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利福布汀与克拉霉素治疗克罗恩病的开放临床试验。

Open clinical trial of rifabutin and clarithromycin therapy in Crohn's disease.

作者信息

Shafran I, Kugler L, El-Zaatari F A K, Naser S A, Sandoval J

机构信息

Department of Molecular Biology and Microbiology, University of Central Florida, Orlando, USA.

出版信息

Dig Liver Dis. 2002 Jan;34(1):22-8. doi: 10.1016/s1590-8658(02)80055-x.

Abstract

BACKGROUND

Crohn's disease, an inflammatory bowel disease in humans, has a suspected aetiology of Mycobacterium avium subsp. Paratuberculosis.

AIMS

To evaluate the role of rifabutin and clarithromycin anti-Mycobacterium avium subsp. Paratuberculosis treatment in Crohn's disease patients using an open clinical trial.

METHODS

. A total of 36 patients with acute presentations of Crohn's disease, whose sera tested positive against p35 and p36 antigens (two recombinant proteins of Mycobacterium avium subsp. Paratuberculosis), were selected for treatment with rifabutin and macrolide antibiotic therapy Rifabutin and macrolide antibiotic therapy medications included 250 mg 1 po bid clarithromycin and 150 mg 1 po bid Ri-fabutin accompanied with a probiotic. Crohn's disease patients' response to rifabutin and macrolide antibiotic therapy was monitored over a period ranging from 4 to 17 months.

RESULTS

Seven patients (19.4%) withdrew from the study since they were unable to tolerate medications. Of the remaining 29 patients, 21 (58.3%) reached a sustained state of improvement, traditionally defined as a decrease of 70 points between their entrance and exit Crohn's disease activity index scores together with the absence of the need of all other Crohn's medications, such as immunosuppressants and corticosteroids. Three Crohn's disease patients [8. 3%) noticed significant improvements, but required other Crohn's medications, concurrently with rifabutin and macrolide antibiotic therapy, to achieve and sustain improvement. Only 5 Crohn's disease patients (13.8%) were non-responders, noticing no marked improvement while on rifabutin and macrolide antibiotic therapy.

CONCLUSION

The data add further evidence to support the role of rifabutin and macrolide antibiotic therapy in the treatment of Crohn's disease specifically in those patients with evidence of Mycobacterium avium subsp. Paratuberculosis infection. A large multi-centre clinical trial is needed to further explore these findings.

摘要

背景

克罗恩病是一种人类炎症性肠病,其病因疑似为副结核分枝杆菌。

目的

通过一项开放性临床试验评估利福布汀和克拉霉素抗副结核分枝杆菌治疗在克罗恩病患者中的作用。

方法

总共36例克罗恩病急性发作患者,其血清针对p35和p36抗原(副结核分枝杆菌的两种重组蛋白)检测呈阳性,被选入接受利福布汀和大环内酯类抗生素治疗。利福布汀和大环内酯类抗生素治疗药物包括250毫克口服每日两次克拉霉素和150毫克口服每日两次利福布汀,并伴有一种益生菌。对克罗恩病患者接受利福布汀和大环内酯类抗生素治疗的反应进行了4至17个月的监测。

结果

7例患者(19.4%)因无法耐受药物而退出研究。在其余29例患者中,21例(58.3%)达到持续改善状态,传统上定义为其克罗恩病活动指数入组和出组评分之间下降70分,且无需使用所有其他克罗恩病药物,如免疫抑制剂和皮质类固醇。3例克罗恩病患者(8.3%)有显著改善,但在接受利福布汀和大环内酯类抗生素治疗的同时需要其他克罗恩病药物来实现并维持改善。只有5例克罗恩病患者(13.8%)无反应,在接受利福布汀和大环内酯类抗生素治疗时未观察到明显改善。

结论

这些数据进一步证明了利福布汀和大环内酯类抗生素治疗在克罗恩病治疗中的作用,特别是在那些有副结核分枝杆菌感染证据的患者中。需要进行一项大型多中心临床试验来进一步探索这些发现。

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