Lazzaroni M, Anderloni A, Bianchi Porro G
L Sacco University Hospital, Milan, Italy.
Eur J Gastroenterol Hepatol. 2001 Jul;13(7):833-9. doi: 10.1097/00042737-200107000-00012.
Amtolmetin-guacyl (AMG) (2-[2[1-methyl-5-(4-methylbenzoyl) pyrrol-2-yl] acetamido] acetic acid 2-methoxyphenyl ester) is a recent drug that, in preliminary studies, has shown effective anti-inflammatory properties with improved gastrointestinal safety. Our study was designed to investigate the effects of AMG and piroxicam on gastroduodenal mucosa in healthy volunteers.
Forty-two healthy volunteers aged 18--45 years were randomized in a double-blind manner to AMG 1200 mg for 2 days and 600 mg for 12 days, or piroxicam 40 mg for 2 days and 20 mg for 12 days. Endoscopic evaluation and laboratory tests were performed at baseline and at the end of the treatment. The mucosa was evaluated by endoscopy using a predefined scale: the score could range from 0 to 4. Only volunteers with endoscopy grade 0-1 entered the trial.
The median post-treatment endoscopy gastric injury scores were 1 (range 0--4) in the AMG-treated volunteers and 3 (range 0--4) in the piroxicam-treated volunteers (P = 0.04). There were two cases with an endoscopic gastric score of 4 in the AMG group, and seven in the piroxicam group (P = 0.1). The corresponding values in the duodenum were 1/21 volunteers in the AMG group and 1/21 in the piroxicam group. Eight out of 11 subjects with an endoscopic score of 4 were Helicobacter pylori negative, and 3/11 were infected by the micro-organism. Different adverse reactions were reported by 15/21 volunteers (71%) in the AMG group and by 12/21 (57%) in the piroxicam group. None of these events resulted in interruption of the study.
AMG is a new anti-inflammatory drug with limited gastric toxicity. If these findings are confirmed on a wider scale in long-term trials, then the drug might become a valid alternative to current treatments, especially for patients such as those with rheumatoid arthritis who need steroids and second-line drugs simultaneously.
安托美汀 - 胍酯(AMG)(2 - [2[1 - 甲基 - 5 - (4 - 甲基苯甲酰基)吡咯 - 2 - 基]乙酰胺基]乙酸2 - 甲氧基苯基酯)是一种新型药物,在初步研究中已显示出有效的抗炎特性且胃肠道安全性有所改善。我们的研究旨在调查AMG和吡罗昔康对健康志愿者胃十二指肠黏膜的影响。
42名年龄在18至45岁的健康志愿者以双盲方式随机分组,分别接受AMG 1200毫克治疗2天、600毫克治疗12天,或吡罗昔康40毫克治疗2天、20毫克治疗12天。在基线和治疗结束时进行内镜评估和实验室检查。通过内镜使用预定义量表评估黏膜:评分范围为0至4分。只有内镜分级为0 - 1级的志愿者进入试验。
AMG治疗组志愿者治疗后内镜下胃损伤评分中位数为1(范围0 - 4),吡罗昔康治疗组为3(范围0 - 4)(P = 0.04)。AMG组有2例内镜下胃评分为4分,吡罗昔康组有7例(P = 0.1)。十二指肠的相应数值在AMG组为1/21名志愿者,吡罗昔康组为1/21名志愿者。内镜评分为4分的11名受试者中,8名幽门螺杆菌阴性,3/11名受该微生物感染。AMG组21名志愿者中有15名(71%)报告了不同的不良反应,吡罗昔康组21名中有12名(57%)。这些事件均未导致研究中断。
AMG是一种胃毒性有限的新型抗炎药物。如果这些发现在长期试验中得到更广泛的证实,那么该药物可能成为当前治疗方法的有效替代药物,特别是对于类风湿关节炎等需要同时使用类固醇和二线药物的患者。