Slowly progressive anti-neutrophil cytoplasmic antibody-associated renal vasculitis: clinico-pathological characterization and outcome

Author:

Trivioli Giorgio1,Gopaluni Seerapani2,Urban Maria L.3,Gianfreda Davide4,Cassia Matthias A.5,Vercelloni Paolo G.6,Calatroni Marta7,Bettiol Alessandra8,Esposito Pasquale9,Murtas Corrado10,Alberici Federico1112,Maritati Federica13,Manenti Lucio14,Palmisano Alessandra14,Emmi Giacomo3,Romagnani Paola1,Moroni Gabriella15,Gregorini Gina16,Sinico Renato A.6,Jayne David R.W.2,Vaglio Augusto1

Affiliation:

1. Department of Biomedical Experimental and Clinical Sciences “Mario Serio”, University of Firenze, and Nephrology Unit, Meyer Children’s Hospital, Firenze, Italy

2. Department of Medicine, University of Cambridge, Cambridge, UK

3. Department of Experimental and Clinical Sciences, University of Firenze, Firenze, Italy

4. Nephrology Unit, Fondazione Panico Hospital, Tricase, Italy

5. Department of Health Science, University of Milan, Italy

6. Nephrology Unit, University Milano Bicocca, Monza, Italy

7. Nephrology Unit, Humanitas Hospital, Rozzano, Italy

8. Department of Neurosciences, Psychology, Pharmacology and Child Health, University of Firenze, Firenze, Italy

9. Department of Internal Medicine and Medical Specialties, University of Genova, Genova, Italy

10. Nephrology Unit, Nephrology Unit, ASSL Oristano, ATS Sardegna, Oristano, Italy

11. Nephrology Unit, ASST Spedali Civili, Brescia, Italy

12. Department of Medical and Surgical Specialities, Radiological Sciences and Public Health, University of Brescia, Brescia, Italy

13. Nephrology, Dialysis and Transplant Unit, Ospedali Riuniti, Ancona, Italy

14. Nephrology Unit, Parma University Hospital, Parma, Italy

15. Nephrology Unit, Policlinico Hospital, Milano, Italy

16. Nephrology Unit, Spedali Civili, Brescia, Italy

Abstract

Abstract Background Although rapidly progressive glomerulonephritis is the main renal phenotype of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV), slow renal disease progression is sometimes observed. These forms have been rarely discussed; we analysed their prevalence, clinico-pathological characteristics and outcome. Methods We screened patients with microscopic  polyangiitis (MPA) and granulomatosis with polyangiitis followed at seven referral centres and selected those with estimated glomerular filtration rate (eGFR) reduction <50% over a 6-month period preceding diagnosis. Data regarding patient features and response to treatment were retrieved. Results Of 856 patients, 41 (5%) had slowly progressive renal AAV. All had MPA and all but one was P-ANCA/myeloperoxidase (MPO) ANCA-positive. At diagnosis, the median age was 70 years [interquartile range (IQR) 64–78] and extra-renal manifestations were absent or subclinical (interstitial lung lesions in 10, 24%). The median (IQR) eGFR was 23 mL/min/1.73 m2 (15–35); six patients (15%) had started renal replacement therapy (RRT). All had proteinuria (median 1180 mg/24 h, IQR 670–2600) and micro-haematuria. Main histologic findings were extracapillary proliferation at chronic stages and glomerulosclerosis; following Berden’s classification, 6/28 biopsies (21%) were ‘focal’, 1/28 (4%) ‘crescentic’, 9/28 (32%) ‘mixed’ and 12/28 (43%) ‘sclerotic’. At last follow-up (median 32 months, IQR 12–52), 20/34 patients (59%) treated with immunosuppression had eGFR improvement >25% as compared with diagnosis, while 4/34 (12%) had started RRT. Conclusions AAV may present with slow renal disease progression; this subset is hallmarked by advanced age at diagnosis, positive MPO-ANCA, subclinical interstitial lung lesions and chronic damage at kidney biopsy. Partial renal recovery may occur following immunosuppression.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

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