Kanda Tatsuo, Sasaki-Tanaka Reina, Abe Hiroyuki, Kimura Naruhiro, Yoshida Tomoaki, Hayashi Kazunao, Sakamaki Akira, Yokoo Takeshi, Kamimura Hiroteru, Tsuchiya Atsunori, Kamimura Kenya, Terai Shuji
Division of Gastroenterology and Hepatology, Uonuma Institute of Community Medicine, Niigata University Medical and Dental Hospital, Uonuma Kikan Hospital, Minamiuonuma 949-7302, Japan.
Division of Gastroenterology and Hepatology, Graduate School of Medical and Dental Sciences, Niigata University, Niigata 951-8520, Japan.
Int J Mol Sci. 2025 May 28;26(11):5164. doi: 10.3390/ijms26115164.
Metabolic dysfunction-associated steatotic liver disease (MASLD) and metabolic dysfunction-associated steatohepatitis (MASH) are spreading worldwide as the most critical causes of cirrhosis and hepatocellular carcinoma (HCC). Thus, improving the screening and managing strategies for patients with MASLD or MASH is necessary. A traditional non-systemic review provided this narrative. Genetic variations associated with the development of MASLD and MASH, such as , , , , , and , were initially reviewed. genetic variants appeared to be strongly associated with the increased pathogenesis of MASLD, MASH, cirrhosis, and HCC. We also reviewed the useful polygenic risk score (PRS) for the development of MASLD, MASH, their related cirrhosis, and the occurrence of HCC. PRSs appeared to be better predictors of MASLD, MASH, the development of cirrhosis, and the occurrence of HCC in patients with MASLD or MASH than any single-nucleotide polymorphisms. RNA interference and antisense nucleotides against the genetic variations of and are also being developed. Multidisciplinary collaboration and cooperation involving hepatologists, geneticists, pharmacologists, and pathologists should resolve complicated problems in MASLD and MASH. This narrative review highlights the importance of the genetic susceptibility and PRS as predictive markers and personalized medicine for patients with MASLD or MASH in the future.
代谢功能障碍相关脂肪性肝病(MASLD)和代谢功能障碍相关脂肪性肝炎(MASH)作为肝硬化和肝细胞癌(HCC)的最主要病因正在全球范围内蔓延。因此,有必要改进MASLD或MASH患者的筛查和管理策略。本叙述性综述提供了这样的内容。最初对与MASLD和MASH发生相关的基因变异进行了综述,如 、 、 、 、 以及 。 基因变异似乎与MASLD、MASH、肝硬化和HCC发病机制的增加密切相关。我们还综述了用于MASLD、MASH、其相关肝硬化发生以及HCC发生的有用多基因风险评分(PRS)。在MASLD或MASH患者中,PRS似乎比任何单核苷酸多态性都能更好地预测MASLD、MASH、肝硬化的发生以及HCC的发生。针对 和 的基因变异的RNA干扰和反义核苷酸也正在研发中。肝病学家、遗传学家、药理学家和病理学家之间的多学科协作应能解决MASLD和MASH中的复杂问题。本叙述性综述强调了基因易感性和PRS作为预测标志物以及未来针对MASLD或MASH患者的个性化医疗的重要性。