Association between kinetic of anti-neutrophil cytoplasmic antibody (ANCA), renal survival and relapse risk in ANCA glomerulonephritis.


Journal

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
ISSN: 1460-2385
Titre abrégé: Nephrol Dial Transplant
Pays: England
ID NLM: 8706402

Informations de publication

Date de publication:
04 05 2023
Historique:
received: 19 02 2022
medline: 5 5 2023
pubmed: 1 9 2022
entrez: 31 8 2022
Statut: ppublish

Résumé

Anti-neutrophil cytoplasmic antibody (ANCA) kinetic in ANCA-associated vasculitis with glomerulonephritis (AAV-GN) has been suggested to be associated with AAV relapse. Few studies have focused on its association with renal prognosis. Thus we aimed to investigate the relationship between ANCA specificity and the evolutive profile and renal outcomes. This multicentric retrospective study included patients diagnosed with ANCA-GN since 1 January 2000. Patients without ANCA at diagnosis and with fewer than three ANCA determinations during follow-up were excluded. We analysed estimated glomerular filtration rate (eGFR) variation, renal-free survival and relapse-free survival according to three ANCA profiles (negative, recurrent and persistent) and to ANCA specificity [myeloperoxidase (MPO) or proteinase 3 (PR3)]. Over a follow-up of 56 months [interquartile range (IQR) 34-101], a median of 19 (IQR 13-25) ANCA determinations were performed for the 134 included patients. Patients with a recurrent/persistent ANCA profile had a lower relapse-free survival (P = .019) and tended to have a lower renal survival (P = .053) compared with those with a negative ANCA profile. Patients with a recurrent/persistent MPO-ANCA profile had the shortest renal survival (P = .015) and those with a recurrent/persistent PR3-ANCA profile had the worst relapse-free survival (P = .013) compared with other profiles. The negative ANCA profile was associated with a greater eGFR recovery. In multivariate regression analysis, it was an independent predictor of a 2-fold increase in eGFR at 2 years [odds ratio 6.79 (95% confidence interval 1.78-31.4), P = .008]). ANCA kinetic after an ANCA-GN diagnosis is associated with outcomes. MPO-ANCA recurrence/persistence identifies patients with a lower potential of renal recovery and a higher risk of kidney failure, while PR3-ANCA recurrence/persistence identifies patients with a greater relapse risk. Thus ANCA kinetics may help identify patients with a smouldering disease.

Sections du résumé

BACKGROUND
Anti-neutrophil cytoplasmic antibody (ANCA) kinetic in ANCA-associated vasculitis with glomerulonephritis (AAV-GN) has been suggested to be associated with AAV relapse. Few studies have focused on its association with renal prognosis. Thus we aimed to investigate the relationship between ANCA specificity and the evolutive profile and renal outcomes.
METHODS
This multicentric retrospective study included patients diagnosed with ANCA-GN since 1 January 2000. Patients without ANCA at diagnosis and with fewer than three ANCA determinations during follow-up were excluded. We analysed estimated glomerular filtration rate (eGFR) variation, renal-free survival and relapse-free survival according to three ANCA profiles (negative, recurrent and persistent) and to ANCA specificity [myeloperoxidase (MPO) or proteinase 3 (PR3)].
RESULTS
Over a follow-up of 56 months [interquartile range (IQR) 34-101], a median of 19 (IQR 13-25) ANCA determinations were performed for the 134 included patients. Patients with a recurrent/persistent ANCA profile had a lower relapse-free survival (P = .019) and tended to have a lower renal survival (P = .053) compared with those with a negative ANCA profile. Patients with a recurrent/persistent MPO-ANCA profile had the shortest renal survival (P = .015) and those with a recurrent/persistent PR3-ANCA profile had the worst relapse-free survival (P = .013) compared with other profiles. The negative ANCA profile was associated with a greater eGFR recovery. In multivariate regression analysis, it was an independent predictor of a 2-fold increase in eGFR at 2 years [odds ratio 6.79 (95% confidence interval 1.78-31.4), P = .008]).
CONCLUSION
ANCA kinetic after an ANCA-GN diagnosis is associated with outcomes. MPO-ANCA recurrence/persistence identifies patients with a lower potential of renal recovery and a higher risk of kidney failure, while PR3-ANCA recurrence/persistence identifies patients with a greater relapse risk. Thus ANCA kinetics may help identify patients with a smouldering disease.

