Department of Clinical and Experimental Medicine, Translational Research Center for Gastrointestinal Disorders, KU Leuven, , Leuven, Belgium.
Gut. 2014 Feb;63(2):262-71. doi: 10.1136/gutjnl-2012-303857. Epub 2013 Mar 8.
OBJECTIVE: Functional dyspepsia (FD) is an extremely common functional gastrointestinal disorder, the pathophysiology of which is poorly understood. We hypothesised that impaired intestinal barrier function is involved in the onset and persistence of this disorder by inducing low-grade inflammation. Therefore, our aim was to evaluate duodenal mucosal integrity and low-grade inflammation in patients with FD. DESIGN: Duodenal biopsy specimens were obtained from 15 patients with FD fulfilling the Rome III criteria and 15 age- and gender-matched healthy volunteers. Transepithelial electrical resistance (TEER) and paracellular permeability were measured in Ussing chambers. Expression of cell-to-cell adhesion proteins was evaluated by real-time PCR, western blot and/or immunofluorescence. Numbers of mast cells, eosinophils and intraepithelial lymphocytes were assessed by immunohistochemistry. RESULTS: Patients with FD displayed lower TEER and increased paracellular passage compared with healthy controls, which is indicative of impaired mucosal integrity. In addition, abnormal expression of cell-to-cell adhesion proteins at the level of tight junctions, adherens junctions and desmosomes was shown. Furthermore, patients were characterised by the presence of low-grade inflammation, as demonstrated by increased infiltration of mucosal mast cells and eosinophils. A significant association between the expression level of several cell-to-cell adhesion proteins, the extent of increased permeability and the severity of low-grade inflammation was found. CONCLUSIONS: These findings challenge the classical paradigm that patients with FD show no structural changes in the gastrointestinal tract. We suggest that impaired intestinal barrier function is a pathophysiological mechanism in FD. Thus, restoration of intestinal barrier integrity may be a potential therapeutic target for treating patients with FD.
目的:功能性消化不良(FD)是一种极为常见的功能性胃肠疾病,其病理生理学尚未完全阐明。我们假设,肠道屏障功能受损通过引发低度炎症而参与这种疾病的发生和持续。因此,我们的目的是评估 FD 患者的十二指肠黏膜完整性和低度炎症。
设计:从符合 Rome III 标准的 15 例 FD 患者和 15 名年龄和性别匹配的健康志愿者中获取十二指肠活检标本。在 Ussing 室中测量跨上皮电阻(TEER)和细胞旁通透性。通过实时 PCR、western blot 和/或免疫荧光评估细胞间黏附蛋白的表达。通过免疫组织化学评估肥大细胞、嗜酸性粒细胞和上皮内淋巴细胞的数量。
结果:与健康对照组相比,FD 患者的 TEER 较低,细胞旁通透性增加,表明黏膜完整性受损。此外,还显示出紧密连接、黏附连接和桥粒处细胞间黏附蛋白的异常表达。此外,患者存在低度炎症,表现为黏膜肥大细胞和嗜酸性粒细胞浸润增加。发现几种细胞间黏附蛋白的表达水平、通透性增加的程度和低度炎症的严重程度之间存在显著相关性。
结论:这些发现挑战了 FD 患者胃肠道无结构变化的经典观点。我们认为,肠道屏障功能受损是 FD 的一种病理生理机制。因此,恢复肠道屏障完整性可能是治疗 FD 患者的潜在治疗靶点。
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