Heart Rate Variability’s Value in Predicting Out-of-Hospital Major Adverse Cardiovascular Events in Patients With Chronic Heart Failure

IF 3.4 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Li Men, Bingxin Chen, Long Yang, Jiangrong Shi, Shuqin Tang, Xing Jiang, Yunhua Chen, Xiao Wang, Ping Fan
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引用次数: 0

Abstract

Background: Chronic heart failure (CHF) involves changes in cardiac structure and function, along with extensive neuroendocrine adaptations and metabolic abnormalities. Heart rate variability (HRV) is a noninvasive measure of autonomic nervous system function and is associated with mortality in CHF. However, the significance of HRV in predicting major adverse cardiovascular events (MACEs) in CHF patients has not been fully explored. This study was aimed at investigating the predictive value of HRV parameters assessed by 24-h Holter monitoring for MACEs in CHF patients.

Methods: This prospective cohort study included 906 CHF patients from five centers in Xinjiang, China, who underwent Holter monitoring and were followed up. Cox proportional hazards regression models were used to assess the independent associations between HRV parameters and the incidence of MACEs. Receiver operating characteristic (ROC) curve analysis was conducted to determine the predictive accuracy of each HRV parameter, and the incremental predictive value of HRV parameters was evaluated using coherence index (C-index), net reclassification improvement (NRI), and integrated discrimination improvement (IDI).

Results: During a median follow-up of 16 months, 211 (23.3%) MACEs occurred. Cox regression analysis indicated that SDNN (HR: 0.976, 95% CI: 0.970~0.981), triangular index (HR: 0.963, 95% CI: 0.953~0.973), SDNN index (HR: 0.983, 95% CI: 0.974~0.992), SDANN index (HR: 0.974, 95% CI: 0.967~0.981), NN50 (HR: 0.859, 95% CI: 0.787~0.937), rMSSD (HR: 0.980, 95% CI: 0.970~0.989), TP (HR: 0.890, 95% CI: 0.816~0.971), VLF (HR: 0.889, 95% CI: 0.815~0.969), LF (HR: 0.817, 95% CI: 0.743~0.898), and HF (HR: 0.806, 95% CI: 0.728~0.893) were independently associated with MACEs. ROC analysis revealed that the triangular index and SDNN had the highest area under the curve (AUC) for predicting MACEs, with values of 0.699 (95% CI: 0.655~0.743) and 0.711 (95% CI: 0.668~0.753), respectively. Incorporation of HRV parameters into traditional risk models improves the C-index, NRI, and IDI of the model’s predictive ability for MACE and cardiovascular mortality to varying degrees.

Conclusion: SDNN and triangular index demonstrated the strongest predictive abilities; other time–domain and frequency–domain parameters also showed certain predictive values for MACEs.

Abstract Image

心率变异性在预测慢性心力衰竭患者院外主要不良心血管事件中的价值
背景:慢性心力衰竭(CHF)涉及心脏结构和功能的改变,以及广泛的神经内分泌适应和代谢异常。心率变异性(HRV)是自主神经系统功能的无创测量,与心力衰竭的死亡率相关。然而,HRV在预测CHF患者主要不良心血管事件(mace)中的意义尚未得到充分探讨。本研究旨在探讨通过24小时动态心电图监测评估的HRV参数对CHF患者mace的预测价值。方法:本前瞻性队列研究纳入来自中国新疆5个中心的906例CHF患者,接受动态心电图监测并随访。采用Cox比例风险回归模型评估HRV参数与mace发生率之间的独立相关性。采用受试者工作特征(ROC)曲线分析确定HRV各参数的预测精度,并采用相干指数(C-index)、净重分类改善(NRI)、综合判别改善(IDI)评价HRV参数的增量预测值。结果:在中位随访16个月期间,发生211例(23.3%)mace。Cox回归分析显示,SDNN (HR: 0.976, 95% CI: 0.970~0.981)、三角指数(HR: 0.963, 95% CI: 0.953~0.973)、SDNN指数(HR: 0.983, 95% CI: 0.967~0.981)、SDANN指数(HR: 0.974, 95% CI: 0.967~0.981)、NN50 (HR: 0.859, 95% CI: 0.787~0.937)、rMSSD (HR: 0.980, 95% CI: 0.970~0.989)、TP (HR: 0.890, 95% CI: 0.816~0.971)、VLF (HR: 0.889, 95% CI: 0.815~0.969)、LF (HR: 0.817, 95% CI: 0.743~0.898)、HF (HR: 0.806, 95% CI: 0.728~0.893)与MACEs独立相关。ROC分析显示,三角形指数和SDNN预测mace的曲线下面积(AUC)最高,分别为0.699 (95% CI: 0.655~0.743)和0.711 (95% CI: 0.668~0.753)。将HRV参数纳入传统风险模型,可不同程度地提高模型对MACE和心血管死亡率预测能力的c指数、NRI和IDI。结论:SDNN和三角指数的预测能力最强;其他时域和频域参数对mace也有一定的预测价值。
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来源期刊
Cardiovascular Therapeutics
Cardiovascular Therapeutics 医学-心血管系统
CiteScore
5.60
自引率
0.00%
发文量
55
审稿时长
6 months
期刊介绍: Cardiovascular Therapeutics (formerly Cardiovascular Drug Reviews) is a peer-reviewed, Open Access journal that publishes original research and review articles focusing on cardiovascular and clinical pharmacology, as well as clinical trials of new cardiovascular therapies. Articles on translational research, pharmacogenomics and personalized medicine, device, gene and cell therapies, and pharmacoepidemiology are also encouraged. Subject areas include (but are by no means limited to): Acute coronary syndrome Arrhythmias Atherosclerosis Basic cardiac electrophysiology Cardiac catheterization Cardiac remodeling Coagulation and thrombosis Diabetic cardiovascular disease Heart failure (systolic HF, HFrEF, diastolic HF, HFpEF) Hyperlipidemia Hypertension Ischemic heart disease Vascular biology Ventricular assist devices Molecular cardio-biology Myocardial regeneration Lipoprotein metabolism Radial artery access Percutaneous coronary intervention Transcatheter aortic and mitral valve replacement.
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