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Implications of DNA Methylation in Parkinson’s Disease

It has been 200 years since Parkinson’s disease (PD) was first described, yet many aspects of its etiopathogenesis remain unclear. PD is a progressive and complex neurodegenerative disorder caused by genetic and environmental factors including aging, nutrition, pesticides and exposure to heavy metal...

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Autores principales: Miranda-Morales, Ernesto, Meier, Karin, Sandoval-Carrillo, Ada, Salas-Pacheco, José, Vázquez-Cárdenas, Paola, Arias-Carrión, Oscar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513956/
https://www.ncbi.nlm.nih.gov/pubmed/28769760
http://dx.doi.org/10.3389/fnmol.2017.00225
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author Miranda-Morales, Ernesto
Meier, Karin
Sandoval-Carrillo, Ada
Salas-Pacheco, José
Vázquez-Cárdenas, Paola
Arias-Carrión, Oscar
author_facet Miranda-Morales, Ernesto
Meier, Karin
Sandoval-Carrillo, Ada
Salas-Pacheco, José
Vázquez-Cárdenas, Paola
Arias-Carrión, Oscar
author_sort Miranda-Morales, Ernesto
collection PubMed
description It has been 200 years since Parkinson’s disease (PD) was first described, yet many aspects of its etiopathogenesis remain unclear. PD is a progressive and complex neurodegenerative disorder caused by genetic and environmental factors including aging, nutrition, pesticides and exposure to heavy metals. DNA methylation may be altered in response to some of these factors; therefore, it is proposed that epigenetic mechanisms, particularly DNA methylation, can have a fundamental role in gene–environment interactions that are related with PD. Epigenetic changes in PD-associated genes are now widely studied in different populations, to discover the mechanisms that contribute to disease development and identify novel biomarkers for early diagnosis and future pharmacological treatment. While initial studies sought to find associations between promoter DNA methylation and the regulation of associated genes in PD brain tissue, more recent studies have described concordant DNA methylation patterns between blood and brain tissue DNA. These data justify the use of peripheral blood samples instead of brain tissue for epigenetic studies. Here, we summarize the current data about DNA methylation changes in PD and discuss the potential of DNA methylation as a potential biomarker for PD. Additionally, we discuss environmental and nutritional factors that have been implicated in DNA methylation. Although the search for significant DNA methylation changes and gene expression analyses of PD-associated genes have yielded inconsistent and contradictory results, epigenetic modifications remain under investigation for their potential to reveal the link between environmental risk factors and the development of PD.
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spelling pubmed-55139562017-08-02 Implications of DNA Methylation in Parkinson’s Disease Miranda-Morales, Ernesto Meier, Karin Sandoval-Carrillo, Ada Salas-Pacheco, José Vázquez-Cárdenas, Paola Arias-Carrión, Oscar Front Mol Neurosci Neuroscience It has been 200 years since Parkinson’s disease (PD) was first described, yet many aspects of its etiopathogenesis remain unclear. PD is a progressive and complex neurodegenerative disorder caused by genetic and environmental factors including aging, nutrition, pesticides and exposure to heavy metals. DNA methylation may be altered in response to some of these factors; therefore, it is proposed that epigenetic mechanisms, particularly DNA methylation, can have a fundamental role in gene–environment interactions that are related with PD. Epigenetic changes in PD-associated genes are now widely studied in different populations, to discover the mechanisms that contribute to disease development and identify novel biomarkers for early diagnosis and future pharmacological treatment. While initial studies sought to find associations between promoter DNA methylation and the regulation of associated genes in PD brain tissue, more recent studies have described concordant DNA methylation patterns between blood and brain tissue DNA. These data justify the use of peripheral blood samples instead of brain tissue for epigenetic studies. Here, we summarize the current data about DNA methylation changes in PD and discuss the potential of DNA methylation as a potential biomarker for PD. Additionally, we discuss environmental and nutritional factors that have been implicated in DNA methylation. Although the search for significant DNA methylation changes and gene expression analyses of PD-associated genes have yielded inconsistent and contradictory results, epigenetic modifications remain under investigation for their potential to reveal the link between environmental risk factors and the development of PD. Frontiers Media S.A. 2017-07-18 /pmc/articles/PMC5513956/ /pubmed/28769760 http://dx.doi.org/10.3389/fnmol.2017.00225 Text en Copyright © 2017 Miranda-Morales, Meier, Sandoval-Carrillo, Salas-Pacheco, Vázquez-Cárdenas and Arias-Carrión. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Miranda-Morales, Ernesto
Meier, Karin
Sandoval-Carrillo, Ada
Salas-Pacheco, José
Vázquez-Cárdenas, Paola
Arias-Carrión, Oscar
Implications of DNA Methylation in Parkinson’s Disease
title Implications of DNA Methylation in Parkinson’s Disease
title_full Implications of DNA Methylation in Parkinson’s Disease
title_fullStr Implications of DNA Methylation in Parkinson’s Disease
title_full_unstemmed Implications of DNA Methylation in Parkinson’s Disease
title_short Implications of DNA Methylation in Parkinson’s Disease
title_sort implications of dna methylation in parkinson’s disease
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513956/
https://www.ncbi.nlm.nih.gov/pubmed/28769760
http://dx.doi.org/10.3389/fnmol.2017.00225
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