Meta-analyses identify DNA methylation associated with kidney function and damage.

Journal Article (Journal Article)

Chronic kidney disease is a major public health burden. Elevated urinary albumin-to-creatinine ratio is a measure of kidney damage, and used to diagnose and stage chronic kidney disease. To extend the knowledge on regulatory mechanisms related to kidney function and disease, we conducted a blood-based epigenome-wide association study for estimated glomerular filtration rate (n = 33,605) and urinary albumin-to-creatinine ratio (n = 15,068) and detected 69 and seven CpG sites where DNA methylation was associated with the respective trait. The majority of these findings showed directionally consistent associations with the respective clinical outcomes chronic kidney disease and moderately increased albuminuria. Associations of DNA methylation with kidney function, such as CpGs at JAZF1, PELI1 and CHD2 were validated in kidney tissue. Methylation at PHRF1, LDB2, CSRNP1 and IRF5 indicated causal effects on kidney function. Enrichment analyses revealed pathways related to hemostasis and blood cell migration for estimated glomerular filtration rate, and immune cell activation and response for urinary albumin-to-creatinineratio-associated CpGs.

Full Text

Duke Authors

Cited Authors

  • Schlosser, P; Tin, A; Matias-Garcia, PR; Thio, CHL; Joehanes, R; Liu, H; Weihs, A; Yu, Z; Hoppmann, A; Grundner-Culemann, F; Min, JL; Adeyemo, AA; Agyemang, C; Ärnlöv, J; Aziz, NA; Baccarelli, A; Bochud, M; Brenner, H; Breteler, MMB; Carmeli, C; Chaker, L; Chambers, JC; Cole, SA; Coresh, J; Corre, T; Correa, A; Cox, SR; de Klein, N; Delgado, GE; Domingo-Relloso, A; Eckardt, K-U; Ekici, AB; Endlich, K; Evans, KL; Floyd, JS; Fornage, M; Franke, L; Fraszczyk, E; Gao, X; Gào, X; Ghanbari, M; Ghasemi, S; Gieger, C; Greenland, P; Grove, ML; Harris, SE; Hemani, G; Henneman, P; Herder, C; Horvath, S; Hou, L; Hurme, MA; Hwang, S-J; Jarvelin, M-R; Kardia, SLR; Kasela, S; Kleber, ME; Koenig, W; Kooner, JS; Kramer, H; Kronenberg, F; Kühnel, B; Lehtimäki, T; Lind, L; Liu, D; Liu, Y; Lloyd-Jones, DM; Lohman, K; Lorkowski, S; Lu, AT; Marioni, RE; März, W; McCartney, DL; Meeks, KAC; Milani, L; Mishra, PP; Nauck, M; Navas-Acien, A; Nowak, C; Peters, A; Prokisch, H; Psaty, BM; Raitakari, OT; Ratliff, SM; Reiner, AP; Rosas, SE; Schöttker, B; Schwartz, J; Sedaghat, S; Smith, JA; Sotoodehnia, N; Stocker, HR; Stringhini, S; Sundström, J; Swenson, BR; Tellez-Plaza, M; van Meurs, JBJ; van Vliet-Ostaptchouk, JV; Venema, A; Verweij, N; Walker, RM; Wielscher, M; Winkelmann, J; Wolffenbuttel, BHR; Zhao, W; Zheng, Y; Estonian Biobank Research Team, ; Genetics of DNA Methylation Consortium, ; Loh, M; Snieder, H; Levy, D; Waldenberger, M; Susztak, K; Köttgen, A; Teumer, A

Published Date

  • December 9, 2021

Published In

Volume / Issue

  • 12 / 1

Start / End Page

  • 7174 -

PubMed ID

  • 34887417

Pubmed Central ID

  • PMC8660832

Electronic International Standard Serial Number (EISSN)

  • 2041-1723

Digital Object Identifier (DOI)

  • 10.1038/s41467-021-27234-3

Language

  • eng

Conference Location

  • England