Cargando…
Association of genetic variants of Glutamate Metabotropic Receptor 5 gene and state-anhedonia
INTRODUCTION: Andedonia is one of the core symptoms of depression. It is known that in case of depressed individuals experiencing anhedonia, the classical antidepressants are often ineffective, thus investigation of this symptom would be essential. Recent studies highlight the possible role of the g...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9566961/ http://dx.doi.org/10.1192/j.eurpsy.2022.398 |
_version_ | 1784809281999077376 |
---|---|
author | Török, D. Gonda, X. Gal, Z. Eszlari, N. Bagdy, G. Juhasz, G. Petschner, P. |
author_facet | Török, D. Gonda, X. Gal, Z. Eszlari, N. Bagdy, G. Juhasz, G. Petschner, P. |
author_sort | Török, D. |
collection | PubMed |
description | INTRODUCTION: Andedonia is one of the core symptoms of depression. It is known that in case of depressed individuals experiencing anhedonia, the classical antidepressants are often ineffective, thus investigation of this symptom would be essential. Recent studies highlight the possible role of the glutamatergic system in anhedonia however, the genetic background of these assumptions is still unclear. OBJECTIVES: Our goal was to investigate the possible associations between state-anhedonia and genetic variants from GRM5 (Glutamate Metabotropic Receptor 5) gene. METHODS: For our analysis we used data from the NewMood (New Molecules in Mood Disorders, LSHM-CT-2004-503474) project. Participants (n = 1820) aged between 18-60, were recruited in Budapest and in Manchester. All volunteers filled out mental-health questionnaires and provided DNA sample. Genotyping was performed by Illumina’s CoreExom PsychChip. Altogether 1282 variants from GRM5 gene survived the genetic quality control steps. State-anhedonia was measured with an item from the Brief Symptom Inventory questionnaire. We performed logistic regression using Plink 2.0. During our analyses, age, gender, population and the top10 principal components of the genome were added into the model as covariates. Correction for linkage-disequilibrium were performed with LDlink. RESULTS: After the correction of linkage-disequilibrium, three independent variables (r(2)<0.2), (rs1827603, rs6483520, rs35669869) yielded significant (p<0.05) results, both in additive and in dominant model. In case of recessive model, only rs11020880 showed significant (p<0.05) effect. CONCLUSIONS: The detected nominally significant associations between state-anhedonia and genetic variants from GRM5 gene strengthen previous assumptions about the possible relationship between glutamatergic system and anhedonia. DISCLOSURE: This study was supported by: MTA-SE Neuropsychopharmacology and Neurochemistry Research Group; 2017-1.2.1-NKP-2017-00002; KTIA_13_NAPA-II/14; KTIA_NAP_13-1-2013- 0001; KTIA_NAP_13-2- 2015-0001; 2020-4.1.1.-TKP2020 and 2019-2.1.7-ERA-NET-2020-00005 (TRAJEC |
format | Online Article Text |
id | pubmed-9566961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-95669612022-10-17 Association of genetic variants of Glutamate Metabotropic Receptor 5 gene and state-anhedonia Török, D. Gonda, X. Gal, Z. Eszlari, N. Bagdy, G. Juhasz, G. Petschner, P. Eur Psychiatry Abstract INTRODUCTION: Andedonia is one of the core symptoms of depression. It is known that in case of depressed individuals experiencing anhedonia, the classical antidepressants are often ineffective, thus investigation of this symptom would be essential. Recent studies highlight the possible role of the glutamatergic system in anhedonia however, the genetic background of these assumptions is still unclear. OBJECTIVES: Our goal was to investigate the possible associations between state-anhedonia and genetic variants from GRM5 (Glutamate Metabotropic Receptor 5) gene. METHODS: For our analysis we used data from the NewMood (New Molecules in Mood Disorders, LSHM-CT-2004-503474) project. Participants (n = 1820) aged between 18-60, were recruited in Budapest and in Manchester. All volunteers filled out mental-health questionnaires and provided DNA sample. Genotyping was performed by Illumina’s CoreExom PsychChip. Altogether 1282 variants from GRM5 gene survived the genetic quality control steps. State-anhedonia was measured with an item from the Brief Symptom Inventory questionnaire. We performed logistic regression using Plink 2.0. During our analyses, age, gender, population and the top10 principal components of the genome were added into the model as covariates. Correction for linkage-disequilibrium were performed with LDlink. RESULTS: After the correction of linkage-disequilibrium, three independent variables (r(2)<0.2), (rs1827603, rs6483520, rs35669869) yielded significant (p<0.05) results, both in additive and in dominant model. In case of recessive model, only rs11020880 showed significant (p<0.05) effect. CONCLUSIONS: The detected nominally significant associations between state-anhedonia and genetic variants from GRM5 gene strengthen previous assumptions about the possible relationship between glutamatergic system and anhedonia. DISCLOSURE: This study was supported by: MTA-SE Neuropsychopharmacology and Neurochemistry Research Group; 2017-1.2.1-NKP-2017-00002; KTIA_13_NAPA-II/14; KTIA_NAP_13-1-2013- 0001; KTIA_NAP_13-2- 2015-0001; 2020-4.1.1.-TKP2020 and 2019-2.1.7-ERA-NET-2020-00005 (TRAJEC Cambridge University Press 2022-09-01 /pmc/articles/PMC9566961/ http://dx.doi.org/10.1192/j.eurpsy.2022.398 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Abstract Török, D. Gonda, X. Gal, Z. Eszlari, N. Bagdy, G. Juhasz, G. Petschner, P. Association of genetic variants of Glutamate Metabotropic Receptor 5 gene and state-anhedonia |
title | Association of genetic variants of Glutamate Metabotropic Receptor 5 gene and state-anhedonia |
title_full | Association of genetic variants of Glutamate Metabotropic Receptor 5 gene and state-anhedonia |
title_fullStr | Association of genetic variants of Glutamate Metabotropic Receptor 5 gene and state-anhedonia |
title_full_unstemmed | Association of genetic variants of Glutamate Metabotropic Receptor 5 gene and state-anhedonia |
title_short | Association of genetic variants of Glutamate Metabotropic Receptor 5 gene and state-anhedonia |
title_sort | association of genetic variants of glutamate metabotropic receptor 5 gene and state-anhedonia |
topic | Abstract |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9566961/ http://dx.doi.org/10.1192/j.eurpsy.2022.398 |
work_keys_str_mv | AT torokd associationofgeneticvariantsofglutamatemetabotropicreceptor5geneandstateanhedonia AT gondax associationofgeneticvariantsofglutamatemetabotropicreceptor5geneandstateanhedonia AT galz associationofgeneticvariantsofglutamatemetabotropicreceptor5geneandstateanhedonia AT eszlarin associationofgeneticvariantsofglutamatemetabotropicreceptor5geneandstateanhedonia AT bagdyg associationofgeneticvariantsofglutamatemetabotropicreceptor5geneandstateanhedonia AT juhaszg associationofgeneticvariantsofglutamatemetabotropicreceptor5geneandstateanhedonia AT petschnerp associationofgeneticvariantsofglutamatemetabotropicreceptor5geneandstateanhedonia |