Disease and treatment-related morbidity in young and elderly patients with granulomatosis with polyangiitis and microscopic polyangiitis.


Journal

Seminars in arthritis and rheumatism
ISSN: 1532-866X
Titre abrégé: Semin Arthritis Rheum
Pays: United States
ID NLM: 1306053

Informations de publication

Date de publication:
12 2020
Historique:
received: 03 07 2019
revised: 26 01 2020
accepted: 13 02 2020
pubmed: 17 3 2020
medline: 30 9 2021
entrez: 17 3 2020
Statut: ppublish

Résumé

Aging may be a risk factor for morbidity in anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV). We compared the rate and better characterized the type of disease- and treatment-related complications affecting young and elderly patients with AAV. All new cases of granulomatosis with polyangiitis or microscopic polyangiitis diagnosed in three referral centers between 2000-2016 were included. Patients were stratified by age into young or elderly (< or ≥65 years old, respectively). Data were collected from diagnosis until end of follow-up, with scheduled annual visits or additional visits in case of relapse or complication requiring hospitalization. Of 141 patients included, 42 were elderly and 99 were young at the time of AAV diagnosis. Median follow-up was 58.0 [25-75% IQR, 31.0-60.0] months in young and 48.0 [23.25-60.0] months in elderly patients (p>0.05). Overall, the elderly group was associated to higher damage accrual assessed by Vasculitis Damage Index during follow-up (β=0.28, p<0.05). Sixty-three (44.7%) patients had acute kidney injury due to AAV-glomerulonephritis at diagnosis. In contrast to elderly, young patients showed significant improvement in renal function over time, particularly in the first 6 months while on induction treatment (ΔeGFR, median [25-75%IQR], 5.3 [0.4-14] versus 22.8 [5.9-52.1] ml/min/1.73m Elderly patients with AAV had higher susceptibility to disease- and treatment-related morbidity than younger patients, particularly to renal and infective morbidity.

Identifiants

pubmed: 32173060
pii: S0049-0172(20)30031-7
doi: 10.1016/j.semarthrit.2020.02.008
pii:
doi:

Substances chimiques

Antibodies, Antineutrophil Cytoplasmic 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1441-1448

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest None.

Auteurs

Alvise Berti (A)

Department of Rheumatology, Santa Chiara Hospital, Trento, Italy; Department of Cellular, Computational and Integrative Biology-CIBIO, University of Trento, Trento, Italy. Electronic address: alvise.berti@apss.tn.it.

Mara Felicetti (M)

Operative Unit of Rheumatology, Department of Medicine DI-MED, University of Padova, Italy.

Sara Monti (S)

Department of Rheumatology, IRCCS Policlinico S. Matteo Foundation, University of Pavia, Italy; Ph.D. in Experimental Medicine, University of Pavia, Pavia, Italy.

Augusta Ortolan (A)

Operative Unit of Rheumatology, Department of Medicine DI-MED, University of Padova, Italy.

Roberto Padoan (R)

Operative Unit of Rheumatology, Department of Medicine DI-MED, University of Padova, Italy.

Giuliano Brunori (G)

Nephrology Department, Santa Chiara Hospital, Trento, Italy.

Roberto Bortolotti (R)

Department of Rheumatology, Santa Chiara Hospital, Trento, Italy.

Roberto Caporali (R)

Department of Clinical Sciences and community health, University of Milan, Italy.

Carlomaurizio Montecucco (C)

Department of Rheumatology, IRCCS Policlinico S. Matteo Foundation, University of Pavia, Italy.

Franco Schiavon (F)

Operative Unit of Rheumatology, Department of Medicine DI-MED, University of Padova, Italy.

Giuseppe Paolazzi (G)

Department of Rheumatology, Santa Chiara Hospital, Trento, Italy.

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