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Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing

BACKGROUND: DNA methylation changes with age. Chronological age predictors built from DNA methylation are termed ‘epigenetic clocks’. The deviation of predicted age from the actual age (‘age acceleration residual’, AAR) has been reported to be associated with death. However, it is currently unclear...

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Autores principales: Zhang, Qian, Vallerga, Costanza L., Walker, Rosie M., Lin, Tian, Henders, Anjali K., Montgomery, Grant W., He, Ji, Fan, Dongsheng, Fowdar, Javed, Kennedy, Martin, Pitcher, Toni, Pearson, John, Halliday, Glenda, Kwok, John B., Hickie, Ian, Lewis, Simon, Anderson, Tim, Silburn, Peter A., Mellick, George D., Harris, Sarah E., Redmond, Paul, Murray, Alison D., Porteous, David J., Haley, Christopher S., Evans, Kathryn L., McIntosh, Andrew M., Yang, Jian, Gratten, Jacob, Marioni, Riccardo E., Wray, Naomi R., Deary, Ian J., McRae, Allan F., Visscher, Peter M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708158/
https://www.ncbi.nlm.nih.gov/pubmed/31443728
http://dx.doi.org/10.1186/s13073-019-0667-1
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author Zhang, Qian
Vallerga, Costanza L.
Walker, Rosie M.
Lin, Tian
Henders, Anjali K.
Montgomery, Grant W.
He, Ji
Fan, Dongsheng
Fowdar, Javed
Kennedy, Martin
Pitcher, Toni
Pearson, John
Halliday, Glenda
Kwok, John B.
Hickie, Ian
Lewis, Simon
Anderson, Tim
Silburn, Peter A.
Mellick, George D.
Harris, Sarah E.
Redmond, Paul
Murray, Alison D.
Porteous, David J.
Haley, Christopher S.
Evans, Kathryn L.
McIntosh, Andrew M.
Yang, Jian
Gratten, Jacob
Marioni, Riccardo E.
Wray, Naomi R.
Deary, Ian J.
McRae, Allan F.
Visscher, Peter M.
author_facet Zhang, Qian
Vallerga, Costanza L.
Walker, Rosie M.
Lin, Tian
Henders, Anjali K.
Montgomery, Grant W.
He, Ji
Fan, Dongsheng
Fowdar, Javed
Kennedy, Martin
Pitcher, Toni
Pearson, John
Halliday, Glenda
Kwok, John B.
Hickie, Ian
Lewis, Simon
Anderson, Tim
Silburn, Peter A.
Mellick, George D.
Harris, Sarah E.
Redmond, Paul
Murray, Alison D.
Porteous, David J.
Haley, Christopher S.
Evans, Kathryn L.
McIntosh, Andrew M.
Yang, Jian
Gratten, Jacob
Marioni, Riccardo E.
Wray, Naomi R.
Deary, Ian J.
McRae, Allan F.
Visscher, Peter M.
author_sort Zhang, Qian
collection PubMed
description BACKGROUND: DNA methylation changes with age. Chronological age predictors built from DNA methylation are termed ‘epigenetic clocks’. The deviation of predicted age from the actual age (‘age acceleration residual’, AAR) has been reported to be associated with death. However, it is currently unclear how a better prediction of chronological age affects such association. METHODS: In this study, we build multiple predictors based on training DNA methylation samples selected from 13,661 samples (13,402 from blood and 259 from saliva). We use the Lothian Birth Cohorts of 1921 (LBC1921) and 1936 (LBC1936) to examine whether the association between AAR (from these predictors) and death is affected by (1) improving prediction accuracy of an age predictor as its training sample size increases (from 335 to 12,710) and (2) additionally correcting for confounders (i.e., cellular compositions). In addition, we investigated the performance of our predictor in non-blood tissues. RESULTS: We found that in principle, a near-perfect age predictor could be developed when the training sample size is sufficiently large. The association between AAR and mortality attenuates as prediction accuracy increases. AAR from our best predictor (based on Elastic Net, https://github.com/qzhang314/DNAm-based-age-predictor) exhibits no association with mortality in both LBC1921 (hazard ratio = 1.08, 95% CI 0.91–1.27) and LBC1936 (hazard ratio = 1.00, 95% CI 0.79–1.28). Predictors based on small sample size are prone to confounding by cellular compositions relative to those from large sample size. We observed comparable performance of our predictor in non-blood tissues with a multi-tissue-based predictor. CONCLUSIONS: This study indicates that the epigenetic clock can be improved by increasing the training sample size and that its association with mortality attenuates with increased prediction of chronological age. