Ma Wen, Wu Wentao, Wen Weixing, Xu Fengshuo, Han Didi, Lyu Jun, Huang Yuli
Department of Cardiology, Shunde Hospital, Southern Medical University, Foshan, P.R. China.
Department of Clinical Research, The First Affiliated Hospital, Jinan University, Guangzhou, P.R. China.
Ther Adv Chronic Dis. 2022 Sep 20;13:20406223221122478. doi: 10.1177/20406223221122478. eCollection 2022.
Nonalcoholic fatty liver disease (NAFLD) is considered as the hepatic manifestation of metabolic syndrome, sharing the similar cardiometabolic risk factors with cardiovascular disease (CVD). Whether NAFLD by itself is associated with increased cardiovascular events and death remain an issue to debate. This study aimed to further investigate the association between NAFLD and adverse CVD outcomes.
Participants were followed up until the end of 2020 in current analysis. NAFLD is defined using fatty liver index (FLI). Cox proportional hazard model was used to analyze the association between NAFLD and all-cause mortality, major adverse cardiovascular events (MACEs), CVD mortality, fatal/nonfatal acute myocardial infarction (AMI), and fatal/nonfatal stroke. C-index was calculated to evaluate the model enhancement when adding NAFLD factor.
After screening the data of 502,492 participants in the original cohort, 215,245 eligible participants were included in this study for MACEs outcome. Compared with non-NAFLD participants, the multivariable adjusted hazard ratios of NAFLD group was 1.25 (1.14-1.36) for MACEs; 1.14 (1.08-1.20) for all-cause mortality; 1.61(1.42-1.82) for CVD mortality; 1.58(1.19-2.11) for AMI mortality; and 1.18 (0.85-1.64) for stroke mortality. When adding FLI, C-index of NAFLD model improved for all-cause mortality, MACEs, and CVD mortality compared with that in the traditional CVD risk factor model.
NAFLD is an independent risk factor for all-cause mortality and adverse CVD outcomes. Based on the traditional CVD risk factor model, additionally screening NAFLD could improve the prediction efficiency for adverse CVD outcomes.
非酒精性脂肪性肝病(NAFLD)被认为是代谢综合征的肝脏表现,与心血管疾病(CVD)具有相似的心脏代谢危险因素。NAFLD本身是否与心血管事件和死亡风险增加相关仍存在争议。本研究旨在进一步探讨NAFLD与不良CVD结局之间的关联。
在本次分析中,对参与者进行随访直至2020年底。使用脂肪肝指数(FLI)定义NAFLD。采用Cox比例风险模型分析NAFLD与全因死亡率、主要不良心血管事件(MACE)、CVD死亡率、致命/非致命急性心肌梗死(AMI)以及致命/非致命性卒中之间的关联。计算C指数以评估添加NAFLD因素时模型的改进情况。
在筛选了原始队列中502,492名参与者的数据后,本研究纳入了215,245名符合条件的参与者以分析MACE结局。与非NAFLD参与者相比,NAFLD组发生MACE的多变量调整风险比为1.25(1.14 - 1.36);全因死亡率为1.14(1.08 - 1.20);CVD死亡率为1.61(1.42 - 1.82);AMI死亡率为1.58(1.19 - 2.11);卒中死亡率为1.18(0.85 - 1.64)。添加FLI后,与传统CVD危险因素模型相比,NAFLD模型的C指数在全因死亡率、MACE和CVD死亡率方面有所改善。
NAFLD是全因死亡率和不良CVD结局的独立危险因素。基于传统CVD危险因素模型,额外筛查NAFLD可提高对不良CVD结局的预测效率。