Impact of age-related changes in buccal epithelial cells on pediatric epigenetic biomarker research

Abstract Cheek swabs, heterogeneous samples consisting primarily of buccal epithelial cells, are widely used in pediatric DNA methylation studies and biomarker creation. However, the decrease in buccal proportion with age in adults remains unexamined in childhood. We analyzed cheek swabs from 4626 t...

Full description

Saved in:
Bibliographic Details
Main Authors: Sarah M. Merrill, Chaini Konwar, Fizza Fatima, Kristy Dever, Julia L. MacIsaac, Nicole Letourneau, Gerald F. Giesbrecht, Deborah Dewey, Gillian England-Mason, Candace R. Lewis, Dennis Wang, Ai Ling Teh, Michael J. Meaney, Andrea Gonzalez, Jennie G. Noll, Carolina De Weerth, Nicole R. Bush, Kieran J. O’Donnell, S. Evelyn Stewart, Michael S. Kobor
Format: Article
Language:English
Published: Nature Portfolio 2025-01-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-025-55909-8
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1841544415066193920
author Sarah M. Merrill
Chaini Konwar
Fizza Fatima
Kristy Dever
Julia L. MacIsaac
Nicole Letourneau
Gerald F. Giesbrecht
Deborah Dewey
Gillian England-Mason
Candace R. Lewis
Dennis Wang
Ai Ling Teh
Michael J. Meaney
Andrea Gonzalez
Jennie G. Noll
Carolina De Weerth
Nicole R. Bush
Kieran J. O’Donnell
S. Evelyn Stewart
Michael S. Kobor
author_facet Sarah M. Merrill
Chaini Konwar
Fizza Fatima
Kristy Dever
Julia L. MacIsaac
Nicole Letourneau
Gerald F. Giesbrecht
Deborah Dewey
Gillian England-Mason
Candace R. Lewis
Dennis Wang
Ai Ling Teh
Michael J. Meaney
Andrea Gonzalez
Jennie G. Noll
Carolina De Weerth
Nicole R. Bush
Kieran J. O’Donnell
S. Evelyn Stewart
Michael S. Kobor
author_sort Sarah M. Merrill
collection DOAJ
description Abstract Cheek swabs, heterogeneous samples consisting primarily of buccal epithelial cells, are widely used in pediatric DNA methylation studies and biomarker creation. However, the decrease in buccal proportion with age in adults remains unexamined in childhood. We analyzed cheek swabs from 4626 typically developing children 2-months to 20-years-old. Estimated buccal proportion declined throughout childhood with both increasing chronological and predicted epigenetic age. However, buccal proportion did not associate with age throughout adolescence. Variability in buccal proportion increased with age through the entire developmental range. These trends held inversely true for neutrophil proportions. Correcting for buccal proportion attenuated the weak association with PedBE age acceleration to non-significance during initial estimation. Notably, correcting for buccal proportion attenuated the association of PedBE age acceleration with obsessive-compulsive disorder and strengthened the association with diurnal cortisol slope. Thus, the age-related change in children’s oral cells is a crucial consideration for cell type-sensitive research.
format Article
id doaj-art-1df6ac6ab68949dabcd433fc73e31218
institution Kabale University
issn 2041-1723
language English
publishDate 2025-01-01
publisher Nature Portfolio
record_format Article
series Nature Communications
spelling doaj-art-1df6ac6ab68949dabcd433fc73e312182025-01-12T12:31:34ZengNature PortfolioNature Communications2041-17232025-01-0116111610.1038/s41467-025-55909-8Impact of age-related changes in buccal epithelial cells on pediatric epigenetic biomarker researchSarah M. Merrill0Chaini Konwar1Fizza Fatima2Kristy Dever3Julia L. MacIsaac4Nicole Letourneau5Gerald F. Giesbrecht6Deborah Dewey7Gillian England-Mason8Candace R. Lewis9Dennis Wang10Ai Ling Teh11Michael J. Meaney12Andrea Gonzalez13Jennie G. Noll14Carolina De Weerth15Nicole R. Bush16Kieran J. O’Donnell17S. Evelyn Stewart18Michael S. Kobor19Department of Psychology, University of Massachusetts LowellBritish Columbia Children’s Hospital Research Institute, University of British ColumbiaBritish Columbia Children’s Hospital Research Institute, University of British ColumbiaBritish Columbia Children’s Hospital Research Institute, University of British ColumbiaBritish Columbia Children’s Hospital Research Institute, University of British ColumbiaFaculty of Nursing and Cumming School of Medicine, Departments of Pediatrics, Community Health Sciences and Psychiatry, University of CalgaryOwerko Centre, Alberta Children’s Hospital Research Institute, University of CalgaryFaculty of Nursing and Cumming School of Medicine, Departments of Pediatrics, Community Health Sciences and Psychiatry, University of CalgaryOwerko Centre, Alberta Children’s Hospital Research Institute, University of CalgarySchool of Life Sciences, Arizona State UniversityInstitute for Human Development and Potential (IHDP), Agency for Science, Technology and Research (A*STAR)Institute for Human Development and Potential (IHDP), Agency for Science, Technology and Research (A*STAR)Institute for Human Development and Potential (IHDP), Agency for Science, Technology and Research (A*STAR)Department of Psychiatry and Behavioural Neurosciences, McMaster