Suppr超能文献

遗传对儿童语言障碍和读写问题的影响:相同还是不同?

Genetic influences on language impairment and literacy problems in children: same or different?

作者信息

Bishop D V

机构信息

Dept. Experimental Psychology, University of Oxford, UK.

出版信息

J Child Psychol Psychiatry. 2001 Feb;42(2):189-98.

Abstract

Data from two twin studies are examined to assess genetic and environmental influences on literacy, and the etiological relationship between language and literacy. Study 1 used children from 86 families previously recruited for a study of the genetics of specific language impairment (see Bishop, North, & Donlan, 1995), who completed tests of single-word reading and spelling. Literacy problems in this sample were common, were strongly heritable, and showed a close genetic relationship with poor nonword repetition. Study 2 included two subsets of children: 37 twin pairs who had taken part in study 1, 3 to 4 years earlier, and 100 twin pairs recruited from the general population by Bishop et al. (1999). All children were given a standardised test of nonword reading. There was no genetic influence on nonword reading ability, either across the normal range, or at the lower extreme, though there were significant associations with some social variables. However, bivariate DeFries Fulker analysis suggested that in this study, as in study 1, there was shared genetic variance between poor nonword repetition and literacy deficits. It is concluded that poor nonword repetition, which is known to be highly heritable, puts the child at risk for literacy problems. However, in a general population sample, such as that included in study 2, poor nonword repetition is a relatively rare correlate of literacy problems, which are more likely to have an environmental origin. Thus the different pattern of results in the two studies can be explained if one assumes that genetic influences are substantial only when literacy problems are severe and/or accompanied by oral language difficulties.

摘要

本文考察了两项双胞胎研究的数据,以评估基因和环境对读写能力的影响,以及语言与读写能力之间的病因学关系。研究1使用了来自86个家庭的儿童,这些家庭此前参与了一项关于特定语言障碍遗传学的研究(见毕晓普、诺思和唐兰,1995),他们完成了单字阅读和拼写测试。该样本中的读写问题很常见,具有很强的遗传性,并且与非词重复能力差存在密切的遗传关系。研究2包括两组儿童:一组是37对双胞胎,他们在3至4年前参与了研究1;另一组是毕晓普等人(1999)从普通人群中招募的100对双胞胎。所有儿童都接受了非词阅读的标准化测试。无论在正常范围内还是在较低水平,非词阅读能力都没有受到基因影响,不过与一些社会变量存在显著关联。然而,双变量德弗里斯-富尔克分析表明,在本研究中,与研究1一样,非词重复能力差和读写能力缺陷之间存在共同的遗传变异。研究得出结论,已知高度可遗传的非词重复能力差会使儿童面临读写问题的风险。然而,在像研究2中所包含的普通人群样本中,非词重复能力差是读写问题相对罕见的关联因素,读写问题更可能源于环境。因此,如果假设只有当读写问题严重和/或伴有口语困难时基因影响才显著,那么可以解释两项研究结果的不同模式。

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