Departamento de Gastroenterología, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
Division of Gastroenterology, Department of Medicine, Schulich School of Medicine, Western University & London Health Sciences Centre, London, Ontario, Canada.
Nat Rev Gastroenterol Hepatol. 2023 Dec;20(12):764-783. doi: 10.1038/s41575-023-00822-y. Epub 2023 Aug 15.
Nonalcoholic fatty liver disease (NAFLD) and alcohol-related liver disease (ALD) are the leading causes of chronic liver disease worldwide. NAFLD and ALD share pathophysiological, histological and genetic features and both alcohol and metabolic dysfunction coexist as aetiological factors in many patients with hepatic steatosis. A diagnosis of NAFLD requires the exclusion of significant alcohol consumption and other causes of liver disease. However, data suggest that significant alcohol consumption is often under-reported in patients classified as having NAFLD and that alcohol and metabolic factors interact to exacerbate the progression of liver disease. In this Review, we analyse existing data on the interaction between alcohol consumption and metabolic syndrome as well as the overlapping features and differences in the pathogenesis of ALD and NAFLD. We also discuss the clinical implications of the coexistence of alcohol consumption, of any degree, in patients with evidence of metabolic derangement as well as the use of alcohol biomarkers to detect alcohol intake. Finally, we summarize the evolving nomenclature of fatty liver disease and describe a recent proposal to classify patients at the intersection of NAFLD and ALD. We propose that, regardless of the presumed aetiology, patients with fatty liver disease should be evaluated for both metabolic syndrome and alcohol consumption to enable better prognostication and a personalized medicine approach.
非酒精性脂肪性肝病 (NAFLD) 和酒精性肝病 (ALD) 是全球慢性肝病的主要病因。NAFLD 和 ALD 具有相同的病理生理、组织学和遗传学特征,并且在许多患有肝脂肪变性的患者中,酒精和代谢功能障碍并存是病因。NAFLD 的诊断需要排除大量饮酒和其他肝病的原因。然而,数据表明,在被归类为患有 NAFLD 的患者中,大量饮酒往往被报告不足,并且酒精和代谢因素相互作用会加剧肝病的进展。在这篇综述中,我们分析了现有关于酒精消费与代谢综合征之间相互作用的的数据,以及 ALD 和 NAFLD 发病机制的重叠特征和差异。我们还讨论了在有代谢紊乱证据的患者中存在任何程度的酒精消费以及使用酒精生物标志物来检测酒精摄入的临床意义。最后,我们总结了不断发展的脂肪性肝病命名法,并描述了最近提出的将 NAFLD 和 ALD 相交处的患者分类的建议。我们建议,无论假定的病因如何,都应评估患有脂肪性肝病的患者的代谢综合征和酒精消费情况,以便更好地预测和采用个性化的治疗方法。