Mai Huanzhuo, Yang Xing, Xie Yulan, Zhou Jie, Wang Qing, Wei Yiru, Yang Yuecong, Lu Dongjia, Ye Li, Cui Ping, Liang Hao, Huang Jiegang
School of Public Health, Guangxi Medical University, Nanning, China.
Guangxi Key Laboratory of AIDS Prevention and Treatment, Guangxi Medical University, Nanning, China.
Front Microbiol. 2024 Jan 5;14:1257903. doi: 10.3389/fmicb.2023.1257903. eCollection 2023.
Non-alcoholic fatty liver disease (NAFLD) is the most prevalent cause of chronic liver disease worldwide, and gut microbes are associated with the development and progression of NAFLD. Despite numerous studies exploring the changes in gut microbes associated with NAFLD, there was no consistent pattern of changes.
We retrieved studies on the human fecal microbiota sequenced by 16S rRNA gene amplification associated with NAFLD from the NCBI database up to April 2023, and re-analyzed them using bioinformatic methods.
We finally screened 12 relevant studies related to NAFLD, which included a total of 1,189 study subjects (NAFLD, = 654; healthy control, = 398; obesity, = 137). Our results revealed a significant decrease in gut microbial diversity with the occurrence and progression of NAFLD (SMD = -0.32; 95% CI -0.42 to -0.21; < 0.001). Alpha diversity and the increased abundance of several crucial genera, including , , and , can serve as an indication of their predictive risk ability for the occurrence and progression of NAFLD (all AUC > 0.7). The occurrence and progression of NAFLD are significantly associated with higher levels of LPS biosynthesis, tryptophan metabolism, glutathione metabolism, and lipid metabolism.
This study elucidated gut microbes relevance to disease development and identified potential risk-associated microbes and functional pathways associated with NAFLD occurrence and progression.
非酒精性脂肪性肝病(NAFLD)是全球慢性肝病最常见的病因,肠道微生物与NAFLD的发生和发展相关。尽管有大量研究探索了与NAFLD相关的肠道微生物变化,但变化模式并不一致。
我们从NCBI数据库中检索了截至2023年4月通过16S rRNA基因扩增测序的与NAFLD相关的人类粪便微生物群研究,并使用生物信息学方法对其进行重新分析。
我们最终筛选出12项与NAFLD相关的研究,共纳入1189名研究对象(NAFLD组654例;健康对照组398例;肥胖组137例)。我们的结果显示,随着NAFLD的发生和发展,肠道微生物多样性显著降低(标准化均数差=-0.32;95%可信区间-0.42至-0.21;P<0.001)。α多样性以及几个关键菌属丰度的增加,包括 、 和 ,可作为它们对NAFLD发生和发展预测风险能力的指标(所有曲线下面积>0.7)。NAFLD的发生和发展与较高水平的脂多糖生物合成、色氨酸代谢、谷胱甘肽代谢和脂质代谢显著相关。
本研究阐明了肠道微生物与疾病发展的相关性,并确定了与NAFLD发生和发展相关的潜在风险相关微生物和功能途径。