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DNA Methylation and All-Cause Mortality in Middle-Aged and Elderly Danish Twins
Several studies have linked DNA methylation at individual CpG sites to aging and various diseases. Recent studies have also identified single CpGs whose methylation levels are associated with all-cause mortality. In this study, we perform an epigenome-wide study of the association between CpG methyl...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852574/ https://www.ncbi.nlm.nih.gov/pubmed/29419728 http://dx.doi.org/10.3390/genes9020078 |
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author | Svane, Anne Marie Soerensen, Mette Lund, Jesper Tan, Qihua Jylhävä, Juulia Wang, Yunzhang Pedersen, Nancy L. Hägg, Sara Debrabant, Birgit Deary, Ian J. Christensen, Kaare Christiansen, Lene Hjelmborg, Jacob B. |
author_facet | Svane, Anne Marie Soerensen, Mette Lund, Jesper Tan, Qihua Jylhävä, Juulia Wang, Yunzhang Pedersen, Nancy L. Hägg, Sara Debrabant, Birgit Deary, Ian J. Christensen, Kaare Christiansen, Lene Hjelmborg, Jacob B. |
author_sort | Svane, Anne Marie |
collection | PubMed |
description | Several studies have linked DNA methylation at individual CpG sites to aging and various diseases. Recent studies have also identified single CpGs whose methylation levels are associated with all-cause mortality. In this study, we perform an epigenome-wide study of the association between CpG methylation and mortality in a population of 435 monozygotic twin pairs from three Danish twin studies. The participants were aged 55–90 at the time of blood sampling and were followed for up to 20 years. We validated our results by comparison with results from a British and a Swedish cohort, as well as results from the literature. We identified 2806 CpG sites associated with mortality (false discovery rate ([Formula: see text]), of which 24 had an association p-value below [Formula: see text]. This was confirmed by intra-pair comparison controlling for confounding effects. Eight of the 24 top sites could be validated in independent datasets or confirmed by previous studies. For all these eight sites, hypomethylation was associated with poor survival prognosis, and seven showed monozygotic correlations above 35%, indicating a potential moderate to strong heritability, but leaving room for substantial shared or unique environmental effects. We also set up a predictor for mortality using least absolute shrinkage and selection operator (LASSO) regression. The predictor showed good performance on the Danish data under cross-validation, but did not perform very well in independent samples. |
format | Online Article Text |
id | pubmed-5852574 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-58525742018-03-19 DNA Methylation and All-Cause Mortality in Middle-Aged and Elderly Danish Twins Svane, Anne Marie Soerensen, Mette Lund, Jesper Tan, Qihua Jylhävä, Juulia Wang, Yunzhang Pedersen, Nancy L. Hägg, Sara Debrabant, Birgit Deary, Ian J. Christensen, Kaare Christiansen, Lene Hjelmborg, Jacob B. Genes (Basel) Article Several studies have linked DNA methylation at individual CpG sites to aging and various diseases. Recent studies have also identified single CpGs whose methylation levels are associated with all-cause mortality. In this study, we perform an epigenome-wide study of the association between CpG methylation and mortality in a population of 435 monozygotic twin pairs from three Danish twin studies. The participants were aged 55–90 at the time of blood sampling and were followed for up to 20 years. We validated our results by comparison with results from a British and a Swedish cohort, as well as results from the literature. We identified 2806 CpG sites associated with mortality (false discovery rate ([Formula: see text]), of which 24 had an association p-value below [Formula: see text]. This was confirmed by intra-pair comparison controlling for confounding effects. Eight of the 24 top sites could be validated in independent datasets or confirmed by previous studies. For all these eight sites, hypomethylation was associated with poor survival prognosis, and seven showed monozygotic correlations above 35%, indicating a potential moderate to strong heritability, but leaving room for substantial shared or unique environmental effects. We also set up a predictor for mortality using least absolute shrinkage and selection operator (LASSO) regression. The predictor showed good performance on the Danish data under cross-validation, but did not perform very well in independent samples. MDPI 2018-02-08 /pmc/articles/PMC5852574/ /pubmed/29419728 http://dx.doi.org/10.3390/genes9020078 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Svane, Anne Marie Soerensen, Mette Lund, Jesper Tan, Qihua Jylhävä, Juulia Wang, Yunzhang Pedersen, Nancy L. Hägg, Sara Debrabant, Birgit Deary, Ian J. Christensen, Kaare Christiansen, Lene Hjelmborg, Jacob B. DNA Methylation and All-Cause Mortality in Middle-Aged and Elderly Danish Twins |
title | DNA Methylation and All-Cause Mortality in Middle-Aged and Elderly Danish Twins |
title_full | DNA Methylation and All-Cause Mortality in Middle-Aged and Elderly Danish Twins |
title_fullStr | DNA Methylation and All-Cause Mortality in Middle-Aged and Elderly Danish Twins |
title_full_unstemmed | DNA Methylation and All-Cause Mortality in Middle-Aged and Elderly Danish Twins |
title_short | DNA Methylation and All-Cause Mortality in Middle-Aged and Elderly Danish Twins |
title_sort | dna methylation and all-cause mortality in middle-aged and elderly danish twins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852574/ https://www.ncbi.nlm.nih.gov/pubmed/29419728 http://dx.doi.org/10.3390/genes9020078 |
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