{"title":"孤立的快速眼动睡眠行为障碍在阶段性快速眼动睡眠中的脑功能网络改变。","authors":"Kang-Min Choi, Tae-Gon Noh, Jun-Sang Sunwoo, Jung-Ick Byun, Ki-Young Jung","doi":"10.1016/j.sleep.2025.106724","DOIUrl":null,"url":null,"abstract":"<p><strong>Study objectives: </strong>Isolated REM sleep behavior disorder (iRBD) is characterized by vivid, emotionally charged, and often aggressive dreams, yet the underlying neural correlates remain poorly understood. This study aimed to investigate alterations in functional brain networks during REM sleep in iRBD patients using electroencephalogram (EEG), which is potentially associated with their dream characteristics.</p><p><strong>Methods: </strong>We analyzed EEG data from 13 drug-naïve iRBD patients and 10 healthy controls (HCs) during phasic and tonic REM sleep. Source-level functional connectivity was computed across 14 cortical regions associated with dream generation, and network topology was evaluated using graph theory metrics.</p><p><strong>Results: </strong>iRBD patients showed significantly increased gamma-band functional connectivity during phasic REM sleep (p = 0.003, network-based statistic). This hyperconnectivity correlated with reduced REM atonia (RAI; R = -0.725, p = 0.007) and trended with increased dream-related symptom severity. Key network hubs included the posterior cingulate cortex (PCC) and right inferior parietal lobule (rIPL)-core nodes of the default mode network-implicated in self-referential and spatial processing. Additionally, increased connectivity between rIPL and salience-motor circuits (anterior cingulate cortex, insula, and M1) may underlie emotional overactivation and aggressive dream content.</p><p><strong>Conclusion: </strong>Our findings suggest that gamma-band hyperconnectivity during phasic REM sleep reflects altered 'dream-related network' dynamics in iRBD, potentially contributing to the intensity and emotional valence of dream experiences. This study provides preliminary evidence that functional network alterations during REM sleep may shape dream characteristics in iRBD, offering new perspectives on its neurophysiological basis.</p>","PeriodicalId":21874,"journal":{"name":"Sleep medicine","volume":"134 ","pages":"106724"},"PeriodicalIF":3.4000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Altered functional brain networks in isolated REM sleep behavior disorder during phasic REM sleep.\",\"authors\":\"Kang-Min Choi, Tae-Gon Noh, Jun-Sang Sunwoo, Jung-Ick Byun, Ki-Young Jung\",\"doi\":\"10.1016/j.sleep.2025.106724\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Study objectives: </strong>Isolated REM sleep behavior disorder (iRBD) is characterized by vivid, emotionally charged, and often aggressive dreams, yet the underlying neural correlates remain poorly understood. This study aimed to investigate alterations in functional brain networks during REM sleep in iRBD patients using electroencephalogram (EEG), which is potentially associated with their dream characteristics.</p><p><strong>Methods: </strong>We analyzed EEG data from 13 drug-naïve iRBD patients and 10 healthy controls (HCs) during phasic and tonic REM sleep. Source-level functional connectivity was computed across 14 cortical regions associated with dream generation, and network topology was evaluated using graph theory metrics.</p><p><strong>Results: </strong>iRBD patients showed significantly increased gamma-band functional connectivity during phasic REM sleep (p = 0.003, network-based statistic). This hyperconnectivity correlated with reduced REM atonia (RAI; R = -0.725, p = 0.007) and trended with increased dream-related symptom severity. Key network hubs included the posterior cingulate cortex (PCC) and right inferior parietal lobule (rIPL)-core nodes of the default mode network-implicated in self-referential and spatial processing. Additionally, increased connectivity between rIPL and salience-motor circuits (anterior cingulate cortex, insula, and M1) may underlie emotional overactivation and aggressive dream content.