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表面积与阅读相关技能和阅读障碍史有关,与灰质体积有关。

Surface area accounts for the relation of gray matter volume to reading-related skills and history of dyslexia.

机构信息

Division of Child and Adolescent Neurology, Department of Pediatrics, University of Texas Health Science Center, Houston, TX 77030, USA.

出版信息

Cereb Cortex. 2010 Nov;20(11):2625-35. doi: 10.1093/cercor/bhq010. Epub 2010 Feb 12.

Abstract

It is unknown whether the abnormalities in brain structure and function observed in dyslexic readers are congenital or arise later in development. Analyzing the 2 components of gray matter volume separately may help in differentiating these possibilities. Gray matter volume is the product of cortical surface area, determined during prenatal brain development, and cortical thickness, determined during postnatal development. For this study, 16 adults with a history of phonological dyslexia and 16 age- and gender-matched controls underwent magnetic resonance imaging and an extensive battery of tests of reading-related skills. Cortical surface area and gray matter volume measures of the whole brain, the inferior frontal gyrus, and the fusiform gyrus were similarly related to phonological skills and a history of dyslexia. There was no relationship between cortical thickness and phonological skills or history of dyslexia. Because cortical surface area reflects cortical folding patterns determined prenatally, this suggests that brain differences in dyslexia are rooted in early cortical development and are not due to compensatory changes that occur during postnatal development and would be expected to influence cortical thickness. This study demonstrates the importance of examining the separate components of gray matter volume when studying developmental abnormalities.

摘要

目前尚不清楚在阅读障碍者中观察到的大脑结构和功能异常是先天的还是在发育后期出现的。分别分析灰质体积的 2 个组成部分可能有助于区分这些可能性。灰质体积是皮质表面积的产物,在产前大脑发育过程中确定,而皮质厚度在产后发育过程中确定。在这项研究中,16 名有语音阅读障碍病史的成年人和 16 名年龄和性别匹配的对照者接受了磁共振成像和一系列广泛的阅读相关技能测试。整个大脑、下额回和梭状回的皮质表面积和灰质体积测量值与语音技能和阅读障碍病史均有类似的相关性。皮质厚度与语音技能或阅读障碍病史之间没有关系。因为皮质表面积反映了产前确定的皮质折叠模式,这表明阅读障碍中的大脑差异源于早期的皮质发育,而不是由于在产后发育过程中发生的代偿性变化,预计这些变化会影响皮质厚度。这项研究表明,在研究发育异常时,检查灰质体积的单独组成部分非常重要。

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