Sutherland L, Singleton J, Sessions J, Hanauer S, Krawitt E, Rankin G, Summers R, Mekhjian H, Greenberger N, Kelly M
Department of Medicine, University of Calgary.
Gut. 1991 Sep;32(9):1071-5. doi: 10.1136/gut.32.9.1071.
A double blind study compared the efficacy of metronidazole in two doses (20 mg/kg, 10 mg/kg) with placebo in patients with Crohn's disease. One hundred and five patients participated but only 56 completed the 16 week study -21 were withdrawn for deterioration of symptoms, 17 for adverse experiences, and 11 for protocol violation. Significant improvement in disease activity as measured by the Crohn's disease activity index (metronidazole 20 mg/kg, 97 units; metronidazole 10 mg/kg, 67 units; placebo -1 unit, p = 0.002) and serum orosomucoid (metronidazole 20 mg/kg/day, 49; 10 mg/kg/day, 38; placebo, -9, p = 0.001)) were detected. Changes in C reactive protein concentrations did not achieve significance when all three groups were considered but were significant when all metronidazole treated patients were grouped and compared with the placebo treated patients (0.8 v -0.9, p less than 0.05). Although patients receiving metronidazole 20 mg/kg/day had a greater improvement in disease activity than those receiving 10 mg/kg/day (difference 30 units (95% confidence intervals -27-87), the small sample size may have precluded the detection of statistical significance. Preliminary analysis suggests that metronidazole was more effective in patients with disease confined to the large intestine or affecting both small and large bowel than in those with small bowel disease only. There were no differences in remission rates between metronidazole and placebo treated patients. We conclude that metronidazole warrants further assessment in the treatment of patients with active Crohn's disease.
一项双盲研究比较了两种剂量(20毫克/千克、10毫克/千克)的甲硝唑与安慰剂对克罗恩病患者的疗效。105名患者参与了研究,但只有56名完成了为期16周的研究——21名因症状恶化退出,17名因不良事件退出,11名因违反方案退出。通过克罗恩病活动指数测量(甲硝唑20毫克/千克组,97单位;甲硝唑10毫克/千克组,67单位;安慰剂组,-1单位,p = 0.002)以及血清类粘蛋白(甲硝唑20毫克/千克/天组,49;10毫克/千克/天组,38;安慰剂组,-9,p = 0.001)发现疾病活动有显著改善。当考虑所有三组时,C反应蛋白浓度的变化无显著意义,但当所有接受甲硝唑治疗的患者分组并与接受安慰剂治疗的患者比较时则有显著意义(0.8对-0.9,p小于0.05)。虽然接受20毫克/千克/天甲硝唑治疗的患者在疾病活动方面的改善比接受10毫克/千克/天治疗的患者更大(差异30单位(95%置信区间-27 - 87)),但样本量较小可能妨碍了统计学显著性的检测。初步分析表明,甲硝唑对局限于大肠或同时累及小肠和大肠的疾病患者比仅患有小肠疾病的患者更有效。甲硝唑治疗组和安慰剂治疗组的缓解率没有差异。我们得出结论,甲硝唑在治疗活动性克罗恩病患者方面值得进一步评估。