4.7 Article

Patients double-seropositive for ANCA and anti-GBM antibodies have varied renal survival, frequency of relapse, and outcomes compared to single-seropositive patients

Journal

KIDNEY INTERNATIONAL
Volume 92, Issue 3, Pages 693-702

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.kint.2017.03.014

Keywords

anti-GBM disease; anti-neutrophil cytoplasm antibody; glomerulonephritis; Goodpasture syndrome; vasculitis

Funding

  1. UK National Institute for Health Research (NIHR) Academic Clinical Lectureship
  2. Wellcome Trust
  3. NIHR Imperial Biomedical Research Centre
  4. Charles University Hospital, Prague, Czech Republic [RVO-VFN64165]
  5. Academy of Medical Sciences (AMS) [SGL014\\1010] Funding Source: researchfish
  6. Medical Research Council [G0901997] Funding Source: researchfish
  7. National Institute for Health Research [ACF-2007-21-019, CL-2014-21-006] Funding Source: researchfish
  8. MRC [G0901997] Funding Source: UKRI

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Co-presentation with both ANCA and anti-GBM antibodies is thought to be relatively rare. Current studies of such 'double-positive' cases report small numbers and variable outcomes. To study this further we retrospectively analyzed clinical features and long-term outcomes of a large cohort of 568 contemporary patients with ANCA-associated vasculitis, 41 patients with anti-GBM disease, and 37 double-positive patients with ANCA and anti-GBM disease from four European centers. Double-positive patients shared characteristics of ANCA-associated vasculitis (AAV), such as older age distribution and longer symptom duration before diagnosis, and features of anti-GBM disease, such as severe renal disease and high frequency of lung hemorrhage at presentation. Despite having more evidence of chronic injury on renal biopsy compared to patients with anti-GBM disease, double-positive patients had a greater tendency to recover from being dialysis-dependent after treatment and had intermediate long-term renal survival compared to the single-positive patients. However, overall patient survival was similar in all three groups. Predictors of poor patient survival included advanced age, severe renal failure, and lung hemorrhage at presentation. No single-positive anti-GBM patients experienced disease relapse, whereas approximately half of surviving patients with AAV and double-positive patients had recurrent disease during a median follow-up of 4.8 years. Thus, double-positive patients have a truly hybrid disease phenotype, requiring aggressive early treatment for anti-GBM disease, and careful long-term follow-up and consideration for maintenance immunosuppression for AAV. Since double-positivity appears common, further work is required to define the underlying mechanisms of this association and define optimum treatment strategies.

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