Epigenetic scores for the circulating proteome as tools for disease prediction

Danni A. Gadd(Edinburgh Cancer Research), Robert F. Hillary(Edinburgh Cancer Research), Daniel L. McCartney(Edinburgh Cancer Research), Shaza B. Zaghlool(Weill Cornell Medical College in Qatar), Anna J. Stevenson(Edinburgh Cancer Research), Yipeng Cheng(Edinburgh Cancer Research), Chloe Fawns‐Ritchie(Edinburgh Cancer Research), Clifford Nangle(Edinburgh Cancer Research), Archie Campbell(Edinburgh Cancer Research), Robin Flaig(Edinburgh Cancer Research), Sarah E. Harris(NHS Lothian), Rosie M. Walker(University of Edinburgh), Liu Shi(University of Oxford), Elliot M. Tucker–Drob(The University of Texas at Austin), Christian Gieger(Center for Environmental Health), Annette Peters(Center for Environmental Health), Mélanie Waldenberger(Center for Environmental Health), Johannes Graumann(Max Planck Institute for Heart and Lung Research), Allan F. McRae(The University of Queensland), Ian J. Deary(NHS Lothian), David J. Porteous(Edinburgh Cancer Research), Caroline Hayward(Edinburgh Cancer Research), Peter M. Visscher(The University of Queensland), Simon R Cox(NHS Lothian), Kathryn L. Evans(Edinburgh Cancer Research), Andrew M. McIntosh(Royal Edinburgh Hospital), Karsten Suhre(Weill Cornell Medical College in Qatar), Riccardo E. Marioni(Edinburgh Cancer Research)
eLife
January 13, 2022
Cited by 137Open Access
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Abstract

Protein biomarkers have been identified across many age-related morbidities. However, characterising epigenetic influences could further inform disease predictions. Here, we leverage epigenome-wide data to study links between the DNA methylation (DNAm) signatures of the circulating proteome and incident diseases. Using data from four cohorts, we trained and tested epigenetic scores (EpiScores) for 953 plasma proteins, identifying 109 scores that explained between 1% and 58% of the variance in protein levels after adjusting for known protein quantitative trait loci (pQTL) genetic effects. By projecting these EpiScores into an independent sample (Generation Scotland; n = 9537) and relating them to incident morbidities over a follow-up of 14 years, we uncovered 137 EpiScore-disease associations. These associations were largely independent of immune cell proportions, common lifestyle and health factors, and biological aging. Notably, we found that our diabetes-associated EpiScores highlighted previous top biomarker associations from proteome-wide assessments of diabetes. These EpiScores for protein levels can therefore be a valuable resource for disease prediction and risk stratification.


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