酒精性脂肪性肝病的肠道菌群失调:不同的微生物群落和生化改变

IF 1.7 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
American journal of translational research Pub Date : 2025-06-15 eCollection Date: 2025-01-01 DOI:10.62347/LDCH9386
Xin Li, Fan Yang, Yuning Shi, Zheng Li, Zhuo Wang, Youqing Xu
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引用次数: 0

摘要

目的:比较酒精性脂肪性肝病(AFLD)患者、无肝损害的酒精使用障碍(AUD)患者和健康对照者的肠道微生物群组成,并探讨微生物谱与肝脏健康之间的相关性。方法:对34例患者进行回顾性分析,其中14例为AFLD, 10例为AUD,无肝损害,10例为健康对照。评估血液生化指标、肝功能测试、脂质谱和肠道微生物群组成。通过高通量16S rRNA基因测序分析肠道菌群。计算α和β多样性指数,确定群落特有的微生物类群。结果:与其他组相比,AFLD患者表现出厚壁菌门/拟杆菌门比例降低,拟杆菌门丰度增加,表明肠道生态失调。生化指标,包括甘油三酯、丙氨酸转氨酶、γ -谷氨酰转移酶和胆碱酯酶,在AFLD患者中显著改变(均P < 0.05)。Beta多样性分析显示,AFLD组中存在不同的微生物群落。值得注意的是,巨型单胞菌(Megamonas)和硒单胞菌(Selenomonadales)等类群AFLD富集,而瘤胃球菌(Ruminococcus)和粪杆菌(Faecalibacterium)等有益类群AFLD显著减少。结论:AFLD与明显的肠道菌群改变和明显的微生物特征相关,这些特征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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gut microbiota dysbiosis in alcoholic fatty liver disease: distinct microbial communities and biochemical alterations.

Objectives: 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.

Methods: 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.

Results: 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.

Conclusion: 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.

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American journal of translational research
American journal of translational research ONCOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
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