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Variants of GRM7 as risk factor and response to antipsychotic therapy in schizophrenia
Genome-wide association study (GWAS) has determined the metabotropic glutamate receptor 7 (GRM7) gene as potential locus for schizophrenia risk variants; However, the relationship between the GRM7 variants and the risk of schizophrenia is still uncertain, and there are significant individual variati...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054263/ https://www.ncbi.nlm.nih.gov/pubmed/32127521 http://dx.doi.org/10.1038/s41398-020-0763-4 |
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author | Liang, Wei Yu, Hao Su, Yi Lu, Tianlan Yan, Hao Yue, Weihua Zhang, Dai |
author_facet | Liang, Wei Yu, Hao Su, Yi Lu, Tianlan Yan, Hao Yue, Weihua Zhang, Dai |
author_sort | Liang, Wei |
collection | PubMed |
description | Genome-wide association study (GWAS) has determined the metabotropic glutamate receptor 7 (GRM7) gene as potential locus for schizophrenia risk variants; However, the relationship between the GRM7 variants and the risk of schizophrenia is still uncertain, and there are significant individual variations in response to the antipsychotic drugs. In order to identify susceptible gene and drug-response-related markers, 2413 subjects in our research were chosen for determining drug-response-related markers in schizophrenia. The rs1516569 variant (OR = 0.95, P < 3.47 × 10(−4)) was a significant risk factor, and a single-nucleotide polymorphism of GRM7 gene- rs9883258 (OR = 0.84, P = 2.18 × 10(−3)) has been determined as potential biomarkers for therapeutic responses of seven commonly used antipsychotic drugs (aripiprazole, haloperidol, olanzapine, perphenazine, quetiapine, risperidone and ziprasidone) in Chinese Han population; Significant associations with treatment response for several single-nucleotide polymorphisms in every antipsychotic drugs, such as rs779746 (OR = 1.39, P = 0.03), rs480409 (OR = 0.73, P = 0.04), rs78137319 (OR = 3.09, P = 0.04), rs1154370 (OR = 1.51, P = 0.006) have been identified in our study. Hence our research elucidates that GRM7 variants play the critical role of predicting the risk of schizophrenia and antipsychotic effect of seven common drugs. |
format | Online Article Text |
id | pubmed-7054263 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70542632020-03-05 Variants of GRM7 as risk factor and response to antipsychotic therapy in schizophrenia Liang, Wei Yu, Hao Su, Yi Lu, Tianlan Yan, Hao Yue, Weihua Zhang, Dai Transl Psychiatry Article Genome-wide association study (GWAS) has determined the metabotropic glutamate receptor 7 (GRM7) gene as potential locus for schizophrenia risk variants; However, the relationship between the GRM7 variants and the risk of schizophrenia is still uncertain, and there are significant individual variations in response to the antipsychotic drugs. In order to identify susceptible gene and drug-response-related markers, 2413 subjects in our research were chosen for determining drug-response-related markers in schizophrenia. The rs1516569 variant (OR = 0.95, P < 3.47 × 10(−4)) was a significant risk factor, and a single-nucleotide polymorphism of GRM7 gene- rs9883258 (OR = 0.84, P = 2.18 × 10(−3)) has been determined as potential biomarkers for therapeutic responses of seven commonly used antipsychotic drugs (aripiprazole, haloperidol, olanzapine, perphenazine, quetiapine, risperidone and ziprasidone) in Chinese Han population; Significant associations with treatment response for several single-nucleotide polymorphisms in every antipsychotic drugs, such as rs779746 (OR = 1.39, P = 0.03), rs480409 (OR = 0.73, P = 0.04), rs78137319 (OR = 3.09, P = 0.04), rs1154370 (OR = 1.51, P = 0.006) have been identified in our study. Hence our research elucidates that GRM7 variants play the critical role of predicting the risk of schizophrenia and antipsychotic effect of seven common drugs. Nature Publishing Group UK 2020-03-03 /pmc/articles/PMC7054263/ /pubmed/32127521 http://dx.doi.org/10.1038/s41398-020-0763-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Liang, Wei Yu, Hao Su, Yi Lu, Tianlan Yan, Hao Yue, Weihua Zhang, Dai Variants of GRM7 as risk factor and response to antipsychotic therapy in schizophrenia |
title | Variants of GRM7 as risk factor and response to antipsychotic therapy in schizophrenia |
title_full | Variants of GRM7 as risk factor and response to antipsychotic therapy in schizophrenia |
title_fullStr | Variants of GRM7 as risk factor and response to antipsychotic therapy in schizophrenia |
title_full_unstemmed | Variants of GRM7 as risk factor and response to antipsychotic therapy in schizophrenia |
title_short | Variants of GRM7 as risk factor and response to antipsychotic therapy in schizophrenia |
title_sort | variants of grm7 as risk factor and response to antipsychotic therapy in schizophrenia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054263/ https://www.ncbi.nlm.nih.gov/pubmed/32127521 http://dx.doi.org/10.1038/s41398-020-0763-4 |
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