UniversityMount Hope Family Center and Department of Psychology, University of RochesterDonders Institute for Brain, Cognition and Behaviour and Radbound UniversityDepartment of Psychiatry and Behavioral Sciences, Department of Pediatrics, University of CaliforniaYale Child Study Center and Department of Obstetrics Gynaecology and Reproductive Sciences, Yale School of MedicineBritish Columbia Children’s Hospital Research Institute, University of British ColumbiaBritish Columbia Children’s Hospital Research Institute, University of British ColumbiaAbstract Cheek swabs, heterogeneous samples consisting primarily of buccal epithelial cells, are widely used in pediatric DNA methylation studies and biomarker creation. However, the decrease in buccal proportion with age in adults remains unexamined in childhood. We analyzed cheek swabs from 4626 typically developing children 2-months to 20-years-old. Estimated buccal proportion declined throughout childhood with both increasing chronological and predicted epigenetic age. However, buccal proportion did not associate with age throughout adolescence. Variability in buccal proportion increased with age through the entire developmental range. These trends held inversely true for neutrophil proportions. Correcting for buccal proportion attenuated the weak association with PedBE age acceleration to non-significance during initial estimation. Notably, correcting for buccal proportion attenuated the association of PedBE age acceleration with obsessive-compulsive disorder and strengthened the association with diurnal cortisol slope. Thus, the age-related change in children’s oral cells is a crucial consideration for cell type-sensitive research.https://doi.org/10.1038/s41467-025-55909-8
spellingShingle Sarah M. Merrill
Chaini Konwar
Fizza Fatima
Kristy Dever
Julia L. MacIsaac
Nicole Letourneau
Gerald F. Giesbrecht
Deborah Dewey
Gillian England-Mason
Candace R. Lewis
Dennis Wang
Ai Ling Teh
Michael J. Meaney
Andrea Gonzalez
Jennie G. Noll
Carolina De Weerth
Nicole R. Bush
Kieran J. O’Donnell
S. Evelyn Stewart
Michael S. Kobor
Impact of age-related changes in buccal epithelial cells on pediatric epigenetic biomarker research
Nature Communications
title Impact of age-related changes in buccal epithelial cells on pediatric epigenetic biomarker research
title_full Impact of age-related changes in buccal epithelial cells on pediatric epigenetic biomarker research
title_fullStr Impact of age-related changes in buccal epithelial cells on pediatric epigenetic biomarker research
title_full_unstemmed Impact of age-related changes in buccal epithelial cells on pediatric epigenetic biomarker research
title_short Impact of age-related changes in buccal epithelial cells on pediatric epigenetic biomarker research
title_sort impact of age related changes in buccal epithelial cells on pediatric epigenetic biomarker research
url https://doi.org/10.1038/s41467-025-55909-8
work_keys_str_mv AT sarahmmerrill impactofagerelatedchangesinbuccalepithelialcellsonpediatricepigeneticbiomarkerresearch
AT chainikonwar impactofagerelatedchangesinbuccalepithelialcellsonpediatricepigeneticbiomarkerresearch
AT fizzafatima impactofagerelatedchangesinbuccalepithelialcellsonpediatricepigeneticbiomarkerresearch
AT kristydever impactofagerelatedchangesinbuccalepithelialcellsonpediatricepigeneticbiomarkerresearch
AT julialmacisaac impactofagerelatedchangesinbuccalepithelialcellsonpediatricepigeneticbiomarkerresearch
AT nicoleletourneau impactofagerelatedchangesinbuccalepithelialcellsonpediatricepigeneticbiomarkerresearch
AT geraldfgiesbrecht impactofagerelatedchangesinbuccalepithelialcellsonpediatricepigeneticbiomarkerresearch
AT deborahdewey impactofagerelatedchangesinbuccalepithelialcellsonpediatricepigeneticbiomarkerresearch
AT gillianenglandmason impactofagerelatedchangesinbuccalepithelialcellsonpediatricepigeneticbiomarkerresearch
AT candacerlewis impactofagerelatedchangesinbuccalepithelialcellsonpediatricepigeneticbiomarkerresearch
AT denniswang impactofagerelatedchangesinbuccalepithelialcellsonpediatricepigeneticbiomarkerresearch
AT ailingteh impactofagerelatedchangesinbuccalepithelialcellsonpediatricepigeneticbiomarkerresearch
AT michaeljmeaney impactofagerelatedchangesinbuccalepithelialcellsonpediatricepigeneticbiomarkerresearch
AT andreagonzalez impactofagerelatedchangesinbuccalepithelialcellsonpediatricepigeneticbiomarkerresearch
AT jenniegnoll impactofagerelatedchangesinbuccalepithelialcellsonpediatricepigeneticbiomarkerresearch
AT carolinadeweerth impactofagerelatedchangesinbuccalepithelialcellsonpediatricepigeneticbiomarkerresearch
AT nicolerbush impactofagerelatedchangesinbuccalepithelialcellsonpediatricepigeneticbiomarkerresearch
AT kieranjodonnell impactofagerelatedchangesinbuccalepithelialcellsonpediatricepigeneticbiomarkerresearch
AT sevelynstewart impactofagerelatedchangesinbuccalepithelialcellsonpediatricepigeneticbiomarkerresearch
AT michaelskobor impactofagerelatedchangesinbuccalepithelialcellsonpediatricepigeneticbiomarkerresearch