Önnerhag Kristina, Hartman Hannes, Nilsson Peter M, Lindgren Stefan
a Department of Gastroenterology and Hepatology , Skåne University Hospital , Malmö , Sweden.
b Department of Clinical Sciences , Lund University Skåne University Hospital , Malmö , Sweden.
Scand J Gastroenterol. 2019 Mar;54(3):328-334. doi: 10.1080/00365521.2019.1583366. Epub 2019 Mar 23.
Progression to fibrosis in non-alcoholic fatty liver disease (NAFLD) is associated with an increased risk of liver-related events, overall mortality and possibly metabolic comorbidities. Our aim was to determine if non-invasive fibrosis scoring systems can predict the future risk of diabetes mellitus, cardiovascular disease (CVD), chronic kidney disease (CKD), liver-related events and overall mortality. Patients with biopsy-proven NAFLD 1978 to 2006 were identified from a computerised register in Malmö, Sweden. Medical records were scrutinised in detail to collect data from inclusion to endpoint (death or end of 2016). Non-invasive fibrosis scoring systems (FIB-4-index, NAFLD fibrosis score (NFS), APRI and BARD score) were calculated and the scores classified into three risk categories (low, intermediate and high risk for advanced fibrosis). Chronic kidney disease was evaluated using the CKD-EPI equation. One hundred and forty-four patients with biopsy-proven NAFLD were included, with a mean age of 53.2 years and a mean follow-up time of 18.8 years. At inclusion, 18% had advanced fibrosis. NFS was the only score that could predict the future risk of all included outcomes with fairly good accuracy (Area-under-ROC curve). Multivariate-adjusted hazard ratios revealed that both the intermediate and high-risk category of FIB-4-index and NFS could significantly predict metabolic outcomes. All four scoring systems significantly predicted overall mortality in the high-risk category. Non-invasive fibrosis scoring systems, especially NFS and FIB-4-index, can be used to identify patients at risk of future liver-related events, overall mortality, metabolic comorbidities and CKD.
非酒精性脂肪性肝病(NAFLD)进展为肝纤维化与肝脏相关事件、全因死亡率以及可能的代谢合并症风险增加相关。我们的目的是确定非侵入性纤维化评分系统能否预测未来患糖尿病、心血管疾病(CVD)、慢性肾脏病(CKD)、肝脏相关事件和全因死亡率的风险。从瑞典马尔默的计算机登记系统中识别出1978年至2006年经活检证实患有NAFLD的患者。详细审查病历以收集从纳入研究到终点(死亡或2016年底)的数据。计算非侵入性纤维化评分系统(FIB-4指数、NAFLD纤维化评分(NFS)、APRI和BARD评分),并将评分分为三个风险类别(晚期纤维化的低、中、高风险)。使用CKD-EPI方程评估慢性肾脏病。纳入了144例经活检证实患有NAFLD的患者,平均年龄为53.2岁,平均随访时间为18.8年。纳入研究时,18%的患者有晚期纤维化。NFS是唯一能够以相当高的准确性预测所有纳入结局未来风险的评分(ROC曲线下面积)。多变量调整后的风险比显示,FIB-4指数和NFS的中、高风险类别均可显著预测代谢结局。所有四个评分系统在高风险类别中均能显著预测全因死亡率。非侵入性纤维化评分系统,尤其是NFS和FIB-4指数,可用于识别未来有肝脏相关事件、全因死亡率、代谢合并症和CKD风险的患者。