医学
纤维化
炎症
非酒精性脂肪肝
肝纤维化
疾病
内科学
病理
胃肠病学
脂肪肝
作者
Eduardo Vilar‐Gómez,Tiebing Liang,Katherine P. Yates,Laura Wilson,Rohit Loomba,Naga Chalasani
标识
DOI:10.1016/j.cgh.2022.11.002
摘要
Hydroxysteroid 17-β dehydrogenase 13 (HSD17B13) splice donor (rs72613567) variant is associated with a lower risk of inflammation and fibrosis among patients with nonalcoholic fatty liver disease (NAFLD).1,2 The mechanism whereby rs72613567 protects against fibrosis development is unclear, but it could be a direct effect and/or indirectly through intermediate histologic lesions such as lobular inflammation, ballooning, and portal inflammation. Understanding the pathways through which rs72613567 might lead to fibrosis is a critical step for the development of more precise and targeted therapies that could halt the disease progression.
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