6, while IL-1 β reduced significantly after treatment with NCL. Treatment with NCL also exerts a significant lowering in the serum level of the E-selectin, ICAM1, and VCAM1 when compared to their value in baseline level. In RA disease, the use of NCL as adjuvant with ETN has resulted in a marked reduction in clinical assessment scoring indices and significantly decreased the E-selectin, ICAM-1, and VCAM-1 with marked improvement in the quality of life of patients.
这项研究旨在确定尼氯柳胺(NCL)在伊拉克接受依那西普(ETN)治疗超过 3 个月且仍处于高或中度活动期类风湿关节炎(RA)的患者中的疗效。110 名接受依那西普(ETN)治疗超过 3 个月且仍处于高或中度活动期类风湿关节炎(RA)的患者被随机分为两组,每组 55 名:一组接受 1000mg/天 NCL 治疗,另一组接受 1000mg/天乳糖胶囊治疗。研究持续 8 周。NCL 的临床疗效根据 28 关节疾病活动评分(DAS28)、简单疾病活动指数(SDAI)、临床疾病活动指数(CDAI)和健康评估问卷残疾指数(HAQ-DI)在基线和 8 周治疗期末的评分来衡量。此外,在基线和治疗 8 周后从患者身上采集血样,用于测量红细胞沉降率(ESR)、C 反应蛋白(CRP)、白细胞介素 1β(IL-1β)、白细胞介素 6、肿瘤坏死因子(TNF-α)、细胞间黏附分子-1(ICAM-1)、血管细胞黏附分子-1(VCAM-1)和 E-选择素。在临床研究结束时,与接受安慰剂药物的患者相比,NCL 联合 ETN 治疗的患者对 NCL 有良好的反应,在 SJC、TJC、DAS-28、CDAI、SDAI 和 HAQ-DI 方面有显著改善。此外,33%的患者达到了 ACR20%反应(ACR20),在 NCL 和 ETN 治疗组中,有 4%的患者达到了 ACR50,另有 4%的患者达到了 ACR70 反应。而在接受安慰剂+ETN 治疗的组中,只有 5%的患者达到了 ACR20 反应,没有人达到 ACR50 或 ACR70 反应。27%接受 NCL 治疗的 RA 患者达到了中度 EULAR 评分,而接受 ETN 联合安慰剂治疗的患者中只有 17%达到了中度反应。另一方面,CRP、ESR、TNF-α 和 IL-6 没有显著降低,而 NCL 治疗后 IL-1β 显著降低。NCL 治疗还可显著降低 E-选择素、ICAM1 和 VCAM1 的血清水平,与基线水平相比。在 RA 疾病中,NCL 联合 ETN 的使用可显著降低临床评估评分指数,并显著降低 E-选择素、ICAM-1 和 VCAM-1,从而显著改善患者的生活质量。