A Genome-Wide Association Study of Chinese and English Language Phenotypes in Hong Kong Chinese Children
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| Title: | A Genome-Wide Association Study of Chinese and English Language Phenotypes in Hong Kong Chinese Children |
|---|---|
| Language: | English |
| Authors: | Yu-Ping Lin (ORCID |
| Source: | npj Science of Learning. 2024 9. |
| Availability: | Nature Portfolio. Available from: Springer Nature. One New York Plaza, Suite 4600, New York, NY 10004. Tel: 800-777-4643; Tel: 212-460-1500; Fax: 212-460-1700; e-mail: customerservice@springernature.com; Web site: https://www.nature.com/npjscilearn/ |
| Peer Reviewed: | Y |
| Page Count: | 18 |
| Publication Date: | 2024 |
| Document Type: | Journal Articles Reports - Research |
| Descriptors: | Genetics, Phenomenology, Chinese, Foreign Countries, Children, Dyslexia, Language Impairments, English Language Learners, English (Second Language), Bilingualism, Correlation, Biological Influences, Reading Skills, Neuropsychology |
| Geographic Terms: | Hong Kong |
| DOI: | 10.1038/s41539-024-00229-7 |
| ISSN: | 2056-7936 |
| Abstract: | Dyslexia and developmental language disorders are important learning difficulties. However, their genetic basis remains poorly understood, and most genetic studies were performed on Europeans. There is a lack of genome-wide association studies (GWAS) on literacy phenotypes of Chinese as a native language and English as a second language (ESL) in a Chinese population. In this study, we conducted GWAS on 34 reading/language-related phenotypes in Hong Kong Chinese bilingual children (including both twins and singletons; total N = 1046). We performed association tests at the single-variant, gene, and pathway levels. In addition, we tested genetic overlap of these phenotypes with other neuropsychiatric disorders, as well as cognitive performance (CP) and educational attainment (EA) using polygenic risk score (PRS) analysis. Totally 5 independent loci (LD-clumped at r[superscript 2] = 0.01; MAF > 0.05) reached genome-wide significance (p < 5e-08; filtered by imputation quality metric Rsq>0.3 and having at least 2 correlated SNPs (r[superscript 2] > 0.5) with p < 1e-3). The loci were associated with a range of language/literacy traits such as Chinese vocabulary, character and word reading, and rapid digit naming, as well as English lexical decision. Several SNPs from these loci mapped to genes that were reported to be associated with EA and other neuropsychiatric phenotypes, such as "MANEA" and "PLXNC1." In PRS analysis, EA and CP showed the most consistent and significant polygenic overlap with a variety of language traits, especially English literacy skills. To summarize, this study revealed the genetic basis of Chinese and English abilities in a group of Chinese bilingual children. Further studies are warranted to replicate the findings. |
| Abstractor: | As Provided |
| Entry Date: | 2024 |
| Accession Number: | EJ1431854 |
| Database: | ERIC |
| FullText | Text: Availability: 0 |
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| Header | DbId: eric DbLabel: ERIC An: EJ1431854 AccessLevel: 3 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: A Genome-Wide Association Study of Chinese and English Language Phenotypes in Hong Kong Chinese Children – Name: Language Label: Language Group: Lang Data: English – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Yu-Ping+Lin%22">Yu-Ping Lin</searchLink> (ORCID <externalLink term="http://orcid.org/0000-0002-9546-3889">0000-0002-9546-3889</externalLink>)<br /><searchLink fieldCode="AR" term="%22Yujia+Shi%22">Yujia Shi</searchLink><br /><searchLink fieldCode="AR" term="%22Ruoyu+Zhang%22">Ruoyu Zhang</searchLink> (ORCID <externalLink term="http://orcid.org/0000-0002-6089-7476">0000-0002-6089-7476</externalLink>)<br /><searchLink fieldCode="AR" term="%22Xiao+Xue%22">Xiao Xue</searchLink><br /><searchLink fieldCode="AR" term="%22Shitao+Rao%22">Shitao Rao</searchLink><br /><searchLink fieldCode="AR" term="%22Liangying+Yin%22">Liangying Yin</searchLink><br /><searchLink fieldCode="AR" term="%22Kelvin+Fai+Hong+Lui%22">Kelvin Fai Hong Lui</searchLink><br /><searchLink fieldCode="AR" term="%22Dora+Jue+Pan%22">Dora Jue Pan</searchLink> (ORCID <externalLink term="http://orcid.org/0000-0001-9764-6454">0000-0001-9764-6454</externalLink>)<br /><searchLink fieldCode="AR" term="%22Urs+Maurer%22">Urs Maurer</searchLink> (ORCID <externalLink term="http://orcid.org/0000-0002-4156-8597">0000-0002-4156-8597</externalLink>)<br /><searchLink fieldCode="AR" term="%22Kwong-Wai+Choy%22">Kwong-Wai Choy</searchLink><br /><searchLink fieldCode="AR" term="%22Silvia+Paracchini%22">Silvia Paracchini</searchLink> (ORCID <externalLink term="http://orcid.org/0000-0001-9934-8602">0000-0001-9934-8602</externalLink>)<br /><searchLink fieldCode="AR" term="%22Catherine+McBride%22">Catherine McBride</searchLink><br /><searchLink fieldCode="AR" term="%22Hon-Cheong+So%22">Hon-Cheong So</searchLink> (ORCID <externalLink term="http://orcid.org/0000-0002-7102-833X">0000-0002-7102-833X</externalLink>) – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="SO" term="%22npj+Science+of+Learning%22"><i>npj Science of Learning</i></searchLink>. 2024 9. – Name: Avail Label: Availability Group: Avail Data: Nature Portfolio. Available from: Springer Nature. One New York Plaza, Suite 4600, New York, NY 10004. Tel: 800-777-4643; Tel: 212-460-1500; Fax: 212-460-1700; e-mail: customerservice@springernature.com; Web site: https://www.nature.com/npjscilearn/ – Name: PeerReviewed Label: Peer Reviewed Group: SrcInfo Data: Y – Name: Pages Label: Page Count Group: Src Data: 18 – Name: DatePubCY Label: Publication Date Group: Date Data: 2024 – Name: TypeDocument Label: Document Type Group: TypDoc Data: Journal Articles<br />Reports - Research – Name: Subject Label: Descriptors Group: Su Data: <searchLink fieldCode="DE" term="%22Genetics%22">Genetics</searchLink><br /><searchLink fieldCode="DE" term="%22Phenomenology%22">Phenomenology</searchLink><br /><searchLink fieldCode="DE" term="%22Chinese%22">Chinese</searchLink><br /><searchLink fieldCode="DE" term="%22Foreign+Countries%22">Foreign Countries</searchLink><br /><searchLink fieldCode="DE" term="%22Children%22">Children</searchLink><br /><searchLink fieldCode="DE" term="%22Dyslexia%22">Dyslexia</searchLink><br /><searchLink fieldCode="DE" term="%22Language+Impairments%22">Language Impairments</searchLink><br /><searchLink fieldCode="DE" term="%22English+Language+Learners%22">English Language Learners</searchLink><br /><searchLink fieldCode="DE" term="%22English+%28Second+Language%29%22">English (Second Language)</searchLink><br /><searchLink fieldCode="DE" term="%22Bilingualism%22">Bilingualism</searchLink><br /><searchLink fieldCode="DE" term="%22Correlation%22">Correlation</searchLink><br /><searchLink fieldCode="DE" term="%22Biological+Influences%22">Biological Influences</searchLink><br /><searchLink fieldCode="DE" term="%22Reading+Skills%22">Reading Skills</searchLink><br /><searchLink fieldCode="DE" term="%22Neuropsychology%22">Neuropsychology</searchLink> – Name: Subject Label: Geographic Terms Group: Su Data: <searchLink fieldCode="DE" term="%22Hong+Kong%22">Hong Kong</searchLink> – Name: DOI Label: DOI Group: ID Data: 10.1038/s41539-024-00229-7 – Name: ISSN Label: ISSN Group: ISSN Data: 2056-7936 – Name: Abstract Label: Abstract Group: Ab Data: Dyslexia and developmental language disorders