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The European Vasculitis Society 2016 Meeting Report

Bajema, Ingeborg M. (author)
Leiden University Medical Centre
Bruijn, Jan A. (author)
Leiden University Medical Centre
Casian, Alina (author)
Guy's and St Thomas' NHS Foundation Trust
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Cid, Maria C. (author)
University of Barcelona
Csernok, Elena (author)
University Hospital of Tubingen
van Daalen, Emma (author)
Leiden University Medical Centre
Harper, Lorraine (author)
University of Birmingham
Hauser, Thomas (author)
Immunologie-Zentrum Zürich
Little, Mark A. (author)
Trinity College Dublin
Luqmani, Raashid A. (author)
University of Oxford
Mahr, Alfred (author)
Cochin Hospital
Ponte, Cristina (author)
University of Lisbon
Salama, Alan (author)
University College London
Segelmark, Mårten (author)
Linköping University
Suzuki, Kazuo (author)
Teikyo University School of Medicine
Sznajd, Jan (author)
University of Aberdeen
Teng, Y. K.Onno (author)
Leiden University Medical Centre
Vaglio, Augusto (author)
Parma University Hospital
Westman, Kerstin (author)
Lund University,Lunds universitet,Autoimmunitet och njursjukdomar,Forskargrupper vid Lunds universitet,Autoimmunity and kidney diseases,Lund University Research Groups
Jayne, David (author)
University of Cambridge
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 (creator_code:org_t)
Elsevier BV, 2017
2017
English 14 s.
In: Kidney International Reports. - : Elsevier BV. - 2468-0249. ; 2:6, s. 1018-1031
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The 2016 European Vasculitis Society (EUVAS) meeting, held in Leiden, the Netherlands, was centered around phenotypic subtyping in antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis (AAV). There were parallel meetings of the EUVAS petals, which here report on disease assessment; database; and long-term follow-up, registries, genetics, histology, biomarker studies, and clinical trials. Studies currently conducted will improve our ability to discriminate between different forms of vasculitis. In a project that involves the 10-year follow-up of AAV patients, we are working on retrieving data on patient and renal survival, relapse rate, the cumulative incidence of malignancies, and comorbidities. Across Europe, several vasculitis registries were developed covering over 10,000 registered patients. In the near future, these registries will facilitate clinical research in AAV on a scale hitherto unknown. Current studies on the genetic background of AAV will explore the potential prognostic significance of genetic markers and further refine genetic associations with distinct disease subsets. The histopathological classification of ANCA-associated glomerulonephritis is currently evaluated in light of data coming out of a large international validation study. In our continuous search for biomarkers to predict clinical outcome, promising new markers are important subjects of current research. Over the last 2 decades, a host of clinical trials have provided evidence for refinement of therapeutic regimens. We give an overview of clinical trials currently under development, and consider refractory vasculitis in detail. The goal of EUVAS is to stimulate ongoing research in clinical, serological, and histological management and techniques for patients with systemic vasculitis, with an outlook on the applicability for clinical trials.

Keyword

ANCA
renal outcome
therapy
vasculitis

Publication and Content Type

art (subject category)
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