• 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

有阅读障碍家族史的学龄前儿童大脑灰质发育改变。

Altered gray matter development in pre-reading children with a family history of reading disorder.

机构信息

Department of Radiology, University of Calgary, Calgary, AB, Canada.

Owerko Centre, Alberta Children Hospital Research Institute, University of Calgary, Calgary, AB, Canada.

出版信息

Dev Sci. 2022 Mar;25(2):e13160. doi: 10.1111/desc.13160. Epub 2021 Jul 26.

DOI:10.1111/desc.13160
PMID:34278658
Abstract

Reading disorders are common in children and can impact academic success, mental health, and career prospects. Reading is supported by network of interconnected left hemisphere brain regions, including temporo-parietal, occipito-temporal, and inferior-frontal circuits. Poor readers often show hypoactivation and reduced gray matter volumes in this reading network, with hyperactivation and increased volumes in the posterior right hemisphere. We assessed gray matter development longitudinally in pre-reading children aged 2-5 years using magnetic resonance imaging (MRI) (N = 32, 110 MRI scans; mean age: 4.40 ± 0.77 years), half of whom had a family history of reading disorder. The family history group showed slower proportional growth (relative to total brain volume) in the left supramarginal and inferior frontal gyri, and faster proportional growth in the right angular, right fusiform, and bilateral lingual gyri. This suggests delayed development of left hemisphere reading areas in children with a family history of dyslexia, along with faster growth in right homologues. This alternate development pattern may predispose the brain to later reading difficulties and may later manifest as the commonly noted compensatory mechanisms. The results of this study further shows our understanding of structural brain alterations that may form the neurological basis of reading difficulties.

摘要

阅读障碍在儿童中很常见,会影响学业成功、心理健康和职业前景。阅读依赖于相互连接的左半球脑区网络,包括颞顶叶、枕颞叶和下额前回回路。阅读障碍患者的阅读网络常表现为低激活和灰质体积减少,而右后半球表现为过度激活和体积增加。我们使用磁共振成像(MRI)对 2-5 岁的阅读前儿童进行了纵向灰质发育评估(N=32,110 次 MRI 扫描;平均年龄:4.40±0.77 岁),其中一半有阅读障碍家族史。家族史组左侧缘上回和额下回的比例增长(相对于总脑容量)较慢,而右侧角回、右侧梭状回和双侧舌回的比例增长较快。这表明有阅读障碍家族史的儿童左半球阅读区发育延迟,而右侧同型区发育较快。这种替代的发育模式可能使大脑容易出现阅读困难,并且可能以后表现为常见的代偿机制。本研究的结果进一步表明,我们对可能构成阅读困难神经基础的结构脑改变的理解。

相似文献

1
Altered gray matter development in pre-reading children with a family history of reading disorder.有阅读障碍家族史的学龄前儿童大脑灰质发育改变。
Dev Sci. 2022 Mar;25(2):e13160. doi: 10.1111/desc.13160. Epub 2021 Jul 26.
2
Functional and morphometric brain dissociation between dyslexia and reading ability.阅读障碍与阅读能力之间的大脑功能及形态测量差异
Proc Natl Acad Sci U S A. 2007 Mar 6;104(10):4234-9. doi: 10.1073/pnas.0609399104. Epub 2007 Feb 23.
3
Atypical gray matter in children with dyslexia before the onset of reading instruction.阅读指导前患有诵读困难症儿童的非典型灰质。
Cortex. 2019 Dec;121:399-413. doi: 10.1016/j.cortex.2019.09.010. Epub 2019 Oct 11.
4
Structural brain alterations associated with dyslexia predate reading onset.与阅读障碍相关的结构性脑改变先于阅读障碍出现。
Neuroimage. 2011 Aug 1;57(3):742-9. doi: 10.1016/j.neuroimage.2010.09.055. Epub 2010 Sep 25.
5
Sex-specific gray matter volume differences in females with developmental dyslexia.发育性阅读障碍女性的性别特异性灰质体积差异。
Brain Struct Funct. 2014 May;219(3):1041-54. doi: 10.1007/s00429-013-0552-4. Epub 2013 Apr 27.
6
Gray-white matter and cerebrospinal fluid volume differences in children with Specific Language Impairment and/or Reading Disability.特定语言障碍和/或阅读障碍儿童的灰白质及脑脊液容量差异
Neuropsychologia. 2014 Apr;56:90-100. doi: 10.1016/j.neuropsychologia.2014.01.004. Epub 2014 Jan 11.
7
White matter but not grey matter predicts change in reading skills after intervention.白质而非灰质可预测干预后阅读技能的变化。
Dyslexia. 2021 May;27(2):224-244. doi: 10.1002/dys.1668. Epub 2020 Sep 22.
8
Anomalous gray matter patterns in specific reading comprehension deficit are independent of dyslexia.特定阅读理解缺陷中的异常灰质模式与阅读障碍无关。
Ann Dyslexia. 2016 Oct;66(3):256-274. doi: 10.1007/s11881-015-0114-y. Epub 2016 Jun 20.
9
Developmental dyslexia: gray matter abnormalities in the occipitotemporal cortex.发育性阅读障碍:枕颞叶皮质的灰质异常。
Hum Brain Mapp. 2008 May;29(5):613-25. doi: 10.1002/hbm.20425.
10
Relationships between gray matter volume and reading ability in typically developing children, adolescents, and young adults.典型发展儿童、青少年和年轻成年人的灰质体积与阅读能力之间的关系。
Dev Cogn Neurosci. 2019 Apr;36:100636. doi: 10.1016/j.dcn.2019.100636. Epub 2019 Mar 12.

引用本文的文献

1
Atypical characteristic changes of surface morphology and structural covariance network in developmental dyslexia.发展性阅读障碍的表面形态和结构协变网络的非典型特征变化。
Neurol Sci. 2024 May;45(5):2261-2270. doi: 10.1007/s10072-023-07193-x. Epub 2023 Nov 23.
2
Arcuate fasciculus and pre-reading language development in children with prenatal alcohol exposure.产前酒精暴露儿童的弓状束与阅读前语言发展
Front Neurosci. 2023 Jun 2;17:1174165. doi: 10.3389/fnins.2023.1174165. eCollection 2023.
3
Dyslexia: Causes and Concomitant Impairments.
阅读障碍:成因与伴随的损伤
Brain Sci. 2023 Mar 10;13(3):472. doi: 10.3390/brainsci13030472.
4
Extraction of discriminative features from EEG signals of dyslexic children; before and after the treatment.诵读困难儿童治疗前后脑电图信号中判别性特征的提取。
Cogn Neurodyn. 2022 Dec;16(6):1249-1259. doi: 10.1007/s11571-022-09794-2. Epub 2022 Mar 7.
5
Patterns of Neural Functional Connectivity in Infants at Familial Risk of Developmental Dyslexia.发育性阅读障碍家族风险婴儿的神经功能连接模式。
JAMA Netw Open. 2022 Oct 3;5(10):e2236102. doi: 10.1001/jamanetworkopen.2022.36102.
6
Multimodal brain features at 3 years of age and their relationship with pre-reading measures 1 year later.3岁时的多模态脑特征及其与1年后阅读前测量指标的关系。
Front Hum Neurosci. 2022 Aug 22;16:965602. doi: 10.3389/fnhum.2022.965602. eCollection 2022.