Current Genetic Advances in NAFLD/NASH: Related Hepatocellular Carcinoma Along with Characteristic Clinical Manifestation

K. Fujioka
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引用次数: 1

Abstract

Non-Alcoholic Fatty Liver Disease (NAFLD) is the common liver disease worldwide because of the increasing rates in parallel to obesity and Type 2 Diabetes Mellitus (T2DM). Mechanically, lipid accumulation and insulin resistance serve as the first hit, second hit is considered as inflammation and fibrosis in NAFLD. NAFLD is attributed to liverrelated morbidity and mortality, there is also growing evidence that NAFLD is a multisystem disease and is associated with hepatic (hepatocellular carcinoma: HCC) and extrahepatic (Cardiovascular Disease: CVD, Coronary Artery Disease: CAD, and Chronic Kidney Disease: CKD) diseases. The author previously suggested that an association between chronic liver disease (NAFLD/NASH and chronic hepatitis C virus infection: HCV infection) and systemic atherosclerosis may be present due to the presence of the inflammation as a common pathway. In this article, the current genetic advances of NAFLD/NASH-related HCC including PNPLA3, TM6SF2, GCKR, MBOAT7, HSD17B13, and the combined effect of these variants along with characteristic clinical manifestation have been reviewed. NAFLDs clinically predispose to occur non-cirrhotic NAFLD-HCC. The study of polygenic risk scores may be attributed to the stratification of the risk of the NAFLD/NASH-related HCC in the near feature. On the basis of the characteristic clinical and genetic evidences, the author suggests that the risk stratification of the medium/high risk in NAFLD-related HCC, especially non-cirrhotic HCC may contribute to the prevention, prediction, and surveillance.
NAFLD/NASH的遗传学进展:相关肝细胞癌及特征性临床表现
非酒精性脂肪性肝病(NAFLD)是世界范围内常见的肝脏疾病,其发病率与肥胖和2型糖尿病(T2DM)平行上升。机械上,脂质积累和胰岛素抵抗是NAFLD的第一个打击,第二个打击被认为是炎症和纤维化。NAFLD归因于肝脏相关的发病率和死亡率,也有越来越多的证据表明NAFLD是一种多系统疾病,与肝脏(肝细胞癌:HCC)和肝外(心血管疾病:CVD,冠状动脉疾病:CAD和慢性肾脏疾病:CKD)疾病相关。作者先前提出,慢性肝病(NAFLD/NASH和慢性丙型肝炎病毒感染:HCV感染)与系统性动脉粥样硬化之间可能存在关联,因为炎症是一种常见的途径。本文综述了PNPLA3、TM6SF2、GCKR、MBOAT7、HSD17B13等NAFLD/ nash相关HCC的遗传学研究进展,以及这些变异与特征性临床表现的联合作用。nafld在临床上易发生非肝硬化NAFLD-HCC。多基因风险评分的研究可能归因于近特征中NAFLD/ nash相关HCC的风险分层。基于这些特征性的临床和遗传学证据,作者建议将nafld相关HCC,特别是非肝硬化HCC的中高危人群进行风险分层,可能有助于预防、预测和监测。
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