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Data-driven sleep structure deciphering based on cardiorespiratory signals

delete2025-07-01
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PRE
AI
M
Ming Huang *
O
Osuke Iwata
K
Kiyoko Yokoyama
T
T. Tamura
DOI:10.1016/j.cmpb.2025.108769delete
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摘要

摘要

En 中文
背景与目的:心肺信号通过心肺耦合的生理机制为理解睡眠结构提供了新颖视角。该机制将耦合谱分为高频(HF)和低频(LF)频带,表明4-8分钟长的信号片段最适于分析。然而,由于缺乏针对这些信号的标签,研究不得不依赖美国睡眠医学会(AASM)的定义,而这些定义主要针对脑电图(EEG)和眼动图(EOG)数据设计。本研究旨在解决从AASM定义的标签向心肺导向标签的转换挑战,并评估使用这些信号进行准确睡眠结构识别的可行性。 方法:为符合心肺信号的生理特征,通过排除N2阶段对AASM标签进行了修改,因其同时包含稳定和不稳定非快速眼动(NREM)阶段,易引入模糊性。修改后的数据集聚焦于清醒、N1、深睡(N3)和快速眼动(REM)阶段。开发了一种基于生理学原理的深度学习模型(PIDM),用于从心肺时间序列中提取特征并分类睡眠阶段。后分析通过评估HF/LF比率和呼吸变异性,检验了模型对N2预测的生理合理性。 结果:结合修改后的标签方案与PIDM模型的流程,在正常组中分别实现了清醒、深睡和REM阶段的平衡准确率0.83、0.86和0.78;在轻度及中度睡眠呼吸暂停组中则达到0.92、0.95和0.90。后分析显示,多数N2样本被归因于稳定NREM睡眠,其特征为较高的HF/LF比率和较低的呼吸变异性,与生理学认知一致。 结论:本研究强调了心肺信号在睡眠结构识别中的生理相关性。通过排除和重新定义以解决N2分类的不确定性,所提流程有效区分了清醒、深睡和REM阶段。这些发现表明,心肺信号可作为稳健、实用且不依赖EEG的睡眠分析工具,尤其在居家医疗场景中具有潜力。
Keyword:
Cardiorespiratory signals
Deep-learning model
Sleep apnea
Sleep structure
Sleep stages

期刊

Computer Methods and Programs in Biomedicine 封面图
Computer Methods and Programs in Biomedicine
IF:
4.8
论文数:
7.0K
被引数:
2.1W

机构

N
Nara Institute of Science and Technology
学者数:
542
论文数: 188
被引数: 3.8K
引用论文

引用论文

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