Complement Activation on Endothelial Cell-Derived Microparticles—A Key Determinant for Cardiovascular Risk in Patients with Systemic Lupus Erythematosus?

dc.cclicenceCC-BYen
dc.contributor.authorMartin, Naomi
dc.contributor.authorTu, Xiaodie
dc.contributor.authorEgan, Alica
dc.contributor.authorStover, Cordula
dc.date.acceptance2020-10-09
dc.date.accessioned2020-11-12T15:47:05Z
dc.date.available2020-11-12T15:47:05Z
dc.date.issued2020-10-13
dc.descriptionopen access articleen
dc.description.abstractSystemic lupus erythematosus is a classical systemic autoimmune disease that overactivates complement and can affect all organs. Early diagnosis and effective management are important in this immune-complex-mediated chronic inflammatory disease, which has a strong component of vasculitis and carries an increased risk of thrombosis, even in the absence of antiphospholipid antibodies. Development of lupus nephritis can be life limiting but is managed with dialysis and renal transplantation. Therefore, data have become available that cardiovascular risk poses a serious feature of systemic lupus erythematosus that requires monitoring and prospective treatment. Cell-derived microparticles circulate in plasma and thereby intersect the humoral and cellular component of inflammation. They are involved in disease pathophysiology, particularly thrombosis, and represent a known cardiovascular risk. This viewpoint argues that a focus on characteristics of circulating microparticles measured in patients with systemic lupus erythematosus may help to classify certain ethnic groups who are especially at additional risk of experiencing cardiovascular complications.en
dc.funderNo external funderen
dc.identifier.citationmartin, N., Tu, X., Egan, A., Stover, C. (2020) Complement Activation on Endothelial Cell-Derived Microparticles—A Key Determinant for Cardiovascular Risk in Patients with Systemic Lupus Erythematosus? Medicina, 56, 533.en
dc.identifier.doihttps://doi.org/10.3390/medicina56100533
dc.identifier.urihttps://dora.dmu.ac.uk/handle/2086/20428
dc.language.isoenen
dc.peerreviewedYesen
dc.publisherMDPIen
dc.researchinstituteInstitute for Allied Health Sciences Researchen
dc.subjectlupusen
dc.subjectcomplementen
dc.subjectmicroparticlesen
dc.subjectcardiovascularen
dc.titleComplement Activation on Endothelial Cell-Derived Microparticles—A Key Determinant for Cardiovascular Risk in Patients with Systemic Lupus Erythematosus?en
dc.typeArticleen

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