Consistent cord blood DNA methylation signatures of gestational age between South Asian and white European cohorts.


Journal

Clinical epigenetics
ISSN: 1868-7083
Titre abrégé: Clin Epigenetics
Pays: Germany
ID NLM: 101516977

Informations de publication

Date de publication:
06 Jun 2024
Historique:
received: 28 02 2024
accepted: 23 05 2024
medline: 6 6 2024
pubmed: 6 6 2024
entrez: 5 6 2024
Statut: epublish

Résumé

Epigenetic modifications, particularly DNA methylation (DNAm) in cord blood, are an important biological marker of how external exposures during gestation can influence the in-utero environment and subsequent offspring development. Despite the recognized importance of DNAm during gestation, comparative studies to determine the consistency of these epigenetic signals across different ethnic groups are largely absent. To address this gap, we first performed epigenome-wide association studies (EWAS) of gestational age (GA) using newborn cord blood DNAm comparatively in a white European (n = 342) and a South Asian (n = 490) birth cohort living in Canada. Then, we capitalized on established cord blood epigenetic GA clocks to examine the associations between maternal exposures, offspring characteristics and epigenetic GA, as well as GA acceleration, defined as the residual difference between epigenetic and chronological GA at birth. Individual EWASs confirmed 1,211 and 1,543 differentially methylated CpGs previously reported to be associated with GA, in white European and South Asian cohorts, respectively, with a similar distribution of effects. We confirmed that Bohlin's cord blood GA clock was robustly correlated with GA in white Europeans (r = 0.71; p = 6.0 × 10 These results demonstrate the consistent DNAm signatures of GA and the utility of Bohlin's GA clock across the two populations. Although the overall pattern of DNAm is similar, its connections with the mother's environment and the baby's anthropometrics can differ between the two groups. Further research is needed to understand these unique relationships.

Sections du résumé

BACKGROUND BACKGROUND
Epigenetic modifications, particularly DNA methylation (DNAm) in cord blood, are an important biological marker of how external exposures during gestation can influence the in-utero environment and subsequent offspring development. Despite the recognized importance of DNAm during gestation, comparative studies to determine the consistency of these epigenetic signals across different ethnic groups are largely absent. To address this gap, we first performed epigenome-wide association studies (EWAS) of gestational age (GA) using newborn cord blood DNAm comparatively in a white European (n = 342) and a South Asian (n = 490) birth cohort living in Canada. Then, we capitalized on established cord blood epigenetic GA clocks to examine the associations between maternal exposures, offspring characteristics and epigenetic GA, as well as GA acceleration, defined as the residual difference between epigenetic and chronological GA at birth.
RESULTS RESULTS
Individual EWASs confirmed 1,211 and 1,543 differentially methylated CpGs previously reported to be associated with GA, in white European and South Asian cohorts, respectively, with a similar distribution of effects. We confirmed that Bohlin's cord blood GA clock was robustly correlated with GA in white Europeans (r = 0.71; p = 6.0 × 10
CONCLUSIONS CONCLUSIONS
These results demonstrate the consistent DNAm signatures of GA and the utility of Bohlin's GA clock across the two populations. Although the overall pattern of DNAm is similar, its connections with the mother's environment and the baby's anthropometrics can differ between the two groups. Further research is needed to understand these unique relationships.

Identifiants

pubmed: 38840168
doi: 10.1186/s13148-024-01684-0
pii: 10.1186/s13148-024-01684-0
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

74

Subventions

Organisme : CIHR
ID : MWG-146332
Pays : Canada
Organisme : CIHR
ID : MWG-146332
Pays : Canada
Organisme : CIHR
ID : MWG-146332
Pays : Canada
Organisme : CIHR
ID : MWG-146332
Pays : Canada

Informations de copyright

© 2024. The Author(s).

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Auteurs

Wei Q Deng (WQ)

Peter Boris Centre for Addictions Research, St. Joseph's Healthcare Hamilton, Hamilton, Canada. dengwq@mcmaster.ca.
Department of Psychiatry and Behavioural Neurosciences, McMaster University, Hamilton, Canada. dengwq@mcmaster.ca.
Department of Medicine, Faculty of Health Sciences, McMaster University, Hamilton, Canada. dengwq@mcmaster.ca.

Marie Pigeyre (M)

Department of Medicine, Faculty of Health Sciences, McMaster University, Hamilton, Canada.
Population Health Research Institute, David Braley Cardiac, Vascular and Stroke Research Institute, Hamilton, Canada.
Thrombosis and Atherosclerosis Research Institute, David Braley Cardiac, Vascular and Stroke Research Institute, Hamilton, ON, Canada.

Sandi M Azab (SM)

Department of Medicine, Faculty of Health Sciences, McMaster University, Hamilton, Canada.
Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Canada.

Samantha L Wilson (SL)

Department of Obstetrics and Gynecology, McMaster University, Hamilton, Canada.

Natalie Campbell (N)

Department of Medicine, Faculty of Health Sciences, McMaster University, Hamilton, Canada.

Nathan Cawte (N)

Population Health Research Institute, David Braley Cardiac, Vascular and Stroke Research Institute, Hamilton, Canada.

Katherine M Morrison (KM)

Department of Pediatrics, McMaster University, Hamilton, Canada.

Stephanie A Atkinson (SA)

Department of Pediatrics, McMaster University, Hamilton, Canada.

Padmaja Subbarao (P)

Department of Medicine, Faculty of Health Sciences, McMaster University, Hamilton, Canada.
Hospital for Sick Children, Department of Pediatrics, University of Toronto, Toronto, Canada.
Program in Translational Medicine, SickKids Research Institute, Toronto, Canada.

Stuart E Turvey (SE)

Department of Pediatrics, BC Children's Hospital, The University of British Columbia, Vancouver, Canada.

Theo J Moraes (TJ)

Hospital for Sick Children, Department of Pediatrics, University of Toronto, Toronto, Canada.
Program in Translational Medicine, SickKids Research Institute, Toronto, Canada.

Piush Mandhane (P)

Department of Pediatrics, University of Alberta, Edmonton, Canada.

Meghan B Azad (MB)

Department of Pediatrics and Child Health, Children's Hospital Research Institute of Manitoba, University of Manitoba, Winnipeg, Canada.

Elinor Simons (E)

Section of Allergy and Immunology, Department of Pediatrics and Child Health, University of Manitoba, Winnipeg, Canada.

Guillaume Pare (G)

Population Health Research Institute, David Braley Cardiac, Vascular and Stroke Research Institute, Hamilton, Canada.
Thrombosis and Atherosclerosis Research Institute, David Braley Cardiac, Vascular and Stroke Research Institute, Hamilton, ON, Canada.
Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Canada.
Department of Pathology and Molecular Medicine, Michael G. DeGroote School of Medicine, McMaster University, Hamilton, Canada.

Sonia S Anand (SS)

Department of Medicine, Faculty of Health Sciences, McMaster University, Hamilton, Canada. anands@mcmaster.ca.
Population Health Research Institute, David Braley Cardiac, Vascular and Stroke Research Institute, Hamilton, Canada. anands@mcmaster.ca.
Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Canada. anands@mcmaster.ca.

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