Riskin W G, Gillings D B, Scarlett J A
University of Miami School of Medicine, Florida.
Ann Intern Med. 1989 Sep 15;111(6):455-65. doi: 10.7326/0003-4819-111-6-455.
To assess the safety and efficacy of amiprilose hydrochloride (HCl), a novel synthetic carbohydrate with anti-inflammatory and immunomodulatory properties, in patients with rheumatoid arthritis.
Prospective, multicenter, randomized, parallel group, double-blind placebo-controlled 12-week trial.
Two hundred and one functional class I and II patients with definite or classic rheumatoid arthritis, previously untreated with disease modifying antirheumatic drugs.
Patients were withdrawn from nonsteroidal anti-inflammatory drug therapy. Those who flared were randomly assigned to amiprilose HCl, 6 g/d, or placebo for 12 weeks. No concomitant anti-inflammatory or antirheumatic drug therapy was permitted during the study. Combination acetaminophen and propoxyphene napsylate was the only supplemental analgesic medication allowed.
The number of painful joints and swollen joints, joint pain and joint swelling indices, left and right grip strength, investigator global assessment, and patient global assessment returned to baseline for the amiprilose group and showed statistically significant (P less than 0.05) differences from the placebo group within 4 to 6 weeks. The protocol criteria for overall therapeutic response were satisfied by 41% of the amiprilose patients, compared with 21% of the placebo group (P = 0.003). Approximately 0.5 tablet per day less analgesic medication was taken by the amiprilose group (P less than 0.05 at weeks 6 and 12). There were no statistically significant differences in morning stiffness, walking time, erythrocyte sedimentation rate, C-reactive protein, or rheumatoid factor between the groups. A similar number of adverse experiences were reported by the patients on amiprilose (67%) and on placebo (63%). One patient on amiprilose developed thrombocytopenia of unknown cause; no other reported adverse effects were serious.
Amiprilose HCl has significant anti-inflammatory activity and a favorable safety profile when used as the sole antirheumatic therapy in patients with active rheumatoid arthritis. Synthetic carbohydrates may represent an important new class of drugs for the treatment of inflammatory, autoimmune diseases.
评估新型合成碳水化合物盐酸氨吡咯司(具有抗炎和免疫调节特性)对类风湿关节炎患者的安全性和疗效。
前瞻性、多中心、随机、平行组、双盲安慰剂对照的12周试验。
201例功能分级为I级和II级的确诊或典型类风湿关节炎患者,此前未接受过改善病情抗风湿药物治疗。
患者停用非甾体抗炎药治疗。病情复发的患者被随机分配接受6g/天的盐酸氨吡咯司或安慰剂治疗,为期12周。研究期间不允许同时使用抗炎或抗风湿药物治疗。对乙酰氨基酚和萘磺酸丙氧芬组合是唯一允许使用的补充镇痛药物。
盐酸氨吡咯司组的疼痛关节数、肿胀关节数、关节疼痛和关节肿胀指数、左右握力、研究者整体评估和患者整体评估在4至6周内恢复至基线水平,且与安慰剂组相比有统计学显著差异(P<0.05)。41%的盐酸氨吡咯司治疗患者达到了总体治疗反应的方案标准,而安慰剂组为21%(P = 0.003)。盐酸氨吡咯司组每天服用的镇痛药比安慰剂组少约0.5片(第6周和第12周时P<0.05)。两组在晨僵、步行时间、红细胞沉降率、C反应蛋白或类风湿因子方面无统计学显著差异。服用盐酸氨吡咯司的患者(67%)和服用安慰剂的患者(63%)报告的不良事件数量相似。1例服用盐酸氨吡咯司的患者出现原因不明的血小板减少症;报告的其他不良反应均不严重。
盐酸氨吡咯司作为活动性类风湿关节炎患者的唯一抗风湿治疗药物时,具有显著的抗炎活性和良好的安全性。合成碳水化合物可能代表一类重要的新型抗炎、自身免疫性疾病治疗药物。