are important learning difficulties. However, their genetic basis remains poorly understood, and most genetic studies were performed on Europeans. There is a lack of genome-wide association studies (GWAS) on literacy phenotypes of Chinese as a native language and English as a second language (ESL) in a Chinese population. In this study, we conducted GWAS on 34 reading/language-related phenotypes in Hong Kong Chinese bilingual children (including both twins and singletons; total N = 1046). We performed association tests at the single-variant, gene, and pathway levels. In addition, we tested genetic overlap of these phenotypes with other neuropsychiatric disorders, as well as cognitive performance (CP) and educational attainment (EA) using polygenic risk score (PRS) analysis. Totally 5 independent loci (LD-clumped at r[superscript 2] = 0.01; MAF > 0.05) reached genome-wide significance (p < 5e-08; filtered by imputation quality metric Rsq>0.3 and having at least 2 correlated SNPs (r[superscript 2] > 0.5) with p < 1e-3). The loci were associated with a range of language/literacy traits such as Chinese vocabulary, character and word reading, and rapid digit naming, as well as English lexical decision. Several SNPs from these loci mapped to genes that were reported to be associated with EA and other neuropsychiatric phenotypes, such as "MANEA" and "PLXNC1." In PRS analysis, EA and CP showed the most consistent and significant polygenic overlap with a variety of language traits, especially English literacy skills. To summarize, this study revealed the genetic basis of Chinese and English abilities in a group of Chinese bilingual children. Further studies are warranted to replicate the findings. – Name: AbstractInfo Label: Abstractor Group: Ab Data: As Provided – Name: DateEntry Label: Entry Date Group: Date Data: 2024 – Name: AN Label: Accession Number Group: ID Data: EJ1431854 |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1038/s41539-024-00229-7 Languages: – Text: English PhysicalDescription: Pagination: PageCount: 18 Subjects: – SubjectFull: Genetics Type: general – SubjectFull: Phenomenology Type: general – SubjectFull: Chinese Type: general – SubjectFull: Foreign Countries Type: general – SubjectFull: Children Type: general – SubjectFull: Dyslexia Type: general – SubjectFull: Language Impairments Type: general – SubjectFull: English Language Learners Type: general – SubjectFull: English (Second Language) Type: general – SubjectFull: Bilingualism Type: general – SubjectFull: Correlation Type: general – SubjectFull: Biological Influences Type: general – SubjectFull: Reading Skills Type: general – SubjectFull: Neuropsychology Type: general – SubjectFull: Hong Kong Type: general Titles: – TitleFull: A Genome-Wide Association Study of Chinese and English Language Phenotypes in Hong Kong Chinese Children Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Yu-Ping Lin – PersonEntity: Name: NameFull: Yujia Shi – PersonEntity: Name: NameFull: Ruoyu Zhang – PersonEntity: Name: NameFull: Xiao Xue – PersonEntity: Name: NameFull: Shitao Rao – PersonEntity: Name: NameFull: Liangying Yin – PersonEntity: Name: NameFull: Kelvin Fai Hong Lui – PersonEntity: Name: NameFull: Dora Jue Pan – PersonEntity: Name: NameFull: Urs Maurer – PersonEntity: Name: NameFull: Kwong-Wai Choy – PersonEntity: Name: NameFull: Silvia Paracchini – PersonEntity: Name: NameFull: Catherine McBride – PersonEntity: Name: NameFull: Hon-Cheong So IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 01 Type: published Y: 2024 Identifiers: – Type: issn-electronic Value: 2056-7936 Numbering: – Type: volume Value: 9 Titles: – TitleFull: npj Science of Learning Type: main |
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