Chronic Kidney Disease, Heart Failure, and Adverse Cardiac Remodeling in Older Adults

医学 心力衰竭 肾功能 射血分数 心脏病学 内科学 比例危险模型 射血分数保留的心力衰竭 肾脏疾病 肌酐 舒张期 心室重构 冲程容积 血压
作者
Leo F. Buckley,Brian Claggett,Kunihiro Matsushita,Gearoid M. McMahon,Hicham Skali,Josef Coresh,Aaron R. Folsom,Suma Konety,Lynne E. Wagenknecht,Thomas H. Mosley,Amil M. Shah
出处
期刊:Jacc-Heart Failure [Elsevier]
卷期号:11 (5): 523-537 被引量:1
标识
DOI:10.1016/j.jchf.2023.01.029
摘要

The associations of kidney dysfunction and damage with heart failure with reduced ejection fraction (HFrEF) and heart failure with preserved ejection fraction (HFpEF), as well as adverse cardiac remodeling, in late-life remain incompletely understood. The authors sought to define the associations between kidney dysfunction and damage and incident HFrEF and HFpEF and cardiac structure and function in late-life. This study included 5,170 adults initially free of a heart failure (HF) diagnosis who had estimated glomerular filtration rate (eGFR) and urine albumin-to-creatinine ratio (UACR) measured at visit 5 (2011-2013) of the ARIC (Atherosclerosis Risk In Communities) study. Multivariable Cox proportional hazards models were used to estimate the associations of eGFR and UACR with incident HF, HFrEF, and HFpEF through 2019. Multivariable linear regression models were used to investigate the associations of eGFR and UACR at visit 5 with changes in cardiac structure and function between visits 5 and 7 in 2,313 participants with available echocardiograms. The mean age of participants was 76 ± 5 years, and 2,225 (43%) were men. The mean eGFR and median UACR were 66 ± 18 mL/min/1.73 m2 and 11 mg/g (25th, 75th percentile: 6, 22 mg/g), respectively. In fully adjusted models, both lower eGFR and higher UACR were associated with greater risk of any HF, HFrEF, and HFpEF. Lower eGFR was associated with larger increases in left ventricular end-diastolic volume index and worsening of diastolic measures. UACR did not associate with changes in cardiac structure or function. Mild to moderate kidney dysfunction and damage associate with incident HF and adverse cardiac remodeling in late-life.
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