Sumida Yoshio, Yoneda Masashi, Seko Yuya, Ishiba Hiroshi, Hara Tasuku, Toyoda Hidenori, Yasuda Satoshi, Kumada Takashi, Hayashi Hideki, Kobayashi Takashi, Imajo Kento, Yoneda Masato, Tada Toshifumi, Kawaguchi Takumi, Eguchi Yuichiro, Oeda Satoshi, Takahashi Hirokazu, Tomita Eiichi, Okanoue Takeshi, Nakajima Atsushi
Division of Hepatology and Pancreatology, Department of Internal Medicine, Aichi Medical University, Nagakute, Aichi 480-1195, Japan.
Department of Gastroenterology and Hepatology, Graduate School of Medicine, Kyoto Prefectural University of Medicine, Kyoto 602-8566, Japan.
Diagnostics (Basel). 2020 Aug 10;10(8):579. doi: 10.3390/diagnostics10080579.
Nonalcoholic fatty liver disease (NAFLD) is becoming the leading cause of hepatocellular carcinoma (HCC), liver-related mortality, and liver transplantation. There is sufficient epidemiological cohort data to recommend the surveillance of patients with NAFLD based upon the incidence of HCC. The American Gastroenterology Association (AGA) expert review published in 2020 recommends that NAFLD patients with cirrhosis or advanced fibrosis estimated by non-invasive tests (NITs) consider HCC surveillance. NITs include the fibrosis-4 (FIB-4) index, the enhanced liver fibrosis (ELF) test, FibroScan, and MR elastography. The recommended surveillance modality is abdominal ultrasound (US), which is cost effective and noninvasive with good sensitivity. However, US is limited in obese patients and those with NAFLD. In NAFLD patients with a high likelihood of having an inadequate US, or if an US is attempted but inadequate, CT or MRI may be utilized. The GALAD score, consisting of age, gender, AFP, the lens culinaris-agglutinin-reactive fraction of AFP (AFP-L3), and the protein induced by the absence of vitamin K or antagonist-II (PIVKA-II), can help identify a high risk of HCC in NAFLD patients. Innovative parameters, including a Mac-2 binding protein glycated isomer, type IV collagen 7S, free apoptosis inhibitor of the macrophage, and a combination of single nucleoside polymorphisms, are expected to be established. Considering the large size of the NAFLD population, optimal screening tests must meet several criteria, including high sensitivity, cost effectiveness, and availability.
非酒精性脂肪性肝病(NAFLD)正成为肝细胞癌(HCC)、肝脏相关死亡率和肝移植的主要原因。有足够的流行病学队列数据支持根据HCC发病率对NAFLD患者进行监测。美国胃肠病学会(AGA)2020年发表的专家综述建议,通过非侵入性检测(NITs)评估为肝硬化或晚期纤维化的NAFLD患者应考虑进行HCC监测。NITs包括纤维化-4(FIB-4)指数、增强肝纤维化(ELF)检测、FibroScan和磁共振弹性成像。推荐的监测方式是腹部超声(US),其具有成本效益且为非侵入性,敏感性良好。然而,US在肥胖患者和NAFLD患者中存在局限性。在US检查可能不充分的NAFLD患者中,或者如果尝试进行US检查但结果不充分时,可使用CT或MRI。由年龄、性别、甲胎蛋白(AFP)、AFP的豆凝集素反应性部分(AFP-L3)以及维生素K缺乏或拮抗剂-II诱导蛋白(PIVKA-II)组成的GALAD评分,有助于识别NAFLD患者发生HCC的高风险。包括Mac-2结合蛋白糖化异构体、IV型胶原7S、巨噬细胞游离凋亡抑制剂以及单核苷酸多态性组合在内的创新参数有望得以确立。考虑到NAFLD患者群体规模庞大,最佳筛查检测必须满足多项标准,包括高敏感性、成本效益和可及性。