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蠲痹强骨颗粒联合甲氨蝶呤对类风湿关节炎关节炎症的影响:一项随机对照试验

The effect of JuanBiQiangGu granules in combination with methotrexate on joint inflammation in rheumatoid arthritis: a randomized controlled trial.

作者信息

Ran Lei, Xu Bo, Han Hai-Hui, Wang Jian-Ye, A Xin-Yu, Cao Bo-Ran, Meng Xiao-Hui, Zhang Cheng-Bo, Xin Peng-Fei, Qiu Guo-Wei, Xiang Zheng, Pei Shao-Qiang, Gao Chen-Xin, Shen Jun, Zhong Sheng, Xu Xi-Rui, Bian Yan-Qin, Xie Jun, Shi Qi, Sun Song-Tao, Xiao Lian-Bo

机构信息

Guanghua Clinical Medical College, Shanghai University of Traditional Chinese Medicine, Shanghai, China.

Department of Orthopedic Surgery, Shanghai Guanghua Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai, China.

出版信息

Front Pharmacol. 2023 Apr 19;14:1132602. doi: 10.3389/fphar.2023.1132602. eCollection 2023.

Abstract

Rheumatoid arthritis (RA) joint inflammation severely affects joint function and quality of life in patients and leads to joint deformities and limb disability. The non-steroidal anti-inflammatory drugs used in the treatment of RA do not fully control the progression of joint inflammation and bone destruction and have notable adverse reactions. Traditional Chinese medicine formula JuanBiQiangGu Granules (JBQG) are commonly used for the treatment of RA inflammation and delay of bone destruction, but has not been evaluated through high-quality clinical studies. There is a pressing need for well-designed, randomized, parallel, controlled clinical studies to evaluate the exact effect of JBQG on RA joint inflammation and improvement of patient quality of life. This is a randomized, parallel, controlled clinical study in which 144 patients with rheumatoid arthritis who met the inclusion criteria were randomly assigned to 2 groups in a 1:1 ratio. The JBQG group received methotrexate 7.5 mg qw and JBQG granules 8 mg tid, while the MTX group received methotrexate 7.5 mg qw. The endpoint was 12 weeks after treatment. Relevant indices at baseline, 4 weeks, 8 weeks, and 12 weeks after treatment were observed and recorded, and DAS28-ESR, HAQ-DI, and Sharp scores were recorded for each patient. Blood samples were collected to test for CRP, ESR, TNF-α, IL-1β, IL-6, IL-17, and INF-γ, and adverse reactions and liver and kidney function (AST, ALT, Cr, BUN) were recorded for safety assessment. After 12 weeks of treatment, the effect of JBQG granules on disease activity, improvement in bone damage, and patient quality of life scores and safety in RA patients were evaluated. A total of 144 subjects completed treatment (71 in the JBQG group and 73 in the MTX group) and were included in the analysis. At baseline, there were no significant differences between the groups in terms of the observed indicators ( > 0.05). After treatment, 76.06% of patients in the JBQG group had DAS28-ESR levels below or equal to Low, including 45.07% in Remission and 5.63% in High, compared to 53.1% in the MTX group below or equal to Low, 12.33% in Remission, and 17.81% in High. CRP was significantly reduced (8.54 ± 5.87 vs. 11.86 ± 7.92, < 0.05, = 0.005), ESR was significantly reduced (15.1 ± 6.11 vs. 21.96 ± 9.19, < 0.0001), TNF-α was significantly reduced (1.44 ± 0.83 vs. 1.85 ± 1.07, < 0.05, = 0.011), IL-17 was significantly reduced (0.53 ± 0.33 vs. 0.71 ± 0.38, < 0.05, = 0.004), and INF-γ was significantly reduced (3.2 ± 1.51 vs. 3.89 ± 1.77, < 0.05, = 0.014). The median (IQR) OPG in the JBQG group was 2.54 (2.21-3.01), significantly higher than in the MTX group 2.06 (1.81-2.32), < 0.0001), and the median (IQR) -CTX in the JBQG group was 0.4 (0.32-0.43), significantly lower than in the MTX group 0.55 (0.47-0.67), < 0.0001). The median (IQR) VSA scores were 2 (1-3), a decrease from 3 (2-4) in the MTX group ( < 0.0001). The median (IQR) Sharp scores were 1 (1-2), a decrease from 2 (1-2) in the MTX group, but the difference was not statistically significant ( > 0.05, = 0.28). The median (IQR) HAQ-DI scores were 11 (8-16), significantly lower than in the MTX group 26 (16-30) ( < 0.0001). The median (IQR) AST in the JBQG group was 16 (12-20), with a significant difference compared to the MTX group 19 (13-25) ( < 0.01, = 0.004); the median (IQR) ALT in the JBQG group was 14 (10-18), with a significant difference compared to the MTX group 16 (11-22.5) ( < 0.05, = 0.015). There were no statistically significant differences in Cr or BUN ( > 0.05). JuanBiQiangGu Granules can be used to treat patients with rheumatoid arthritis, alleviate joint inflammation, reduce the incidence of adverse reactions to methotrexate, and has good safety. http://www.chinadrugtrials.org.cn/index.html; identifier: ChiCTR2100046373.

