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A genetic interaction of NRXN2 with GABRE, SYT1 and CASK in migraine patients: a case-control study

BACKGROUND: Migraine is a multifactorial disorder that is more frequent (two to four times) in women than in men. In recent years, our research group has focused on the role of neurotransmitter release and its regulation. Neurexin (NRXN2) is one of the components of the synaptic vesicle machinery, r...

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Autores principales: Alves-Ferreira, Miguel, Quintas, Marlene, Sequeiros, Jorge, Sousa, Alda, Pereira-Monteiro, José, Alonso, Isabel, Neto, João Luís, Lemos, Carolina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Milan 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8201896/
https://www.ncbi.nlm.nih.gov/pubmed/34126933
http://dx.doi.org/10.1186/s10194-021-01266-y
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author Alves-Ferreira, Miguel
Quintas, Marlene
Sequeiros, Jorge
Sousa, Alda
Pereira-Monteiro, José
Alonso, Isabel
Neto, João Luís
Lemos, Carolina
author_facet Alves-Ferreira, Miguel
Quintas, Marlene
Sequeiros, Jorge
Sousa, Alda
Pereira-Monteiro, José
Alonso, Isabel
Neto, João Luís
Lemos, Carolina
author_sort Alves-Ferreira, Miguel
collection PubMed
description BACKGROUND: Migraine is a multifactorial disorder that is more frequent (two to four times) in women than in men. In recent years, our research group has focused on the role of neurotransmitter release and its regulation. Neurexin (NRXN2) is one of the components of the synaptic vesicle machinery, responsible for connecting intracellular fusion proteins and synaptic vesicles. Our aim was to continue exploring the role and interaction of proteins involved in the control and promotion of neurotransmission in migraine susceptibility. METHODS: A case-control study was performed comprising 183 migraineurs (148 females and 35 males) and 265 migraine-free controls (202 females and 63 males). Tagging single nucleotide polymorphisms of NRXN2 were genotyped to assess the association between NRXN2 and migraine susceptibility. The χ(2) test was used to compare allele frequencies in cases and controls and odds ratios were estimated with 95% confidence intervals. Haplotype frequencies were compared between groups. Gene-gene interactions were analysed using the Multifactor Dimensionality Reduction v2.0. RESULTS: We found a statistically significant interaction model (p = 0.009) in the female group between the genotypes CG of rs477138 (NRXN2) and CT of rs1158605 (GABRE). This interaction was validated by logistic regression, showing a significant risk effect [OR = 4.78 (95%CI: 1.76–12.97)] after a Bonferroni correction. Our data also supports a statistically significant interaction model (p = 0.011) in the female group between the GG of rs477138 in NRXN2 and, the rs2244325's GG genotype and rs2998250’s CC genotype of CASK. This interaction was also validated by logistic regression, with a protective effect [OR = 0.08 (95%CI: 0.01–0.75)]. A weak interaction model was found between NRXN2-SYT1. We have not found any statistically significant allelic or haplotypic associations between NRXN2 and migraine susceptibility. CONCLUSIONS: This study unravels, for the first time, the gene-gene interactions between NRXN2, GABRE - a GABA(A)-receptor - and CASK, importantly it shows the synergetic effect between those genes and its relation with migraine susceptibility. These gene interactions, which may be a part of a larger network, can potentially help us in better understanding migraine aetiology and in development of new therapeutic approaches. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s10194-021-01266-y.
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spelling pubmed-82018962021-06-16 A genetic interaction of NRXN2 with GABRE, SYT1 and CASK in migraine patients: a case-control study Alves-Ferreira, Miguel Quintas, Marlene Sequeiros, Jorge Sousa, Alda Pereira-Monteiro, José Alonso, Isabel Neto, João Luís Lemos, Carolina J Headache Pain Research Article BACKGROUND: Migraine is a multifactorial disorder that is more frequent (two to four times) in women than in men. In recent years, our research group has focused on the role of neurotransmitter release and its regulation. Neurexin (NRXN2) is one of the components of the synaptic vesicle machinery, responsible for connecting intracellular fusion proteins and synaptic vesicles. Our aim was to continue exploring the role and interaction of proteins involved in the control and promotion of neurotransmission in migraine susceptibility. METHODS: A case-control study was performed comprising 183 migraineurs (148 females and 35 males) and 265 migraine-free controls (202 females and 63 males). Tagging single nucleotide polymorphisms of NRXN2 were genotyped to assess the association between NRXN2 and migraine susceptibility. The χ(2) test was used to compare allele frequencies in cases and controls and odds ratios were estimated with 95% confidence intervals. Haplotype frequencies were compared between groups. Gene-gene interactions were analysed using the Multifactor Dimensionality Reduction v2.0. RESULTS: We found a statistically significant interaction model (p = 0.009) in the female group between the genotypes CG of rs477138 (NRXN2) and CT of rs1158605 (GABRE). This interaction was validated by logistic regression, showing a significant risk effect [OR = 4.78 (95%CI: 1.76–12.97)] after a Bonferroni correction. Our data also supports a statistically significant interaction model (p = 0.011) in the female group between the GG of rs477138 in NRXN2 and, the rs2244325's GG genotype and rs2998250’s CC genotype of CASK. This interaction was also validated by logistic regression, with a protective effect [OR = 0.08 (95%CI: 0.01–0.75)]. A weak interaction model was found between NRXN2-SYT1. We have not found any statistically significant allelic or haplotypic associations between NRXN2 and migraine susceptibility. CONCLUSIONS: This study unravels, for the first time, the gene-gene interactions between NRXN2, GABRE - a GABA(A)-receptor - and CASK, importantly it shows the synergetic effect between those genes and its relation with migraine susceptibility. These gene interactions, which may be a part of a larger network, can potentially help us in better understanding migraine aetiology and in development of new therapeutic approaches. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s10194-021-01266-y. Springer Milan 2021-06-14 /pmc/articles/PMC8201896/ /pubmed/34126933 http://dx.doi.org/10.1186/s10194-021-01266-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Alves-Ferreira, Miguel
Quintas, Marlene
Sequeiros, Jorge
Sousa, Alda
Pereira-Monteiro, José
Alonso, Isabel
Neto, João Luís
Lemos, Carolina
A genetic interaction of NRXN2 with GABRE, SYT1 and CASK in migraine patients: a case-control study
title A genetic interaction of NRXN2 with GABRE, SYT1 and CASK in migraine patients: a case-control study
title_full A genetic interaction of NRXN2 with GABRE, SYT1 and CASK in migraine patients: a case-control study
title_fullStr A genetic interaction of NRXN2 with GABRE, SYT1 and CASK in migraine patients: a case-control study
title_full_unstemmed A genetic interaction of NRXN2 with GABRE, SYT1 and CASK in migraine patients: a case-control study
title_short A genetic interaction of NRXN2 with GABRE, SYT1 and CASK in migraine patients: a case-control study
title_sort genetic interaction of nrxn2 with gabre, syt1 and cask in migraine patients: a case-control study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8201896/
https://www.ncbi.nlm.nih.gov/pubmed/34126933
http://dx.doi.org/10.1186/s10194-021-01266-y
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