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Family-based association study of ZNF804A polymorphisms and autism in a Han Chinese population
BACKGROUND: Autism is a complex neurodevelopmental disorder with high heritability. Zinc finger protein 804A (ZNF804A) was suggested to play important roles in neurodevelopment. Previous studies indicated that single-nucleotide polymorphism (SNP) rs1344706 in ZNF804A was strongly associated with sch...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6533675/ https://www.ncbi.nlm.nih.gov/pubmed/31122238 http://dx.doi.org/10.1186/s12888-019-2144-1 |
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author | Wang, Ziqi Zhang, Tian Liu, Jing Wang, Han Lu, Tianlan Jia, Meixiang Zhang, Dai Wang, Lifang Li, Jun |
author_facet | Wang, Ziqi Zhang, Tian Liu, Jing Wang, Han Lu, Tianlan Jia, Meixiang Zhang, Dai Wang, Lifang Li, Jun |
author_sort | Wang, Ziqi |
collection | PubMed |
description | BACKGROUND: Autism is a complex neurodevelopmental disorder with high heritability. Zinc finger protein 804A (ZNF804A) was suggested to play important roles in neurodevelopment. Previous studies indicated that single-nucleotide polymorphism (SNP) rs1344706 in ZNF804A was strongly associated with schizophrenia and might influence social interaction. Only one study explored the significance of ZNF804A polymorphisms in autism, which discovered that rs7603001 was nominally associated with autism. Moreover, no previous study investigated the association between ZNF804A and autism in a Han Chinese population. Here, we investigated whether these two SNPs (rs1344706 and rs7603001) in ZNF804A contribute to the risk of autism in a Han Chinese population. METHODS: We performed a family-based association study in 640 Han Chinese autism trios. Sanger sequencing was used for sample genotyping. Then, single marker association analyses were conducted using the family-based association test (FBAT) program. RESULTS: No significant association was found between the two SNPs (rs1344706 and rs7603001) in ZNF804A and autism (P > 0.05). CONCLUSIONS: Our findings suggested that rs1344706 and rs7603001 in ZNF804A might not be associated with autism in a Han Chinese population. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12888-019-2144-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6533675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65336752019-05-29 Family-based association study of ZNF804A polymorphisms and autism in a Han Chinese population Wang, Ziqi Zhang, Tian Liu, Jing Wang, Han Lu, Tianlan Jia, Meixiang Zhang, Dai Wang, Lifang Li, Jun BMC Psychiatry Research Article BACKGROUND: Autism is a complex neurodevelopmental disorder with high heritability. Zinc finger protein 804A (ZNF804A) was suggested to play important roles in neurodevelopment. Previous studies indicated that single-nucleotide polymorphism (SNP) rs1344706 in ZNF804A was strongly associated with schizophrenia and might influence social interaction. Only one study explored the significance of ZNF804A polymorphisms in autism, which discovered that rs7603001 was nominally associated with autism. Moreover, no previous study investigated the association between ZNF804A and autism in a Han Chinese population. Here, we investigated whether these two SNPs (rs1344706 and rs7603001) in ZNF804A contribute to the risk of autism in a Han Chinese population. METHODS: We performed a family-based association study in 640 Han Chinese autism trios. Sanger sequencing was used for sample genotyping. Then, single marker association analyses were conducted using the family-based association test (FBAT) program. RESULTS: No significant association was found between the two SNPs (rs1344706 and rs7603001) in ZNF804A and autism (P > 0.05). CONCLUSIONS: Our findings suggested that rs1344706 and rs7603001 in ZNF804A might not be associated with autism in a Han Chinese population. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12888-019-2144-1) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-23 /pmc/articles/PMC6533675/ /pubmed/31122238 http://dx.doi.org/10.1186/s12888-019-2144-1 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Wang, Ziqi Zhang, Tian Liu, Jing Wang, Han Lu, Tianlan Jia, Meixiang Zhang, Dai Wang, Lifang Li, Jun Family-based association study of ZNF804A polymorphisms and autism in a Han Chinese population |
title | Family-based association study of ZNF804A polymorphisms and autism in a Han Chinese population |
title_full | Family-based association study of ZNF804A polymorphisms and autism in a Han Chinese population |
title_fullStr | Family-based association study of ZNF804A polymorphisms and autism in a Han Chinese population |
title_full_unstemmed | Family-based association study of ZNF804A polymorphisms and autism in a Han Chinese population |
title_short | Family-based association study of ZNF804A polymorphisms and autism in a Han Chinese population |
title_sort | family-based association study of znf804a polymorphisms and autism in a han chinese population |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6533675/ https://www.ncbi.nlm.nih.gov/pubmed/31122238 http://dx.doi.org/10.1186/s12888-019-2144-1 |
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