Lückhoff Hilmar K, Kruger Frederik C, Kotze Maritha J
Hilmar K Lückhoff, Maritha J Kotze, Division of Anatomical Pathology, Department of Pathology, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, Bellville 7530, Cape Town, Western Cape, South Africa.
World J Hepatol. 2015 May 28;7(9):1192-208. doi: 10.4254/wjh.v7.i9.1192.
Heterogeneity in clinical presentation, histological severity, prognosis and therapeutic outcomes characteristic of non-alcoholic fatty liver disease (NAFLD) necessitates the development of scientifically sound classification schemes to assist clinicians in stratifying patients into meaningful prognostic subgroups. The need for replacement of invasive liver biopsies as the standard method whereby NAFLD is diagnosed, graded and staged with biomarkers of histological severity injury led to the development of composite prognostic models as potentially viable surrogate alternatives. In the present article, we review existing scoring systems used to (1) confirm the presence of undiagnosed hepatosteatosis; (2) distinguish between simple steatosis and NASH; and (3) predict advanced hepatic fibrosis, with particular emphasis on the role of NAFLD as an independent cardio-metabolic risk factor. In addition, the incorporation of functional genomic markers and application of emerging imaging technologies are discussed as a means to improve the diagnostic accuracy and predictive performance of promising composite models found to be most appropriate for widespread clinical adoption.
非酒精性脂肪性肝病(NAFLD)在临床表现、组织学严重程度、预后和治疗结果方面存在异质性,因此有必要制定科学合理的分类方案,以帮助临床医生将患者分层为有意义的预后亚组。由于需要用组织学严重损伤的生物标志物取代侵入性肝活检作为诊断、分级和分期NAFLD的标准方法,因此开发了复合预后模型作为潜在可行的替代方法。在本文中,我们回顾了用于(1)确认未诊断的肝脂肪变性的存在;(2)区分单纯性脂肪变性和非酒精性脂肪性肝炎(NASH);以及(3)预测晚期肝纤维化的现有评分系统,特别强调NAFLD作为独立的心脑血管代谢危险因素的作用。此外,还讨论了功能基因组标记的纳入和新兴成像技术的应用,以此作为提高已发现最适合广泛临床应用的有前景的复合模型的诊断准确性和预测性能的一种手段。