Centre for Liver Disease Research, Faculty of Medicine, University of Queensland, Translational Research Institute, Woolloongabba, QLD, Australia.
Department of Gastroenterology and Hepatology, Princess Alexandra Hospital, Woolloongabba, QLD, Australia.
Hepatol Commun. 2022 Apr;6(4):728-739. doi: 10.1002/hep4.1852. Epub 2021 Nov 15.
It remains unclear whether screening for advanced fibrosis in the community can identify the subgroup of people with nonalcoholic fatty liver disease (NAFLD) at higher risk for development of liver-related complications. We aimed to determine the prognostic value of baseline noninvasive fibrosis tests for predicting liver-related outcomes and mortality in patients with NAFLD from type 2 diabetes (T2D) clinics or primary care. Patients (n = 243) who were screened for NAFLD with advanced fibrosis by using NAFLD fibrosis score (NFS), fibrosis 4 score (FIB-4), enhanced liver fibrosis (ELF) test, and liver stiffness measurements (LSMs) were followed up for clinical outcomes by review of electronic medical records. During a median follow-up of 50 months, decompensated liver disease or primary liver cancer occurred in 6 of 35 (17.1%) patients with baseline LSM > 13 kPa, 1 of 17 (5.9%) patients with LSM 9.5-13 kPa, and in no patients with LSM < 9.5 kPa. No patient with low-risk NFS developed liver decompensation or liver-related mortality. Following repeat NFSs at the end of follow-up, all patients with a liver-related complication were in the high-risk NFS category. Patients who developed liver-related complications were also more likely to have baseline high-risk FIB-4 scores or ELF test ≥9.8 compared to patients who did not develop liver outcomes. Conclusion: Liver fibrosis risk stratification in non-hepatology settings can identify the subset of patients at risk of liver-related complications. Although the rate of development of a decompensation event or hepatocellular carcinoma was low (2.1% per year) in our patients with compensated cirrhosis (LSM > 13 kPa), these events are projected to lead to a substantial increase in NAFLD-related disease burden over the next decade due to the high prevalence of NAFLD in people with obesity and T2D.
目前尚不清楚在社区中筛查晚期纤维化是否能识别出非酒精性脂肪性肝病(NAFLD)患者中发生肝脏相关并发症风险较高的亚组人群。我们旨在确定基线非侵入性纤维化检测对预测来自 2 型糖尿病(T2D)诊所或初级保健的 NAFLD 患者的肝脏相关结局和死亡率的预后价值。通过使用 NAFLD 纤维化评分(NFS)、纤维化 4 评分(FIB-4)、增强型肝纤维化(ELF)试验和肝硬度测量(LSM)筛查 NAFLD 伴晚期纤维化的患者(n=243),通过电子病历回顾进行临床结局随访。在中位随访 50 个月期间,基线 LSM>13kPa 的 35 例患者中有 6 例(17.1%)发生失代偿性肝病或原发性肝癌,9.5-13kPa 的 17 例患者中有 1 例(5.9%)发生,LSM<9.5kPa 的患者无一例发生。没有低危 NFS 的患者发生肝失代偿或与肝脏相关的死亡率。在随访结束时重复进行 NFS 后,所有发生肝脏相关并发症的患者均处于高危 NFS 类别。与未发生肝脏结局的患者相比,发生肝脏相关并发症的患者基线时更可能具有高危 FIB-4 评分或 ELF 试验≥9.8。结论:在非肝病环境中进行肝纤维化风险分层可识别出发生肝脏相关并发症风险较高的患者亚组。尽管我们的代偿性肝硬化患者(LSM>13kPa)发生失代偿事件或肝细胞癌的发生率较低(每年 2.1%),但由于肥胖和 T2D 人群中 NAFLD 的高患病率,预计在未来十年内,这些事件将导致与 NAFLD 相关的疾病负担显著增加。