Drisko Jeanne, Bischoff Bette, Hall Matthew, McCallum Richard
University of Kansas Medical Center, Kansas City, KS 66160, USA.
J Am Coll Nutr. 2006 Dec;25(6):514-22. doi: 10.1080/07315724.2006.10719567.
In Irritable Bowel Syndrome, the gut-associated immune system may be up-regulated resulting in immune complex production, low-grade inflammation, loss of Class I bacteria, and translocation of inflammatory mediators and macromolecules outside of the GI lumen. Since food intolerance may be one of the reasons for this upregulation, our goal was to investigate the role of food intolerance in IBS patients.
In this open label pilot study, we enrolled 20 patients with IBS by Rome II criteria (15 women, ages 24-81) who had failed standard medical therapies in a tertiary care GI clinic. Baseline serum IgE and IgG food and mold panels, and comprehensive stool analysis (CSA) were performed. Breath-hydrogen testing and IBS Quality-of-Life (QOL) questionnaires were obtained. Patients underwent food elimination diets based on the results of food and mold panels followed by controlled food challenge. Probiotics were also introduced. Repeat testing was performed at 6-months. We followed up with this cohort at 1 year after trial completion to assess the reported intervention and for placebo effect.
Baseline abnormalities were identified on serum IgG food and mold panels in 100% of the study subjects with significant improvement after food elimination and rotation diet (p < 0.05). Significant improvements were seen in stool frequency (p < 0.05), pain (p < 0.05), and IBS-QOL scores (p < 0.0001). Imbalances of beneficial flora and dysbiotic flora were identified in 100% of subjects by CSA. There was a trend to improvement of beneficial flora after treatment but no change in dysbiotic flora. The 1-year follow up demonstrated significant continued adherence to the food rotation diet (4.00 +/- 1.45), minimal symptomatic problems with IBS (4.00 +/- 1.17), and perception of control over IBS (4.15 +/- 1.23). The continued use of probiotics was considered less helpful (3.40 +/- 1.60).
These data demonstrate that identifying and appropriately addressing food sensitivity in IBS patients not previously responding to standard therapy results in a sustained clinical response and impacts on overall well being and quality of life in this challenging entity.
在肠易激综合征中,肠道相关免疫系统可能上调,导致免疫复合物产生、低度炎症、一类细菌丧失以及炎症介质和大分子移位至胃肠道管腔外。由于食物不耐受可能是这种上调的原因之一,我们的目标是研究食物不耐受在肠易激综合征患者中的作用。
在这项开放标签的试点研究中,我们通过罗马II标准招募了20名肠易激综合征患者(15名女性,年龄24 - 81岁),这些患者在三级医疗胃肠诊所的标准药物治疗中失败。进行了基线血清IgE和IgG食物及霉菌检测,以及综合粪便分析(CSA)。获取了呼气氢测试和肠易激综合征生活质量(QOL)问卷。患者根据食物及霉菌检测结果进行食物排除饮食,随后进行对照食物激发试验。还引入了益生菌。在6个月时进行重复检测。在试验完成后1年对该队列进行随访,以评估所报告的干预措施及安慰剂效应。
100%的研究对象血清IgG食物及霉菌检测出现基线异常,在食物排除和轮换饮食后有显著改善(p < 0.05)。在大便频率(p < 0.05)、疼痛(p < 0.05)和肠易激综合征生活质量评分(p < 0.0001)方面有显著改善。通过CSA在100%的受试者中发现有益菌群和失调菌群失衡。治疗后有益菌群有改善趋势,但失调菌群无变化。1年随访显示对食物轮换饮食有显著持续依从性(4.00 +/- 1.45),肠易激综合征的症状问题极少(4.00 +/- 1.17),以及对肠易激综合征有控制感(4.15 +/- 1.23)。继续使用益生菌被认为帮助较小(3.40 +/- 1.60)。
这些数据表明,识别并适当处理先前对标准治疗无反应的肠易激综合征患者的食物敏感性会导致持续的临床反应,并对这个具有挑战性的疾病的整体健康和生活质量产生影响。