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Analyzing a single nucleotide polymorphism in schizophrenia: a meta-analysis approach

BACKGROUND: Schizophrenia is a severe mental disorder affecting >21 million people worldwide. Some genetic studies reported that single nucleotide polymorphism (SNP) involving variant rs1344706 from the ZNF804A gene in human beings is associated with the risk of schizophrenia in several populatio...

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Autores principales: Falola, Oluwadamilare, Osamor, Victor Chukwudi, Adebiyi, Marion, Adebiyi, Ezekiel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5574680/
https://www.ncbi.nlm.nih.gov/pubmed/28883732
http://dx.doi.org/10.2147/NDT.S111900
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author Falola, Oluwadamilare
Osamor, Victor Chukwudi
Adebiyi, Marion
Adebiyi, Ezekiel
author_facet Falola, Oluwadamilare
Osamor, Victor Chukwudi
Adebiyi, Marion
Adebiyi, Ezekiel
author_sort Falola, Oluwadamilare
collection PubMed
description BACKGROUND: Schizophrenia is a severe mental disorder affecting >21 million people worldwide. Some genetic studies reported that single nucleotide polymorphism (SNP) involving variant rs1344706 from the ZNF804A gene in human beings is associated with the risk of schizophrenia in several populations. Similar results tend to conflict with other reports in literature, indicating that no true significant association exists between rs1344706 and schizophrenia. We seek to determine the level of association of this SNP with schizophrenia in the Asian population using more recent genome-wide association study (GWAS) datasets. METHODS: Applying a computational approach with inclusion of more recent GWAS datasets, we conducted a meta-analysis to examine the level of association of SNP rs1344706 and the risk of schizophrenia disorder among the Asian population constituting Chinese, Indonesians, Japanese, Kazakhs and Singaporeans. For a total of 21 genetic studies, including a total of 28,842 cases and 35,630 controls, regression analysis, publication bias, Cochran’s Q and I(2) tests were performed. The DerSimonian and Laird random-effects model was used to assess the association of the genetic variant to schizophrenia. Leave-one-out sensitivity analysis was also conducted to determine the influence of each study on the final outcome of the association study. RESULTS: Our summarized analysis for Asian population revealed a pooled odds ratio of 1.06, 95% confidence interval of 1.01–1.11 and two-tailed P-value of 0.0228. Our test for heterogeneity showed the presence of large heterogeneity (I(2)=53.44%, P =0.00207) and Egger’s regression test (P =0.8763) and Begg’s test (P =0.8347), indicating no presence of publication bias among our selected studies. In our sensitivity analysis, 10 different studies comprising of ~50% of the entire study had an impact on our final results as each leave-one-out test became insignificant. Our result suggests that genetic variant rs1344706 might be associated with the development of schizophrenia in Asians.
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spelling pubmed-55746802017-09-07 Analyzing a single nucleotide polymorphism in schizophrenia: a meta-analysis approach Falola, Oluwadamilare Osamor, Victor Chukwudi Adebiyi, Marion Adebiyi, Ezekiel Neuropsychiatr Dis Treat Original Research BACKGROUND: Schizophrenia is a severe mental disorder affecting >21 million people worldwide. Some genetic studies reported that single nucleotide polymorphism (SNP) involving variant rs1344706 from the ZNF804A gene in human beings is associated with the risk of schizophrenia in several populations. Similar results tend to conflict with other reports in literature, indicating that no true significant association exists between rs1344706 and schizophrenia. We seek to determine the level of association of this SNP with schizophrenia in the Asian population using more recent genome-wide association study (GWAS) datasets. METHODS: Applying a computational approach with inclusion of more recent GWAS datasets, we conducted a meta-analysis to examine the level of association of SNP rs1344706 and the risk of schizophrenia disorder among the Asian population constituting Chinese, Indonesians, Japanese, Kazakhs and Singaporeans. For a total of 21 genetic studies, including a total of 28,842 cases and 35,630 controls, regression analysis, publication bias, Cochran’s Q and I(2) tests were performed. The DerSimonian and Laird random-effects model was used to assess the association of the genetic variant to schizophrenia. Leave-one-out sensitivity analysis was also conducted to determine the influence of each study on the final outcome of the association study. RESULTS: Our summarized analysis for Asian population revealed a pooled odds ratio of 1.06, 95% confidence interval of 1.01–1.11 and two-tailed P-value of 0.0228. Our test for heterogeneity showed the presence of large heterogeneity (I(2)=53.44%, P =0.00207) and Egger’s regression test (P =0.8763) and Begg’s test (P =0.8347), indicating no presence of publication bias among our selected studies. In our sensitivity analysis, 10 different studies comprising of ~50% of the entire study had an impact on our final results as each leave-one-out test became insignificant. Our result suggests that genetic variant rs1344706 might be associated with the development of schizophrenia in Asians. Dove Medical Press 2017-08-23 /pmc/articles/PMC5574680/ /pubmed/28883732 http://dx.doi.org/10.2147/NDT.S111900 Text en © 2017 Falola et al. 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.
spellingShingle Original Research
Falola, Oluwadamilare
Osamor, Victor Chukwudi
Adebiyi, Marion
Adebiyi, Ezekiel
Analyzing a single nucleotide polymorphism in schizophrenia: a meta-analysis approach
title Analyzing a single nucleotide polymorphism in schizophrenia: a meta-analysis approach
title_full Analyzing a single nucleotide polymorphism in schizophrenia: a meta-analysis approach
title_fullStr Analyzing a single nucleotide polymorphism in schizophrenia: a meta-analysis approach
title_full_unstemmed Analyzing a single nucleotide polymorphism in schizophrenia: a meta-analysis approach
title_short Analyzing a single nucleotide polymorphism in schizophrenia: a meta-analysis approach
title_sort analyzing a single nucleotide polymorphism in schizophrenia: a meta-analysis approach
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5574680/
https://www.ncbi.nlm.nih.gov/pubmed/28883732
http://dx.doi.org/10.2147/NDT.S111900
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