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Epigenome-Wide DNA Methylation in Hearing Ability: New Mechanisms for an Old Problem

Epigenetic regulation of gene expression has been shown to change over time and may be associated with environmental exposures in common complex traits. Age-related hearing impairment is a complex disorder, known to be heritable, with heritability estimates of 57–70%. Epigenetic regulation might exp...

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Autores principales: Wolber, Lisa E., Steves, Claire J., Tsai, Pei-Chien, Deloukas, Panos, Spector, Tim D., Bell, Jordana T., Williams, Frances M. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4153547/
https://www.ncbi.nlm.nih.gov/pubmed/25184702
http://dx.doi.org/10.1371/journal.pone.0105729
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author Wolber, Lisa E.
Steves, Claire J.
Tsai, Pei-Chien
Deloukas, Panos
Spector, Tim D.
Bell, Jordana T.
Williams, Frances M. K.
author_facet Wolber, Lisa E.
Steves, Claire J.
Tsai, Pei-Chien
Deloukas, Panos
Spector, Tim D.
Bell, Jordana T.
Williams, Frances M. K.
author_sort Wolber, Lisa E.
collection PubMed
description Epigenetic regulation of gene expression has been shown to change over time and may be associated with environmental exposures in common complex traits. Age-related hearing impairment is a complex disorder, known to be heritable, with heritability estimates of 57–70%. Epigenetic regulation might explain the observed difference in age of onset and magnitude of hearing impairment with age. Epigenetic epidemiology studies using unrelated samples can be limited in their ability to detect small effects, and recent epigenetic findings in twins underscore the power of this well matched study design. We investigated the association between venous blood DNA methylation epigenome-wide and hearing ability. Pure-tone audiometry (PTA) and Illumina HumanMethylation array data were obtained from female twin volunteers enrolled in the TwinsUK register. Two study groups were explored: first, an epigenome-wide association scan (EWAS) was performed in a discovery sample (n = 115 subjects, age range: 47–83 years, Illumina 27 k array), then replication of the top ten associated probes from the discovery EWAS was attempted in a second unrelated sample (n = 203, age range: 41–86 years, Illumina 450 k array). Finally, a set of monozygotic (MZ) twin pairs (n = 21 pairs) within the discovery sample (Illumina 27 k array) was investigated in more detail in an MZ discordance analysis. Hearing ability was strongly associated with DNA methylation levels in the promoter regions of several genes, including TCF25 (cg01161216, p = 6.6×10(−6)), FGFR1 (cg15791248, p = 5.7×10(−5)) and POLE (cg18877514, p = 6.3×10(−5)). Replication of these results in a second sample confirmed the presence of differential methylation at TCF25 (p(replication) = 6×10(−5)) and POLE (p(replication) = 0.016). In the MZ discordance analysis, twins' intrapair difference in hearing ability correlated with DNA methylation differences at ACP6 (cg01377755, r = −0.75, p = 1.2×10(−4)) and MEF2D (cg08156349, r = −0.75, p = 1.4×10(−4)). Examination of gene expression in skin, suggests an influence of differential methylation on expression, which may account for the variation in hearing ability with age.
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spelling pubmed-41535472014-09-05 Epigenome-Wide DNA Methylation in Hearing Ability: New Mechanisms for an Old Problem Wolber, Lisa E. Steves, Claire J. Tsai, Pei-Chien Deloukas, Panos Spector, Tim D. Bell, Jordana T. Williams, Frances M. K. PLoS One Research Article Epigenetic regulation of gene expression has been shown to change over time and may be associated with environmental exposures in common complex traits. Age-related hearing impairment is a complex disorder, known to be heritable, with heritability estimates of 57–70%. Epigenetic regulation might explain the observed difference in age of onset and magnitude of hearing impairment with age. Epigenetic epidemiology studies using unrelated samples can be limited in their ability to detect small effects, and recent epigenetic findings in twins underscore the power of this well matched study design. We investigated the association between venous blood DNA methylation epigenome-wide and hearing ability. Pure-tone audiometry (PTA) and Illumina HumanMethylation array data were obtained from female twin volunteers enrolled in the TwinsUK register. Two study groups were explored: first, an epigenome-wide association scan (EWAS) was performed in a discovery sample (n = 115 subjects, age range: 47–83 years, Illumina 27 k array), then replication of the top ten associated probes from the discovery EWAS was attempted in a second unrelated sample (n = 203, age range: 41–86 years, Illumina 450 k array). Finally, a set of monozygotic (MZ) twin pairs (n = 21 pairs) within the discovery sample (Illumina 27 k array) was investigated in more detail in an MZ discordance analysis. Hearing ability was strongly associated with DNA methylation levels in the promoter regions of several genes, including TCF25 (cg01161216, p = 6.6×10(−6)), FGFR1 (cg15791248, p = 5.7×10(−5)) and POLE (cg18877514, p = 6.3×10(−5)). Replication of these results in a second sample confirmed the presence of differential methylation at TCF25 (p(replication) = 6×10(−5)) and POLE (p(replication) = 0.016). In the MZ discordance analysis, twins' intrapair difference in hearing ability correlated with DNA methylation differences at ACP6 (cg01377755, r = −0.75, p = 1.2×10(−4)) and MEF2D (cg08156349, r = −0.75, p = 1.4×10(−4)). Examination of gene expression in skin, suggests an influence of differential methylation on expression, which may account for the variation in hearing ability with age. Public Library of Science 2014-09-03 /pmc/articles/PMC4153547/ /pubmed/25184702 http://dx.doi.org/10.1371/journal.pone.0105729 Text en © 2014 Wolber et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Wolber, Lisa E.
Steves, Claire J.
Tsai, Pei-Chien
Deloukas, Panos
Spector, Tim D.
Bell, Jordana T.
Williams, Frances M. K.
Epigenome-Wide DNA Methylation in Hearing Ability: New Mechanisms for an Old Problem
title Epigenome-Wide DNA Methylation in Hearing Ability: New Mechanisms for an Old Problem
title_full Epigenome-Wide DNA Methylation in Hearing Ability: New Mechanisms for an Old Problem
title_fullStr Epigenome-Wide DNA Methylation in Hearing Ability: New Mechanisms for an Old Problem
title_full_unstemmed Epigenome-Wide DNA Methylation in Hearing Ability: New Mechanisms for an Old Problem
title_short Epigenome-Wide DNA Methylation in Hearing Ability: New Mechanisms for an Old Problem
title_sort epigenome-wide dna methylation in hearing ability: new mechanisms for an old problem
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4153547/
https://www.ncbi.nlm.nih.gov/pubmed/25184702
http://dx.doi.org/10.1371/journal.pone.0105729
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