• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

慢性失眠障碍皮质结构变化的转录特征。

Transcriptional signatures of cortical structural changes in chronic insomnia disorder.

机构信息

School of Acupuncture and Tuina, Chengdu University of Traditional Chinese Medicine, Chengdu, China.

Department of Traditional Chinese Medicine Rehabilitation, Chongqing University Three Gorges Hospital, Chongqing, China.

出版信息

Psychophysiology. 2024 Dec;61(12):e14671. doi: 10.1111/psyp.14671. Epub 2024 Aug 19.

DOI:10.1111/psyp.14671
PMID:39160694
Abstract

Chronic insomnia disorder (CID) is a multidimensional disease that may influence various levels of brain organization, spanning the macroscopic structural connectome to microscopic gene expression. However, the connection between genomic variations and morphological alterations in CID remains unclear. Here, we investigated brain structural changes in CID patients at the whole-brain level and whether these link to transcriptional characteristics. Brain structural data from 104 CID patients and 102 matched healthy controls (HC) were acquired to examine cortical structural alterations using morphometric similarity (MS) analysis. Partial least squares (PLS) regression and transcriptome data from the Allen Human Brain Atlas were used to extract genomes related to MS changes. Gene-category enrichment analysis (GCEA) was used to identify potential molecular mechanisms behind the observed structural changes. We found that CID patients exhibited MS reductions in the parietal and limbic regions, along with enhancements in the temporal and frontal regions compared to HCs (p < .05). Subsequently, PLS and GCEA revealed that these MS alterations were spatially correlated with a set of genes, especially those significantly correlated with excitatory and inhibitory neurons and chronic neuroinflammation. This neuroimaging-transcriptomic study bridges the gap between cortical structural changes and the molecular mechanisms in CID patients, providing novel insight into the pathophysiology of insomnia and targeted treatments.

摘要

慢性失眠障碍(CID)是一种多维疾病,可能影响大脑组织的各个层次,从宏观的结构连接组到微观的基因表达。然而,基因组变异与 CID 形态改变之间的联系尚不清楚。在这里,我们在全脑水平上研究了 CID 患者的大脑结构变化,以及这些变化是否与转录特征相关。我们获得了 104 名 CID 患者和 102 名匹配的健康对照者(HC)的大脑结构数据,使用形态相似性(MS)分析来检查皮质结构的改变。我们使用偏最小二乘(PLS)回归和艾伦人类大脑图谱的转录组数据来提取与 MS 变化相关的基因组。基因类别富集分析(GCEA)用于确定观察到的结构变化背后的潜在分子机制。我们发现,与 HC 相比,CID 患者的顶叶和边缘区域的 MS 降低,而颞叶和额叶区域的 MS 增强(p<0.05)。随后,PLS 和 GCEA 表明,这些 MS 改变与一组基因在空间上相关,特别是那些与兴奋性和抑制性神经元和慢性神经炎症显著相关的基因。这项神经影像学-转录组学研究弥合了 CID 患者皮质结构变化与分子机制之间的差距,为失眠的病理生理学和靶向治疗提供了新的见解。

