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Epigenome-wide meta-analysis identifies DNA methylation biomarkers associated with diabetic kidney disease.

Authors :
Smyth, Laura J.
Dahlström, Emma H.
Syreeni, Anna
Kerr, Katie
Kilner, Jill
Doyle, Ross
Brennan, Eoin
Nair, Viji
Fermin, Damian
Nelson, Robert G.
Looker, Helen C.
Wooster, Christopher
Andrews, Darrell
Anderson, Kerry
McKay, Gareth J.
Cole, Joanne B.
Salem, Rany M.
Conlon, Peter J.
Kretzler, Matthias
Hirschhorn, Joel N.
Source :
Nature Communications; 12/22/2022, Vol. 13 Issue 1, p1-16, 16p
Publication Year :
2022

Abstract

Type 1 diabetes affects over nine million individuals globally, with approximately 40% developing diabetic kidney disease. Emerging evidence suggests that epigenetic alterations, such as DNA methylation, are involved in diabetic kidney disease. Here we assess differences in blood-derived genome-wide DNA methylation associated with diabetic kidney disease in 1304 carefully characterised individuals with type 1 diabetes and known renal status from two cohorts in the United Kingdom-Republic of Ireland and Finland. In the meta-analysis, we identify 32 differentially methylated CpGs in diabetic kidney disease in type 1 diabetes, 18 of which are located within genes differentially expressed in kidneys or correlated with pathological traits in diabetic kidney disease. We show that methylation at 21 of the 32 CpGs predict the development of kidney failure, extending the knowledge and potentially identifying individuals at greater risk for diabetic kidney disease in type 1 diabetes. Approximately 40 percent of people with type 1 diabetes develop kidney disease, but the risk factors are not well understood. Here, the authors identify DNA methylation signatures associated with diabetic kidney disease, of which 21 biomarkers predict the development of kidney failure. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20411723
Volume :
13
Issue :
1
Database :
Complementary Index
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
160936969
Full Text :
https://doi.org/10.1038/s41467-022-34963-6