Winding down for the night: changes in thalamocortical connectivity before bed are associated with subsequent sleep-stage duration.

IF 2.1 4区 医学 Q4 NEUROSCIENCES
Neuroreport Pub Date : 2026-03-04 Epub Date: 2025-02-11 DOI:10.1097/WNR.0000000000002245
William D S Killgore, Kymberly Henderson-Arredondo, Samantha Jankowski, Salma I Patel, Michael A Grandner, Lindsey L Hildebrand, Kathryn E R Kennedy, Jungwon Cha, David C Negelspach, Alisa Huskey
{"title":"Winding down for the night: changes in thalamocortical connectivity before bed are associated with subsequent sleep-stage duration.","authors":"William D S Killgore, Kymberly Henderson-Arredondo, Samantha Jankowski, Salma I Patel, Michael A Grandner, Lindsey L Hildebrand, Kathryn E R Kennedy, Jungwon Cha, David C Negelspach, Alisa Huskey","doi":"10.1097/WNR.0000000000002245","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>The transition from wakefulness to sleep depends on dynamic thalamocortical interactions that regulate arousal and sensory gating. While thalamic coordination of cortical activity during sleep is well established, little is known about how presleep thalamocortical connectivity relates to subsequent sleep architecture. This study examined whether short-term changes in thalamocortical coupling during the early evening predict polysomnographically measured sleep later that night.</p><p><strong>Methods: </strong>Twenty adults (8 men, 12 women; age 19-39 years) with clinically significant insomnia symptoms completed two resting-state functional MRI scans ~2 hours apart (~6 : 30 and 8 : 30 p.m.) before an overnight in-lab sleep study. Whole-brain seed-to-voxel analyses using a bilateral thalamic region of interest assessed changes in functional connectivity between scans, which were then correlated with polysomnographic sleep-stage metrics [i.e. time in wake, N1, N2, N3, rapid eye movement (REM)].</p><p><strong>Results: </strong>Increased thalamocortical connectivity with occipital, posterior middle temporal, and left frontal cortices before sleep predicted greater time in N2 sleep, whereas decreased connectivity with insula, putamen, and frontal regions predicted more N3 sleep. Reduced thalamic coupling with the left lateral occipital gyrus predicted greater REM sleep, and decreased thalamocerebellar connectivity was associated with increased wake time while in bed. No associations were observed for N1, total sleep time, or sleep efficiency.</p><p><strong>Conclusion: </strong>Fluctuations in presleep thalamocortical connectivity predicted distinct features of subsequent sleep architecture. These findings suggest that presleep thalamocortical network dynamics may facilitate some aspects of later restorative sleep the same night, providing insight into how waking brain patterns influence subsequent sleep quality and continuity.</p>","PeriodicalId":19213,"journal":{"name":"Neuroreport","volume":"37 4","pages":"139-144"},"PeriodicalIF":2.1000,"publicationDate":"2026-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12888901/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuroreport","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1097/WNR.0000000000002245","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/11 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: The transition from wakefulness to sleep depends on dynamic thalamocortical interactions that regulate arousal and sensory gating. While thalamic coordination of cortical activity during sleep is well established, little is known about how presleep thalamocortical connectivity relates to subsequent sleep architecture. This study examined whether short-term changes in thalamocortical coupling during the early evening predict polysomnographically measured sleep later that night.

Methods: Twenty adults (8 men, 12 women; age 19-39 years) with clinically significant insomnia symptoms completed two resting-state functional MRI scans ~2 hours apart (~6 : 30 and 8 : 30 p.m.) before an overnight in-lab sleep study. Whole-brain seed-to-voxel analyses using a bilateral thalamic region of interest assessed changes in functional connectivity between scans, which were then correlated with polysomnographic sleep-stage metrics [i.e. time in wake, N1, N2, N3, rapid eye movement (REM)].

Results: Increased thalamocortical connectivity with occipital, posterior middle temporal, and left frontal cortices before sleep predicted greater time in N2 sleep, whereas decreased connectivity with insula, putamen, and frontal regions predicted more N3 sleep. Reduced thalamic coupling with the left lateral occipital gyrus predicted greater REM sleep, and decreased thalamocerebellar connectivity was associated with increased wake time while in bed. No associations were observed for N1, total sleep time, or sleep efficiency.

Conclusion: Fluctuations in presleep thalamocortical connectivity predicted distinct features of subsequent sleep architecture. These findings suggest that presleep thalamocortical network dynamics may facilitate some aspects of later restorative sleep the same night, providing insight into how waking brain patterns influence subsequent sleep quality and continuity.

Abstract Image

睡前放松:睡前丘脑皮质连通性的变化与随后的睡眠阶段持续时间有关。
目的:从清醒到睡眠的转变依赖于调节觉醒和感觉门控的动态丘脑皮质相互作用。虽然睡眠期间丘脑皮质活动的协调已经得到了很好的证实,但人们对睡眠前丘脑皮质连接与随后的睡眠结构之间的关系知之甚少。这项研究调查了在傍晚早期丘脑皮质耦合的短期变化是否预示着当晚多导睡眠仪测量的睡眠。方法:20名有明显失眠症状的成年人(8名男性,12名女性,年龄19-39岁)在夜间实验室睡眠研究前间隔约2小时(约6:30和8:30)完成两次静息状态功能MRI扫描。全脑种子到体素分析使用双侧丘脑感兴趣区域评估扫描之间功能连通性的变化,然后将其与多导睡眠图睡眠阶段指标(即清醒时间,N1, N2, N3,快速眼动(REM))相关联。结果:睡眠前丘脑皮质与枕叶、中颞叶后叶和左额叶皮质的连通性增加预示着更长的N2睡眠时间,而与岛叶、壳核和额叶区域的连通性减少预示着更多的N3睡眠。丘脑与左侧枕侧回耦合的减少预示着更长的快速眼动睡眠,丘脑-小脑连接的减少预示着在床上醒来的时间增加。没有观察到N1、总睡眠时间或睡眠效率之间的关联。结论:睡眠前丘脑皮质连通性的波动预测了随后睡眠结构的明显特征。这些发现表明,睡眠前的丘脑皮质网络动态可能会促进当晚后期恢复性睡眠的某些方面,从而深入了解清醒的大脑模式如何影响随后的睡眠质量和连续性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Neuroreport
Neuroreport 医学-神经科学
CiteScore
3.20
自引率
0.00%
发文量
150
审稿时长
1 months
期刊介绍: NeuroReport is a channel for rapid communication of new findings in neuroscience. It is a forum for the publication of short but complete reports of important studies that require very fast publication. Papers are accepted on the basis of the novelty of their finding, on their significance for neuroscience and on a clear need for rapid publication. Preliminary communications are not suitable for the Journal. Submitted articles undergo a preliminary review by the editor. Some articles may be returned to authors without further consideration. Those being considered for publication will undergo further assessment and peer-review by the editors and those invited to do so from a reviewer pool. The core interest of the Journal is on studies that cast light on how the brain (and the whole of the nervous system) works. We aim to give authors a decision on their submission within 2-5 weeks, and all accepted articles appear in the next issue to press.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书