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Association between ADORA2A gene polymorphisms and schizophrenia in the North Chinese Han population
BACKGROUND: A large number of studies have shown a close relationship between ADORA2A and the pathological mechanism of schizophrenia. However, to our knowledge, there has been no studies examining the association between the ADORA2A gene and schizophrenia in Chinese Han population. PURPOSE: The obj...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718062/ https://www.ncbi.nlm.nih.gov/pubmed/31695381 http://dx.doi.org/10.2147/NDT.S205014 |
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author | Miao, Junxiao Liu, Lu Yan, Ci Zhu, Xiaotong Fan, Mengqi Yu, Peitong Ji, Keming Huang, Yinglin Wang, Yuan Zhu, Gang |
author_facet | Miao, Junxiao Liu, Lu Yan, Ci Zhu, Xiaotong Fan, Mengqi Yu, Peitong Ji, Keming Huang, Yinglin Wang, Yuan Zhu, Gang |
author_sort | Miao, Junxiao |
collection | PubMed |
description | BACKGROUND: A large number of studies have shown a close relationship between ADORA2A and the pathological mechanism of schizophrenia. However, to our knowledge, there has been no studies examining the association between the ADORA2A gene and schizophrenia in Chinese Han population. PURPOSE: The objective of this study was to examine the relationship between adenosine A2A receptor (ADORA2A) single nucleotide polymorphisms and schizophrenia in the North Chinese Han population. PATIENTS AND METHODS: We detected ADORA2A single nucleotide polymorphisms (SNPs) using polymerase chain reaction-restriction fragment length polymorphism analyses and summarized our results using SPSS statistical software and Haploview in schizophrenia case group (n=398) and healthy control group (n=535). RESULTS: The frequency of the CC homozygote genotype of SNP rs2298383T/C were significantly higher in the case than the control group (p=0.005, OR=1.712, 95% CI=1.172–2.502). After linkage disequilibrium analysis, SNPs rs5996696A/C and rs2298383T/C displayed strong linkage disequilibrium. We found that the frequencies of haplotypes TA (χ(2)=6.268, p=0.0123) and CA (χ(2)=7.012, p=0.0081) were significantly higher in the case group than in the control group. CONCLUSION: In conclusion, SNPs in the ADORA2A gene may be associated with schizophrenia in the northern Chinese Han population. |
format | Online Article Text |
id | pubmed-6718062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-67180622019-11-06 Association between ADORA2A gene polymorphisms and schizophrenia in the North Chinese Han population Miao, Junxiao Liu, Lu Yan, Ci Zhu, Xiaotong Fan, Mengqi Yu, Peitong Ji, Keming Huang, Yinglin Wang, Yuan Zhu, Gang Neuropsychiatr Dis Treat Original Research BACKGROUND: A large number of studies have shown a close relationship between ADORA2A and the pathological mechanism of schizophrenia. However, to our knowledge, there has been no studies examining the association between the ADORA2A gene and schizophrenia in Chinese Han population. PURPOSE: The objective of this study was to examine the relationship between adenosine A2A receptor (ADORA2A) single nucleotide polymorphisms and schizophrenia in the North Chinese Han population. PATIENTS AND METHODS: We detected ADORA2A single nucleotide polymorphisms (SNPs) using polymerase chain reaction-restriction fragment length polymorphism analyses and summarized our results using SPSS statistical software and Haploview in schizophrenia case group (n=398) and healthy control group (n=535). RESULTS: The frequency of the CC homozygote genotype of SNP rs2298383T/C were significantly higher in the case than the control group (p=0.005, OR=1.712, 95% CI=1.172–2.502). After linkage disequilibrium analysis, SNPs rs5996696A/C and rs2298383T/C displayed strong linkage disequilibrium. We found that the frequencies of haplotypes TA (χ(2)=6.268, p=0.0123) and CA (χ(2)=7.012, p=0.0081) were significantly higher in the case group than in the control group. CONCLUSION: In conclusion, SNPs in the ADORA2A gene may be associated with schizophrenia in the northern Chinese Han population. Dove 2019-08-28 /pmc/articles/PMC6718062/ /pubmed/31695381 http://dx.doi.org/10.2147/NDT.S205014 Text en © 2019 Miao et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Miao, Junxiao Liu, Lu Yan, Ci Zhu, Xiaotong Fan, Mengqi Yu, Peitong Ji, Keming Huang, Yinglin Wang, Yuan Zhu, Gang Association between ADORA2A gene polymorphisms and schizophrenia in the North Chinese Han population |
title | Association between ADORA2A gene polymorphisms and schizophrenia in the North Chinese Han population |
title_full | Association between ADORA2A gene polymorphisms and schizophrenia in the North Chinese Han population |
title_fullStr | Association between ADORA2A gene polymorphisms and schizophrenia in the North Chinese Han population |
title_full_unstemmed | Association between ADORA2A gene polymorphisms and schizophrenia in the North Chinese Han population |
title_short | Association between ADORA2A gene polymorphisms and schizophrenia in the North Chinese Han population |
title_sort | association between adora2a gene polymorphisms and schizophrenia in the north chinese han population |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718062/ https://www.ncbi.nlm.nih.gov/pubmed/31695381 http://dx.doi.org/10.2147/NDT.S205014 |
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