微生物群
失调
队列
医学
炎症性肠病
生物
肠道菌群
免疫学
队列研究
内科学
疾病
生物信息学
作者
Victoria Pascal,Marta Pozuelo,Natalia Borruel,Francesc Casellas,David Campos,Alba Santiago,Xavier Martínez,Encarna Varela,Guillaume Sarrabayrouse,Kathleen Machiels,Séverine Vermeire,Harry Sokol,Francisco Guarner,Chaysavanh Manichanh
出处
期刊:Gut
[BMJ]
日期:2017-02-07
卷期号:66 (5): 813-822
被引量:725
标识
DOI:10.1136/gutjnl-2016-313235
摘要
Objective
A decade of microbiome studies has linked IBD to an alteration in the gut microbial community of genetically predisposed subjects. However, existing profiles of gut microbiome dysbiosis in adult IBD patients are inconsistent among published studies, and did not allow the identification of microbial signatures for CD and UC. Here, we aimed to compare the faecal microbiome of CD with patients having UC and with non-IBD subjects in a longitudinal study. Design
We analysed a cohort of 2045 non-IBD and IBD faecal samples from four countries (Spain, Belgium, the UK and Germany), applied a 16S rRNA sequencing approach and analysed a total dataset of 115 million sequences. Results
In the Spanish cohort, dysbiosis was found significantly greater in patients with CD than with UC, as shown by a more reduced diversity, a less stable microbial community and eight microbial groups were proposed as a specific microbial signature for CD. Tested against the whole cohort, the signature achieved an overall sensitivity of 80% and a specificity of 94%, 94%, 89% and 91% for the detection of CD versus healthy controls, patients with anorexia, IBS and UC, respectively. Conclusions
Although UC and CD share many epidemiologic, immunologic, therapeutic and clinical features, our results showed that they are two distinct subtypes of IBD at the microbiome level. For the first time, we are proposing microbiomarkers to discriminate between CD and non-CD independently of geographical regions.
科研通智能强力驱动
Strongly Powered by AbleSci AI