摘要

类风湿性关节炎(RA)关节炎症严重影响患者的关节功能和生活质量,并导致关节畸形和肢体残疾。用于治疗RA的非甾体抗炎药不能完全控制关节炎症和骨质破坏的进展,且有明显的不良反应。中药方剂蠲痹强骨颗粒(JBQG)常用于治疗RA炎症和延缓骨质破坏,但尚未通过高质量的临床研究进行评估。迫切需要设计良好的随机、平行、对照临床研究来评估JBQG对RA关节炎症的确切疗效以及患者生活质量的改善情况。这是一项随机、平行、对照临床研究,将144例符合纳入标准的类风湿性关节炎患者按1:1比例随机分为两组。JBQG组接受甲氨蝶呤7.5mg每周一次及JBQG颗粒8mg每日三次,而MTX组仅接受甲氨蝶呤7.5mg每周一次。终点为治疗12周后。观察并记录治疗前、治疗后4周、8周和12周的相关指标,记录每位患者的DAS28-ESR、HAQ-DI和Sharp评分。采集血样检测CRP、ESR、TNF-α、IL-1β、IL-6、IL-17和INF-γ,并记录不良反应及肝肾功能(AST、ALT、Cr、BUN)以进行安全性评估。治疗12周后,评估JBQG颗粒对RA患者疾病活动度、骨损伤改善情况、生活质量评分及安全性的影响。共有144名受试者完成治疗(JBQG组71例,MTX组73例)并纳入分析。治疗前,两组观察指标无显著差异(P>0.05)。治疗后,JBQG组76.06%的患者DAS28-ESR水平低于或等于低疾病活动度,其中缓解期占45.07%,高疾病活动度占5.63%;而MTX组分别为53.1%低于或等于低疾病活动度,缓解期占12.33%,高疾病活动度占17.81%。CRP显著降低(8.54±5.87 vs. 11.86±7.92,P<0.05,t=0.005),ESR显著降低(15.1±6.11 vs. 21.96±9.19,P<0.0001),TNF-α显著降低(1.44±0.83 vs. 1.85±1.07,P<0.05,t=0.011),IL-17显著降低(0.53±0.33 vs. 0.71±0.38,P<0.05,t=0.004),INF-γ显著降低(3.2±1.51 vs. 3.89±1.77,P<0.05,t=0.014)。JBQG组OPG中位数(IQR)为2.54(2.21 - 3.01),显著高于MTX组的2.06(1.81 - 2.32),P<0.0001;JBQG组-CTX中位数(IQR)为0.4(0.32 - 0.43),显著低于MTX组的0.55(0.47 - 0.67),P<0.0001。VSA评分中位数(IQR)为2(1 - 3),较MTX组的3(2 - 4)有所降低(P<0.0001)。Sharp评分中位数(IQR)为1(1 - 2),较MTX组的2(1 - 2)有所降低,但差异无统计学意义(P>0.05,t=0.28)。HAQ-DI评分中位数(IQR)为11(8 - 16),显著低于MTX组的26(16 - 30)(P<0.0001)。JBQG组AST中位数(IQR)为16(12 - 20),与MTX组的19(13 - 25)相比有显著差异(P<0.01,t=0.004);JBQG组ALT中位数(IQR)为14(10 - 18),与MTX组的16(11 - 22.5)相比有显著差异(P<0.05,t=0.015)。Cr或BUN无统计学显著差异(P>0.05)。蠲痹强骨颗粒可用于治疗类风湿性关节炎患者,减轻关节炎症,降低甲氨蝶呤不良反应的发生率,且安全性良好。http://www.chinadrugtrials.org.cn/index.html;标识符:ChiCTR2100046373

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ec/10167420/a1ede4681e7c/fphar-14-1132602-g001.jpg

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