Parental ages and levels of DNA methylation in the newborn are correlated

<p>Abstract</p> <p>Background</p> <p>Changes in DNA methylation patterns with age frequently have been observed and implicated in the normal aging process and its associated increasing risk of disease, particularly cancer. Additionally, the offspring of older parents ar...

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Main Authors: Tylavsky Frances A, Thomas Fridtjof, Adkins Ronald M, Krushkal Julia
Format: Article
Language:English
Published: BMC 2011-03-01
Series:BMC Medical Genetics
Online Access:http://www.biomedcentral.com/1471-2350/12/47
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spelling doaj-fb89fc97f0184789affb64423eb8a50a2021-04-02T15:03:39ZengBMCBMC Medical Genetics1471-23502011-03-011214710.1186/1471-2350-12-47Parental ages and levels of DNA methylation in the newborn are correlatedTylavsky Frances AThomas FridtjofAdkins Ronald MKrushkal Julia<p>Abstract</p> <p>Background</p> <p>Changes in DNA methylation patterns with age frequently have been observed and implicated in the normal aging process and its associated increasing risk of disease, particularly cancer. Additionally, the offspring of older parents are at significantly increased risk of cancer, diabetes, and neurodevelopmental disorders. Only a proportion of these increased risks among the children of older parents can be attributed to nondisjunction and chromosomal rearrangements.</p> <p>Results</p> <p>Using a genome-wide survey of 27,578 CpG dinucleotides in a cohort of 168 newborns, we examined the relationship between DNA methylation in newborns and a variety of parental and newborn traits. We found that methylation levels of 144 CpGs belonging to 142 genes were significantly correlated with maternal age. A weaker correlation was observed with paternal age. Among these genes, processes related to cancer were over-represented, as were functions related to neurological regulation, glucose/carbohydrate metabolism, nucleocytoplasmic transport, and transcriptional regulation. CpGs exhibiting gender differences in methylation were overwhelmingly located on the X chromosome, although a small subset of autosomal CpGs were found in genes previously shown to exhibit gender-specific differences in methylation levels.</p> <p>Conclusions</p> <p>These results indicate that there are differences in CpG methylation levels at birth that are related to parental age and that could influence disease risk in childhood and throughout life.</p> http://www.biomedcentral.com/1471-2350/12/47
collection DOAJ
language English
format Article
sources DOAJ
author Tylavsky Frances A
Thomas Fridtjof
Adkins Ronald M
Krushkal Julia
spellingShingle Tylavsky Frances A
Thomas Fridtjof
Adkins Ronald M
Krushkal Julia
Parental ages and levels of DNA methylation in the newborn are correlated
BMC Medical Genetics
author_facet Tylavsky Frances A
Thomas Fridtjof
Adkins Ronald M
Krushkal Julia
author_sort Tylavsky Frances A
title Parental ages and levels of DNA methylation in the newborn are correlated
title_short Parental ages and levels of DNA methylation in the newborn are correlated
title_full Parental ages and levels of DNA methylation in the newborn are correlated
title_fullStr Parental ages and levels of DNA methylation in the newborn are correlated
title_full_unstemmed Parental ages and levels of DNA methylation in the newborn are correlated
title_sort parental ages and levels of dna methylation in the newborn are correlated
publisher BMC
series BMC Medical Genetics
issn 1471-2350
publishDate 2011-03-01
description <p>Abstract</p> <p>Background</p> <p>Changes in DNA methylation patterns with age frequently have been observed and implicated in the normal aging process and its associated increasing risk of disease, particularly cancer. Additionally, the offspring of older parents are at significantly increased risk of cancer, diabetes, and neurodevelopmental disorders. Only a proportion of these increased risks among the children of older parents can be attributed to nondisjunction and chromosomal rearrangements.</p> <p>Results</p> <p>Using a genome-wide survey of 27,578 CpG dinucleotides in a cohort of 168 newborns, we examined the relationship between DNA methylation in newborns and a variety of parental and newborn traits. We found that methylation levels of 144 CpGs belonging to 142 genes were significantly correlated with maternal age. A weaker correlation was observed with paternal age. Among these genes, processes related to cancer were over-represented, as were functions related to neurological regulation, glucose/carbohydrate metabolism, nucleocytoplasmic transport, and transcriptional regulation. CpGs exhibiting gender differences in methylation were overwhelmingly located on the X chromosome, although a small subset of autosomal CpGs were found in genes previously shown to exhibit gender-specific differences in methylation levels.</p> <p>Conclusions</p> <p>These results indicate that there are differences in CpG methylation levels at birth that are related to parental age and that could influence disease risk in childhood and throughout life.</p>
url http://www.biomedcentral.com/1471-2350/12/47
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