非酒精性脂肪肝
纤维化
基因组
微生物群
肝活检
内科学
医学
胃肠病学
疾病
生物
脂肪肝
生物信息学
活检
基因
遗传学
作者
Rohit Loomba,Victor Seguritan,Weizhong Li,Tao Long,Niels Klitgord,Archana Bhatt,Parambir S. Dulai,Cyrielle Caussy,Richele Bettencourt,Sarah K. Highlander,Marcus B. Jones,Claude B. Sirlin,Bernd Schnabl,Lauren Brinkac,Nicholas J. Schork,Chi‐Hua Chen,David A. Brenner,William Biggs,Shibu Yooseph,J. Craig Venter,Karen E. Nelson
出处
期刊:Cell Metabolism
[Elsevier]
日期:2017-05-01
卷期号:25 (5): 1054-1062.e5
被引量:787
标识
DOI:10.1016/j.cmet.2017.04.001
摘要
The presence of advanced fibrosis in nonalcoholic fatty liver disease (NAFLD) is the most important predictor of liver mortality. There are limited data on the diagnostic accuracy of gut microbiota-derived signature for predicting the presence of advanced fibrosis. In this prospective study, we characterized the gut microbiome compositions using whole-genome shotgun sequencing of DNA extracted from stool samples. This study included 86 uniquely well-characterized patients with biopsy-proven NAFLD, of which 72 had mild/moderate (stage 0–2 fibrosis) NAFLD, and 14 had advanced fibrosis (stage 3 or 4 fibrosis). We identified a set of 40 features (p < 0.006), which included 37 bacterial species that were used to construct a Random Forest classifier model to distinguish mild/moderate NAFLD from advanced fibrosis. The model had a robust diagnostic accuracy (AUC 0.936) for detecting advanced fibrosis. This study provides preliminary evidence for a fecal-microbiome-derived metagenomic signature to detect advanced fibrosis in NAFLD.
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