脂肪肝
脂毒性
疾病
慢性肝病
营养基因学
生物信息学
表型
肝病
生物
医学
内科学
基因
肝硬化
遗传学
肥胖
胰岛素抵抗
作者
Alessandro Cherubini,Elia Casirati,Melissa Tomasi,Luca Valenti
标识
DOI:10.1080/14728222.2021.2018418
摘要
The main therapeutic strategies under development for NAFLD have shown variable efficacy and side-effects likely due to disease heterogeneity and lack of engagement of the main pathogenic drivers of liver disease. To overcome these limitations, new strategies are becoming available for targeting PNPLA3 p.I148M, responsible for a large fraction of disease susceptibility.
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