Idalsoaga Francisco, Kulkarni Anand V, Mousa Omar Y, Arrese Marco, Arab Juan Pablo
Departamento de Gastroenterología, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
Department of Hepatology, Asian Institute of Gastroenterology, Hyderabad, India.
Front Med (Lausanne). 2020 Aug 20;7:448. doi: 10.3389/fmed.2020.00448. eCollection 2020.
Non-alcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver disease worldwide, with a prevalence of 25-30%. Since its first description in 1980, NAFLD has been conceived as a different entity from alcohol-related fatty liver disease (ALD), despite that, both diseases have an overlap in the pathophysiology, share genetic-epigenetic factors, and frequently coexist. Both entities are characterized by a broad spectrum of histological features ranging from isolated steatosis to steatohepatitis and cirrhosis. Distinction between NAFLD and ALD is based on the amount of consumed alcohol, which has been arbitrarily established. In this context, a proposal of positive criteria for NAFLD diagnosis not considering exclusion of alcohol consumption as a prerequisite criterion for diagnosis had emerged, recognizing the possibility of a dual etiology of fatty liver in some individuals. The impact of moderate alcohol use on the severity of NAFLD is ill-defined. Some studies suggest protective effects in moderate doses, but current evidence shows that there is no safe threshold for alcohol consumption for NAFLD. In fact, given the synergistic effect between alcohol consumption, obesity, and metabolic dysfunction, it is likely that alcohol use serves as a significant risk factor for the progression of liver disease in NAFLD and metabolic syndrome. This also affects the incidence of hepatocellular carcinoma. In this review, we summarize the overlapping pathophysiology of NAFLD and ALD, the current data on alcohol consumption in patients with NAFLD, and the effects of metabolic dysfunction and overweight in ALD.
非酒精性脂肪性肝病(NAFLD)是全球慢性肝病最常见的病因,患病率为25%-30%。自1980年首次被描述以来,NAFLD被认为是一种与酒精性脂肪性肝病(ALD)不同的疾病,尽管如此,这两种疾病在病理生理学上存在重叠,共享遗传-表观遗传因素,且经常同时存在。这两种疾病都具有广泛的组织学特征,从单纯性脂肪变性到脂肪性肝炎和肝硬化。NAFLD和ALD的区分基于酒精摄入量,这是任意确定的。在这种背景下,出现了一项不将排除饮酒作为诊断前提标准的NAFLD诊断阳性标准提案,认识到某些个体存在脂肪肝双重病因的可能性。适度饮酒对NAFLD严重程度的影响尚不明确。一些研究表明适度剂量有保护作用,但目前的证据表明,对于NAFLD不存在安全的饮酒阈值。事实上,鉴于饮酒、肥胖和代谢功能障碍之间的协同作用,饮酒很可能是NAFLD和代谢综合征中肝病进展的重要危险因素。这也会影响肝细胞癌的发病率。在本综述中,我们总结了NAFLD和ALD重叠的病理生理学、NAFLD患者饮酒的现有数据,以及代谢功能障碍和超重对ALD的影响。