Disruption of structural connectome hierarchy in age-related hearing loss.

IF 3.2 3区 医学 Q2 NEUROSCIENCES
Frontiers in Neuroscience Pub Date : 2025-03-17 eCollection Date: 2025-01-01 DOI:10.3389/fnins.2025.1555553
Yi Zhen, Hongwei Zheng, Yi Zheng, Zhiming Zheng, Yaqian Yang, Shaoting Tang
{"title":"Disruption of structural connectome hierarchy in age-related hearing loss.","authors":"Yi Zhen, Hongwei Zheng, Yi Zheng, Zhiming Zheng, Yaqian Yang, Shaoting Tang","doi":"10.3389/fnins.2025.1555553","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Age-related hearing loss (ARHL) is a common sensory disability among older adults and is considered a risk factor for the development of dementia. Previous work has shown altered brain connectome topology in ARHL, including abnormal nodal strength and clustering coefficient. However, whether ARHL affects the hierarchical organization of structural connectome and how these alterations relate to transcriptomic signatures remain unknown.</p><p><strong>Methods: </strong>Here, we apply a gradient mapping framework to the structural connectome derived from diffusion magnetic resonance imaging. We focus on the first three structural gradients that reflect distinct hierarchical organization of structural connectome, and assess ARHL-related changes.</p><p><strong>Results: </strong>We find that, compared to controls, ARHL patients exhibit widespread disruptions of structural connectome organization, spanning from primary sensory areas (e.g., somatomotor network) to high-order association areas (e.g., default mode network). Subsequently, by employing subcortical-weighted gradients derived from weighting cortical gradients by subcortical-cortical connectivity, we observe that ARHL patients show significantly altered subcortical-cortical connectivity in the left caudate, left nucleus accumbens, right hippocampus, and right amygdala. Finally, we investigate the relationship between gene expression and alterations in structural gradients. We observe that these alterations in structural gradients are associated with weighted gene expression profiles, with relevant genes preferentially enriched for inorganic ion transmembrane transport and terms related to regulating biological processes.</p><p><strong>Discussion: </strong>Taken together, these findings highlight that ARHL is associated with abnormal structural connectome hierarchy and reveal the transcriptomic relevance of these abnormalities, contributing to a richer understanding of the neurobiological substrates in ARHL.</p>","PeriodicalId":12639,"journal":{"name":"Frontiers in Neuroscience","volume":"19 ","pages":"1555553"},"PeriodicalIF":3.2000,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11955685/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3389/fnins.2025.1555553","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Age-related hearing loss (ARHL) is a common sensory disability among older adults and is considered a risk factor for the development of dementia. Previous work has shown altered brain connectome topology in ARHL, including abnormal nodal strength and clustering coefficient. However, whether ARHL affects the hierarchical organization of structural connectome and how these alterations relate to transcriptomic signatures remain unknown.

Methods: Here, we apply a gradient mapping framework to the structural connectome derived from diffusion magnetic resonance imaging. We focus on the first three structural gradients that reflect distinct hierarchical organization of structural connectome, and assess ARHL-related changes.

Results: We find that, compared to controls, ARHL patients exhibit widespread disruptions of structural connectome organization, spanning from primary sensory areas (e.g., somatomotor network) to high-order association areas (e.g., default mode network). Subsequently, by employing subcortical-weighted gradients derived from weighting cortical gradients by subcortical-cortical connectivity, we observe that ARHL patients show significantly altered subcortical-cortical connectivity in the left caudate, left nucleus accumbens, right hippocampus, and right amygdala. Finally, we investigate the relationship between gene expression and alterations in structural gradients. We observe that these alterations in structural gradients are associated with weighted gene expression profiles, with relevant genes preferentially enriched for inorganic ion transmembrane transport and terms related to regulating biological processes.

Discussion: Taken together, these findings highlight that ARHL is associated with abnormal structural connectome hierarchy and reveal the transcriptomic relevance of these abnormalities, contributing to a richer understanding of the neurobiological substrates in ARHL.

年龄相关性听力损失中结构连接体层级的破坏。
年龄相关性听力损失(ARHL)是老年人中常见的感觉障碍,被认为是痴呆发展的危险因素。先前的研究表明,ARHL患者的脑连接体拓扑结构发生改变,包括异常的节点强度和聚类系数。然而,ARHL是否影响结构连接组的层次组织以及这些改变与转录组特征的关系尚不清楚。方法:在这里,我们将梯度映射框架应用于来自扩散磁共振成像的结构连接体。我们关注反映结构连接体不同层次组织的前三个结构梯度,并评估arhl相关的变化。结果:我们发现,与对照组相比,ARHL患者表现出广泛的结构连接体组织破坏,从初级感觉区域(例如,躯体运动网络)到高阶关联区域(例如,默认模式网络)。随后,通过使用皮质下-皮质连通性加权梯度得出的皮质下加权梯度,我们观察到ARHL患者在左侧尾状核、左侧伏隔核、右侧海马和右侧杏仁核的皮质下-皮质连通性显著改变。最后,我们研究了基因表达与结构梯度变化之间的关系。我们观察到这些结构梯度的改变与加权基因表达谱有关,相关基因优先富集于无机离子跨膜运输和调节生物过程相关的术语。综上所述,这些发现强调了ARHL与异常结构连接组层次相关,并揭示了这些异常的转录组相关性,有助于更丰富地了解ARHL的神经生物学底物。
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
Frontiers in Neuroscience
Frontiers in Neuroscience NEUROSCIENCES-
CiteScore
6.20
自引率
4.70%
发文量
2070
审稿时长
14 weeks
期刊介绍: Neural Technology is devoted to the convergence between neurobiology and quantum-, nano- and micro-sciences. In our vision, this interdisciplinary approach should go beyond the technological development of sophisticated methods and should contribute in generating a genuine change in our discipline.
×
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:481959085
Book学术官方微信