Wright Emily K, Kamm Michael A, Teo Shu Mei, Inouye Michael, Wagner Josef, Kirkwood Carl D
*Department of Gastroenterology, St Vincent's Hospital Melbourne, Australia; †Department of Pathology, University of Melbourne, Australia; ‡Imperial College, London, United Kingdom; and §Enteric Virus Group, Murdoch Children's Research Institute, Melbourne, Australia.
Inflamm Bowel Dis. 2015 Jun;21(6):1219-28. doi: 10.1097/MIB.0000000000000382.
The intestinal microbiota is involved in the pathogenesis of inflammatory bowel disease. A reduction in the diversity of the intestinal microbiota as well as specific taxonomic and functional shifts have been reported in Crohn's disease and may play a central role in the inflammatory process. The aim was to systematically review recent developments in the structural and functional changes observed in the gastrointestinal microbiome in patients with Crohn's Disease.
Seventy-two abstracts were included in this review. The effects of host genetics, disease phenotype, and inflammatory bowel disease treatment on the gastrointestinal microbiome in Crohn's disease were reviewed, and taxonomic shifts in patients with early and established disease were described. The relative abundance of Bacteroidetes is increased and Firmicutes decreased in Crohn's disease compared with healthy controls. Enterobacteriaceae, specifically Eschericia coli, is enriched in Crohn's disease. Faecalibacterium prausnitzii is found at lower abundance in Crohn's disease and in those with postoperative recurrence. Observed functional changes include major shifts in oxidative stress pathways, a decrease in butanoate and propanoate metabolism gene expression, lower levels of butyrate, and other short-chain fatty acids, decreased carbohydrate metabolism, and decreased amino acid biosynthesis.
Changes in microbial composition and function have been described, although a causative role remains to be established. Larger, prospective, and longitudinal studies are required with deep interrogation of the microbiome if causality is to be determined, and refined microbial manipulation is to emerge as a focused therapy.
肠道微生物群参与炎症性肠病的发病机制。据报道,克罗恩病患者肠道微生物群的多样性降低,以及特定的分类学和功能发生了变化,这些变化可能在炎症过程中起核心作用。目的是系统回顾克罗恩病患者胃肠道微生物组结构和功能变化的最新进展。
本综述纳入了72篇摘要。回顾了宿主遗传学、疾病表型和炎症性肠病治疗对克罗恩病患者胃肠道微生物组的影响,并描述了疾病早期和确诊患者的分类学变化。与健康对照相比,克罗恩病患者中拟杆菌门的相对丰度增加,厚壁菌门减少。肠杆菌科,特别是大肠杆菌,在克罗恩病中富集。在克罗恩病患者及术后复发患者中,普拉梭菌的丰度较低。观察到的功能变化包括氧化应激途径的重大改变、丁酸和丙酸代谢基因表达的降低、丁酸和其他短链脂肪酸水平的降低、碳水化合物代谢的减少以及氨基酸生物合成的减少。
尽管因果关系尚待确定,但已经描述了微生物组成和功能的变化。如果要确定因果关系并使精准的微生物调控成为一种有针对性的治疗方法,则需要开展更大规模的前瞻性纵向研究,并对微生物组进行深入研究。