Eleven genomic loci affect plasma levels of chronic inflammation marker soluble urokinase-type plasminogen activator receptor

Soluble urokinase-type plasminogen activator receptor (suPAR) is a chronic inflammation marker associated with the development of a range of diseases, including cancer and cardiovascular disease. The genetics of suPAR remain unexplored but may shed light on the biology of the marker and its connecti...

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Published in:Communications Biology
Main Authors: Dowsett, Joseph, Ferkingstad, Egil, Rasmussen, Line Jee Hartmann, Thørner, Lise Wegner, Magnússon, Magnús K., Sugden, Karen, Thorleifsson, Gudmar, Frigge, Mike, Burgdorf, Kristoffer Sølvsten, Ostrowski, Sisse Rye, Sørensen, Erik, Erikstrup, Christian, Pedersen, Ole Birger, Hansen, Thomas Folkmann, Banasik, Karina, Brunak, Søren, Tragante, Vinicius, Lund, Sigrun Helga, Stefansdottir, Lilja, Gunnarson, Bjarni, Poulton, Richie, Arseneault, Louise, Caspi, Avshalom, Moffitt, Terrie E., Gudbjartsson, Daníel, Eugen-Olsen, Jesper, Stefánsson, Hreinn, Stefánsson, Kári, Ullum, Henrik
Format: Text
Language:English
Published: Nature Publishing Group UK 2021
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Article
Iceland
Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8172928/
http://www.ncbi.nlm.nih.gov/pubmed/34079037
https://doi.org/10.1038/s42003-021-02144-8
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Summary:Soluble urokinase-type plasminogen activator receptor (suPAR) is a chronic inflammation marker associated with the development of a range of diseases, including cancer and cardiovascular disease. The genetics of suPAR remain unexplored but may shed light on the biology of the marker and its connection to outcomes. We report a heritability estimate of 60% for the variation in suPAR and performed a genome-wide association meta-analysis on suPAR levels measured in Iceland (N = 35,559) and in Denmark (N = 12,177). We identified 13 independently genome-wide significant sequence variants associated with suPAR across 11 distinct loci. Associated variants were found in and around genes encoding uPAR (PLAUR), its ligand uPA (PLAU), the kidney-disease-associated gene PLA2R1 as well as genes with relations to glycosylation, glycoprotein biosynthesis, and the immune response. These findings provide new insight into the causes of variation in suPAR plasma levels, which may clarify suPAR’s potential role in associated diseases, as well as the underlying mechanisms that give suPAR its prognostic value as a unique marker of chronic inflammation.

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