Department of Gastroenterology and Hepatology, Jikei University, Tokyo, Japan.
Am J Gastroenterol. 2010 Aug;105(8):1820-9. doi: 10.1038/ajg.2010.84. Epub 2010 Mar 9.
Fusobacterium varium may contribute to ulcerative colitis (UC). We conducted a double-blind placebo-controlled multicenter trial to determine whether antibiotic combination therapy induces and/or maintains remission of active UC.
Patients with chronic mild-to-severe relapsing UC were randomly assigned to oral amoxicillin 1500 mg/day, tetracycline 1500 mg/day, and metronidazole 750 mg/day, vs. placebo, for 2 weeks, and then followed up. The primary study end point was clinical response (Mayo score at 3 months after treatment completion) and secondary end points were clinical and endoscopic score improvements at 12 months. Anti-F. varium antibodies were measured by enzyme-linked immunosorbent assay.
Treatment and placebo groups each had 105 subjects. At the primary end point, response rates were significantly greater with antibiotics than with placebo (44.8 vs. 22.8%, P=0.0011). Endoscopic scores significantly improved at 3 months (P=0.002 vs. placebo). Remission rates were 19.0% (antibiotics) vs. 15.8% (placebo) at 3 months (P=0.59). At the secondary end point, response rates were significantly greater with antibiotics than with placebo (49.5 vs. 21.8%, respectively, P<0.0001). Endoscopic scores were significantly improved at 12 months after antibiotic treatment (P=0.002 vs. placebo). Remission rates had improved to 26.7% with antibiotics vs. 14.9% for placebo, at 12 months (P=0.041). F. varium antibody titers decreased in responders but not in nonresponders, and more in the antibiotic than in the placebo group. More pretreatment steroid-dependent UC patients discontinued corticosteroids after treatment completion (6 months: 28.6 vs. 11.8%, respectively, P=0.046; 9 months: 34.7 vs. 13.7%, respectively, P=0.019; and 12 months: 34.7 vs. 13.7%, respectively, P=0.019). These effects were greater in the subanalysis of the active group (Mayo scores of 6-12) than in that of total cases (0-12). No serious drug-related toxicities occurred.
The 2-week triple antibiotic therapy produced improvement, remission, and steroid withdrawal in active UC more effectively than a placebo.
变异梭杆菌可能与溃疡性结肠炎(UC)有关。我们进行了一项双盲安慰剂对照的多中心试验,以确定抗生素联合治疗是否能诱导和/或维持活动期 UC 的缓解。
将慢性轻至重度复发的 UC 患者随机分配至口服阿莫西林 1500mg/天、四环素 1500mg/天和甲硝唑 750mg/天,或安慰剂治疗 2 周,然后进行随访。主要研究终点为治疗结束后 3 个月时的临床应答(Mayo 评分),次要终点为 12 个月时的临床和内镜评分改善。通过酶联免疫吸附试验测量抗 F. varium 抗体。
治疗组和安慰剂组各有 105 例患者。在主要终点,抗生素组的应答率明显高于安慰剂组(44.8%比 22.8%,P=0.0011)。3 个月时内镜评分显著改善(P=0.002 比安慰剂)。3 个月时缓解率分别为 19.0%(抗生素)和 15.8%(安慰剂)(P=0.59)。在次要终点,抗生素组的应答率明显高于安慰剂组(分别为 49.5%比 21.8%,P<0.0001)。抗生素治疗 12 个月后内镜评分显著改善(P=0.002 比安慰剂)。缓解率分别为 26.7%(抗生素)和 14.9%(安慰剂),在 12 个月时(P=0.041)。应答者的 F. varium 抗体滴度下降,但非应答者没有下降,而且在抗生素组下降更明显。更多的皮质类固醇依赖的 UC 患者在治疗完成后(6 个月:28.6%比 11.8%,分别为 P=0.046;9 个月:34.7%比 13.7%,分别为 P=0.019;和 12 个月:34.7%比 13.7%,分别为 P=0.019)停止使用皮质类固醇。这些效果在活动组(Mayo 评分为 6-12)的亚分析中比总病例(0-12)更明显。没有发生严重的与药物相关的毒性。
两周三联抗生素治疗比安慰剂更有效地改善、缓解活动期 UC,并且能停用皮质类固醇。