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dc.contributor.authorIglesias, Maria Jesus
dc.contributor.authorSanchez-Rivera, Laura
dc.contributor.authorIbrahim-Kosta, Manal
dc.contributor.authorNaudin, Clément
dc.contributor.authorMunsch, Gaëlle
dc.contributor.authorGoumidi, Louisa
dc.contributor.authorFarm, Maria
dc.contributor.authorSmith, Philip M.
dc.contributor.authorThibord, Florian
dc.contributor.authorKral-Pointner, Julia Barbara
dc.contributor.authorHong, Mun-Gwan
dc.contributor.authorSuchon, Pierre
dc.contributor.authorGermain, Marine
dc.contributor.authorSchottmaier, Waltraud
dc.contributor.authorDusart, Philip James
dc.contributor.authorBoland, Anne
dc.contributor.authorKotol, David
dc.contributor.authorEdfors, Fredrik
dc.contributor.authorKoprulu, Mine
dc.contributor.authorPietzner, Maik
dc.contributor.authorLangenberg, Claudia
dc.contributor.authorDamrauer, Scott M.
dc.contributor.authorJohnson, Andrew D.
dc.contributor.authorKlarin, Derek M.
dc.contributor.authorSmith, Nicholas L.
dc.contributor.authorSmadja, David M.
dc.contributor.authorHolmström, Margareta
dc.contributor.authorMagnusson, Maria
dc.contributor.authorSilveira, Angela
dc.contributor.authorUhlén, Mathias
dc.contributor.authorRenné, Thomas
dc.contributor.authorMartinez-Perez, Angel
dc.contributor.authorEmmerich, Joseph
dc.contributor.authorDeleuze, Jean-Francois
dc.contributor.authorAntovic, Jovan
dc.contributor.authorSoria Fernandez, Jose Manuel
dc.contributor.authorAssinger, Alice
dc.contributor.authorSchwenk, Jochen M.
dc.contributor.authorSouto Andres, Joan Carles
dc.contributor.authorMorange, Pierre-Emmanuel
dc.contributor.authorButler, Lynn
dc.contributor.authorTrégouët, David-Alexandre
dc.contributor.authorOdeberg, Jacob
dc.date.accessioned2023-08-10T12:04:52Z
dc.date.available2023-08-10T12:04:52Z
dc.date.issued2023-06-07
dc.description.abstractVenous thromboembolism (VTE) is a common, multi-causal disease with potentially serious short- and long-term complications. In clinical practice, there is a need for improved plasma biomarker-based tools for VTE diagnosis and risk prediction. Here we show, using proteomics profiling to screen plasma from patients with suspected acute VTE, and several case-control studies for VTE, how Complement Factor H Related 5 protein (CFHR5), a regulator of the alternative pathway of complement activation, is a VTE-associated plasma biomarker. In plasma, higher CFHR5 levels are associated with increased thrombin generation potential and recombinant CFHR5 enhanced platelet activation in vitro. GWAS analysis of ~52,000 participants identifies six loci associated with CFHR5 plasma levels, but Mendelian randomization do not demonstrate causality between CFHR5 and VTE. Our results indicate an important role for the regulation of the alternative pathway of complement activation in VTE and that CFHR5 represents a potential diagnostic and/or risk predictive plasma biomarker.en_US
dc.identifier.citationIglesias, Sanchez-Rivera, Ibrahim-Kosta, Naudin, Munsch, Goumidi, Farm, Smith, Thibord, Kral-Pointner, Hong, Suchon, Germain, Schottmaier, Dusart, Boland, Kotol, Edfors, Koprulu, Pietzner, Langenberg, Damrauer, Johnson, Klarin, Smith, Smadja, Holmström, Magnusson, Silveira, Uhlén, Renné, Martinez-Perez, Emmerich, Deleuze, Antovic, Soria Fernandez, Assinger, Schwenk, Souto Andres, Morange, Butler, Trégouët, Odeberg. Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism. Nature Communications. 2023;14(1)en_US
dc.identifier.cristinIDFRIDAID 2159152
dc.identifier.doi10.1038/s41467-023-38383-y
dc.identifier.issn2041-1723
dc.identifier.urihttps://hdl.handle.net/10037/29856
dc.language.isoengen_US
dc.publisherSpringer Natureen_US
dc.relation.journalNature Communications
dc.rights.accessRightsopenAccessen_US
dc.rights.holderCopyright 2023 The Author(s)en_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0en_US
dc.rightsAttribution 4.0 International (CC BY 4.0)en_US
dc.titleElevated plasma complement factor H related 5 protein is associated with venous thromboembolismen_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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Attribution 4.0 International (CC BY 4.0)
Med mindre det står noe annet, er denne innførselens lisens beskrevet som Attribution 4.0 International (CC BY 4.0)