Department of Endocrinology and Nutrition, Virgen de la Victoria University Hospital, Malaga University, Campus Teatinos S/N, 29010, Málaga, Spain.
Instituto de Investigación Biomédica de Málaga-Plataforma BIONAND (IBIMA), Virgen de la Victoria University Hospital, Malaga University, 2ª Planta, Campus Teatinos S/N, 29010, Málaga, Spain.
J Gastroenterol. 2024 Apr;59(4):329-341. doi: 10.1007/s00535-023-02075-7. Epub 2024 Jan 24.
BACKGROUND/AIM: Alterations in gut microbiota are associated with the pathogenesis of metabolic diseases, including metabolic-associated fatty liver disease (MAFLD). The aim of this study was to evaluate gut microbiota composition and functionality in patients with morbid obesity with different degrees of MAFLD, as assessed by biopsy. SUBJECTS/METHODS: 110 patients with morbid obesity were evaluated by biopsy obtained during bariatric surgery for MAFLD. Stool samples were collected prior to surgery for microbiota analysis. RESULTS: Gut microbiota from patients with steatosis and non-alcoholic steatohepatitis (NASH) were characterized by an enrichment in Enterobacteriaceae (an ethanol-producing bacteria), Acidaminococcus and Megasphaera and the depletion of Eggerthellaceae and Ruminococcaceae (SCFA-producing bacteria). MAFLD was also associated with enrichment of pathways related to proteinogenic amino acid degradation, succinate production, menaquinol-7 (K2-vitamin) biosynthesis, and saccharolytic and proteolytic fermentation. Basic histological hepatic alterations (steatosis, necroinflammatory activity, or fibrosis) were associated with specific changes in microbiota patterns. Overall, the core microbiome related to basic histological alterations in MAFLD showed an increase in Enterobacteriaceae and a decrease in Ruminococcaceae. Specifically, Escherichia coli was associated with steatosis and necroinflammatory activity, whilst Escherichia-shigella was associated with fibrosis and necroinflammatory activity. CONCLUSIONS: We established a link between gut microbiota alterations and histological injury in liver diagnosis using biopsy. Harmful products such as ethanol or succinate may be involved in the pathogenesis and progression of MAFLD. Thus, these alterations in gut microbiota patterns and their possible metabolic pathways could add information to the classical predictors of MAFLD severity and suggest novel metabolic targets.
背景/目的:肠道微生物群的改变与代谢性疾病的发病机制有关,包括代谢相关脂肪性肝病(MAFLD)。本研究旨在评估通过活检评估的不同 MAFLD 严重程度的病态肥胖患者的肠道微生物群组成和功能。 受试者/方法:对 110 例病态肥胖患者进行了 MAFLD 活检评估。在减重手术前采集粪便样本进行微生物分析。 结果:脂肪变性和非酒精性脂肪性肝炎(NASH)患者的肠道微生物群特征是肠杆菌科(产乙醇细菌)、产酸菌属和巨球形菌属富集,而 Eggerthellaceae 和 Ruminococcaceae(产生 SCFA 的细菌)减少。MAFLD 还与与蛋白源氨基酸降解、琥珀酸产生、menaquinol-7(K2 维生素)生物合成以及糖解和蛋白水解发酵相关途径的富集有关。基本组织学肝改变(脂肪变性、坏死性炎症活动或纤维化)与微生物群模式的特定变化有关。总体而言,与 MAFLD 基本组织学改变相关的核心微生物群表现为肠杆菌科增加和 Ruminococcaceae 减少。具体而言,大肠杆菌与脂肪变性和坏死性炎症活动有关,而大肠埃希氏菌-志贺氏菌与纤维化和坏死性炎症活动有关。 结论:我们通过活检建立了肠道微生物群改变与肝脏诊断组织学损伤之间的联系。有害产物,如乙醇或琥珀酸,可能参与 MAFLD 的发病机制和进展。因此,这些肠道微生物群模式及其可能的代谢途径的改变可以为 MAFLD 严重程度的经典预测指标提供信息,并为新的代谢靶点提供建议。
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