</p><p><strong>Conclusion: </strong>Our findings suggest that gamma-band hyperconnectivity during phasic REM sleep reflects altered 'dream-related network' dynamics in iRBD, potentially contributing to the intensity and emotional valence of dream experiences. This study provides preliminary evidence that functional network alterations during REM sleep may shape dream characteristics in iRBD, offering new perspectives on its neurophysiological basis.</p>\",\"PeriodicalId\":21874,\"journal\":{\"name\":\"Sleep medicine\",\"volume\":\"134 \",\"pages\":\"106724\"},\"PeriodicalIF\":3.4000,\"publicationDate\":\"2025-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Sleep medicine\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.sleep.2025.106724\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/8/5 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sleep medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.sleep.2025.106724","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/5 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
摘要
研究目标:孤立的快速眼动睡眠行为障碍(iRBD)的特征是生动的、情绪化的、经常是攻击性的梦,但潜在的神经关联仍然知之甚少。本研究旨在利用脑电图(EEG)研究iRBD患者快速眼动睡眠期间脑功能网络的变化,这可能与他们的梦境特征有关。方法:我们分析了13例drug-naïve iRBD患者和10例健康对照(hc)在相性和强直性REM睡眠期间的脑电图数据。通过14个与梦境产生相关的皮质区域计算源级功能连通性,并使用图论指标评估网络拓扑。结果:iRBD患者在相期REM睡眠时γ波段功能连通性显著增加(p = 0.003,基于网络统计)。这种超连通性与快速眼动期弛缓症(RAI;R = -0.725, p = 0.007),且与梦相关症状严重程度增加有关。关键的网络枢纽包括后扣带皮层(PCC)和右下顶叶(rIPL)——默认模式网络的核心节点,涉及自我参照和空间处理。此外,rIPL和突出运动回路(前扣带皮层、脑岛和M1)之间的连通性增加可能是情绪过度激活和攻击性梦境内容的基础。结论:我们的研究结果表明,在阶段性快速眼动睡眠期间,伽玛波段的超连通性反映了iRBD中“梦相关网络”动态的改变,可能有助于梦经历的强度和情绪效价。本研究为快速眼动睡眠期间的功能网络改变可能影响iRBD的梦特征提供了初步证据,为其神经生理学基础提供了新的视角。
Altered functional brain networks in isolated REM sleep behavior disorder during phasic REM sleep.
Study objectives: Isolated REM sleep behavior disorder (iRBD) is characterized by vivid, emotionally charged, and often aggressive dreams, yet the underlying neural correlates remain poorly understood. This study aimed to investigate alterations in functional brain networks during REM sleep in iRBD patients using electroencephalogram (EEG), which is potentially associated with their dream characteristics.
Methods: We analyzed EEG data from 13 drug-naïve iRBD patients and 10 healthy controls (HCs) during phasic and tonic REM sleep. Source-level functional connectivity was computed across 14 cortical regions associated with dream generation, and network topology was evaluated using graph theory metrics.
Results: iRBD patients showed significantly increased gamma-band functional connectivity during phasic REM sleep (p = 0.003, network-based statistic). This hyperconnectivity correlated with reduced REM atonia (RAI; R = -0.725, p = 0.007) and trended with increased dream-related symptom severity. Key network hubs included the posterior cingulate cortex (PCC) and right inferior parietal lobule (rIPL)-core nodes of the default mode network-implicated in self-referential and spatial processing. Additionally, increased connectivity between rIPL and salience-motor circuits (anterior cingulate cortex, insula, and M1) may underlie emotional overactivation and aggressive dream content.
Conclusion: Our findings suggest that gamma-band hyperconnectivity during phasic REM sleep reflects altered 'dream-related network' dynamics in iRBD, potentially contributing to the intensity and emotional valence of dream experiences. This study provides preliminary evidence that functional network alterations during REM sleep may shape dream characteristics in iRBD, offering new perspectives on its neurophysiological basis.
期刊介绍:
Sleep Medicine aims to be a journal no one involved in clinical sleep medicine can do without.
A journal primarily focussing on the human aspects of sleep, integrating the various disciplines that are involved in sleep medicine: neurology, clinical neurophysiology, internal medicine (particularly pulmonology and cardiology), psychology, psychiatry, sleep technology, pediatrics, neurosurgery, otorhinolaryngology, and dentistry.
The journal publishes the following types of articles: Reviews (also intended as a way to bridge the gap between basic sleep research and clinical relevance); Original Research Articles; Full-length articles; Brief communications; Controversies; Case reports; Letters to the Editor; Journal search and commentaries; Book reviews; Meeting announcements; Listing of relevant organisations plus web sites.