Jamialahmadi Oveis, De Vincentis Antonio, Tavaglione Federica, Malvestiti Francesco, Li-Gao Ruifang, Mancina Rosellina M, Alvarez Marcus, Gelev Kyla, Maurotti Samantha, Vespasiani-Gentilucci Umberto, Rosendaal Frits Richard, Kozlitina Julia, Pajukanta Päivi, Pattou François, Valenti Luca, Romeo Stefano
Department of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, Wallenberg Laboratory, University of Gothenburg, Gothenburg, Sweden.
Operative Unit of Internal Medicine, Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy.
Nat Med. 2024 Dec;30(12):3614-3623. doi: 10.1038/s41591-024-03284-0. Epub 2024 Dec 9.
Metabolic dysfunction-associated steatotic liver disease (MASLD) is characterized by an excess of lipids, mainly triglycerides, in the liver and components of the metabolic syndrome, which can lead to cirrhosis and liver cancer. While there is solid epidemiological evidence that MASLD clusters with cardiometabolic disease, several leading genetic risk factors for MASLD do not increase the risk of cardiovascular disease, suggesting no causal relationship between MASLD and cardiometabolic derangement. In this work, we leveraged measurements of visceral adiposity identifying 27 previously unknown genetic loci associated with MASLD (n = 36,394), six replicated in four independent cohorts (n = 3,903). Next, we generated two partitioned polygenic risk scores based on the presence of lipoprotein retention in the liver. The two polygenic risk scores suggest the presence of at least two distinct types of MASLD, one confined to the liver resulting in a more aggressive liver disease and one that is systemic and results in a higher risk of cardiometabolic disease. These findings shed light on the heterogeneity of MASLD and have the potential to improve the prediction of clinical trajectories and inform precision medicine approaches.
代谢功能障碍相关脂肪性肝病(MASLD)的特征是肝脏中存在过量脂质,主要是甘油三酯,以及代谢综合征的组成部分,这可能导致肝硬化和肝癌。虽然有确凿的流行病学证据表明MASLD与心脏代谢疾病聚集,但MASLD的几个主要遗传风险因素并不会增加心血管疾病的风险,这表明MASLD与心脏代谢紊乱之间没有因果关系。在这项研究中,我们利用内脏脂肪测量方法,确定了27个与MASLD相关的先前未知的基因位点(n = 36,394),其中6个在四个独立队列(n = 3,903)中得到重复验证。接下来,我们根据肝脏中脂蛋白潴留情况生成了两个分区多基因风险评分。这两个多基因风险评分表明至少存在两种不同类型的MASLD,一种局限于肝脏,导致更具侵袭性的肝脏疾病,另一种是全身性的,导致心脏代谢疾病风险更高。这些发现揭示了MASLD的异质性,并有可能改善临床病程预测,为精准医学方法提供依据。