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Genetic association and gene expression studies suggest that genetic variants in the SYNE1 and TNF genes are related to menstrual migraine

BACKGROUND: Menstrual migraine (MM) encompasses pure menstrual migraine (PMM) and menstrually-related migraine (MRM). This study was aimed at investigating genetic variants that are potentially related to MM, specifically undertaking genotyping and mRNA expression analysis of the ESR1, PGR, SYNE1 an...

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Autores principales: Rodriguez-Acevedo, Astrid J, Smith, Robert A, Roy, Bishakha, Sutherland, Heidi, Lea, Rod A, Frith, Alison, MacGregor, E Anne, Griffiths, Lyn R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196204/
https://www.ncbi.nlm.nih.gov/pubmed/25315199
http://dx.doi.org/10.1186/1129-2377-15-62
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author Rodriguez-Acevedo, Astrid J
Smith, Robert A
Roy, Bishakha
Sutherland, Heidi
Lea, Rod A
Frith, Alison
MacGregor, E Anne
Griffiths, Lyn R
author_facet Rodriguez-Acevedo, Astrid J
Smith, Robert A
Roy, Bishakha
Sutherland, Heidi
Lea, Rod A
Frith, Alison
MacGregor, E Anne
Griffiths, Lyn R
author_sort Rodriguez-Acevedo, Astrid J
collection PubMed
description BACKGROUND: Menstrual migraine (MM) encompasses pure menstrual migraine (PMM) and menstrually-related migraine (MRM). This study was aimed at investigating genetic variants that are potentially related to MM, specifically undertaking genotyping and mRNA expression analysis of the ESR1, PGR, SYNE1 and TNF genes in MM cases and non-migraine controls. METHODS: A total of 37 variants distributed across 14 genes were genotyped in 437 DNA samples (282 cases and 155 controls). In addition levels of gene expression were determined in 74 cDNA samples (41 cases and 33 controls). Association and correlation analysis were performed using Plink and RStudio. RESULTS: SNPs rs3093664 and rs9371601 in TNF and SYNE1 genes respectively, were significantly associated with migraine in the MM population (p = 0.008; p = 0.009 respectively). Analysis of qPCR results found no significant difference in levels of gene expression between cases and controls. However, we found a significant correlation between the expression of ESR1 and SYNE1, ESR1 and PGR and TNF and SYNE1 in samples taken during the follicular phase of the menstrual cycle. CONCLUSIONS: Our results show that SNPs rs9371601 and rs3093664 in the SYNE1 and TNF genes respectively, are associated with MM. The present study also provides strong evidence to support the correlation of ESR1, PGR, SYNE1 and TNF gene expression in MM.
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spelling pubmed-41962042014-10-14 Genetic association and gene expression studies suggest that genetic variants in the SYNE1 and TNF genes are related to menstrual migraine Rodriguez-Acevedo, Astrid J Smith, Robert A Roy, Bishakha Sutherland, Heidi Lea, Rod A Frith, Alison MacGregor, E Anne Griffiths, Lyn R J Headache Pain Research Article BACKGROUND: Menstrual migraine (MM) encompasses pure menstrual migraine (PMM) and menstrually-related migraine (MRM). This study was aimed at investigating genetic variants that are potentially related to MM, specifically undertaking genotyping and mRNA expression analysis of the ESR1, PGR, SYNE1 and TNF genes in MM cases and non-migraine controls. METHODS: A total of 37 variants distributed across 14 genes were genotyped in 437 DNA samples (282 cases and 155 controls). In addition levels of gene expression were determined in 74 cDNA samples (41 cases and 33 controls). Association and correlation analysis were performed using Plink and RStudio. RESULTS: SNPs rs3093664 and rs9371601 in TNF and SYNE1 genes respectively, were significantly associated with migraine in the MM population (p = 0.008; p = 0.009 respectively). Analysis of qPCR results found no significant difference in levels of gene expression between cases and controls. However, we found a significant correlation between the expression of ESR1 and SYNE1, ESR1 and PGR and TNF and SYNE1 in samples taken during the follicular phase of the menstrual cycle. CONCLUSIONS: Our results show that SNPs rs9371601 and rs3093664 in the SYNE1 and TNF genes respectively, are associated with MM. The present study also provides strong evidence to support the correlation of ESR1, PGR, SYNE1 and TNF gene expression in MM. Springer 2014 2014-10-14 /pmc/articles/PMC4196204/ /pubmed/25315199 http://dx.doi.org/10.1186/1129-2377-15-62 Text en Copyright © 2014 Rodriguez-Acevedo et al.; licensee Springer. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research Article
Rodriguez-Acevedo, Astrid J
Smith, Robert A
Roy, Bishakha
Sutherland, Heidi
Lea, Rod A
Frith, Alison
MacGregor, E Anne
Griffiths, Lyn R
Genetic association and gene expression studies suggest that genetic variants in the SYNE1 and TNF genes are related to menstrual migraine
title Genetic association and gene expression studies suggest that genetic variants in the SYNE1 and TNF genes are related to menstrual migraine
title_full Genetic association and gene expression studies suggest that genetic variants in the SYNE1 and TNF genes are related to menstrual migraine
title_fullStr Genetic association and gene expression studies suggest that genetic variants in the SYNE1 and TNF genes are related to menstrual migraine
title_full_unstemmed Genetic association and gene expression studies suggest that genetic variants in the SYNE1 and TNF genes are related to menstrual migraine
title_short Genetic association and gene expression studies suggest that genetic variants in the SYNE1 and TNF genes are related to menstrual migraine
title_sort genetic association and gene expression studies suggest that genetic variants in the syne1 and tnf genes are related to menstrual migraine
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196204/
https://www.ncbi.nlm.nih.gov/pubmed/25315199
http://dx.doi.org/10.1186/1129-2377-15-62
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