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Alterations observed in the interferon α and β signaling pathway in MDD patients are marginally influenced by cis-acting alleles

Major depressive disorder (MDD) is a common psychiatric disorder with a multifactorial aetiology determined by the interaction between genetic and environmental risk factors. Pieces of evidence indicate that inflammation and immune activation may contribute to the onset of MDD playing a role in the...

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Autores principales: Magri, Chiara, Giacopuzzi, Edoardo, Sacco, Chiara, Bocchio-Chiavetto, Luisella, Minelli, Alessandra, Gennarelli, Massimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804189/
https://www.ncbi.nlm.nih.gov/pubmed/33436853
http://dx.doi.org/10.1038/s41598-020-80374-2
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author Magri, Chiara
Giacopuzzi, Edoardo
Sacco, Chiara
Bocchio-Chiavetto, Luisella
Minelli, Alessandra
Gennarelli, Massimo
author_facet Magri, Chiara
Giacopuzzi, Edoardo
Sacco, Chiara
Bocchio-Chiavetto, Luisella
Minelli, Alessandra
Gennarelli, Massimo
author_sort Magri, Chiara
collection PubMed
description Major depressive disorder (MDD) is a common psychiatric disorder with a multifactorial aetiology determined by the interaction between genetic and environmental risk factors. Pieces of evidence indicate that inflammation and immune activation may contribute to the onset of MDD playing a role in the pathogenetic mechanism. To date, it is not known to which extent the association between MDD and inflammation is shaped by the genetic background or by the presence of environmental factors. To clarify this issue, we analyzed genotype and blood RNA profiles of 463 MDD cases and 459 controls (NIMH-Study 88/Site621) estimating the Genetic and Environmental Regulated eXpression component of gene expression (GReX and EReX respectively). Both components were tested for association with MDD. Many genes belonging to the α/β interferon signaling pathway showed an association between MDD and EReX, only two between MDD and GReX. Also other MDD differentially expressed genes were more influenced by the EReX than by GReX. These results suggest that impact of the genetic background on MDD blood gene expression alterations is much lower than the contribution of environmental factors and almost absent for the genes of the interferon pathway.
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spelling pubmed-78041892021-01-13 Alterations observed in the interferon α and β signaling pathway in MDD patients are marginally influenced by cis-acting alleles Magri, Chiara Giacopuzzi, Edoardo Sacco, Chiara Bocchio-Chiavetto, Luisella Minelli, Alessandra Gennarelli, Massimo Sci Rep Article Major depressive disorder (MDD) is a common psychiatric disorder with a multifactorial aetiology determined by the interaction between genetic and environmental risk factors. Pieces of evidence indicate that inflammation and immune activation may contribute to the onset of MDD playing a role in the pathogenetic mechanism. To date, it is not known to which extent the association between MDD and inflammation is shaped by the genetic background or by the presence of environmental factors. To clarify this issue, we analyzed genotype and blood RNA profiles of 463 MDD cases and 459 controls (NIMH-Study 88/Site621) estimating the Genetic and Environmental Regulated eXpression component of gene expression (GReX and EReX respectively). Both components were tested for association with MDD. Many genes belonging to the α/β interferon signaling pathway showed an association between MDD and EReX, only two between MDD and GReX. Also other MDD differentially expressed genes were more influenced by the EReX than by GReX. These results suggest that impact of the genetic background on MDD blood gene expression alterations is much lower than the contribution of environmental factors and almost absent for the genes of the interferon pathway. Nature Publishing Group UK 2021-01-12 /pmc/articles/PMC7804189/ /pubmed/33436853 http://dx.doi.org/10.1038/s41598-020-80374-2 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Magri, Chiara
Giacopuzzi, Edoardo
Sacco, Chiara
Bocchio-Chiavetto, Luisella
Minelli, Alessandra
Gennarelli, Massimo
Alterations observed in the interferon α and β signaling pathway in MDD patients are marginally influenced by cis-acting alleles
title Alterations observed in the interferon α and β signaling pathway in MDD patients are marginally influenced by cis-acting alleles
title_full Alterations observed in the interferon α and β signaling pathway in MDD patients are marginally influenced by cis-acting alleles
title_fullStr Alterations observed in the interferon α and β signaling pathway in MDD patients are marginally influenced by cis-acting alleles
title_full_unstemmed Alterations observed in the interferon α and β signaling pathway in MDD patients are marginally influenced by cis-acting alleles
title_short Alterations observed in the interferon α and β signaling pathway in MDD patients are marginally influenced by cis-acting alleles
title_sort alterations observed in the interferon α and β signaling pathway in mdd patients are marginally influenced by cis-acting alleles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804189/
https://www.ncbi.nlm.nih.gov/pubmed/33436853
http://dx.doi.org/10.1038/s41598-020-80374-2
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