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Efficacy of an Andrographis paniculata composition for the relief of rheumatoid arthritis symptoms: a prospective randomized placebo-controlled trial

机译:穿心莲的组合物缓解类风湿关节炎症状的功效:一项前瞻性随机安慰剂对照试验

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摘要

Andrographis paniculata (Burm. f.) Wall ex Nees (Acanthaceae) possesses anti-inflammatory effects, attributed to the main constituent andrographolide proposed as alternative in the treatment of autoimmune disease. A prospective, randomized, double blind, and placebo-controlled study in patients with rheumatoid arthritis (RA) was performed. Tablets (Paractin®) made of an extract of A. paniculata (30% total andrographolides) were administered three times a day for 14 weeks, after a 2-week washout period to 60 patients with active RA. The primary outcomes were pain intensity measured using a horizontal visual analog pain scale (VAPS). In addition, ACR, EULAR, and SF36 clinical parameters were recorded. The intensity of joint pain decreased in the active vs placebo group at the end of treatment, although these differences were not statistically significant. A significant diminishing for week in tender joint −0.13 95% confidence interval (CI; −0.22 to 0.06; p = 0.001), number of swollen joints −0.15 95%CI (−0.29 to −0.02; p = 0.02), total grade of swollen joint −0.27 95%CI (−0.48 to −0.07; p = 0.010), number of tender joints −0.25 95%CI (−0.48 to −0.02; p = 0.033), total grade of swollen joints −0.27 95%CI (−0.48 to −0.07; p = 0.01), total grade of tender joints −0.47 95%CI (−0.77 to −0.17; p = 0.002) and HAQ −0.52 95%CI (−0.82 to −0.21; p < 0.001) and SF36 0.02 95%CI (0.01 to 0.02; p < 0.001) health questionnaires was observed within the group with the active drug. Moreover, it was associated to a reduction of rheumatoid factor, IgA, and C4. These findings suggest that A. paniculata could be a useful “natural complement” in the treatment of AR; however, a larger trial and a more extended period of treatment is necessary in order to corroborate these results.
机译:穿心莲(穿心莲)具有抗炎作用,这归因于穿心莲内酯的主要成分被提议作为自身免疫性疾病的治疗方法。对风湿性关节炎(RA)患者进行了一项前瞻性,随机,双盲和安慰剂对照研究。在2周的冲洗期后,对60例活动性RA患者每天服用3次,由Pan.uliculata(总穿心莲内酯含量为30%)制成的片剂(Paractin®),持续14周。主要结果是使用水平视觉模拟疼痛量表(VAPS)测量的疼痛强度。此外,还记录了ACR,EULAR和SF36临床参数。在治疗结束时,活性组与安慰剂组的关节痛强度有所降低,尽管这些差异在统计学上并不显着。嫩关节的-0.13 95%置信区间(CI; -0.22至0.06; p = 0.001)的一周显着减少,肿胀的关节数-0.15 95%CI(-0.29至-0.02; p = 0.02),总等级肿胀关节数-0.27 95%CI(-0.48至-0.07; p = 0.010),嫩关节数-0.25 95%CI(-0.48 to -0.02; p = 0.033),肿胀关节的总等级-0.27 95% CI(-0.48至-0.07; p = 0.01),嫩关节的总等级-0.47 95%CI(-0.77至-0.17; p = 0.002)和HAQ -0.52 95%CI(-0.82至-0.21; p <活性药物组中观察到0.001)和SF36 0.02 95%CI(0.01至0.02; p <0.001)健康调查表。此外,它与类风湿因子,IgA和C4减少有关。这些发现表明,沙棘曲霉在AR的治疗中可能是有用的“天然补体”。然而,为了证实这些结果,有必要进行更大的试验并延长治疗时间。

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