Vaz Karl, Kemp William, Majeed Ammar, Lubel John, Magliano Dianna J, Glenister Kristen M, Bourke Lisa, Simmons David, Roberts Stuart K
Department of Gastroenterology and Hepatology, Alfred Health, Ground Floor Alfred Centre,55 Commercial Road, Melbourne, VIC, 3004, Australia.
Central Clinical School, Monash University, Melbourne, VIC, Australia.
Hepatol Int. 2025 Apr;19(2):384-394. doi: 10.1007/s12072-024-10748-5. Epub 2024 Dec 14.
Controversy remains whether the mortality risk in people with fatty liver disease (FLD) including metabolic-(dysfunction) associated steatotic liver disease (MASLD) and metabolic-(dysfunction) associated fatty liver disease (MAFLD) is higher than observed in those without FLD. We aimed to determine the mortality rate and mortality rate ratio (MRR) for these FLDs.
The study population was a randomly selected cohort of community-dwelling adults in regional Victoria, Australia between 2001 and 2003 with sufficient data evaluable for Fatty Liver Index and determination on alcohol consumption. MASLD and MAFLD were diagnosed by established criteria. The primary outcome was overall mortality and main secondary outcome was major adverse liver outcomes (MALO) (i.e., decompensated liver disease, primary liver cancer and liver-related death). Non-fatal and fatal outcomes were captured via data linkage to hospital admission, cancer registry, and death registries. MRR was calculated with non-FLD participants as the comparator.
1444 (99.3%) and 1324 (91.1%) individuals from a total of 1454 were included in the final MAFLD and MASLD analyses. The median follow-up was 19.7 years (IQR 19.1-20.1) and there were 298 deaths. The MRR for MAFLD and MASLD was 1.39 (95% CI 1.10-1.76) and 1.25 (95% CI 0.96-1.61), respectively. MAFLD persisted as a risk factor for all-cause death on multivariable models correcting for lifestyle and socioeconomic variables, but not when adjusted for metabolic risk factors. MALOs were increased in MAFLD [incidence rate ratio (IRR) 3.03, 95% CI 1.22-8.18] and MASLD (IRR 2.80, 95% CI 1.05-7.90). Metabolic risk factors increased the risk of overall mortality and MALO, and cancer (34.3-34.6%) and cardiovascular disease (30.1-33.7%) were the most common cause of death in FLD.
In this population-based longitudinal study, MAFLD but not MASLD increases the risk of overall mortality, with metabolic syndrome components key risk factors increasing risk of death.
包括代谢(功能障碍)相关脂肪性肝病(MASLD)和代谢(功能障碍)相关脂肪肝(MAFLD)在内的脂肪性肝病(FLD)患者的死亡风险是否高于非FLD患者,目前仍存在争议。我们旨在确定这些FLD的死亡率和死亡率比(MRR)。
研究人群为2001年至2003年间在澳大利亚维多利亚州地区随机选取的社区居住成年人队列,其具有可用于评估脂肪肝指数和确定酒精摄入量的充分数据。MASLD和MAFLD通过既定标准进行诊断。主要结局为全因死亡率,主要次要结局为主要不良肝脏结局(MALO)(即失代偿性肝病、原发性肝癌和肝脏相关死亡)。通过与医院入院、癌症登记和死亡登记的数据链接获取非致命和致命结局。以非FLD参与者作为对照计算MRR。
在总共1454名个体中,1444名(99.3%)和1324名(91.1%)个体被纳入最终的MAFLD和MASLD分析。中位随访时间为19.7年(IQR 19.1 - 20.1),共有298例死亡。MAFLD和MASLD的MRR分别为1.39(95%CI 1.10 - 1.76)和1.25(95%CI 0.96 - 1.61)。在对生活方式和社会经济变量进行校正的多变量模型中,MAFLD仍然是全因死亡的危险因素,但在调整代谢危险因素后则不是。MAFLD[发病率比(IRR)3.03,95%CI 1.22 - 8.18]和MASLD(IRR 2.80,95%CI 1.05 - 7.90)的MALO增加。代谢危险因素增加了全因死亡率和MALO的风险,癌症(34.3 - 34.6%)和心血管疾病(30.1 - 33.7%)是FLD中最常见的死亡原因。
在这项基于人群的纵向研究中,MAFLD而非MASLD增加了全因死亡风险,代谢综合征组分是增加死亡风险的关键危险因素。