NIHR Biomedical Research Unit, Nottingham Digestive Diseases Centre, University Hospital, Nottingham NG7 2UH, United Kingdom.
Curr Opin Pharmacol. 2011 Dec;11(6):586-92. doi: 10.1016/j.coph.2011.09.009. Epub 2011 Oct 13.
Recent data developing from the study of postinfectious IBS has challenged the belief that IBS is a purely psychological disorder. Distinct abnormalities of the gut mucosa have been reported including immune activation and increased release of inflammatory mediators with some overlap with IBD. New studies show that genetic factors which predispose to IBD are also associated with IBS. A common feature is impaired gut barrier function which appears to precede the development of IBD while in IBS it may be the result of either a preceding infection or psychosocial stress. Stress can activate mast cells which are a feature in most but not all IBS series. Anti-inflammatory treatments targeting activated mast cells may benefit IBS patients but currently the evidence is weak and larger trials are needed. Changes in the commensal microbiota have been recently described with a "dysbiosis" in CD characterised by reduced diversity. Inconsistent changes have also been described in IBS but studies controlling for antibiotic use and differences in diet and bowel habit are needed before definitive conclusions can be made.
最近从感染后肠易激综合征(IBS)的研究中得出的数据,对肠易激综合征完全是一种心理障碍的观点提出了挑战。据报道,肠道黏膜有明显的异常,包括免疫激活和炎症介质释放增加,与炎症性肠病(IBD)有一些重叠。新的研究表明,易患 IBD 的遗传因素也与肠易激综合征有关。一个共同的特征是肠道屏障功能受损,这似乎先于 IBD 的发展,而在肠易激综合征中,它可能是先前感染或心理社会压力的结果。压力会激活肥大细胞,肥大细胞是大多数但不是所有肠易激综合征患者的特征。针对活化肥大细胞的抗炎治疗可能对肠易激综合征患者有益,但目前证据薄弱,需要进行更大规模的试验。最近描述了共生微生物群的变化,CD 表现为多样性减少的“失调”。在肠易激综合征中也描述了不一致的变化,但需要在控制抗生素使用、饮食和肠道习惯差异的情况下进行研究,然后才能得出明确的结论。