Exploratory Analysis of Sleep Deprivation Effects on Gene Expression and Regional Brain Metabolism.

Complex psychiatry Pub Date : 2025-03-24 eCollection Date: 2025-01-01 DOI:10.1159/000545461
Lily Bai, Ramanuj Sarkar, Faith Lee, Joseph Chong-Sang Wu, Marquis P Vawter
{"title":"Exploratory Analysis of Sleep Deprivation Effects on Gene Expression and Regional Brain Metabolism.","authors":"Lily Bai, Ramanuj Sarkar, Faith Lee, Joseph Chong-Sang Wu, Marquis P Vawter","doi":"10.1159/000545461","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Sleep deprivation affects cognitive performance and immune function, yet its mechanisms and biomarkers remain unclear. This study explored the relationships among gene expression, brain metabolism, sleep deprivation, and sex differences.</p><p><strong>Methods: </strong>Fluorodeoxyglucose-18 positron emission tomography measured brain metabolism in regions of interest, and RNA analysis of blood samples assessed gene expression pre- and post-sleep deprivation. Mixed model regression and principal component analysis identified significant genes and regional metabolic changes.</p><p><strong>Results: </strong>There were 23 and 28 differentially expressed probe sets for the main effects of sex and sleep deprivation, respectively, and 55 probe sets for their interaction (FDR-corrected <i>p</i> < 0.05). Functional analysis of genes affected by sleep deprivation revealed pathway enrichment in nucleoplasm- and UBL conjugation-related genes. Genes with significant sex effects mapped to chromosomes Y and 19 (Benjamini-Hochberg FDR <i>p</i> < 0.05), with 11 genes (4%) and 29 genes (10.5%) involved, respectively. Differential gene expression highlighted sex-based differences in innate and adaptive immunity. For brain metabolism, sleep deprivation resulted in significant decreases in the left insula, left medial prefrontal cortex (BA32), left somatosensory cortex (BA1/2), and left motor premotor cortex (BA6) and increases in the right inferior longitudinal fasciculus, right primary visual cortex (BA17), right amygdala, left cerebellum, and bilateral pons.</p><p><strong>Conclusion: </strong>Sleep deprivation broadly impacts brain metabolism, gene expression, and immune function, revealing cellular stress responses and hemispheric vulnerability. These findings enhance our understanding of the molecular and functional effects of sleep deprivation.</p>","PeriodicalId":72654,"journal":{"name":"Complex psychiatry","volume":"11 1","pages":"50-71"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12054991/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Complex psychiatry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1159/000545461","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Sleep deprivation affects cognitive performance and immune function, yet its mechanisms and biomarkers remain unclear. This study explored the relationships among gene expression, brain metabolism, sleep deprivation, and sex differences.

Methods: Fluorodeoxyglucose-18 positron emission tomography measured brain metabolism in regions of interest, and RNA analysis of blood samples assessed gene expression pre- and post-sleep deprivation. Mixed model regression and principal component analysis identified significant genes and regional metabolic changes.

Results: There were 23 and 28 differentially expressed probe sets for the main effects of sex and sleep deprivation, respectively, and 55 probe sets for their interaction (FDR-corrected p < 0.05). Functional analysis of genes affected by sleep deprivation revealed pathway enrichment in nucleoplasm- and UBL conjugation-related genes. Genes with significant sex effects mapped to chromosomes Y and 19 (Benjamini-Hochberg FDR p < 0.05), with 11 genes (4%) and 29 genes (10.5%) involved, respectively. Differential gene expression highlighted sex-based differences in innate and adaptive immunity. For brain metabolism, sleep deprivation resulted in significant decreases in the left insula, left medial prefrontal cortex (BA32), left somatosensory cortex (BA1/2), and left motor premotor cortex (BA6) and increases in the right inferior longitudinal fasciculus, right primary visual cortex (BA17), right amygdala, left cerebellum, and bilateral pons.

Conclusion: Sleep deprivation broadly impacts brain metabolism, gene expression, and immune function, revealing cellular stress responses and hemispheric vulnerability. These findings enhance our understanding of the molecular and functional effects of sleep deprivation.

睡眠剥夺对基因表达和脑区域代谢影响的探索性分析。
睡眠剥夺会影响认知能力和免疫功能,但其机制和生物标志物尚不清楚。这项研究探讨了基因表达、脑代谢、睡眠剥夺和性别差异之间的关系。方法:氟脱氧葡萄糖-18正电子发射断层扫描测量感兴趣区域的脑代谢,血液样本的RNA分析评估睡眠剥夺前和睡眠剥夺后的基因表达。混合模型回归和主成分分析发现了显著的基因和区域代谢变化。结果:性剥夺和睡眠剥夺的主效应分别有23和28个差异表达探针集,交互作用有55个差异表达探针集(经fdr校正p < 0.05)。对受睡眠剥夺影响的基因的功能分析揭示了核质和UBL偶联相关基因的通路富集。性别效应显著的基因定位于Y染色体和19染色体(Benjamini-Hochberg FDR p < 0.05),分别涉及11个基因(4%)和29个基因(10.5%)。差异基因表达突出了先天免疫和适应性免疫的性别差异。在脑代谢方面,睡眠剥夺导致左侧脑岛、左侧内侧前额叶皮质(BA32)、左侧体感皮质(BA1/2)和左侧运动前皮质(BA6)显著减少,右侧下纵束、右侧初级视觉皮质(BA17)、右侧杏仁核、左侧小脑和双侧脑桥显著增加。结论:睡眠剥夺广泛影响脑代谢、基因表达和免疫功能,揭示细胞应激反应和半球易感性。这些发现增强了我们对睡眠剥夺的分子和功能影响的理解。
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
CiteScore
2.80
自引率
0.00%
发文量
0
×
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