Department of Cardiovascular Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Institute of Cardiovascular Disease, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Dis Markers. 2022 Oct 15;2022:9927254. doi: 10.1155/2022/9927254. eCollection 2022.
Left ventricular (LV) diastolic dysfunction (LVDD) is the defining feature of heart failure with preserved ejection fraction (HFpEF) and predicts subsequent incident heart failure (HF) and all-cause mortality. Mounting evidence reveals that cardiometabolic risk factors play critical roles in the development of LVDD. In this study, we sought to investigate the relation between serum uric acid (SUA) level and the progression of LVDD in apparently healthy patients.
A total of 1082 apparently healthy subjects without diagnosed cardiovascular disease and LVDD were consecutively enrolled. SUA levels were measured, and repeat echocardiography and tissue Doppler imaging (TDI) were performed at baseline and during 1-year follow-up.
By dividing the study population based on quartiles of SUA, we found subjects in higher quartiles had greater increases in TDI-derived early diastolic velocity (e') and E (peak LV filling velocity)/e' ratios during 1-year follow-up. After multivariate adjustment, high SUA persisted to be an independent predictor for the subsequent worsening of LVDD (odds ratio: 1.351 [95% CI 1.125~1.625], per 100 mol/L SUA). Subgroup analysis suggested that the association between SUA and LVDD development was more pronounced in subjects without other cardiometabolic risk factors involved. Factor analysis demonstrated that high SUA was the major cardiometabolic attribute in patients with LVDD progression.
Our findings suggest that high SUA is an independent cardiometabolic risk factor for the progression of LVDD in apparently healthy subjects.
左心室(LV)舒张功能障碍(LVDD)是射血分数保留的心力衰竭(HFpEF)的特征,并预测随后发生心力衰竭(HF)和全因死亡率。越来越多的证据表明,心脏代谢危险因素在 LVDD 的发展中起着关键作用。在这项研究中,我们试图研究血清尿酸(SUA)水平与明显健康患者 LVDD 进展之间的关系。
共连续纳入 1082 名无诊断心血管疾病和 LVDD 的明显健康受试者。测量 SUA 水平,并在基线和 1 年随访时进行重复超声心动图和组织多普勒成像(TDI)。
根据 SUA 的四分位数将研究人群进行分组,我们发现较高四分位数的受试者在 1 年随访期间 TDI 衍生的早期舒张速度(e')和 E(峰值左室充盈速度)/e'比值增加更大。经过多变量调整后,高 SUA 仍然是 LVDD 恶化的独立预测因素(比值比:1.351[95%CI 1.125~1.625],每增加 100μmol/L SUA)。亚组分析表明,SUA 与 LVDD 发展之间的关联在没有其他心脏代谢危险因素的受试者中更为明显。因子分析表明,高 SUA 是 LVDD 进展患者的主要心脏代谢特征。
我们的研究结果表明,高 SUA 是明显健康受试者 LVDD 进展的独立心脏代谢危险因素。