Identifiants

pubmed: 36043422
pii: 6679399
doi: 10.1093/ndt/gfac240
doi:

Substances chimiques

Antibodies, Antineutrophil Cytoplasmic 0
Myeloblastin EC 3.4.21.76
Peroxidase EC 1.11.1.7

Types de publication

Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1192-1203

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the ERA.

Auteurs

Clément Samoreau (C)

Service de Néphrologie-Dialyse-Transplantation, Université d'Angers, CHU Angers, Angers, France.

Giorgina Barbara Piccoli (GB)

Service de Néphrologie-Dialyse, Centre Hospitalier du Mans, Le Mans, France.

Cécile Martin (C)

Service de Néphrologie-Dialyse-Transplantation, CHU de Poitiers, Poitiers, France.

Philippe Gatault (P)

Service de Néphrologie-Dialyse-Transplantation, CHU de Tours, Tours, France.

Emeline Vinatier (E)

Laboratoire d'Immunologie et Allergologie, CHU Angers, Angers, France.
Université d'Angers, Inserm, CNRS, Nantes Université, CRCI2NA, Angers, France.

Frank Bridoux (F)

Service de Néphrologie-Dialyse-Transplantation, CHU de Poitiers, Poitiers, France.

Jérémie Riou (J)

Methodology and Biostatistics Department, Delegation to Clinical Research and Innovation, CHU Angers, Angers, France.

Alice Desouche (A)

Service de Néphrologie-Dialyse-Transplantation, Université d'Angers, CHU Angers, Angers, France.

Pierre Jourdain (P)

Service de Néphrologie-Dialyse-Transplantation, Université d'Angers, CHU Angers, Angers, France.

Jean-Philippe Coindre (JP)

Service de Néphrologie-Dialyse, Centre Hospitalier du Mans, Le Mans, France.

Samuel Wacrenier (S)

Service de Néphrologie-Dialyse-Transplantation, Université d'Angers, CHU Angers, Angers, France.
Service de Néphrologie-Dialyse, Centre Hospitalier du Mans, Le Mans, France.

Fanny Guibert (F)

Service de Néphrologie-Dialyse-Transplantation, Université d'Angers, CHU Angers, Angers, France.
Service de Néphrologie-Dialyse, Centre Hospitalier de Cholet, Cholet, France.

Nicolas Henry (N)

Service de Néphrologie-Dialyse-Transplantation, Université d'Angers, CHU Angers, Angers, France.
Service de Néphrologie-Dialyse, Centre Hospitalier de Laval, Laval, France.

Odile Blanchet (O)

Centre de Resources Biologiques, BB-0033-00038, CHU Angers, Angers, France.

Anne Croué (A)

Département de Pathologie Cellulaire et Tissulaire, Université d'Angers, CHU Angers, Angers, France.

Assia Djema (A)

Service de Néphrologie-Dialyse, Centre Hospitalier de Cholet, Cholet, France.

Lise-Marie Pouteau (LM)

Service de Néphrologie-Dialyse, Centre Hospitalier de Cholet, Cholet, France.

Marie-Christine Copin (MC)

Université d'Angers, Inserm, CNRS, Nantes Université, CRCI2NA, Angers, France.
Département de Pathologie Cellulaire et Tissulaire, Université d'Angers, CHU Angers, Angers, France.

Céline Beauvillain (C)

Laboratoire d'Immunologie et Allergologie, CHU Angers, Angers, France.
Université d'Angers, Inserm, CNRS, Nantes Université, CRCI2NA, Angers, France.

Jean-François Subra (JF)

Service de Néphrologie-Dialyse-Transplantation, Université d'Angers, CHU Angers, Angers, France.
Université d'Angers, Inserm, CNRS, Nantes Université, CRCI2NA, Angers, France.

Jean-François Augusto (JF)

Service de Néphrologie-Dialyse-Transplantation, Université d'Angers, CHU Angers, Angers, France.
Université d'Angers, Inserm, CNRS, Nantes Université, CRCI2NA, Angers, France.

Benoit Brilland (B)

Service de Néphrologie-Dialyse-Transplantation, Université d'Angers, CHU Angers, Angers, France.
Université d'Angers, Inserm, CNRS, Nantes Université, CRCI2NA, Angers, France.

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Classifications MeSH