"Touching" the brain: braille reading mitigates the SC-FC decoupling of brain networks in congenital blindness.

IF 2.7 3区 医学 Q1 ANATOMY & MORPHOLOGY
Saiyi Jiao, Ke Wang, Jiahong Zeng, Zhenjiang Cui, Yudan Luo, Zaizhu Han
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引用次数: 0

Abstract

Acquired experiences are crucial for brain structure and function development, with a strong covariance between them. However, how experience deprivation reorganizes the covariance between structural connectivity (SC) and functional connectivity (FC), and how newly acquired experience influences this plastic reorganization remain unclear. To address these, we recruited 21 congenitally blind (CB) participants and 21 normally sighted (NS) controls. Using multi-modal MRI and graph-theoretical analyses, we examined the topological properties, and then investigated the SC-FC coupling reorganization and its relationship with braille reading ability. Compared to the NS group, the CB group showed significant topological reorganization in structural networks and disrupted intra-hemispheric SC-FC coupling. Importantly, braille reading proficiency and earlier braille onset mitigated SC-FC decoupling, suggesting that braille reading partially rescued disrupted network. Our findings highlight dynamic network plasticity in compensating for visual loss, and underscore the importance of early braille acquisition in maintaining brain networks stability in congenital blindness.

“触摸”大脑:盲文阅读减轻先天失明的大脑网络SC-FC脱钩。
获得性经验对大脑结构和功能的发展至关重要,两者之间存在很强的协方差。然而,经验剥夺如何重组结构连通性(SC)和功能连通性(FC)之间的协方差,以及新获得的经验如何影响这种塑性重组尚不清楚。为了解决这些问题,我们招募了21名先天性失明(CB)参与者和21名正常视力(NS)对照组。通过多模态MRI和图理论分析,研究了盲文阅读能力与SC-FC耦合重组的关系。与NS组相比,CB组在结构网络中表现出明显的拓扑重组,并破坏了半球内SC-FC耦合。重要的是,盲文阅读能力和早期盲文发病减轻了SC-FC脱钩,表明盲文阅读部分地挽救了中断的网络。我们的研究结果强调了动态网络可塑性在补偿视觉损失方面的作用,并强调了先天性失明患者早期盲文习得在维持大脑网络稳定性方面的重要性。
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来源期刊
Brain Structure & Function
Brain Structure & Function 医学-解剖学与形态学
CiteScore
6.00
自引率
6.50%
发文量
168
审稿时长
8 months
期刊介绍: Brain Structure & Function publishes research that provides insight into brain structure−function relationships. Studies published here integrate data spanning from molecular, cellular, developmental, and systems architecture to the neuroanatomy of behavior and cognitive functions. Manuscripts with focus on the spinal cord or the peripheral nervous system are not accepted for publication. Manuscripts with focus on diseases, animal models of diseases, or disease-related mechanisms are only considered for publication, if the findings provide novel insight into the organization and mechanisms of normal brain structure and function.
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