Are anti-proteinase-3 ANCA a useful marker of granulomatosis with polyangiitis (Wegener's) relapses? Results of a retrospective study on 126 patients

Abstract Objectives Predicting granulomatosis with polyangiitis (Wegener's) (GPA) relapses based on ANCA titers remains a source of debate. Our objective was to evaluate the relevance of monitoring PR3-ANCA titers for GPA management. Methods This retrospective study included 126 patients fulfil...

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Veröffentlicht in:Autoimmunity reviews 2014-03, Vol.13 (3), p.313-318
Hauptverfasser: Thai, Lan-Huong, Charles, Pierre, Resche-Rigon, Matthieu, Desseaux, Kristell, Guillevin, Loïc
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Sprache:eng
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Zusammenfassung:Abstract Objectives Predicting granulomatosis with polyangiitis (Wegener's) (GPA) relapses based on ANCA titers remains a source of debate. Our objective was to evaluate the relevance of monitoring PR3-ANCA titers for GPA management. Methods This retrospective study included 126 patients fulfilling the 1990 ACR criteria for GPA and PR3-ANCA-positive at the time of diagnosis. Disease activity was assessed with BVAS/WG and Disease Extent Index. For each patient, a median of 12 serum samples was analyzed, i.e., one every 5.5 months. Results Induction therapy obtained remission in 88% of the patients. ANCA became negative by IF for 70/115 (60.9%) patients and by ELISA for 90/115 (78.3%). After median follow-up of 70 months, 85/126 (67.5%) patients had 154 clinical relapses associated with cANCA and PR3-ANCA-positivity for 122 (79.2%) and 102 (66.2%) of them, respectively. Relapse-free survival was significantly longer for patients who remained PR3-ANCA-negative (HR 0.60 [95% CI 0.39–0.92], P = 0.02). Individual ANCA-profile analysis revealed that, for 60% of GPA patients, clinical outcomes and ANCA-titer changes were closely associated, i.e., ANCA were always positive during relapses and negative during remission. The 35 patients with fluctuating ANCA-positivity during remission were in partial remission or had developed grumbling GPA. Conclusion Although ANCA were positive during most systemic relapses or residual disease, no strict clinical–immunological correspondence was observed for 25% of the patients. Thus, GPA management cannot be based on ANCA levels alone.
ISSN:1568-9972
1873-0183
DOI:10.1016/j.autrev.2013.11.003