Nonalcoholic Fatty Liver Disease: Changes in Gut Microbiota and Blood Lipids.

IF 3.1 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Keen Yang, Jieying Zeng, Huaiyu Wu, Huiyu Liu, Zhimin Ding, Weiyu Liang, Linghu Wu, Ziwei Lin, Wenhui Huang, Jinfeng Xu, Fajin Dong
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Abstract

Background and aims: The global prevalence of nonalcoholic fatty liver disease (NAFLD) is 25%. This study aimed to explore differences in the gut microbial community and blood lipids between normal livers and those affected by NAFLD using 16S ribosomal deoxyribonucleic acid sequencing.

Methods: Gut microbiome profiles of 40 NAFLD and 20 non-NAFLD controls were analyzed. Information about four blood lipids and 13 other clinical features was collected. Patients were divided into three groups by ultrasound and FibroScan, those with a normal liver, mild FL (FL1), and moderate-to-severe FL (FL2). FL1 and FL2 patients were divided into two groups, those with either hyperlipidemia or non-hyperlipidemia based on their blood lipids. Potential keystone species within the groups were identified using univariate analysis and a specificity-occupancy plot. Significant difference in biochemical parameters ion NAFLD patients and healthy individuals were identified by detrended correspondence analysis and canonical correspondence analysis.

Results: Decreased gut bacterial diversity was found in patients with NAFLD. Firmicutes/Bacteroidetes decreased as NAFLD progressed. Faecalibacterium and Ruminococcus 2 were the most representative fatty-related bacteria. Glutamate pyruvic transaminase, aspartate aminotransferase, and white blood cell count were selected as the most significant biochemical indexes. Calculation of areas under the curve identified two microbiomes combined with the three biochemical indexes that identified normal liver and FL2 very well but performed poorly in diagnosing FL1.

Conclusions: Faecalibacterium and Ruminococcus 2, combined with glutamate pyruvic transaminase, aspartate aminotransferase, and white blood cell count distinguished NAFLD. We speculate that regulating the health of gut microbiota may release NAFLD, in addition to providing new targets for clinicians to treat NAFLD.

非酒精性脂肪肝:肠道微生物群和血脂的变化。
背景和目的:非酒精性脂肪肝(NAFLD)的全球发病率为25%。本研究旨在利用 16S 核糖体脱氧核糖核酸测序技术,探讨正常肝脏与非酒精性脂肪肝患者的肠道微生物群落和血脂之间的差异:方法: 分析了40名非酒精性脂肪肝患者和20名非非酒精性脂肪肝对照者的肠道微生物群谱。收集了有关四种血脂和 13 种其他临床特征的信息。通过超声波和纤维扫描将患者分为三组:肝脏正常组、轻度非酒精性脂肪肝组(FL1)和中重度非酒精性脂肪肝组(FL2)。FL1和FL2患者根据血脂分为两组,即高脂血症组和非高脂血症组。通过单变量分析和特异性占位图确定了组内潜在的关键物种。通过去趋势对应分析和典型对应分析,确定了非酒精性脂肪肝患者和健康人之间生化指标的显著差异:结果:发现非酒精性脂肪肝患者肠道细菌多样性减少。随着非酒精性脂肪肝的进展,固缩菌/类杆菌减少。粪杆菌和反刍球菌 2 是最具代表性的脂肪相关细菌。谷氨酸丙酮酸转氨酶、天冬氨酸氨基转移酶和白细胞计数被选为最重要的生化指标。通过计算曲线下面积发现,两种微生物群与三种生化指标相结合,能很好地识别正常肝脏和FL2,但在诊断FL1时表现不佳:结论:粪便细菌和反刍球菌 2 与谷氨酸丙酮酸转氨酶、天门冬氨酸氨基转移酶和白细胞计数相结合,可区分非酒精性脂肪肝。我们推测,除了为临床医生治疗非酒精性脂肪肝提供新的靶点外,调节肠道微生物群的健康也可能缓解非酒精性脂肪肝。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Clinical and Translational Hepatology
Journal of Clinical and Translational Hepatology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
6.40
自引率
2.80%
发文量
496
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