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DNA methylation age of blood predicts future onset of lung cancer in the women's health initiative
Lung cancer is considered an age-associated disease, whose progression is in part due to accumulation of genomic instability as well as age-related decline in system integrity and function. Thus even among individuals exposed to high levels of genotoxic carcinogens, such as those found in cigarette...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4600626/ https://www.ncbi.nlm.nih.gov/pubmed/26411804 |
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author | Levine, Morgan E. Hosgood, H. Dean Chen, Brian Absher, Devin Assimes, Themistocles Horvath, Steve |
author_facet | Levine, Morgan E. Hosgood, H. Dean Chen, Brian Absher, Devin Assimes, Themistocles Horvath, Steve |
author_sort | Levine, Morgan E. |
collection | PubMed |
description | Lung cancer is considered an age-associated disease, whose progression is in part due to accumulation of genomic instability as well as age-related decline in system integrity and function. Thus even among individuals exposed to high levels of genotoxic carcinogens, such as those found in cigarette smoke, lung cancer susceptibility may vary as a function of individual differences in the rate of biological aging. We recently developed a highly accurate candidate biomarker of aging based on DNA methylation (DNAm) levels, which may prove useful in assessing risk of aging-related diseases, such as lung cancer. Using data on 2,029 females from the Women's Health Initiative, we examined whether baseline measures of “intrinsic epigenetic age acceleration” (IEAA) predicted subsequent lung cancer incidence. We observed 43 lung cancer cases over the nearly twenty years of follow-up. Results showed that standardized measures of IEAA were significantly associated with lung cancer incidence (HR: 1.50, P = 3.4×10(−3)). Furthermore, stratified Cox proportional hazard models suggested that the association may be even stronger among older individuals (70 years or above) or those who are current smokers. Overall, our results suggest that IEAA may be a useful biomarker for evaluating lung cancer susceptibility from a biological aging perspective. |
format | Online Article Text |
id | pubmed-4600626 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-46006262015-10-22 DNA methylation age of blood predicts future onset of lung cancer in the women's health initiative Levine, Morgan E. Hosgood, H. Dean Chen, Brian Absher, Devin Assimes, Themistocles Horvath, Steve Aging (Albany NY) Research Paper Lung cancer is considered an age-associated disease, whose progression is in part due to accumulation of genomic instability as well as age-related decline in system integrity and function. Thus even among individuals exposed to high levels of genotoxic carcinogens, such as those found in cigarette smoke, lung cancer susceptibility may vary as a function of individual differences in the rate of biological aging. We recently developed a highly accurate candidate biomarker of aging based on DNA methylation (DNAm) levels, which may prove useful in assessing risk of aging-related diseases, such as lung cancer. Using data on 2,029 females from the Women's Health Initiative, we examined whether baseline measures of “intrinsic epigenetic age acceleration” (IEAA) predicted subsequent lung cancer incidence. We observed 43 lung cancer cases over the nearly twenty years of follow-up. Results showed that standardized measures of IEAA were significantly associated with lung cancer incidence (HR: 1.50, P = 3.4×10(−3)). Furthermore, stratified Cox proportional hazard models suggested that the association may be even stronger among older individuals (70 years or above) or those who are current smokers. Overall, our results suggest that IEAA may be a useful biomarker for evaluating lung cancer susceptibility from a biological aging perspective. Impact Journals LLC 2015-09-24 /pmc/articles/PMC4600626/ /pubmed/26411804 Text en Copyright: © 2015 Levine et al. http://creativecommons.org/licenses/by/2.5/ 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 credited. |
spellingShingle | Research Paper Levine, Morgan E. Hosgood, H. Dean Chen, Brian Absher, Devin Assimes, Themistocles Horvath, Steve DNA methylation age of blood predicts future onset of lung cancer in the women's health initiative |
title | DNA methylation age of blood predicts future onset of lung cancer in the women's health initiative |
title_full | DNA methylation age of blood predicts future onset of lung cancer in the women's health initiative |
title_fullStr | DNA methylation age of blood predicts future onset of lung cancer in the women's health initiative |
title_full_unstemmed | DNA methylation age of blood predicts future onset of lung cancer in the women's health initiative |
title_short | DNA methylation age of blood predicts future onset of lung cancer in the women's health initiative |
title_sort | dna methylation age of blood predicts future onset of lung cancer in the women's health initiative |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4600626/ https://www.ncbi.nlm.nih.gov/pubmed/26411804 |
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