Department of Gastroenterology, Medical School of National and Kapodistrian University of Athens, General Hospital of Athens "Laiko", Athens, Greece.
First Department of Internal Medicine, Medical School of National & Kapodistrian University, General Hospital of Athens "Laiko", Athens, Greece.
Curr Pharm Des. 2018;24(38):4574-4586. doi: 10.2174/1381612825666190117102111.
Nonalcoholic fatty liver disease (NAFLD) ranges from simple hepatic steatosis to non-alcoholic steatohepatitis (NASH) and cirrhosis. The majority of NAFLD patients do not progress to NASH and their morbidity risk is low. However, clinical and economic burden of the disease is considerable since the prevalence of the disease is estimated as high as 25% of the general population. Liver biopsy remains the current gold standard for diagnosis, despite limitations regarding sampling variability, invasive nature, and high cost. However, numerous non-invasive biomarkers, including mainly serum markers or imaging modalities, intend to detect the presence of steatosis, NASH or advanced fibrosis. To date, ultrasound is suggested as first-line screening tool for defining steatosis in a selected population, while diagnosis of NAFLD requires exclusion of other chronic liver disease etiology or other steatosis causes. A crucial step in the management of NAFLD patients is the identification of advanced fibrosis, which may be reliably excluded by using NAFLD-Fibrosis score or FIB-4 score or by performing transient elastography. The most robust modalities implement Magnetic Resonance technology and manage to accurately quantify steatosis or identify fibrosis stage, but are not yet applicable in routine practice. The most challenging endpoint has proved to be a non-invasive diagnosis of NASH since no reliable biomarkers have been found to detect or predict inflammation in NAFLD. Lately, research focuses on validating existing markers as robust diagnostic tools for clinical use and investigating novel experimental markers of disease. Current strategies concepts aim to safely diagnose NAFLD patients, aid drug development and finally, guide personalised treatment.
非酒精性脂肪性肝病(NAFLD)的范围从单纯性肝脂肪变性到非酒精性脂肪性肝炎(NASH)和肝硬化。大多数 NAFLD 患者不会进展为 NASH,其发病风险较低。然而,由于该病的患病率估计高达普通人群的 25%,因此该病的临床和经济负担相当大。尽管存在取样变异性、侵袭性和高成本等局限性,但肝活检仍然是目前诊断的金标准。然而,许多非侵入性生物标志物,包括主要的血清标志物或成像方式,旨在检测脂肪变性、NASH 或晚期纤维化的存在。迄今为止,超声被建议作为筛选工具,用于在特定人群中定义脂肪变性,而 NAFLD 的诊断需要排除其他慢性肝病病因或其他脂肪变性原因。NAFLD 患者管理的关键步骤是识别晚期纤维化,这可以通过使用 NAFLD-Fibrosis 评分或 FIB-4 评分或进行瞬时弹性成像来可靠排除。最有效的方法是使用磁共振技术,能够准确地定量脂肪变性或识别纤维化阶段,但尚未在常规实践中应用。最具挑战性的终点是对 NASH 的非侵入性诊断,因为尚未发现可靠的生物标志物来检测或预测 NAFLD 中的炎症。最近,研究的重点是验证现有的标志物作为临床应用的可靠诊断工具,并研究疾病的新型实验标志物。目前的策略概念旨在安全地诊断 NAFLD 患者,帮助药物开发,最终指导个体化治疗。