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Linking environmental risk factors with epigenetic mechanisms in Parkinson’s disease

Sporadic Parkinson’s disease (PD) is a progressive neurodegenerative disease, with a complex risk structure thought to be influenced by interactions between genetic variants and environmental exposures, although the full aetiology is unknown. Environmental factors, including pesticides, have been re...

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Autores principales: Tsalenchuk, Maria, Gentleman, Steve M., Marzi, Sarah J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10457362/
https://www.ncbi.nlm.nih.gov/pubmed/37626097
http://dx.doi.org/10.1038/s41531-023-00568-z
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author Tsalenchuk, Maria
Gentleman, Steve M.
Marzi, Sarah J.
author_facet Tsalenchuk, Maria
Gentleman, Steve M.
Marzi, Sarah J.
author_sort Tsalenchuk, Maria
collection PubMed
description Sporadic Parkinson’s disease (PD) is a progressive neurodegenerative disease, with a complex risk structure thought to be influenced by interactions between genetic variants and environmental exposures, although the full aetiology is unknown. Environmental factors, including pesticides, have been reported to increase the risk of developing the disease. Growing evidence suggests epigenetic changes are key mechanisms by which these environmental factors act upon gene regulation, in disease-relevant cell types. We present a systematic review critically appraising and summarising the current body of evidence of the relationship between epigenetic mechanisms and environmental risk factors in PD to inform future research in this area. Epigenetic studies of relevant environmental risk factors in animal and cell models have yielded promising results, however, research in humans is just emerging. While published studies in humans are currently relatively limited, the importance of the field for the elucidation of molecular mechanisms of pathogenesis opens clear and promising avenues for the future of PD research. Carefully designed epidemiological studies carried out in PD patients hold great potential to uncover disease-relevant gene regulatory mechanisms. Therefore, to advance this burgeoning field, we recommend broadening the scope of investigations to include more environmental exposures, increasing sample sizes, focusing on disease-relevant cell types, and recruiting more diverse cohorts.
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spelling pubmed-104573622023-08-27 Linking environmental risk factors with epigenetic mechanisms in Parkinson’s disease Tsalenchuk, Maria Gentleman, Steve M. Marzi, Sarah J. NPJ Parkinsons Dis Review Article Sporadic Parkinson’s disease (PD) is a progressive neurodegenerative disease, with a complex risk structure thought to be influenced by interactions between genetic variants and environmental exposures, although the full aetiology is unknown. Environmental factors, including pesticides, have been reported to increase the risk of developing the disease. Growing evidence suggests epigenetic changes are key mechanisms by which these environmental factors act upon gene regulation, in disease-relevant cell types. We present a systematic review critically appraising and summarising the current body of evidence of the relationship between epigenetic mechanisms and environmental risk factors in PD to inform future research in this area. Epigenetic studies of relevant environmental risk factors in animal and cell models have yielded promising results, however, research in humans is just emerging. While published studies in humans are currently relatively limited, the importance of the field for the elucidation of molecular mechanisms of pathogenesis opens clear and promising avenues for the future of PD research. Carefully designed epidemiological studies carried out in PD patients hold great potential to uncover disease-relevant gene regulatory mechanisms. Therefore, to advance this burgeoning field, we recommend broadening the scope of investigations to include more environmental exposures, increasing sample sizes, focusing on disease-relevant cell types, and recruiting more diverse cohorts. Nature Publishing Group UK 2023-08-25 /pmc/articles/PMC10457362/ /pubmed/37626097 http://dx.doi.org/10.1038/s41531-023-00568-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review Article
Tsalenchuk, Maria
Gentleman, Steve M.
Marzi, Sarah J.
Linking environmental risk factors with epigenetic mechanisms in Parkinson’s disease
title Linking environmental risk factors with epigenetic mechanisms in Parkinson’s disease
title_full Linking environmental risk factors with epigenetic mechanisms in Parkinson’s disease
title_fullStr Linking environmental risk factors with epigenetic mechanisms in Parkinson’s disease
title_full_unstemmed Linking environmental risk factors with epigenetic mechanisms in Parkinson’s disease
title_short Linking environmental risk factors with epigenetic mechanisms in Parkinson’s disease
title_sort linking environmental risk factors with epigenetic mechanisms in parkinson’s disease
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10457362/
https://www.ncbi.nlm.nih.gov/pubmed/37626097
http://dx.doi.org/10.1038/s41531-023-00568-z
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