Sex-Specific DNA Methylation in Saliva from the Multi-Ethnic Future of Families and Child Wellbeing Study
-
2024/01/01
-
Details
-
Personal Author:Bakulski KM ; Dou JF ; Fisher JD ; Mitchell C ; Notterman DA ; Reiner A ; Schneper L ; Ware EB ; Zawistowski M
-
Description:The prevalence and severity of many diseases differs by sex, potentially due to sex-specific patterns in DNA methylation. Autosomal sex-specific differences in DNA methylation have been observed in cord blood and placental tissue but are not well studied in saliva or in diverse populations. We sought to characterize sex-specific DNA methylation on autosomal chromosomes in saliva samples from children in the Future of Families and Child Wellbeing Study, a multi-ethnic prospective birth cohort containing an oversampling of Black, Hispanic and low-income families. DNA methylation from saliva samples was analysed on 796 children (50.6% male) at both ages 9 and 15 with DNA methylation measured using the Illumina HumanMethylation 450k array. An epigenome-wide association analysis of the age 9 samples identified 8,430 sex-differentiated autosomal DNA methylation sites (P < 2.4 × 10-7), of which 76.2% had higher DNA methylation in female children. The strongest sex-difference was in the cg26921482 probe, in the AMDHD2 gene, with 30.6% higher DNA methylation in female compared to male children (P < 1 × 10-300). Treating the age 15 samples as an internal replication set, we observed highly consistent results between the ages 9 and 15 measurements, indicating stable and replicable sex-differentiation. Further, we directly compared our results to previously published DNA methylation sex differences in both cord blood and saliva and again found strong consistency. Our findings support widespread and robust sex-differential DNA methylation across age, human tissues, and populations. These findings help inform our understanding of potential biological processes contributing to sex differences in human physiology and disease. [Description provided by NIOSH]
-
Subjects:
-
Keywords:
-
ISSN:1559-2294
-
Document Type:
-
Funding:
-
Genre:
-
Place as Subject:
-
CIO:
-
Topic:
-
Location:
-
Volume:18
-
Issue:1
-
NIOSHTIC Number:nn:20070591
-
Citation:Epigenetics 2024 Jan; 18(1):2222244
-
Contact Point Address:Erin B. Ware, Survey Research Center, Institute for Social Research, University of Michigan, 426 Thompson St, Ann Arbor, Michigan, MI 48104, USA
-
Email:ebakshis@umich.edu
-
Federal Fiscal Year:2024
-
Performing Organization:University of Michigan, Ann Arbor
-
Peer Reviewed:True
-
Start Date:20050701
-
Source Full Name:Epigenetics
-
End Date:20280630
-
Collection(s):
-
Main Document Checksum:urn:sha-512:b39c33f4451a9a4c2e2986030313964dbedf624f033c74d3dbb59933dedfe9edca36c16fefa4cc1839c4c8cbe93ebe7d71abdd19b26e23fbaa8ca797e97e8289
-
Download URL:
-
File Type:
ON THIS PAGE
CDC STACKS serves as an archival repository of CDC-published products including
scientific findings,
journal articles, guidelines, recommendations, or other public health information authored or
co-authored by CDC or funded partners.
As a repository, CDC STACKS retains documents in their original published format to ensure public access to scientific information.
As a repository, CDC STACKS retains documents in their original published format to ensure public access to scientific information.
You May Also Like