相似文献

1
Transcriptional signatures of cortical structural changes in chronic insomnia disorder.慢性失眠障碍皮质结构变化的转录特征。
Psychophysiology. 2024 Dec;61(12):e14671. doi: 10.1111/psyp.14671. Epub 2024 Aug 19.
2
Altered morphometric similarity networks in insomnia disorder.失眠障碍中形态相似性网络的改变。
Brain Struct Funct. 2024 Jul;229(6):1433-1445. doi: 10.1007/s00429-024-02809-0. Epub 2024 May 27.
3
Electroencephalography connectome changes in chronic insomnia disorder are correlated with neurochemical signatures.慢性失眠障碍的脑电图连接组变化与神经化学特征相关。
Sleep. 2024 Jul 11;47(7). doi: 10.1093/sleep/zsae080.
4
Multimodal neuroimaging exploration of the mechanisms of sleep quality deterioration after SARS-CoV-2 Omicron infection.多模态神经影像学探索 SARS-CoV-2 奥密克戎感染后睡眠质量恶化的机制。
BMC Med. 2024 Jun 26;22(1):271. doi: 10.1186/s12916-024-03487-9.
5
Cortical morphological changes and associated transcriptional signatures in post-traumatic stress disorder and psychological resilience.创伤后应激障碍和心理弹性中的皮质形态变化及相关转录特征。
BMC Med. 2024 Oct 8;22(1):431. doi: 10.1186/s12916-024-03657-9.
6
Functional connectome gradient predicts clinical symptoms of chronic insomnia disorder.功能连接梯度可预测慢性失眠障碍的临床症状。
Prog Neuropsychopharmacol Biol Psychiatry. 2024 Dec 20;135:111120. doi: 10.1016/j.pnpbp.2024.111120. Epub 2024 Aug 21.
7
Amygdala Changes in Chronic Insomnia and Their Association with Sleep and Anxiety Symptoms: Insight from Shape Analysis.杏仁核变化与慢性失眠及其与睡眠和焦虑症状的关系:来自形状分析的见解。
Neural Plast. 2019 Dec 1;2019:8549237. doi: 10.1155/2019/8549237. eCollection 2019.
8
Altered cingulate gyrus subregions functional connectivity in chronic insomnia disorder with anxiety.慢性失眠伴焦虑障碍患者扣带回 gyrus 亚区功能连接改变。
Sleep Med. 2024 Nov;123:42-48. doi: 10.1016/j.sleep.2024.08.031. Epub 2024 Aug 30.
9
Frequency-dependent changes in local intrinsic oscillations in chronic primary insomnia: A study of the amplitude of low-frequency fluctuations in the resting state.慢性原发性失眠中局部内在振荡的频率依赖性变化:静息状态下低频波动幅度的研究
Neuroimage Clin. 2016 May 26;15:458-465. doi: 10.1016/j.nicl.2016.05.011. eCollection 2017.
10
Cortical thickness alterations are associated with astrocytes and excitatory neuron-specific transcriptome signatures in pediatric bipolar disorder.皮质厚度的改变与儿科双相情感障碍中的星形胶质细胞和兴奋性神经元特异性转录组特征有关。
Cereb Cortex. 2023 Jun 8;33(12):7540-7552. doi: 10.1093/cercor/bhad059.

引用本文的文献

1
Exploratory GABAa-informed control network modulates hyperarousal brain dynamics in chronic insomnia.探索性γ-氨基丁酸A受体(GABAa)信息控制网络调节慢性失眠中的过度觉醒脑动力学。
Commun Biol. 2025 Jul 3;8(1):991. doi: 10.1038/s42003-025-08439-4.
2
Molecular mechanisms explaining sex-specific functional connectivity changes in chronic insomnia disorder.解释慢性失眠障碍中性别特异性功能连接变化的分子机制。
BMC Med. 2025 May 6;23(1):261. doi: 10.1186/s12916-025-04089-9.
3
Cerebral Blood Flow Changes and Their Spatial Correlations With GABAa and Dopamine-D1 Receptor Explaining Individual Differences in Chronic Insomnia and the Therapeutic Effects of Acupuncture.
脑血流变化及其与GABAa和多巴胺D1受体的空间相关性,解释慢性失眠的个体差异及针灸的治疗效果。
Hum Brain Mapp. 2025 Mar;46(4):e70183. doi: 10.1002/hbm.70183.
4
Age-Specific Functional Connectivity Changes After Partial Sleep Deprivation Are Correlated With Neurocognitive and Molecular Signatures.部分睡眠剥夺后特定年龄的功能连接变化与神经认知和分子特征相关。
CNS Neurosci Ther. 2025 Feb;31(2):e70272. doi: 10.1111/cns.70272.