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Genetic and environmental causes of variation in epigenetic aging across the lifespan

BACKGROUND: DNA methylation-based biological age (DNAm age) is an important biomarker for adult health. Studies in specific age ranges have found widely varying results about its genetic and environmental causes of variation. However, these studies are not able to provide a comprehensive view of the...

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Autores principales: Li, Shuai, Nguyen, Tuong L., Wong, Ee Ming, Dugué, Pierre-Antoine, Dite, Gillian S., Armstrong, Nicola J., Craig, Jeffrey M., Mather, Karen A., Sachdev, Perminder S., Saffery, Richard, Sung, Joohon, Tan, Qihua, Thalamuthu, Anbupalam, Milne, Roger L., Giles, Graham G., Southey, Melissa C., Hopper, John L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7583207/
https://www.ncbi.nlm.nih.gov/pubmed/33092643
http://dx.doi.org/10.1186/s13148-020-00950-1
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author Li, Shuai
Nguyen, Tuong L.
Wong, Ee Ming
Dugué, Pierre-Antoine
Dite, Gillian S.
Armstrong, Nicola J.
Craig, Jeffrey M.
Mather, Karen A.
Sachdev, Perminder S.
Saffery, Richard
Sung, Joohon
Tan, Qihua
Thalamuthu, Anbupalam
Milne, Roger L.
Giles, Graham G.
Southey, Melissa C.
Hopper, John L.
author_facet Li, Shuai
Nguyen, Tuong L.
Wong, Ee Ming
Dugué, Pierre-Antoine
Dite, Gillian S.
Armstrong, Nicola J.
Craig, Jeffrey M.
Mather, Karen A.
Sachdev, Perminder S.
Saffery, Richard
Sung, Joohon
Tan, Qihua
Thalamuthu, Anbupalam
Milne, Roger L.
Giles, Graham G.
Southey, Melissa C.
Hopper, John L.
author_sort Li, Shuai
collection PubMed
description BACKGROUND: DNA methylation-based biological age (DNAm age) is an important biomarker for adult health. Studies in specific age ranges have found widely varying results about its genetic and environmental causes of variation. However, these studies are not able to provide a comprehensive view of the causes of variation over the lifespan. RESULTS: In order to investigate the genetic and environmental causes of DNAm age variation across the lifespan, we pooled genome-wide DNA methylation data for 4217 people aged 0–92 years from 1871 families. DNAm age was calculated using the Horvath epigenetic clock. We estimated familial correlations in DNAm age for monozygotic (MZ) twin, dizygotic (DZ) twin, sibling, parent–offspring, and spouse pairs by cohabitation status. Genetic and environmental variance components models were fitted and compared. We found that twin pair correlations were − 0.12 to 0.18 around birth, not different from zero (all P > 0.29). For all pairs of relatives, their correlations increased with time spent living together (all P < 0.02) at different rates (MZ > DZ and siblings > parent–offspring; P < 0.001) and decreased with time spent living apart (P = 0.02) at similar rates. These correlation patterns were best explained by cohabitation-dependent shared environmental factors, the effects of which were 1.41 (95% confidence interval [CI] 1.16 to 1.66) times greater for MZ pairs than for DZ and sibling pairs, and the latter were 2.03 (95% CI 1.13 to 9.47) times greater than for parent–offspring pairs. Genetic factors explained 13% (95% CI − 10 to 35%) of variation (P = 0.27). Similar results were found for another two epigenetic clocks, suggesting that our observations are robust to how DNAm age is measured. In addition, results for the other clocks were consistent with there also being a role for prenatal environmental factors in determining their variation. CONCLUSIONS: Variation in DNAm age is mostly caused by environmental factors, including those shared to different extents by relatives while living together and whose effects persist into old age. The equal environment assumption of the classic twin study might not hold for epigenetic aging.
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spelling pubmed-75832072020-10-26 Genetic and environmental causes of variation in epigenetic aging across the lifespan Li, Shuai Nguyen, Tuong L. Wong, Ee Ming Dugué, Pierre-Antoine Dite, Gillian S. Armstrong, Nicola J. Craig, Jeffrey M. Mather, Karen A. Sachdev, Perminder S. Saffery, Richard Sung, Joohon Tan, Qihua Thalamuthu, Anbupalam Milne, Roger L. Giles, Graham G. Southey, Melissa C. Hopper, John L. Clin Epigenetics Research BACKGROUND: DNA methylation-based biological age (DNAm age) is an important biomarker for adult health. Studies in specific age ranges have found widely varying results about its genetic and environmental causes of variation. However, these studies are not able to provide a comprehensive view of the causes of variation over the lifespan. RESULTS: In order to investigate the genetic and environmental causes of DNAm age variation across the lifespan, we pooled genome-wide DNA methylation data for 4217 people aged 0–92 years from 1871 families. DNAm age was calculated using the Horvath epigenetic clock. We estimated familial correlations in DNAm age for monozygotic (MZ) twin, dizygotic (DZ) twin, sibling, parent–offspring, and spouse pairs by cohabitation status. Genetic and environmental variance components models were fitted and compared. We found that twin pair correlations were − 0.12 to 0.18 around birth, not different from zero (all P > 0.29). For all pairs of relatives, their correlations increased with time spent living together (all P < 0.02) at different rates (MZ > DZ and siblings > parent–offspring; P < 0.001) and decreased with time spent living apart (P = 0.02) at similar rates. These correlation patterns were best explained by cohabitation-dependent shared environmental factors, the effects of which were 1.41 (95% confidence interval [CI] 1.16 to 1.66) times greater for MZ pairs than for DZ and sibling pairs, and the latter were 2.03 (95% CI 1.13 to 9.47) times greater than for parent–offspring pairs. Genetic factors explained 13% (95% CI − 10 to 35%) of variation (P = 0.27). Similar results were found for another two epigenetic clocks, suggesting that our observations are robust to how DNAm age is measured. In addition, results for the other clocks were consistent with there also being a role for prenatal environmental factors in determining their variation. CONCLUSIONS: Variation in DNAm age is mostly caused by environmental factors, including those shared to different extents by relatives while living together and whose effects persist into old age. The equal environment assumption of the classic twin study might not hold for epigenetic aging. BioMed Central 2020-10-22 /pmc/articles/PMC7583207/ /pubmed/33092643 http://dx.doi.org/10.1186/s13148-020-00950-1 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research
Li, Shuai
Nguyen, Tuong L.
Wong, Ee Ming
Dugué, Pierre-Antoine
Dite, Gillian S.
Armstrong, Nicola J.
Craig, Jeffrey M.
Mather, Karen A.
Sachdev, Perminder S.
Saffery, Richard
Sung, Joohon
Tan, Qihua
Thalamuthu, Anbupalam
Milne, Roger L.
Giles, Graham G.
Southey, Melissa C.
Hopper, John L.
Genetic and environmental causes of variation in epigenetic aging across the lifespan
title Genetic and environmental causes of variation in epigenetic aging across the lifespan
title_full Genetic and environmental causes of variation in epigenetic aging across the lifespan
title_fullStr Genetic and environmental causes of variation in epigenetic aging across the lifespan
title_full_unstemmed Genetic and environmental causes of variation in epigenetic aging across the lifespan
title_short Genetic and environmental causes of variation in epigenetic aging across the lifespan
title_sort genetic and environmental causes of variation in epigenetic aging across the lifespan
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7583207/
https://www.ncbi.nlm.nih.gov/pubmed/33092643
http://dx.doi.org/10.1186/s13148-020-00950-1
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