Department of Pediatric Research, Faculty of Medicine, University of Oslo, Oslo, Norway.
Celiac Disease Research Center, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Aliment Pharmacol Ther. 2024 Oct;60(8):988-1004. doi: 10.1111/apt.18234. Epub 2024 Sep 5.
In coeliac disease and environmental enteropathy, dietary gluten and enteric infections cause reversible inflammation and morphological changes to the small intestinal mucosa that can be detected in biopsy samples obtained by endoscopy. However, there is a clear need for non-invasive biomarkers. Constant shedding of mucosal material into the bowel lumen and faeces, together with easy availability of stool, makes it an interesting sample matrix.
To conduct a systematic literature search and summarize the existing evidence for host mucosa-derived faecal biomarkers in evaluating small intestinal damage.
We searched for studies on PubMed (MEDLINE) until 1 March 2024.
We identified 494 studies and included 35 original case-control and cohort studies. These assessed host mucosal transcripts and 14 other markers aiming specifically to reflect inflammation and cell-mediated, innate and gluten-induced immune responses. In coeliac disease, faecal calprotectin and anti-gliadin, tissue transglutaminase, endomysium and deamidated gliadin peptide antibodies were the most studied but with inconsistent results. Single studies reported positive findings about microRNA transcripts, β-defensin-2, lipocalin-2, zonulin-related proteins and angiotensin-converting enzyme. In environmental enteropathy, a non-significant association was reported between calprotectin and urine lactulose/mannitol ratio; there were conflicting results for neopterin, myeloperoxidase and host transcripts. Single studies reported a positive association for lactoferrin, and a negative association for regenerating islet-derived protein 1. Studies comparing faecal markers against small intestinal biopsy findings were not identified in environmental enteropathy.
Further studies are needed to determine reliable faecal markers as a proxy for small intestinal mucosal damage.
在乳糜泻和肠病性肢端皮炎中,饮食中的麸质和肠道感染会引起小肠黏膜的炎症和形态学改变,这些改变可在通过内镜获得的活检样本中检测到。然而,目前非常需要非侵入性的生物标志物。黏膜物质不断脱落到肠腔和粪便中,再加上粪便易于获得,这使其成为一个有趣的样本基质。
进行系统的文献检索,总结目前用于评估小肠损伤的宿主黏膜衍生粪便生物标志物的证据。
我们在 PubMed(MEDLINE)上进行了检索,检索时间截至 2024 年 3 月 1 日。
我们共识别出 494 项研究,并纳入了 35 项原始病例对照和队列研究。这些研究评估了宿主黏膜转录物和 14 种其他标志物,旨在专门反映炎症以及细胞介导、固有和麸质诱导的免疫反应。在乳糜泻中,粪便钙卫蛋白和抗麦胶蛋白、组织转谷氨酰胺酶、内肌丝和脱酰胺麦胶肽抗体是研究最多的,但结果不一致。有单项研究报告了 microRNA 转录物、β-防御素-2、脂联素、紧密连接相关蛋白和血管紧张素转换酶的阳性发现。在肠病性肢端皮炎中,粪便钙卫蛋白与尿乳果糖/甘露醇比值之间的相关性无统计学意义;而对于新蝶呤、髓过氧化物酶和宿主转录物,结果则存在矛盾。有单项研究报告乳铁蛋白呈正相关,再生胰岛衍生蛋白 1 呈负相关。在肠病性肢端皮炎中,未发现比较粪便标志物和小肠活检结果的研究。
需要进一步研究以确定可靠的粪便标志物作为小肠黏膜损伤的替代指标。