Neurometabolism and Ventricular Dyssynchrony in Patients With Heart Failure and Reduced Ejection Fraction

被引:8
|
作者
Bai, Yujie [1 ]
Yun, Mingkai [1 ]
Nie, Binbin [2 ]
Shan, Liang [3 ]
Liu, Wenxian [3 ]
Hacker, Marcus [4 ]
Nie, Shaoping [3 ]
Zhou, Yujie [3 ]
Li, Sijin [5 ]
Shan, Baoci [2 ]
Zhang, Xiaoli [1 ]
Li, Xiang [1 ,4 ]
机构
[1] Capital Med Univ, Beijing Anzhen Hosp, Dept Nucl Med, Mol Imaging Lab, Beijing, Peoples R China
[2] Chinese Acad Sci, Inst High Energy Phys, Div Nucl Technol & Applicat, Beijing, Peoples R China
[3] Capital Med Univ, Beijing Anzhen Hosp, Dept Cardiol, Beijing, Peoples R China
[4] Med Univ Vienna, Vienna Gen Hosp, Dept Biomed Imaging & Image Guided Therapy, Div Nucl Med, Vienna, Austria
[5] Shanxi Med Univ, Dept Nucl Med, Hosp 1, Taiyuan, Shanxi, Peoples R China
关键词
F-18-fluorodeoxyglucose positron emission tomography; brain-heart axis; brain network; heart failure; AUTONOMIC NERVOUS-SYSTEM; QT INTERVAL; BRAIN; ASSOCIATION; ARRHYTHMIAS; VARIABILITY; DYSFUNCTION; ACTIVATION; RISK;
D O I
10.1016/j.jacc.2022.08.801
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND The brain coordinates the heart through the autonomic nervous system (ANS). Numerous mediator signals along the brain-heart axis interact with the neuronal-metabolic system in heart failure (HF). Disturbances in cardio-neural interactions influence the disease progression in patients with HF. OBJECTIVES The purpose of this study was to investigate the interactome between ANS-associated neurometabolism and ventricular dyssynchrony in patients with heart failure with reduced ejection fraction (HFrEF). Further, we studied the association of neurometabolism with major arrhythmic events (MAEs). METHODS A total of 197 patients with HFrEF who underwent gated single-photon emission computed tomography myocardial perfusion imaging and the brain F-18-fluorodeoxyglucose positron emission tomography/computed tomography were prospectively enrolled. Relationships between the brain metabolism and MAEs were assessed using Cox models and mediation analyses. Finally, metabolic central autonomic networks were constructed and statistically compared between patients with and without MAEs. RESULTS In total, 35 (17.8%) patients experienced MAEs during a median follow-up of 3.1 years. In patients with HFrEF (age 58 years [IQR: 50-64 years], left ventricular ejection fraction: 20.0% [IQR: 15.0%-25.0%]), glucose hypometabolism in the insula, hippocampus, amygdala, cingulate gyrus, and caudate nucleus were independent predictors for MAEs (all P < 0.05). Cerebral hypometabolism was related to ventricular dyssynchrony, which was the predominant risk factor of MAEs. Additionally, patients who experienced MAEs presented hypoconnectivity in the metabolic central autonomic network compared with those without MAEs (P < 0.05). CONCLUSIONS We found an interaction of the neuronal metabolic-ventricular dyssynchronization axis in HF, which might be related to MAEs. This new brain-heart axis could expand our understanding of the distinct pathomechanisms of HFrEF. (c) 2022 by the American College of Cardiology Foundation.
引用
收藏
页码:1884 / 1896
页数:13
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