Reinshagen Mona, Kabisch Stefan, Pfeiffer Andreas F H, Spranger Joachim
Department of Endocrinology and Metabolism, Campus Benjamin Franklin, Charité University Medicine, Berlin, Germany.
Deutsches Zentrum für Diabetesforschung e.V., Geschäftsstelle am Helmholtz-Zentrum München, Neuherberg, Germany.
J Clin Transl Hepatol. 2023 Oct 28;11(5):1212-1227. doi: 10.14218/JCTH.2022.00019. Epub 2023 May 31.
Nonalcoholic fatty liver disease (NAFLD) is strongly associated with the metabolic syndrome and type 2 diabetes and independently contributes to long-term complications. Being often asymptomatic but reversible, it would require population-wide screening, but direct diagnostics are either too invasive (liver biopsy), costly (MRI) or depending on the examiner's expertise (ultrasonography). Hepatosteatosis is usually accommodated by features of the metabolic syndrome (e.g. obesity, disturbances in triglyceride and glucose metabolism), and signs of hepatocellular damage, all of which are reflected by biomarkers, which poorly predict NAFLD as single item, but provide a cheap diagnostic alternative when integrated into composite liver fat indices. Fatty liver index, NAFLD LFS, and hepatic steatosis index are common and accurate indices for NAFLD prediction, but show limited accuracy for liver fat quantification. Other indices are rarely used. Hepatic scores are commonly used in clinical practice, but their mandatory reflection of fibrotic reorganization, hepatic injury or systemic sequelae reduces sensitivity for the diagnosis of simple steatosis. Diet-induced liver fat changes are poorly reflected by liver fat indices, depending on the intervention and its specific impact of weight loss on NAFLD. This limited validity in longitudinal settings stimulates research for new equations. Adipokines, hepatokines, markers of cellular integrity, genetic variants but also simple and inexpensive routine parameters might be potential components. Currently, liver fat indices lack precision for NAFLD prediction or monitoring in individual patients, but in large cohorts they may substitute nonexistent imaging data and serve as a compound biomarker of metabolic syndrome and its cardiometabolic sequelae.
非酒精性脂肪性肝病(NAFLD)与代谢综合征和2型糖尿病密切相关,并独立导致长期并发症。它通常无症状但可逆转,需要进行全人群筛查,但直接诊断方法要么侵入性太强(肝活检)、成本太高(磁共振成像),要么依赖检查者的专业知识(超声检查)。肝脂肪变性通常伴有代谢综合征的特征(如肥胖、甘油三酯和葡萄糖代谢紊乱)以及肝细胞损伤的迹象,所有这些都可通过生物标志物反映出来,这些生物标志物单独预测NAFLD的能力较差,但整合到综合肝脂肪指数中时可提供一种廉价的诊断方法。脂肪肝指数、NAFLD LFS和肝脂肪变性指数是预测NAFLD常用且准确的指标,但在肝脂肪定量方面准确性有限。其他指标很少使用。肝脏评分在临床实践中常用,但其对纤维化重塑、肝损伤或全身后遗症的必然反映降低了对单纯脂肪变性诊断的敏感性。饮食引起的肝脏脂肪变化在肝脂肪指数中反映不佳,这取决于干预措施及其对体重减轻对NAFLD的具体影响。这种在纵向研究中的有限有效性促使人们研究新的方程。脂肪因子、肝细胞因子、细胞完整性标志物、基因变异以及简单廉价的常规参数可能是潜在的组成部分。目前,肝脂肪指数在个体患者中预测或监测NAFLD缺乏精确性,但在大型队列研究中,它们可以替代不存在的影像学数据,并作为代谢综合征及其心脏代谢后遗症的复合生物标志物。