普通人群中非酒精性脂肪肝与亚临床左心室功能障碍的关系。

European heart journal open Pub Date : 2023-10-17 eCollection Date: 2023-11-01 DOI:10.1093/ehjopen/oead108
Kazutoshi Hirose, Koki Nakanishi, Marco R Di Tullio, Shunichi Homma, Naoko Sawada, Yuriko Yoshida, Megumi Hirokawa, Katsuhiro Koyama, Koichi Kimura, Tomoko Nakao, Masao Daimon, Hiroyuki Morita, Makoto Kurano, Issei Komuro
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引用次数: 0

摘要

目的:新出现的证据表明非酒精性脂肪性肝病(NAFLD)与心力衰竭(HF)之间存在关联。我们在没有明显心脏和肝脏疾病的普通人群样本中研究了NAFLD与左心室(LV)功能重塑之间的关系。方法和结果:我们纳入了481名没有大量饮酒的人,他们自愿接受了广泛的心血管健康检查。计算每个参与者的脂肪肝指数(FLI),NAFLD定义为FLI≥60。所有参与者均接受了二维经胸超声心动图检查;左心室整体纵向应变(LVGLS)通过散斑跟踪分析进行评估。构建了单变量和多变量线性回归模型,以研究NAFLD和LVGLS之间的可能关联。71名(14.8%)参与者被诊断为NAFLD。NAFLD患者的左心室大小和左心室质量指数比无NAFLD的患者大,尽管左心房大小和E/E'比率在各组之间没有差异。患有和不患有NAFLD的参与者的左心室整体纵向应变显著降低(分别为17.1%±2.4%和19.5%±3.1%;P<0.001)。NAFLD组的LVGLS异常频率显著较高(P<0.001),多变量线性回归分析表明,FLI评分越高与LVGLS受损显著相关,与年龄无关,性别、常规心血管危险因素和超声心动图参数(标准化β-0.11,P=0.031)。结论:在没有明显心脏和肝脏疾病的普通人群中,NAFLD的存在与亚临床左心室功能障碍显著相关,这可能部分解释了NAFLD患者HF风险升高的原因。
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Association between non-alcoholic fatty liver disease and subclinical left ventricular dysfunction in the general population.

Aims: Emerging evidence suggests an association between non-alcoholic fatty liver disease (NAFLD) and heart failure (HF). We investigated the relationship between NAFLD and left ventricular (LV) functional remodelling in a general population sample without overt cardiac and liver disease.

Methods and results: We included 481 individuals without significant alcohol consumption who voluntarily underwent an extensive cardiovascular health check. The fatty liver index (FLI) was calculated for each participant, and NAFLD was defined as FLI ≥ 60. All participants underwent 2D transthoracic echocardiography; LV global longitudinal strain (LVGLS) was assessed with speckle-tracking analysis. Univariable and multivariable linear regression models were constructed to investigate the possible association between NAFLD and LVGLS. Seventy-one (14.8%) participants were diagnosed with NAFLD. Individuals with NAFLD exhibited larger LV size and LV mass index than those without NAFLD, although left atrial size and E/e' ratio did not differ between groups. Left ventricular global longitudinal strain was significantly reduced in participants with vs. without NAFLD (17.1% ± 2.4% vs. 19.5% ± 3.1%, respectively; P < 0.001). The NAFLD group had a significantly higher frequency of abnormal LVGLS (<16%) than the non-NAFLD group (31.0% vs. 10.7%, respectively; P < 0.001). Multivariable linear regression analysis demonstrated that higher FLI score was significantly associated with impaired LVGLS independent of age, sex, conventional cardiovascular risk factors, and echocardiographic parameters (standardized β -0.11, P = 0.031).

Conclusion: In the general population without overt cardiac and liver disease, the presence of NAFLD was significantly associated with subclinical LV dysfunction, which may partly explain the elevated risk of HF in individuals with NAFLD.

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