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Non-alcoholic Fatty Liver Disease and Alcohol-Related Liver Disease: Two Intertwined Entities

机译:非酒精性脂肪肝疾病和酒精相关肝病:两个交织在一起的实体

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摘要

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.
机译:非酒精性脂肪肝病(NAFLD)是全世界慢性肝病最常见的原因,患病率为25-30%。自1980年首次说明以来,NAFLD已被认为是与酒精相关的脂肪肝疾病(ALD)的不同实体,尽管,这两种疾病都有在病理生理学,份额遗传 - 表观因素和经常共存中的重叠。两个实体的特征在于广泛的组织学特征,从孤立的脂肪变性与胫骨肝炎和肝硬化等处。 NAFLD和ALD之间的区别基于已被任意建立的消耗酒精的数量。在这种情况下,没有考虑禁止饮酒作为先决条件的诊断标准的核心诊断的阳性标准的提案,识别在一些人中脂肪肝的双重病因的可能性。中度酒精对NAFLD的严重程度的影响是不明定义的。一些研究表明,适度剂量的保护作用,但目前的证据表明,NAFLD没有安全的酒精消耗阈值。事实上,鉴于酒精消耗,肥胖和代谢功能障碍之间的协同效应,醇类可能是NAFLD和代谢综合征在肝病进展的重要风险因素。这也影响肝细胞癌的发生率。在这篇综述中,我们总结了NAFLD和ALD的重叠病理生理学,NAFLD患者的醇消耗数据以及代谢功能障碍和ALD超重的影响。

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