Suppr超能文献

特定语言障碍样本中阅读、语言及相关指标的遗传协变。

Genetic covariation underlying reading, language and related measures in a sample selected for specific language impairment.

机构信息

Department of Human Development and Family Science, The Ohio State University, Columbus, OH 43205, USA.

出版信息

Behav Genet. 2011 Sep;41(5):651-9. doi: 10.1007/s10519-010-9435-0. Epub 2010 Dec 31.

Abstract

Specific language impairment is a developmental language disorder characterized by failure to develop language normally in the absence of a specific cause. Previous twin studies have documented the heritability of reading and language measures as well as the genetic correlation between those measures. This paper presents results from an alternative to the classical twin designs by estimating heritability from extended pedigrees. These pedigrees were previously studied as part of series of molecular genetic studies of specific language impairment where the strongest genetic findings were with reading phenotypes rather than language despite selecting pedigrees based on language impairments. To explore the relationship between reading and language in these pedigrees, variance components estimates of heritability of reading and language measures were conducted showing general agreement with the twin literature, as were genetics correlations between reading and language. Phonological short-term memory, phonological awareness and auditory processing were evaluated as candidate mediators of the reading-language genetic correlations. Only phonological awareness showed significant genetic correlations with all reading measures and several language measures while phonological short-term memory and auditory processing did not.

摘要

特定语言障碍是一种发育性语言障碍,其特征是在不存在特定原因的情况下语言无法正常发育。先前的双胞胎研究记录了阅读和语言测量的遗传性,以及这些测量之间的遗传相关性。本文介绍了一种替代经典双胞胎设计的方法的结果,该方法通过扩展系谱来估计遗传性。这些系谱先前曾作为特定语言障碍的一系列分子遗传学研究的一部分进行研究,尽管选择系谱是基于语言障碍,但最强的遗传发现是与阅读表型而非语言相关。为了探索这些系谱中阅读和语言之间的关系,对阅读和语言测量的遗传变异分量估计进行了研究,结果与双胞胎文献一致,阅读和语言之间的遗传相关性也是如此。语音短时记忆、语音意识和听觉处理被评估为阅读-语言遗传相关性的候选中介。只有语音意识与所有阅读测量和一些语言测量都显示出显著的遗传相关性,而语音短时记忆和听觉处理则没有。

相似文献

1
Genetic covariation underlying reading, language and related measures in a sample selected for specific language impairment.
Behav Genet. 2011 Sep;41(5):651-9. doi: 10.1007/s10519-010-9435-0. Epub 2010 Dec 31.
2
Impairment in non-word repetition: a marker for language impairment or reading impairment?
Dev Med Child Neurol. 2011 Aug;53(8):711-6. doi: 10.1111/j.1469-8749.2011.03936.x. Epub 2011 May 18.
3
The role of genes in the etiology of specific language impairment.
J Commun Disord. 2002 Jul-Aug;35(4):311-28. doi: 10.1016/s0021-9924(02)00087-4.
4
Heritability estimation for speech-sound traits with developmental trajectories.
Behav Genet. 2011 Mar;41(2):184-91. doi: 10.1007/s10519-010-9378-5. Epub 2010 Jul 10.
9
Distinct genetic influences on grammar and phonological short-term memory deficits: evidence from 6-year-old twins.
Genes Brain Behav. 2006 Mar;5(2):158-69. doi: 10.1111/j.1601-183X.2005.00148.x.
10
CMIP and ATP2C2 modulate phonological short-term memory in language impairment.
Am J Hum Genet. 2009 Aug;85(2):264-72. doi: 10.1016/j.ajhg.2009.07.004. Epub 2009 Jul 30.

引用本文的文献

1
Examining Procedural Learning and Corticostriatal Pathways for Individual Differences in Language: Testing Endophenotypes of .
Lang Cogn Neurosci. 2016;31(9):1098-1114. doi: 10.1080/23273798.2015.1089359. Epub 2015 Oct 7.
2
Behavioral and Molecular Genetics of Reading-Related AM and FM Detection Thresholds.
Behav Genet. 2017 Mar;47(2):193-201. doi: 10.1007/s10519-016-9821-3. Epub 2016 Nov 9.
3
Cross-Study Differences in the Etiology of Reading Comprehension: a Meta-Analytical Review of Twin Studies.
Behav Genet. 2017 Jan;47(1):52-76. doi: 10.1007/s10519-016-9810-6. Epub 2016 Sep 14.
4
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes.
J Neurodev Disord. 2016 Jun 14;8:24. doi: 10.1186/s11689-016-9157-6. eCollection 2016.
5
Genome-wide screening for DNA variants associated with reading and language traits.
Genes Brain Behav. 2014 Sep;13(7):686-701. doi: 10.1111/gbb.12158. Epub 2014 Aug 29.
6
Genome-wide association study of receptive language ability of 12-year-olds.
J Speech Lang Hear Res. 2014 Feb;57(1):96-105. doi: 10.1044/1092-4388(2013/12-0303).
7
Gene × gene interaction in shared etiology of autism and specific language impairment.
Biol Psychiatry. 2012 Oct 15;72(8):692-9. doi: 10.1016/j.biopsych.2012.05.019. Epub 2012 Jun 15.
8
Defining the genetic architecture of human developmental language impairment.
Life Sci. 2012 Apr 9;90(13-14):469-75. doi: 10.1016/j.lfs.2012.01.016. Epub 2012 Feb 17.

本文引用的文献

3
Longitudinal genetic analysis of early reading: The Western Reserve Reading Project.
Read Writ. 2007 Feb 1;20(1-2):127-146. doi: 10.1007/s11145-006-9021-2.
4
CMIP and ATP2C2 modulate phonological short-term memory in language impairment.
Am J Hum Genet. 2009 Aug;85(2):264-72. doi: 10.1016/j.ajhg.2009.07.004. Epub 2009 Jul 30.
6
The heritability of general cognitive ability increases linearly from childhood to young adulthood.
Mol Psychiatry. 2010 Nov;15(11):1112-20. doi: 10.1038/mp.2009.55. Epub 2009 Jun 2.
7
Children who read words accurately despite language impairment: who are they and how do they do it?
Child Dev. 2009 Mar-Apr;80(2):593-605. doi: 10.1111/j.1467-8624.2009.01281.x.
8
Genetic and Environmental Effects of Serial Naming and Phonological Awareness on Early Reading Outcomes.
J Educ Psychol. 2006 Feb 1;98(1):112-121. doi: 10.1037/0022-0663.98.1.112.
9
Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia.
Eur J Hum Genet. 2009 Oct;17(10):1354-8. doi: 10.1038/ejhg.2009.43. Epub 2009 Apr 8.
10
Why do preschool language abilities correlate with later reading? A twin study.
J Speech Lang Hear Res. 2008 Jun;51(3):688-705. doi: 10.1044/1092-4388(2008/049).

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验