Madisch Ahmed, Miehlke Stephan, Eichele Otto, Mrwa Jenny, Bethke Birgit, Kuhlisch Eberhard, Bästlein Elke, Wilhelms Georg, Morgner Andrea, Wigginghaus Bernd, Stolte Manfred
Medical Department I, Technical University Hospital, Fetscherstrasse 74, 01307, Dresden, Germany.
Int J Colorectal Dis. 2007 Dec;22(12):1445-51. doi: 10.1007/s00384-007-0364-1. Epub 2007 Sep 2.
The objective of this study was to investigate the effect of Boswellia serrata extract (BSE) on symptoms, quality of life, and histology in patients with collagenous colitis.
Patients with chronic diarrhea and histologically proven collagenous colitis were randomized to receive either oral BSE 400 mg three times daily for 6 weeks or placebo. Complete colonoscopy and histology were performed before and after treatment. Clinical symptoms and quality of life were assessed by standardized questionnaires and SF-36. The primary endpoint was the percentage of patients with clinical remission after 6 weeks (stool frequency<or=3 soft /solid stools per day on average during the last week). Patients of the placebo group with persistent diarrhea received open-label BSE therapy for a further 6 weeks.
Thirty-one patients were randomized; 26 patients were available for per-protocol-analysis. After 6 weeks, the proportion of patients in clinical remission was higher in the BSE group than in the placebo group (per protocol 63.6%; 95%CI, 30.8-89.1 vs 26.7%, 95%CI, 7.7-55.1; p=0.04; intention-to-treat 43.8% vs 26.7%, p=0.25). Compared to placebo, BSE treatment had no effect on histology and quality of life. Five patients discontinued BSE treatment prematurely. Discontinuation was due to adverse events (n=1), unwillingness to continue (n=3), or loss to follow-up for unknown reasons (n=1). Seven patients received open-label BSE therapy, five of whom achieved complete remission.
Our study suggests that BSE might be clinically effective in patients with collagenous colitis. Larger trials are clearly necessary to establish the clinical efficacy of BSE.
本研究旨在探讨锯叶棕提取物(BSE)对胶原性结肠炎患者症状、生活质量及组织学的影响。
慢性腹泻且经组织学证实为胶原性结肠炎的患者被随机分为两组,一组每日口服400毫克BSE,共3次,持续6周;另一组服用安慰剂。治疗前后均进行全结肠镜检查及组织学检查。通过标准化问卷和SF-36评估临床症状及生活质量。主要终点为6周后临床缓解患者的百分比(过去一周平均每天排便频率≤3次软便/固体便)。安慰剂组中持续腹泻的患者接受为期6周的开放标签BSE治疗。
31例患者被随机分组;26例患者可进行符合方案分析。6周后,BSE组临床缓解患者的比例高于安慰剂组(符合方案分析为63.6%;95%可信区间,30.8 - 89.1 vs 26.7%,95%可信区间,7.7 - 55.1;p = 0.04;意向性分析为43.8% vs 26.7%,p = 0.25)。与安慰剂相比,BSE治疗对组织学及生活质量无影响。5例患者提前终止BSE治疗。终止原因包括不良事件(n = 1)、不愿继续(n = 3)或不明原因失访(n = 1)。7例患者接受开放标签BSE治疗,其中5例实现完全缓解。
我们的研究表明,BSE可能对胶原性结肠炎患者具有临床疗效。显然需要进行更大规模的试验来确定BSE的临床疗效。