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13073-019-0667-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-67081582019-08-28 Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing Zhang, Qian Vallerga, Costanza L. Walker, Rosie M. Lin, Tian Henders, Anjali K. Montgomery, Grant W. He, Ji Fan, Dongsheng Fowdar, Javed Kennedy, Martin Pitcher, Toni Pearson, John Halliday, Glenda Kwok, John B. Hickie, Ian Lewis, Simon Anderson, Tim Silburn, Peter A. Mellick, George D. Harris, Sarah E. Redmond, Paul Murray, Alison D. Porteous, David J. Haley, Christopher S. Evans, Kathryn L. McIntosh, Andrew M. Yang, Jian Gratten, Jacob Marioni, Riccardo E. Wray, Naomi R. Deary, Ian J. McRae, Allan F. Visscher, Peter M. Genome Med Research BACKGROUND: DNA methylation changes with age. Chronological age predictors built from DNA methylation are termed ‘epigenetic clocks’. The deviation of predicted age from the actual age (‘age acceleration residual’, AAR) has been reported to be associated with death. However, it is currently unclear how a better prediction of chronological age affects such association. METHODS: In this study, we build multiple predictors based on training DNA methylation samples selected from 13,661 samples (13,402 from blood and 259 from saliva). We use the Lothian Birth Cohorts of 1921 (LBC1921) and 1936 (LBC1936) to examine whether the association between AAR (from these predictors) and death is affected by (1) improving prediction accuracy of an age predictor as its training sample size increases (from 335 to 12,710) and (2) additionally correcting for confounders (i.e., cellular compositions). In addition, we investigated the performance of our predictor in non-blood tissues. RESULTS: We found that in principle, a near-perfect age predictor could be developed when the training sample size is sufficiently large. The association between AAR and mortality attenuates as prediction accuracy increases. AAR from our best predictor (based on Elastic Net, https://github.com/qzhang314/DNAm-based-age-predictor) exhibits no association with mortality in both LBC1921 (hazard ratio = 1.08, 95% CI 0.91–1.27) and LBC1936 (hazard ratio = 1.00, 95% CI 0.79–1.28). Predictors based on small sample size are prone to confounding by cellular compositions relative to those from large sample size. We observed comparable performance of our predictor in non-blood tissues with a multi-tissue-based predictor. CONCLUSIONS: This study indicates that the epigenetic clock can be improved by increasing the training sample size and that its association with mortality attenuates with increased prediction of chronological age. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13073-019-0667-1) contains supplementary material, which is available to authorized users. BioMed Central 2019-08-23 /pmc/articles/PMC6708158/ /pubmed/31443728 http://dx.doi.org/10.1186/s13073-019-0667-1 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Zhang, Qian
Vallerga, Costanza L.
Walker, Rosie M.
Lin, Tian
Henders, Anjali K.
Montgomery, Grant W.
He, Ji
Fan, Dongsheng
Fowdar, Javed
Kennedy, Martin
Pitcher, Toni
Pearson, John
Halliday, Glenda
Kwok, John B.
Hickie, Ian
Lewis, Simon
Anderson, Tim
Silburn, Peter A.
Mellick, George D.
Harris, Sarah E.
Redmond, Paul
Murray, Alison D.
Porteous, David J.
Haley, Christopher S.
Evans, Kathryn L.
McIntosh, Andrew M.
Yang, Jian
Gratten, Jacob
Marioni, Riccardo E.
Wray, Naomi R.
Deary, Ian J.
McRae, Allan F.
Visscher, Peter M.
Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing
title Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing
title_full Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing
title_fullStr Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing
title_full_unstemmed Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing
title_short Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing
title_sort improved precision of epigenetic clock estimates across tissues and its implication for biological ageing
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708158/
https://www.ncbi.nlm.nih.gov/pubmed/31443728
http://dx.doi.org/10.1186/s13073-019-0667-1
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