Leeds Gastroenterology Institute, D Floor, Clarendon Wing, Leeds General Infirmary, Great George Street, Leeds LS1 3EX, UK.
J Gastroenterol. 2011 Apr;46(4):421-31. doi: 10.1007/s00535-011-0379-9. Epub 2011 Feb 18.
The causes of irritable bowel syndrome (IBS) remain obscure. Some investigators have proposed chronic low-grade mucosal inflammation as a potential etiological factor. We performed a systematic review to examine this issue in detail.
MEDLINE, EMBASE, and EMBASE classic were searched up to December 2010 to identify studies of case-control design applying tests for low-grade inflammation to either full-thickness intestinal or endoscopic mucosal biopsies from patients with IBS. Controls were required to be healthy individuals, or asymptomatic patients undergoing investigation for reasons other than the reporting of upper or lower gastrointestinal symptoms. Individual study results were summarized descriptively.
The literature search identified 1388 citations, of which 16 studies were eligible for inclusion. Individual study results were diverse, partly as a consequence of the different surrogate markers for inflammatory mechanisms studied. Mast cells, T lymphocytes, B lymphocytes, and mucosal cytokine production all appeared altered among cases with IBS in individual studies, while no study demonstrated a significant difference in numbers of plasma cells, neutrophils, or eosinophils. Some studies suggested a relationship between mast cell abnormalities and symptom severity and frequency, as well as co-existent fatigue and depression. Studies were limited by the lack of comparability of controls, and the fact that most were conducted in highly selected groups of patients with IBS.
Low-grade mucosal inflammation, particularly mast cell activation, may be a contributory factor in the pathogenesis of IBS. Mast cell stabilizers warrant further assessment as a potential therapy in the condition.
肠易激综合征(IBS)的病因仍不清楚。一些研究人员提出慢性低度黏膜炎症可能是潜在的病因。我们进行了系统评价,以详细研究这个问题。
检索 MEDLINE、EMBASE 和 EMBASE classic,以确定截至 2010 年 12 月应用低度炎症检测方法对 IBS 患者全层肠或内镜黏膜活检的病例对照研究。对照需要为健康个体或因上消化道或下消化道症状以外的原因接受检查的无症状患者。对单个研究的结果进行描述性总结。
文献检索共确定了 1388 条引用,其中 16 项研究符合纳入标准。个别研究的结果存在差异,部分原因是研究的炎症机制替代标志物不同。在个别研究中,IBS 患者的肥大细胞、T 淋巴细胞、B 淋巴细胞和黏膜细胞因子产生均发生改变,而没有研究显示浆细胞、中性粒细胞或嗜酸性粒细胞数量存在显著差异。一些研究表明肥大细胞异常与症状严重程度和频率以及共存的疲劳和抑郁之间存在关系。研究受到对照缺乏可比性以及大多数研究都是在高度选择的 IBS 患者群体中进行的限制。
低度黏膜炎症,特别是肥大细胞激活,可能是 IBS 发病机制中的一个促成因素。肥大细胞稳定剂作为该疾病的潜在治疗方法值得进一步评估。