以布罗卡区为目标的背侧纤维束的侧化与语言技能的发育过程有关

IF 6.7 2区 医学 Q1 NEUROSCIENCES
Cornelius Eichner , Philipp Berger , Cheslie C. Klein , Angela D. Friederici
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引用次数: 0

摘要

在成人大脑中,语言被限制在左半球,而且在发育早期就能观察到功能侧化。在此,我们研究了白质结构语言网络的侧向化是否与之同步。我们分析了连接颞叶和额叶皮层的语言相关纤维束的强度和微结构特性,并分离出两条背侧纤维束,一条以布罗卡后区(BA44)为目标,另一条以中央前回(BA6)为目标。在一个大样本的幼儿(3-6 岁)中,我们发现,与 BA6 目标纤维束不同,BA44 目标纤维束的微观结构不对称性与局部发育的不同方面有显著相关性。前段的不对称反映了年龄,而后段的不对称则与儿童的语言能力有关。这些发现证明了侧化网络中结构与功能的精细映射,超越了我们目前对与语言相关的人类大脑成熟的看法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lateralization of dorsal fiber tract targeting Broca’s area concurs with language skills during development

Language is bounded to the left hemisphere in the adult brain and the functional lateralization can already be observed early during development. Here we investigate whether this is paralleled by a lateralization of the white matter structural language network. We analyze the strength and microstructural properties of language-related fiber tracts connecting temporal and frontal cortices with a separation of two dorsal tracts, one targeting the posterior Broca’s area (BA44) and one targeting the precentral gyrus (BA6). In a large sample of young children (3–6 years), we demonstrate that, in contrast to the BA6-targeting tract, the microstructural asymmetry of the BA44-targeting fiber tract significantly correlates locally with different aspects of development. While the asymmetry in its anterior segment reflects age, the asymmetry in its posterior segment is associated with the children’s language skills. These findings demonstrate a fine-grained structure-to-function mapping in the lateralized network and go beyond our current view of language-related human brain maturation.

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来源期刊
Progress in Neurobiology
Progress in Neurobiology 医学-神经科学
CiteScore
12.80
自引率
1.50%
发文量
107
审稿时长
33 days
期刊介绍: Progress in Neurobiology is an international journal that publishes groundbreaking original research, comprehensive review articles and opinion pieces written by leading researchers. The journal welcomes contributions from the broad field of neuroscience that apply neurophysiological, biochemical, pharmacological, molecular biological, anatomical, computational and behavioral analyses to problems of molecular, cellular, developmental, systems, and clinical neuroscience.
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