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Circulating Angiopoietin-2 as a Biomarker in ANCA-Associated Vasculitis

Authors :
Cees G. M. Kallenberg
Steven R. Ytterberg
Nadia K. Tchao
Simon Carette
Peter A. Merkel
Philipp Kümpers
Alexander Lukasz
Nader Khalidi
David Ikle
Robert Spiera
Linna Ding
E. William St. Clair
John H. Stone
Marion Haubitz
Gary S. Hoffman
Ulrich Specks
David Cuthbertson
Philip Seo
Jeffrey P. Krischer
Carol A. Langford
Gunnar Tomasson
Paul A. Monach
Source :
PLoS ONE, Vol 7, Iss 1, p e30197 (2012), PLoS ONE, 7(1):e30197. PUBLIC LIBRARY SCIENCE, PLoS ONE
Publication Year :
2012
Publisher :
Public Library of Science (PLoS), 2012.

Abstract

The endothelial-specific Angiopoietin-Tie2 ligand-receptor system is an important regulator of endothelial activation. Binding of angiopoietin-2 (Ang-2) to Tie2 receptor renders the endothelial barrier responsive to pro-inflammatory cytokines. We previously showed that circulating Ang-2 correlated with disease severity in a small cohort of critically ill patients with anti-neutrophil cytoplasmic antibody (ANCA)-associated glomerulonephritis. The current study reassessed Ang-2 as a biomarker of disease activity and relapse in AAV. Circulating Ang-2 was measured in 162 patients with severe AAV (BVAS/WG >= 3, with or without glomerulonephritis) in a clinical trial. Ang-2 levels during active AAV were compared to levels in the same patients during remission (BVAS/WG = 0). Levels in clinical subsets of AAV were compared, and association with future disease course was assessed. Ang-2 levels were elevated in severe disease (median 3.0 ng/ml, interquartile range 1.9-4.4) compared to healthy controls (1.2, 0.9-1.5). However, they did not reliably decline with successful treatment (median 2.6 ng/ml, interquartile range 1.9-3.8, median change -0.1). Ang-2 correlated weakly with BVAS/WG score (r = 0.17), moderately with markers of systemic inflammation (r = 0.25-0.41), and inversely with renal function (r = -0.36). Levels were higher in patients with glomerulonephritis, but levels adjusted for renal dysfunction were no different in patients with or without glomerulonephritis. Levels were higher in patients with newly diagnosed AAV and lower in patients in whom treatment had recently been started. Ang-2 levels during active disease did not predict response to treatment, and Ang-2 levels in remission did not predict time to flare. Thus, Ang-2 appears to have limited practical value in AAV as a biomarker of disease activity at time of measurement or for predicting future activity.

Details

ISSN :
19326203
Volume :
7
Database :
OpenAIRE
Journal :
PLoS ONE
Accession number :
edsair.doi.dedup.....f38ca86d15fd5c292da6257f07ac7ae7