Identifying epigenetic aging moderators using the epigenetic pacemaker

Epigenetic clocks are DNA methylation-based chronological age prediction models that are commonly employed to study age-related biology. The difference between the predicted and observed age is often interpreted as a form of biological age acceleration, and many studies have measured the impact of e...

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Main Authors: Colin Farrell, Chanyue Hu, Kalsuda Lapborisuth, Kyle Pu, Sagi Snir, Matteo Pellegrini
Format: Article
Language:English
Published: Frontiers Media S.A. 2024-01-01
Series:Frontiers in Bioinformatics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fbinf.2023.1308680/full
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author Colin Farrell
Chanyue Hu
Kalsuda Lapborisuth
Kyle Pu
Sagi Snir
Matteo Pellegrini
author_facet Colin Farrell
Chanyue Hu
Kalsuda Lapborisuth
Kyle Pu
Sagi Snir
Matteo Pellegrini
author_sort Colin Farrell
collection DOAJ
description Epigenetic clocks are DNA methylation-based chronological age prediction models that are commonly employed to study age-related biology. The difference between the predicted and observed age is often interpreted as a form of biological age acceleration, and many studies have measured the impact of environmental and disease-associated factors on epigenetic age. Most epigenetic clocks are fit using approaches that minimize the error between the predicted and observed chronological age, and as a result, they may not accurately model the impact of factors that moderate the relationship between the actual and epigenetic age. Here, we compare epigenetic clocks that are constructed using penalized regression methods to an evolutionary framework of epigenetic aging with the epigenetic pacemaker (EPM), which directly models DNA methylation as a function of a time-dependent epigenetic state. In simulations, we show that the value of the epigenetic state is impacted by factors such as age, sex, and cell-type composition. Next, in a dataset aggregated from previous studies, we show that the epigenetic state is also moderated by sex and the cell type. Finally, we demonstrate that the epigenetic state is also moderated by toxins in a study on polybrominated biphenyl exposure. Thus, we find that the pacemaker provides a robust framework for the study of factors that impact epigenetic age acceleration and that the effect of these factors may be obscured in traditional clocks based on linear regression models.
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spelling doaj.art-7993b398fa074937a0b107b14bc31d892024-01-03T04:34:42ZengFrontiers Media S.A.Frontiers in Bioinformatics2673-76472024-01-01310.3389/fbinf.2023.13086801308680Identifying epigenetic aging moderators using the epigenetic pacemakerColin Farrell0Chanyue Hu1Kalsuda Lapborisuth2Kyle Pu3Sagi Snir4Matteo Pellegrini5Department of Molecular, Cell and Developmental Biology, University of California, Los Angeles, Los Angeles, CA, United StatesDepartment of Molecular, Cell and Developmental Biology, University of California, Los Angeles, Los Angeles, CA, United StatesDepartment of Molecular, Cell and Developmental Biology, University of California, Los Angeles, Los Angeles, CA, United StatesDepartment of Molecular, Cell and Developmental Biology, University of California, Los Angeles, Los Angeles, CA, United StatesDepartment of Evolutionary Biology, University of Haifa, Haifa, IsraelDepartment of Molecular, Cell and Developmental Biology, University of California, Los Angeles, Los Angeles, CA, United StatesEpigenetic clocks are DNA methylation-based chronological age prediction models that are commonly employed to study age-related biology. The difference between the predicted and observed age is often interpreted as a form of biological age acceleration, and many studies have measured the impact of environmental and disease-associated factors on epigenetic age. Most epigenetic clocks are fit using approaches that minimize the error between the predicted and observed chronological age, and as a result, they may not accurately model the impact of factors that moderate the relationship between the actual and epigenetic age. Here, we compare epigenetic clocks that are constructed using penalized regression methods to an evolutionary framework of epigenetic aging with the epigenetic pacemaker (EPM), which directly models DNA methylation as a function of a time-dependent epigenetic state. In simulations, we show that the value of the epigenetic state is impacted by factors such as age, sex, and cell-type composition. Next, in a dataset aggregated from previous studies, we show that the epigenetic state is also moderated by sex and the cell type. Finally, we demonstrate that the epigenetic state is also moderated by toxins in a study on polybrominated biphenyl exposure. Thus, we find that the pacemaker provides a robust framework for the study of factors that impact epigenetic age acceleration and that the effect of these factors may be obscured in traditional clocks based on linear regression models.https://www.frontiersin.org/articles/10.3389/fbinf.2023.1308680/fullepigeneticagingepigenetic clockDNA methylationepigenome
spellingShingle Colin Farrell
Chanyue Hu
Kalsuda Lapborisuth
Kyle Pu
Sagi Snir
Matteo Pellegrini
Identifying epigenetic aging moderators using the epigenetic pacemaker
Frontiers in Bioinformatics
epigenetic
aging
epigenetic clock
DNA methylation
epigenome
title Identifying epigenetic aging moderators using the epigenetic pacemaker
title_full Identifying epigenetic aging moderators using the epigenetic pacemaker
title_fullStr Identifying epigenetic aging moderators using the epigenetic pacemaker
title_full_unstemmed Identifying epigenetic aging moderators using the epigenetic pacemaker
title_short Identifying epigenetic aging moderators using the epigenetic pacemaker
title_sort identifying epigenetic aging moderators using the epigenetic pacemaker
topic epigenetic
aging
epigenetic clock
DNA methylation
epigenome
url https://www.frontiersin.org/articles/10.3389/fbinf.2023.1308680/full
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