脂肪变性
失调
微生物群
脂肪肝
肠道菌群
基因组
代谢组学
生物
混淆
疾病
生物信息学
计算生物学
医学
免疫学
遗传学
内科学
内分泌学
基因
作者
Müjdat Zeybel,Muhammad Arif,Xiangyü Li,Özlem Altay,Hong Yang,Mengnan Shi,Murat Akyıldız,Burçin Sağlam,Mehmet Gökhan Gönenli,Buket Yiğit,Bürge Ulukan,Dilek Ural,Saeed Shoaie,Hasan Türkez,Jens Nielsen,Cheng Zhang,Mathias Uhlén,Jan Borén,Adil Mardinoğlu
出处
期刊:Advanced Science
[Wiley]
日期:2022-02-07
卷期号:9 (11): e2104373-e2104373
被引量:72
标识
DOI:10.1002/advs.202104373
摘要
Metabolic dysfunction-associated fatty liver disease (MAFLD) is a complex disease involving alterations in multiple biological processes regulated by the interactions between obesity, genetic background, and environmental factors including the microbiome. To decipher hepatic steatosis (HS) pathogenesis by excluding critical confounding factors including genetic variants and diabetes, 56 heterogenous MAFLD patients are characterized by generating multiomics data including oral and gut metagenomics as well as plasma metabolomics and inflammatory proteomics data. The dysbiosis in the oral and gut microbiome is explored and the host-microbiome interactions based on global metabolic and inflammatory processes are revealed. These multiomics data are integrated using the biological network and HS's key features are identified using multiomics data. HS is finally predicted using these key features and findings are validated in a follow-up cohort, where 22 subjects with varying degree of HS are characterized.
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