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基于活动记录仪的阵发性心房颤动患者睡眠中断与自主神经功能的昼夜生物标志物

Actigraphy-based sleep disruption and diurnal biomarkers of autonomic function in paroxysmal atrial fibrillation.

作者信息

Khazaie Sepideh, Wang Lu, Kaffashi Farhad, Chung Mina K, Heinzinger Catherine M, Van Wagoner David R, Loparo Kenneth A, Walia Harneet K, Mehra Reena

机构信息

Sleep Disorders Center, Neurological Institute, Cleveland Clinic, Cleveland, OH, USA.

Department of Quantitative Health Sciences, Cleveland Clinic, Cleveland, OH, USA.

出版信息

Sleep Breath. 2025 Apr 22;29(2):166. doi: 10.1007/s11325-025-03293-4.

Abstract

INTRODUCTION

Sleep architectural disruption is associated with atrial fibrillation (AF); however, associated autonomic influences remain unclear and it is unknown if this detriment persists during wakefulness. We hypothesize sleep disruption and autonomic dysfunction have diurnal patterning in patients with paroxysmal AF.

METHODS

We analyzed data from the Sleep Apnea and Atrial Fibrillation Biomarkers and Electrophysiologic Atrial Triggers (SAFEBEAT) study designed to examine paroxysmal AF and sleep apnea, including simultaneous collection of continuous electrocardiogram monitoring (Heartrak Telemetry) and actigraphy (Actiwatch GTX) for 7-21 days. Heart rate variability (HRV) measures in time-domain (standard deviation of normal-to-normal (NN) intervals (SDNN), coefficient of variation (CV)) and frequency-domain (low frequency power (LFP), high frequency power (HFP)) were used as surrogates of autonomic function and averaged per sleep/wake per day. A linear mixed-effects model assuming compound symmetry correlation structure was used to assess the relationship of HRV with actigraphy-derived sleep data.

RESULTS

The analytic sample (age 60.1 ± 12.0 years, body mass index 32.6 ± 6.7 kg/m2, 36% female, 75% White) included 100 participants with paroxysmal AF. Longer sleep latency was associated with lower HFP during wakefulness (coefficient - 0.0501, p = 0.031). Higher sleep efficiency was associated with increased SDNN (coefficient 0.0007, p = 0.014) and CV (coefficient 0.0167, p = 0.047). Higher arousal index was associated with increased CV (coefficient 0.0166, p = 0.007) and LFP (coefficient 0.0232, p = 0.003). During sleep, longer average awakenings duration was associated with increased LFP/HFP ratio (coefficient 0.1977, p < 0.001) and reduced HFP (coefficient - 0.1338, p < 0.001). Significant sleep-wake interactions were observed for sleep latency with HFP (p = 0.024), sleep efficiency with SDNN and CV (both p < 0.01), WASO with SDNN, CV, and LFP (all p < 0.05), and frequency of awakenings with CV and LFP (both p < 0.05).

CONCLUSIONS

Actigraphy-based measures of sleep disruption were associated with autonomic function alterations exhibiting diurnal variability in paroxysmal AF. Greater overall HRV and parasympathetic modulation were related to better sleep quality. Increased sympathetic activation was associated with sleep fragmentation. Results provide insights into differential autonomic dysfunction related to sleep disruption that may contribute to atrial arrhythmogenesis.

摘要

引言

睡眠结构紊乱与心房颤动(AF)相关;然而,相关的自主神经影响仍不明确,且尚不清楚这种损害在清醒时是否持续存在。我们假设阵发性房颤患者的睡眠中断和自主神经功能障碍具有昼夜模式。

方法

我们分析了睡眠呼吸暂停与心房颤动生物标志物及电生理心房触发因素(SAFEBEAT)研究的数据,该研究旨在检查阵发性房颤和睡眠呼吸暂停,包括同时收集连续7至21天的心电图监测(Heartrak遥测)和活动记录仪(Actiwatch GTX)数据。时域心率变异性(HRV)测量指标(正常到正常(NN)间期的标准差(SDNN)、变异系数(CV))和频域指标(低频功率(LFP)、高频功率(HFP))被用作自主神经功能的替代指标,并按每天的睡眠/清醒状态进行平均。采用假设复合对称相关结构的线性混合效应模型来评估HRV与活动记录仪得出的睡眠数据之间的关系。

结果

分析样本(年龄60.1±12.0岁,体重指数32.6±6.7kg/m²,36%为女性,75%为白人)包括100名阵发性房颤患者。清醒时较长的睡眠潜伏期与较低的HFP相关(系数-0.0501,p = 0.031)。较高的睡眠效率与增加的SDNN(系数0.0007,p = 0.014)和CV(系数0.0167,p = 0.047)相关。较高的觉醒指数与增加的CV(系数0.0166,p = 0.007)和LFP(系数0.0232,p = 0.003)相关。在睡眠期间,较长的平均觉醒持续时间与增加的LFP/HFP比值(系数0.1977,p < 0.001)和降低的HFP(系数-0.1338,p < 0.001)相关。观察到睡眠潜伏期与HFP(p = 0.024)、睡眠效率与SDNN和CV(均p < 0.01)、清醒时间与SDNN、CV和LFP(均p < 0.05)以及觉醒频率与CV和LFP(均p < 0.05)之间存在显著的睡眠-清醒交互作用。

结论

基于活动记录仪的睡眠中断测量指标与自主神经功能改变相关,在阵发性房颤中表现出昼夜变异性。总体HRV和副交感神经调节增强与更好的睡眠质量相关。交感神经激活增加与睡眠碎片化相关。研究结果为与睡眠中断相关的不同自主神经功能障碍提供了见解,这可能有助于心房心律失常的发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/931e/12014697/d93774b6c937/11325_2025_3293_Fig1_HTML.jpg

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