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Epigenetic regulation of Parkinson’s disease risk variant GPNMB cg17274742 methylation by sex and exercise from Taiwan Biobank

BACKGROUND: Parkinson’s disease (PD) is a complex neurodegenerative disease with an elusive etiology that involves the interaction between genetic, behavioral, and environmental factors. Recently, epigenetic modifications, particularly DNA methylation, have been recognized to play an important role...

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Autores principales: Chen, Yen-Chung, Liaw, Yi-Chia, Nfor, Oswald Ndi, Hsiao, Chih-Hsuan, Zhong, Ji-Han, Wu, Shey-Lin, Liaw, Yung-Po
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10513104/
https://www.ncbi.nlm.nih.gov/pubmed/37744396
http://dx.doi.org/10.3389/fnagi.2023.1235840
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author Chen, Yen-Chung
Liaw, Yi-Chia
Nfor, Oswald Ndi
Hsiao, Chih-Hsuan
Zhong, Ji-Han
Wu, Shey-Lin
Liaw, Yung-Po
author_facet Chen, Yen-Chung
Liaw, Yi-Chia
Nfor, Oswald Ndi
Hsiao, Chih-Hsuan
Zhong, Ji-Han
Wu, Shey-Lin
Liaw, Yung-Po
author_sort Chen, Yen-Chung
collection PubMed
description BACKGROUND: Parkinson’s disease (PD) is a complex neurodegenerative disease with an elusive etiology that involves the interaction between genetic, behavioral, and environmental factors. Recently, epigenetic modifications, particularly DNA methylation, have been recognized to play an important role in the onset of PD. Glycoprotein non-metastatic melanoma protein B (GPNMB), a type I transmembrane protein crucial for immune cell activation and maturation, has emerged as a potential biomarker for the risk of PD. This research aims to investigate the influence of exercise and gender on the regulation of methylation levels of GPNMB cg17274742 in individuals. METHODS: We analyze data from 2,474 participants in the Taiwan Biobank, collected from 2008 and 2016. Methylation levels at the GPNMB cg17274742 CpG site were measured using Illumina Infinium MethylationEPIC beads. After excluding individuals with incomplete data or missing information on possible risk factors, our final analysis included 1,442 participants. We used multiple linear regression models to assess the association between sex and exercise with adjusted levels of GPNMB cg17274742 for age, BMI, smoking, drinking, coffee consumption, serum uric acid levels, and hypertension. RESULTS: Our results demonstrated that exercise significantly influenced the methylation levels of GPNMB cg17274742 in males (β = −0.00242; p = 0.0026), but not in females (β = −0.00002362; p = 0.9785). Furthermore, male participants who exercised showed significantly lower levels of methylation compared to the reference groups of the female and non-exercising reference groups (β = −0.00357; p = 0.0079). The effect of the interaction between gender and exercise on the methylation of GPNMB cg17274742 was statistically significant (p = 0.0078). CONCLUSION: This study suggests that gender and exercise can modulate GPNMB cg17274742, with hypomethylation observed in exercise men. More research is needed to understand the underlying mechanisms and implications of these epigenetic changes in the context of risk and prevention strategies.
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spelling pubmed-105131042023-09-22 Epigenetic regulation of Parkinson’s disease risk variant GPNMB cg17274742 methylation by sex and exercise from Taiwan Biobank Chen, Yen-Chung Liaw, Yi-Chia Nfor, Oswald Ndi Hsiao, Chih-Hsuan Zhong, Ji-Han Wu, Shey-Lin Liaw, Yung-Po Front Aging Neurosci Aging Neuroscience BACKGROUND: Parkinson’s disease (PD) is a complex neurodegenerative disease with an elusive etiology that involves the interaction between genetic, behavioral, and environmental factors. Recently, epigenetic modifications, particularly DNA methylation, have been recognized to play an important role in the onset of PD. Glycoprotein non-metastatic melanoma protein B (GPNMB), a type I transmembrane protein crucial for immune cell activation and maturation, has emerged as a potential biomarker for the risk of PD. This research aims to investigate the influence of exercise and gender on the regulation of methylation levels of GPNMB cg17274742 in individuals. METHODS: We analyze data from 2,474 participants in the Taiwan Biobank, collected from 2008 and 2016. Methylation levels at the GPNMB cg17274742 CpG site were measured using Illumina Infinium MethylationEPIC beads. After excluding individuals with incomplete data or missing information on possible risk factors, our final analysis included 1,442 participants. We used multiple linear regression models to assess the association between sex and exercise with adjusted levels of GPNMB cg17274742 for age, BMI, smoking, drinking, coffee consumption, serum uric acid levels, and hypertension. RESULTS: Our results demonstrated that exercise significantly influenced the methylation levels of GPNMB cg17274742 in males (β = −0.00242; p = 0.0026), but not in females (β = −0.00002362; p = 0.9785). Furthermore, male participants who exercised showed significantly lower levels of methylation compared to the reference groups of the female and non-exercising reference groups (β = −0.00357; p = 0.0079). The effect of the interaction between gender and exercise on the methylation of GPNMB cg17274742 was statistically significant (p = 0.0078). CONCLUSION: This study suggests that gender and exercise can modulate GPNMB cg17274742, with hypomethylation observed in exercise men. More research is needed to understand the underlying mechanisms and implications of these epigenetic changes in the context of risk and prevention strategies. Frontiers Media S.A. 2023-09-07 /pmc/articles/PMC10513104/ /pubmed/37744396 http://dx.doi.org/10.3389/fnagi.2023.1235840 Text en Copyright © 2023 Chen, Liaw, Nfor, Hsiao, Zhong, Wu and Liaw. https://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) and the copyright owner(s) 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 Aging Neuroscience
Chen, Yen-Chung
Liaw, Yi-Chia
Nfor, Oswald Ndi
Hsiao, Chih-Hsuan
Zhong, Ji-Han
Wu, Shey-Lin
Liaw, Yung-Po
Epigenetic regulation of Parkinson’s disease risk variant GPNMB cg17274742 methylation by sex and exercise from Taiwan Biobank
title Epigenetic regulation of Parkinson’s disease risk variant GPNMB cg17274742 methylation by sex and exercise from Taiwan Biobank
title_full Epigenetic regulation of Parkinson’s disease risk variant GPNMB cg17274742 methylation by sex and exercise from Taiwan Biobank
title_fullStr Epigenetic regulation of Parkinson’s disease risk variant GPNMB cg17274742 methylation by sex and exercise from Taiwan Biobank
title_full_unstemmed Epigenetic regulation of Parkinson’s disease risk variant GPNMB cg17274742 methylation by sex and exercise from Taiwan Biobank
title_short Epigenetic regulation of Parkinson’s disease risk variant GPNMB cg17274742 methylation by sex and exercise from Taiwan Biobank
title_sort epigenetic regulation of parkinson’s disease risk variant gpnmb cg17274742 methylation by sex and exercise from taiwan biobank
topic Aging Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10513104/
https://www.ncbi.nlm.nih.gov/pubmed/37744396
http://dx.doi.org/10.3389/fnagi.2023.1235840
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