DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases.

Wielscher, MORCID logo; Mandaviya, PR; Kuehnel, B; Joehanes, R; Mustafa, RORCID logo; Robinson, OORCID logo; Zhang, Y; Bodinier, BORCID logo; Walton, EORCID logo; Mishra, PP; +80 more...Schlosser, PORCID logo; Wilson, RORCID logo; Tsai, P; Palaniswamy, SORCID logo; Marioni, RE; Fiorito, G; Cugliari, G; Karhunen, VORCID logo; Ghanbari, MORCID logo; Psaty, BMORCID logo; Loh, MORCID logo; Bis, JCORCID logo; Lehne, B; Sotoodehnia, N; Deary, IJ; Chadeau-Hyam, MORCID logo; Brody, JAORCID logo; Cardona, AORCID logo; Selvin, E; Smith, AKORCID logo; Miller, AHORCID logo; Torres, MA; Marouli, EORCID logo; Gào, XORCID logo; van Meurs, JB; Graf-Schindler, J; Rathmann, W; Koenig, WORCID logo; Peters, AORCID logo; Weninger, W; Farlik, MORCID logo; Zhang, T; Chen, WORCID logo; Xia, YORCID logo; Teumer, AORCID logo; Nauck, MORCID logo; Grabe, HJ; Doerr, MORCID logo; Lehtimäki, TORCID logo; Guan, W; Milani, LORCID logo; Tanaka, T; Fisher, KORCID logo; Waite, LL; Kasela, S; Vineis, P; Verweij, N; van der Harst, PORCID logo; Iacoviello, L; Sacerdote, C; Panico, S; Krogh, VORCID logo; Tumino, R; Tzala, E; Matullo, G; Hurme, MA; Raitakari, OT; Colicino, E; Baccarelli, AA; Kähönen, M; Herzig, KORCID logo; Li, SORCID logo; BIOS consortium; Conneely, KN; Kooner, JS; Köttgen, AORCID logo; Heijmans, BTORCID logo; Deloukas, PORCID logo; Relton, CORCID logo; Ong, KKORCID logo; Bell, JTORCID logo; Boerwinkle, E; Elliott, PORCID logo; Brenner, HORCID logo; Beekman, MORCID logo; Levy, D; Waldenberger, MORCID logo; Chambers, JCORCID logo; Dehghan, AORCID logo; Järvelin, MORCID logo and (2022) DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases. Nature communications, 13 (1). 2408-. ISSN 2041-1723 DOI: 10.1038/s41467-022-29792-6
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We performed a multi-ethnic Epigenome Wide Association study on 22,774 individuals to describe the DNA methylation signature of chronic low-grade inflammation as measured by C-Reactive protein (CRP). We find 1,511 independent differentially methylated loci associated with CRP. These CpG sites show correlation structures across chromosomes, and are primarily situated in euchromatin, depleted in CpG islands. These genomic loci are predominantly situated in transcription factor binding sites and genomic enhancer regions. Mendelian randomization analysis suggests altered CpG methylation is a consequence of increased blood CRP levels. Mediation analysis reveals obesity and smoking as important underlying driving factors for changed CpG methylation. Finally, we find that an activated CpG signature significantly increases the risk for cardiometabolic diseases and COPD.


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