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CACNA1C (rs1006737) may be a susceptibility gene for schizophrenia: An updated meta‐analysis
INTRODUCTION: Schizophrenia is a serious mental illness with a genetic predisposition. Genome‐wide association studies (GWAS) have identified the α‐1C subunit of the L‐type voltage‐gated calcium channel (CACNA1C) gene as a significant risk gene for schizophrenia. However, there are inconsistent conc...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6576147/ https://www.ncbi.nlm.nih.gov/pubmed/31033230 http://dx.doi.org/10.1002/brb3.1292 |
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author | Zhu, Dongjian Yin, Jingwen Liang, Chunmei Luo, Xudong Lv, Dong Dai, Zhun Xiong, Susu Fu, Jiawu Li, You Lin, Juda Lin, Zhixiong Wang, Yajun Ma, Guoda |
author_facet | Zhu, Dongjian Yin, Jingwen Liang, Chunmei Luo, Xudong Lv, Dong Dai, Zhun Xiong, Susu Fu, Jiawu Li, You Lin, Juda Lin, Zhixiong Wang, Yajun Ma, Guoda |
author_sort | Zhu, Dongjian |
collection | PubMed |
description | INTRODUCTION: Schizophrenia is a serious mental illness with a genetic predisposition. Genome‐wide association studies (GWAS) have identified the α‐1C subunit of the L‐type voltage‐gated calcium channel (CACNA1C) gene as a significant risk gene for schizophrenia. However, there are inconsistent conclusions in case–control studies. METHODS: We performed a comprehensive meta‐analysis of all available samples from existing studies under four different genetic models (recessive model, dominant model, additive model and allele model) to further confirm whether CACNA1C rs1006737 is an authentic risk single nucleotide polymorphism (SNP) for schizophrenia. RESULTS: A statistically significant difference under the four models (all p < 0.05) was observed by pooling nine Asian and European studies, including a total of 12,744 cases and 16,460 controls. For European‐decent samples, a significant difference was identified between patients and controls for the four models (all p < 0.05). We observed a significant difference between patients and controls for the recessive model and allele model (GG vs. GA + AA: p < 0.00001; G vs. A: p < 0.00001) using a fixed effect model, but the dominant model (GG + GA vs. AA: OR: p = 0.15) and additive model (GG vs. AA: p = 0.11) showed no significant difference between patients and controls in the Asian samples. CONCLUSION: Our findings provide important evidence for the establishment of CACNA1C as a susceptibility gene for schizophrenia across world populations, but its roles in the pathogenesis of schizophrenia need to be further investigated. |
format | Online Article Text |
id | pubmed-6576147 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65761472019-06-20 CACNA1C (rs1006737) may be a susceptibility gene for schizophrenia: An updated meta‐analysis Zhu, Dongjian Yin, Jingwen Liang, Chunmei Luo, Xudong Lv, Dong Dai, Zhun Xiong, Susu Fu, Jiawu Li, You Lin, Juda Lin, Zhixiong Wang, Yajun Ma, Guoda Brain Behav Review INTRODUCTION: Schizophrenia is a serious mental illness with a genetic predisposition. Genome‐wide association studies (GWAS) have identified the α‐1C subunit of the L‐type voltage‐gated calcium channel (CACNA1C) gene as a significant risk gene for schizophrenia. However, there are inconsistent conclusions in case–control studies. METHODS: We performed a comprehensive meta‐analysis of all available samples from existing studies under four different genetic models (recessive model, dominant model, additive model and allele model) to further confirm whether CACNA1C rs1006737 is an authentic risk single nucleotide polymorphism (SNP) for schizophrenia. RESULTS: A statistically significant difference under the four models (all p < 0.05) was observed by pooling nine Asian and European studies, including a total of 12,744 cases and 16,460 controls. For European‐decent samples, a significant difference was identified between patients and controls for the four models (all p < 0.05). We observed a significant difference between patients and controls for the recessive model and allele model (GG vs. GA + AA: p < 0.00001; G vs. A: p < 0.00001) using a fixed effect model, but the dominant model (GG + GA vs. AA: OR: p = 0.15) and additive model (GG vs. AA: p = 0.11) showed no significant difference between patients and controls in the Asian samples. CONCLUSION: Our findings provide important evidence for the establishment of CACNA1C as a susceptibility gene for schizophrenia across world populations, but its roles in the pathogenesis of schizophrenia need to be further investigated. John Wiley and Sons Inc. 2019-04-29 /pmc/articles/PMC6576147/ /pubmed/31033230 http://dx.doi.org/10.1002/brb3.1292 Text en © 2019 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Zhu, Dongjian Yin, Jingwen Liang, Chunmei Luo, Xudong Lv, Dong Dai, Zhun Xiong, Susu Fu, Jiawu Li, You Lin, Juda Lin, Zhixiong Wang, Yajun Ma, Guoda CACNA1C (rs1006737) may be a susceptibility gene for schizophrenia: An updated meta‐analysis |
title | CACNA1C (rs1006737) may be a susceptibility gene for schizophrenia: An updated meta‐analysis |
title_full | CACNA1C (rs1006737) may be a susceptibility gene for schizophrenia: An updated meta‐analysis |
title_fullStr | CACNA1C (rs1006737) may be a susceptibility gene for schizophrenia: An updated meta‐analysis |
title_full_unstemmed | CACNA1C (rs1006737) may be a susceptibility gene for schizophrenia: An updated meta‐analysis |
title_short | CACNA1C (rs1006737) may be a susceptibility gene for schizophrenia: An updated meta‐analysis |
title_sort | cacna1c (rs1006737) may be a susceptibility gene for schizophrenia: an updated meta‐analysis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6576147/ https://www.ncbi.nlm.nih.gov/pubmed/31033230 http://dx.doi.org/10.1002/brb3.1292 |
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