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Genome-wide association study of antipsychotic-induced sinus bradycardia in Chinese schizophrenia patients

Second-generation antipsychotics (SGAs) play a critical role in current treatment of schizophrenia (SCZ). It has been observed that sinus bradycardia, rare but in certain situations life threatening adverse drug reaction, can be induced by SGAs across different schizophrenia populations. However, th...

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Autores principales: Weng, Saizheng, Wang, Bo, Li, Mo, Chao, Shan, Lin, Ruiqian, Zheng, Rongyan, Yu, Yinliang, Guo, Shaonan, Lin, Xianhao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8084176/
https://www.ncbi.nlm.nih.gov/pubmed/33914752
http://dx.doi.org/10.1371/journal.pone.0249997
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author Weng, Saizheng
Wang, Bo
Li, Mo
Chao, Shan
Lin, Ruiqian
Zheng, Rongyan
Yu, Yinliang
Guo, Shaonan
Lin, Xianhao
author_facet Weng, Saizheng
Wang, Bo
Li, Mo
Chao, Shan
Lin, Ruiqian
Zheng, Rongyan
Yu, Yinliang
Guo, Shaonan
Lin, Xianhao
author_sort Weng, Saizheng
collection PubMed
description Second-generation antipsychotics (SGAs) play a critical role in current treatment of schizophrenia (SCZ). It has been observed that sinus bradycardia, rare but in certain situations life threatening adverse drug reaction, can be induced by SGAs across different schizophrenia populations. However, the roles of genetic factors in this phenomenon have not been studied yet. In the present study, a genome-wide association study of single nucleotide polymorphisms (SNPs) was performed on Chinese Han SCZ patients to identify susceptibility loci that were associated with sinus bradycardia induced by SGAs. This study applied microarray to obtain genotype profiles of 88 Han Chinese SCZ patients. Our results found that there were no SNPs had genome-wide significant association with sinus bradycardia induced by SGAs. The top GWAS hit located in gene KIAA0247, which mainly regulated by the tumor suppressor P53 and thus plays a role in carcinogenesis based on resent research and it should not be a susceptibility locus to sinus bradycardia induced by SGAs. Using gene-set functional analysis, we tested that if top 500 SNPs mapped genes were relevant to sinus bradycardia. The result of gene prioritization analysis showed CTNNA3 was strongly correlated with sinus bradycardia, hinting it was a susceptibility gene of this ADR. Our study provides a preliminary study of genetic variants associated with sinus bradycardia induced by SGAs in Han Chinese SCZ patients. The discovery of a possible susceptibility gene shed light on further study of this adverse drug reaction in Han Chinese SCZ patients.
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spelling pubmed-80841762021-05-06 Genome-wide association study of antipsychotic-induced sinus bradycardia in Chinese schizophrenia patients Weng, Saizheng Wang, Bo Li, Mo Chao, Shan Lin, Ruiqian Zheng, Rongyan Yu, Yinliang Guo, Shaonan Lin, Xianhao PLoS One Research Article Second-generation antipsychotics (SGAs) play a critical role in current treatment of schizophrenia (SCZ). It has been observed that sinus bradycardia, rare but in certain situations life threatening adverse drug reaction, can be induced by SGAs across different schizophrenia populations. However, the roles of genetic factors in this phenomenon have not been studied yet. In the present study, a genome-wide association study of single nucleotide polymorphisms (SNPs) was performed on Chinese Han SCZ patients to identify susceptibility loci that were associated with sinus bradycardia induced by SGAs. This study applied microarray to obtain genotype profiles of 88 Han Chinese SCZ patients. Our results found that there were no SNPs had genome-wide significant association with sinus bradycardia induced by SGAs. The top GWAS hit located in gene KIAA0247, which mainly regulated by the tumor suppressor P53 and thus plays a role in carcinogenesis based on resent research and it should not be a susceptibility locus to sinus bradycardia induced by SGAs. Using gene-set functional analysis, we tested that if top 500 SNPs mapped genes were relevant to sinus bradycardia. The result of gene prioritization analysis showed CTNNA3 was strongly correlated with sinus bradycardia, hinting it was a susceptibility gene of this ADR. Our study provides a preliminary study of genetic variants associated with sinus bradycardia induced by SGAs in Han Chinese SCZ patients. The discovery of a possible susceptibility gene shed light on further study of this adverse drug reaction in Han Chinese SCZ patients. Public Library of Science 2021-04-29 /pmc/articles/PMC8084176/ /pubmed/33914752 http://dx.doi.org/10.1371/journal.pone.0249997 Text en © 2021 Weng et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Weng, Saizheng
Wang, Bo
Li, Mo
Chao, Shan
Lin, Ruiqian
Zheng, Rongyan
Yu, Yinliang
Guo, Shaonan
Lin, Xianhao
Genome-wide association study of antipsychotic-induced sinus bradycardia in Chinese schizophrenia patients
title Genome-wide association study of antipsychotic-induced sinus bradycardia in Chinese schizophrenia patients
title_full Genome-wide association study of antipsychotic-induced sinus bradycardia in Chinese schizophrenia patients
title_fullStr Genome-wide association study of antipsychotic-induced sinus bradycardia in Chinese schizophrenia patients
title_full_unstemmed Genome-wide association study of antipsychotic-induced sinus bradycardia in Chinese schizophrenia patients
title_short Genome-wide association study of antipsychotic-induced sinus bradycardia in Chinese schizophrenia patients
title_sort genome-wide association study of antipsychotic-induced sinus bradycardia in chinese schizophrenia patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8084176/
https://www.ncbi.nlm.nih.gov/pubmed/33914752
http://dx.doi.org/10.1371/journal.pone.0249997
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