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DNA methylation signatures associated with cardiometabolic risk factors in children from India and The Gambia: results from the EMPHASIS study.

Authors :
Antoun E
Issarapu P
di Gravio C
Shrestha S
Betts M
Saffari A
Sahariah SA
Sankareswaran A
Arumalla M
Prentice AM
Fall CHD
Silver MJ
Chandak GR
Lillycrop KA
Source :
Clinical epigenetics [Clin Epigenetics] 2022 Jan 09; Vol. 14 (1), pp. 6. Date of Electronic Publication: 2022 Jan 09.
Publication Year :
2022

Abstract

Background: The prevalence of cardiometabolic disease (CMD) is rising globally, with environmentally induced epigenetic changes suggested to play a role. Few studies have investigated epigenetic associations with CMD risk factors in children from low- and middle-income countries. We sought to identify associations between DNA methylation (DNAm) and CMD risk factors in children from India and The Gambia.<br />Results: Using the Illumina Infinium HumanMethylation 850 K Beadchip array, we interrogated DNAm in 293 Gambian (7-9 years) and 698 Indian (5-7 years) children. We identified differentially methylated CpGs (dmCpGs) associated with systolic blood pressure, fasting insulin, triglycerides and LDL-Cholesterol in the Gambian children; and with insulin sensitivity, insulinogenic index and HDL-Cholesterol in the Indian children. There was no overlap of the dmCpGs between the cohorts. Meta-analysis identified dmCpGs associated with insulin secretion and pulse pressure that were different from cohort-specific dmCpGs. Several differentially methylated regions were associated with diastolic blood pressure, insulin sensitivity and fasting glucose, but these did not overlap with the dmCpGs. We identified significant cis-methQTLs at three LDL-Cholesterol-associated dmCpGs in Gambians; however, methylation did not mediate genotype effects on the CMD outcomes.<br />Conclusion: This study identified cardiometabolic biomarkers associated with differential DNAm in Indian and Gambian children. Most associations were cohort specific, potentially reflecting environmental and ethnic differences.<br /> (© 2022. The Author(s).)

Details

Language :
English
ISSN :
1868-7083
Volume :
14
Issue :
1
Database :
MEDLINE
Journal :
Clinical epigenetics
Publication Type :
Academic Journal
Accession number :
35000590
Full Text :
https://doi.org/10.1186/s13148-021-01213-3