A Genome-Wide Association Study of Chinese and English Language Phenotypes in Hong Kong Chinese Children

Saved in:
Bibliographic Details
Title: A Genome-Wide Association Study of Chinese and English Language Phenotypes in Hong Kong Chinese Children
Language: English
Authors: Yu-Ping Lin (ORCID 0000-0002-9546-3889), Yujia Shi, Ruoyu Zhang (ORCID 0000-0002-6089-7476), Xiao Xue, Shitao Rao, Liangying Yin, Kelvin Fai Hong Lui, Dora Jue Pan (ORCID 0000-0001-9764-6454), Urs Maurer (ORCID 0000-0002-4156-8597), Kwong-Wai Choy, Silvia Paracchini (ORCID 0000-0001-9934-8602), Catherine McBride, Hon-Cheong So (ORCID 0000-0002-7102-833X)
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
Be the first to leave a comment!
You must be logged in first