Carulli Lucia, Zanca Giulia, Schepis Filippo, Villa Erica
Division of Gastroenterology, Department of Medical Specialties, University of Modena and Reggio Emilia, 41124 Modena, Italy.
Metabolites. 2019 Feb 1;9(2):25. doi: 10.3390/metabo9020025.
Nonalcoholic fatty liver disease (NAFLD) is a common cause of hepatic abnormalities worldwide. Nonalcoholic steatohepatitis (NASH) is part of the spectrum of NAFLD and leads to progressive liver disease, such as cirrhosis and hepatocellular carcinoma. In NASH patient, fibrosis represents the major predictor of liver-related mortality; therefore, it is important to have an early and accurate diagnosis of NASH. The current gold standard for the diagnosis of NASH is still liver biopsy. The development of biomarkers able to predict disease severity, prognosis, as well as response to therapy without the need for a biopsy is the focus of most up-to-date genomic, transcriptomic, proteomic, and metabolomic research. In the future, patients might be diagnosed and treated according to their molecular signatures. In this short review, we discuss how information from genomics, proteomics, and metabolomics contribute to the understanding of NAFLD pathogenesis.
非酒精性脂肪性肝病(NAFLD)是全球肝脏异常的常见原因。非酒精性脂肪性肝炎(NASH)是NAFLD的一部分,可导致进行性肝病,如肝硬化和肝细胞癌。在NASH患者中,纤维化是肝脏相关死亡率的主要预测指标;因此,早期准确诊断NASH很重要。目前诊断NASH的金标准仍然是肝活检。能够预测疾病严重程度、预后以及无需活检即可预测治疗反应的生物标志物的开发是最新的基因组学、转录组学、蛋白质组学和代谢组学研究的重点。未来,患者可能会根据其分子特征进行诊断和治疗。在这篇简短的综述中,我们讨论了来自基因组学、蛋白质组学和代谢组学的信息如何有助于理解NAFLD的发病机制。