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A Genome-Wide Association Study Identifies Genetic Variants Associated with Mathematics Ability

Mathematics ability is a complex cognitive trait with polygenic heritability. Genome-wide association study (GWAS) has been an effective approach to investigate genetic components underlying mathematic ability. Although previous studies reported several candidate genetic variants, none of them excee...

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Autores principales: Chen, Huan, Gu, Xiao-hong, Zhou, Yuxi, Ge, Zeng, Wang, Bin, Siok, Wai Ting, Wang, Guoqing, Huen, Michael, Jiang, Yuyang, Tan, Li-Hai, Sun, Yimin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5290743/
https://www.ncbi.nlm.nih.gov/pubmed/28155865
http://dx.doi.org/10.1038/srep40365
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author Chen, Huan
Gu, Xiao-hong
Zhou, Yuxi
Ge, Zeng
Wang, Bin
Siok, Wai Ting
Wang, Guoqing
Huen, Michael
Jiang, Yuyang
Tan, Li-Hai
Sun, Yimin
author_facet Chen, Huan
Gu, Xiao-hong
Zhou, Yuxi
Ge, Zeng
Wang, Bin
Siok, Wai Ting
Wang, Guoqing
Huen, Michael
Jiang, Yuyang
Tan, Li-Hai
Sun, Yimin
author_sort Chen, Huan
collection PubMed
description Mathematics ability is a complex cognitive trait with polygenic heritability. Genome-wide association study (GWAS) has been an effective approach to investigate genetic components underlying mathematic ability. Although previous studies reported several candidate genetic variants, none of them exceeded genome-wide significant threshold in general populations. Herein, we performed GWAS in Chinese elementary school students to identify potential genetic variants associated with mathematics ability. The discovery stage included 494 and 504 individuals from two independent cohorts respectively. The replication stage included another cohort of 599 individuals. In total, 28 of 81 candidate SNPs that met validation criteria were further replicated. Combined meta-analysis of three cohorts identified four SNPs (rs1012694, rs11743006, rs17778739 and rs17777541) of SPOCK1 gene showing association with mathematics ability (minimum p value 5.67 × 10(−10), maximum β −2.43). The SPOCK1 gene is located on chromosome 5q31.2 and encodes a highly conserved glycoprotein testican-1 which was associated with tumor progression and prognosis as well as neurogenesis. This is the first study to report genome-wide significant association of individual SNPs with mathematics ability in general populations. Our preliminary results further supported the role of SPOCK1 during neurodevelopment. The genetic complexities underlying mathematics ability might contribute to explain the basis of human cognition and intelligence at genetic level.
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spelling pubmed-52907432017-02-07 A Genome-Wide Association Study Identifies Genetic Variants Associated with Mathematics Ability Chen, Huan Gu, Xiao-hong Zhou, Yuxi Ge, Zeng Wang, Bin Siok, Wai Ting Wang, Guoqing Huen, Michael Jiang, Yuyang Tan, Li-Hai Sun, Yimin Sci Rep Article Mathematics ability is a complex cognitive trait with polygenic heritability. Genome-wide association study (GWAS) has been an effective approach to investigate genetic components underlying mathematic ability. Although previous studies reported several candidate genetic variants, none of them exceeded genome-wide significant threshold in general populations. Herein, we performed GWAS in Chinese elementary school students to identify potential genetic variants associated with mathematics ability. The discovery stage included 494 and 504 individuals from two independent cohorts respectively. The replication stage included another cohort of 599 individuals. In total, 28 of 81 candidate SNPs that met validation criteria were further replicated. Combined meta-analysis of three cohorts identified four SNPs (rs1012694, rs11743006, rs17778739 and rs17777541) of SPOCK1 gene showing association with mathematics ability (minimum p value 5.67 × 10(−10), maximum β −2.43). The SPOCK1 gene is located on chromosome 5q31.2 and encodes a highly conserved glycoprotein testican-1 which was associated with tumor progression and prognosis as well as neurogenesis. This is the first study to report genome-wide significant association of individual SNPs with mathematics ability in general populations. Our preliminary results further supported the role of SPOCK1 during neurodevelopment. The genetic complexities underlying mathematics ability might contribute to explain the basis of human cognition and intelligence at genetic level. Nature Publishing Group 2017-02-03 /pmc/articles/PMC5290743/ /pubmed/28155865 http://dx.doi.org/10.1038/srep40365 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Chen, Huan
Gu, Xiao-hong
Zhou, Yuxi
Ge, Zeng
Wang, Bin
Siok, Wai Ting
Wang, Guoqing
Huen, Michael
Jiang, Yuyang
Tan, Li-Hai
Sun, Yimin
A Genome-Wide Association Study Identifies Genetic Variants Associated with Mathematics Ability
title A Genome-Wide Association Study Identifies Genetic Variants Associated with Mathematics Ability
title_full A Genome-Wide Association Study Identifies Genetic Variants Associated with Mathematics Ability
title_fullStr A Genome-Wide Association Study Identifies Genetic Variants Associated with Mathematics Ability
title_full_unstemmed A Genome-Wide Association Study Identifies Genetic Variants Associated with Mathematics Ability
title_short A Genome-Wide Association Study Identifies Genetic Variants Associated with Mathematics Ability
title_sort genome-wide association study identifies genetic variants associated with mathematics ability
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5290743/
https://www.ncbi.nlm.nih.gov/pubmed/28155865
http://dx.doi.org/10.1038/srep40365
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