Li Xin, Yang Fan, Shi Yuning, Li Zheng, Wang Zhuo, Xu Youqing
Department of Gastroenterology, Beijing Tiantan Hospital, Capital Medical University Beijing 100070, P. R. China.
Department of Gastroenterology, Beijing Chuiyangliu Hospital Beijing 100022, P. R. China.
Am J Transl Res. 2025 Jun 15;17(6):4213-4224. doi: 10.62347/LDCH9386. eCollection 2025.
To compare the gut microbiota composition among patients with alcoholic fatty liver disease (AFLD), individuals with alcohol use disorder (AUD) without liver damage, and healthy controls, and to investigate correlations between microbial profiles and liver health.
A retrospective analysis was conducted on 34 participants: 14 with AFLD, 10 with AUD without liver damage, and 10 healthy controls. Blood biochemical markers, liver function tests, lipid profiles, and gut microbiota composition were assessed. Gut microbiota was analyzed via high-throughput 16S rRNA gene sequencing. Alpha and beta diversity indices were calculated, and group-specific microbial taxa were identified.
AFLD patients showed a decreased Firmicutes/Bacteroidetes ratio and an increased abundance of Bacteroidetes, indicating gut dysbiosis compared to the other groups. Biochemical markers, including triglycerides, alanine aminotransferase, gamma-glutamyl transferase, and cholinesterase, were significantly altered in AFLD patients (all P > 0.05). Beta diversity analysis revealed distinct microbial communities in the AFLD group. Notably, taxa such as Megamonas and Selenomonadales were enriched in AFLD, while beneficial genera like Ruminococcus and Faecalibacterium were significantly reduced.
AFLD is associated with marked gut microbiota alterations and distinct microbial signatures, which correlate with liver dysfunction and biochemical abnormalities, highlighting the role of dysbiosis in disease pathogenesis.
比较酒精性脂肪性肝病(AFLD)患者、无肝损伤的酒精使用障碍(AUD)个体和健康对照者的肠道微生物群组成,并研究微生物谱与肝脏健康之间的相关性。
对34名参与者进行回顾性分析:14名AFLD患者、10名无肝损伤的AUD患者和10名健康对照者。评估血液生化标志物、肝功能测试、血脂谱和肠道微生物群组成。通过高通量16S rRNA基因测序分析肠道微生物群。计算α和β多样性指数,并鉴定特定组的微生物分类群。
与其他组相比,AFLD患者的厚壁菌门/拟杆菌门比值降低,拟杆菌门丰度增加,表明肠道生态失调。AFLD患者的生化标志物,包括甘油三酯、丙氨酸转氨酶、γ-谷氨酰转移酶和胆碱酯酶,均有显著改变(均P>0.05)。β多样性分析显示AFLD组有独特的微生物群落。值得注意的是,巨单胞菌属和月形单胞菌目等分类群在AFLD中富集,而瘤胃球菌属和粪杆菌属等有益菌属显著减少。
AFLD与明显的肠道微生物群改变和独特的微生物特征相关,这些与肝功能障碍和生化异常相关,突出了生态失调在疾病发病机制中的作用。