Facultad de Química, Unidad de Genómica de Poblaciones Aplicada a la Salud, Universidad Nacional Autónoma de México (UNAM)/Instituto Nacional de Medicina Genómica (INMEGEN), Mexico City, Mexico.
Departamento de Alimentos y Biotecnologia, Facultad de Química, Universidad Nacional Autónoma de Mexico, Mexico City, Mexico.
J Gastroenterol Hepatol. 2023 May;38(5):791-799. doi: 10.1111/jgh.16147. Epub 2023 Mar 2.
Non-alcoholic fatty liver disease (NAFLD) is the most common cause of liver disease. Increasing evidence indicates that the gut microbiota can play an important role in the pathophysiology of NAFLD. Recently, several studies have tested the predictive value of gut microbiome profiles in NAFLD progression; however, comparisons of microbial signatures in NAFLD or non-alcoholic steatohepatitis (NASH) have produced discrepant results, possibly due to ethnic and environmental factors. Thus, we aimed to characterize the gut metagenome composition of patients with fatty liver disease.
Gut microbiome of 45 well-characterized patients with obesity and biopsy-proven NAFLD was evaluated using shot-gun sequencing: 11 non-alcoholic fatty liver controls (non-NAFL), 11 with fatty liver, and 23 with NASH.
Our study showed that Parabacteroides distasonis and Alistipes putredenis were enriched in fatty liver but not in NASH patients. Notably, in a hierarchical clustering analysis, microbial profiles were differentially distributed among groups, and membership to a Prevotella copri dominant cluster was associated with a greater risk of developing NASH. Functional analyses showed that although no differences in LPS biosynthesis pathways were observed, Prevotella-dominant subjects had higher circulating levels of LPS and a lower abundance of pathways encoding butyrate production.
Our findings suggest that a Prevotella copri dominant bacterial community is associated with a greater risk for NAFLD disease progression, probably linked to higher intestinal permeability and lower capacity for butyrate production.
非酒精性脂肪性肝病(NAFLD)是最常见的肝病病因。越来越多的证据表明,肠道微生物群在 NAFLD 的病理生理学中可能发挥重要作用。最近,有几项研究测试了肠道微生物群谱在 NAFLD 进展中的预测价值;然而,NAFLD 或非酒精性脂肪性肝炎(NASH)中微生物特征的比较产生了不一致的结果,这可能是由于种族和环境因素。因此,我们旨在描述脂肪性肝病患者的肠道宏基因组组成。
使用 shotgun 测序评估了 45 例特征明确的肥胖和活检证实的 NAFLD 患者的肠道微生物群:11 例非酒精性脂肪肝对照(非 NAFL)、11 例脂肪性肝病和 23 例 NASH。
我们的研究表明,拟杆菌属和艾克曼菌属在脂肪性肝病中丰富,但在 NASH 患者中不丰富。值得注意的是,在层次聚类分析中,微生物谱在各组中差异分布,而普雷沃氏菌属优势簇的成员与发生 NASH 的风险增加相关。功能分析表明,尽管 LPS 生物合成途径没有差异,但普雷沃氏菌属优势的受试者循环 LPS 水平更高,丁酸产生途径的丰度更低。
我们的发现表明,普雷沃氏菌属主导的细菌群落与 NAFLD 疾病进展的风险增加相关,这可能与更高的肠道通透性和更低的丁酸产生能力有关。