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Combined study of genetic and epigenetic biomarker risperidone treatment efficacy in Chinese Han schizophrenia patients
Nowadays, risperidone is an atypical antipsychotic drug that has been increasingly used for treatment and maintenance therapy in schizophrenia. However, partially affected by genetic or environmental factors, there is significant difference in treatment outcomes among patients. In this study, we aim...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5538123/ https://www.ncbi.nlm.nih.gov/pubmed/28696411 http://dx.doi.org/10.1038/tp.2017.143 |
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author | Shi, Y Li, M Song, C Xu, Q Huo, R Shen, L Xing, Q Cui, D Li, W Zhao, J He, L Qin, S |
author_facet | Shi, Y Li, M Song, C Xu, Q Huo, R Shen, L Xing, Q Cui, D Li, W Zhao, J He, L Qin, S |
author_sort | Shi, Y |
collection | PubMed |
description | Nowadays, risperidone is an atypical antipsychotic drug that has been increasingly used for treatment and maintenance therapy in schizophrenia. However, partially affected by genetic or environmental factors, there is significant difference in treatment outcomes among patients. In this study, we aimed to interpret the difference between good and poor responders treated with risperidone in both genetic and epigenetic levels in 288 mainland Chinese patients. We recruited a Henan cohort including 98 patients as initial discovery group and then confirmed our results in Shanghai cohort. In genetic studies, we found 10 candidate single-nucleotide polymorphisms (SNPs) and 2 rare variants in Henan cohort by next-generation sequencing of 100 risperidone-response-related genes. After replication in Shanghai cohort by massarray platform, ultimately, rs6706232 and rs4818 were significantly associated with risperidone response in the two cohort meta-analysis (P=0.024 and 0.04, respectively). Besides, we also selected another reported 17 candidate SNPs associated with risperidone drug response to replicate in our mainland Chinese samples, while, we found no significant SNPs after Bonferroni correction. In epigenetic studies, we investigated the methylation status in promoters or gene-coding region of risperidone drug response-related genes including CYP3A4, CYP2D6, ABCB1, HTR2A, DRD2. Totally we found seven significant CpG sites in the meta-analysis with Bonferroni-corrected P(CYP3A4_CpG_-36)=0.0014, P(CYP3A4_CpG_-258)=0.0013, P(CYP3A4_CpG_-296)=0.0014, P(CYP3A4_CpG_-367:-372:-374)=0.028, P(CYP2D6_CpG_193)=0.012, P(CYP2D6_CpG_242:244:250)=0.00076 and P(CYP2D6_CpG_284)=0.034, respectively. As genetic and epigenetic factors may interactively affect drug response, we finally carried out a multivariant interaction analysis with multifactor dimensionality reduction and discovered a significant four-locus model (CYP3A4_CpG_-82:-86 +rs6280+rs1800497+rs6265, P=0.038) affecting drug response. These findings could partially explain different risperidone response outcome in Chinese population in a systematic level. |
format | Online Article Text |
id | pubmed-5538123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-55381232017-08-02 Combined study of genetic and epigenetic biomarker risperidone treatment efficacy in Chinese Han schizophrenia patients Shi, Y Li, M Song, C Xu, Q Huo, R Shen, L Xing, Q Cui, D Li, W Zhao, J He, L Qin, S Transl Psychiatry Original Article Nowadays, risperidone is an atypical antipsychotic drug that has been increasingly used for treatment and maintenance therapy in schizophrenia. However, partially affected by genetic or environmental factors, there is significant difference in treatment outcomes among patients. In this study, we aimed to interpret the difference between good and poor responders treated with risperidone in both genetic and epigenetic levels in 288 mainland Chinese patients. We recruited a Henan cohort including 98 patients as initial discovery group and then confirmed our results in Shanghai cohort. In genetic studies, we found 10 candidate single-nucleotide polymorphisms (SNPs) and 2 rare variants in Henan cohort by next-generation sequencing of 100 risperidone-response-related genes. After replication in Shanghai cohort by massarray platform, ultimately, rs6706232 and rs4818 were significantly associated with risperidone response in the two cohort meta-analysis (P=0.024 and 0.04, respectively). Besides, we also selected another reported 17 candidate SNPs associated with risperidone drug response to replicate in our mainland Chinese samples, while, we found no significant SNPs after Bonferroni correction. In epigenetic studies, we investigated the methylation status in promoters or gene-coding region of risperidone drug response-related genes including CYP3A4, CYP2D6, ABCB1, HTR2A, DRD2. Totally we found seven significant CpG sites in the meta-analysis with Bonferroni-corrected P(CYP3A4_CpG_-36)=0.0014, P(CYP3A4_CpG_-258)=0.0013, P(CYP3A4_CpG_-296)=0.0014, P(CYP3A4_CpG_-367:-372:-374)=0.028, P(CYP2D6_CpG_193)=0.012, P(CYP2D6_CpG_242:244:250)=0.00076 and P(CYP2D6_CpG_284)=0.034, respectively. As genetic and epigenetic factors may interactively affect drug response, we finally carried out a multivariant interaction analysis with multifactor dimensionality reduction and discovered a significant four-locus model (CYP3A4_CpG_-82:-86 +rs6280+rs1800497+rs6265, P=0.038) affecting drug response. These findings could partially explain different risperidone response outcome in Chinese population in a systematic level. Nature Publishing Group 2017-07 2017-07-11 /pmc/articles/PMC5538123/ /pubmed/28696411 http://dx.doi.org/10.1038/tp.2017.143 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Original Article Shi, Y Li, M Song, C Xu, Q Huo, R Shen, L Xing, Q Cui, D Li, W Zhao, J He, L Qin, S Combined study of genetic and epigenetic biomarker risperidone treatment efficacy in Chinese Han schizophrenia patients |
title | Combined study of genetic and epigenetic biomarker risperidone treatment efficacy in Chinese Han schizophrenia patients |
title_full | Combined study of genetic and epigenetic biomarker risperidone treatment efficacy in Chinese Han schizophrenia patients |
title_fullStr | Combined study of genetic and epigenetic biomarker risperidone treatment efficacy in Chinese Han schizophrenia patients |
title_full_unstemmed | Combined study of genetic and epigenetic biomarker risperidone treatment efficacy in Chinese Han schizophrenia patients |
title_short | Combined study of genetic and epigenetic biomarker risperidone treatment efficacy in Chinese Han schizophrenia patients |
title_sort | combined study of genetic and epigenetic biomarker risperidone treatment efficacy in chinese han schizophrenia patients |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5538123/ https://www.ncbi.nlm.nih.gov/pubmed/28696411 http://dx.doi.org/10.1038/tp.2017.143 |
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