A predictive mortality score in ANCA-associated renal vasculitis.

AAV ANCA glomerulonephritis mortality prediction scores vasculitis

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:
07 Feb 2024
Historique:
medline: 8 2 2024
pubmed: 8 2 2024
entrez: 8 2 2024
Statut: aheadofprint

Résumé

Several scores have been developed to predict mortality at ANCA-Associated Vasculitis (AAV) diagnosis. Their prognostic value in Caucasian patients with kidney involvement (AAV-GN) remains uncertain as none have been developed in this specific population. We aimed to propose a novel and more accurate score specific for them. This multicentric study included patients diagnosed with AAV-GN since January 2000 in 4 nephrology Centers (recorded in the Maine-Anjou AAV-GN Registry). Existing scores and baseline characteristics were assessed at diagnosis before any therapeutic intervention. A multivariable analysis was performed to build a new predictive score for death. Its prognosis performance (AUROC and C-index) and accuracy (Brier score) was compared to existing scores. 185 patients with AAV-GN from the RENVAS registry were used as a validation cohort. 228 patients with AAV-GN from the Maine-Anjou registry were included to build the new score. It included the 4 components most associated with death: age, history of hypertension or cardiac disease, creatinine, and hemoglobin levels at diagnosis. 194 patients had all the data available to determine the performance of the new score and existing scores. The new score performed better than the previous ones in the development and in the validation cohort. Among the scores tested, only FFS (Five-Factor Score) and JVAS (Japanese Vasculitis Activity Score) had good performance in predicting death in AAV-GN. This original score, named DANGER (Death in ANCA Glomerulonephritis -Estimating the Risk), may be useful to predict the risk of death in AAV-GN patients. Validation in different populations is needed to clarify its role in assisting clinical decisions.

Sections du résumé

BACKGROUND BACKGROUND
Several scores have been developed to predict mortality at ANCA-Associated Vasculitis (AAV) diagnosis. Their prognostic value in Caucasian patients with kidney involvement (AAV-GN) remains uncertain as none have been developed in this specific population. We aimed to propose a novel and more accurate score specific for them.
METHODS METHODS
This multicentric study included patients diagnosed with AAV-GN since January 2000 in 4 nephrology Centers (recorded in the Maine-Anjou AAV-GN Registry). Existing scores and baseline characteristics were assessed at diagnosis before any therapeutic intervention. A multivariable analysis was performed to build a new predictive score for death. Its prognosis performance (AUROC and C-index) and accuracy (Brier score) was compared to existing scores. 185 patients with AAV-GN from the RENVAS registry were used as a validation cohort.
RESULTS RESULTS
228 patients with AAV-GN from the Maine-Anjou registry were included to build the new score. It included the 4 components most associated with death: age, history of hypertension or cardiac disease, creatinine, and hemoglobin levels at diagnosis. 194 patients had all the data available to determine the performance of the new score and existing scores. The new score performed better than the previous ones in the development and in the validation cohort. Among the scores tested, only FFS (Five-Factor Score) and JVAS (Japanese Vasculitis Activity Score) had good performance in predicting death in AAV-GN.
CONCLUSIONS CONCLUSIONS
This original score, named DANGER (Death in ANCA Glomerulonephritis -Estimating the Risk), may be useful to predict the risk of death in AAV-GN patients. Validation in different populations is needed to clarify its role in assisting clinical decisions.

Identifiants

pubmed: 38327221
pii: 7603376
doi: 10.1093/ndt/gfae035
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Investigateurs

Jean-François Augusto (JF)
Céline Beauvillain (C)
Benoit Brilland (B)
Jean-Philippe Coindre (JP)
Marie-Christine Copin (MC)
Maud Cousin (M)
Anne Croué (A)
Assia Djema (A)
Fanny Guibert (F)
Nicolas Henry (N)
Giorgina Barbara Piccoli (GB)
Lise-Marie Pouteau (LM)
Samuel Wacrenier (S)
Emeline Vinatier (E)

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the ERA.

Auteurs

Nicolas Fage (N)

Service de Néphrologie-Dialyse-Transplantation, Université d'Angers, CHU Angers, Angers, France.
Laboratoire MITOVASC UMR INSERM 1083 - CNRS 6015, Université d'Angers, Angers, France.

Thomas Quéméneur (T)

Nephrology and Internal Medicine Department, Hospital of Valenciennes, Valenciennes, France.

Jérémie Riou (J)

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

Charlotte Boud'hors (C)

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

Alice Desouche (A)

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

Emeline Vinatier (E)

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

Clément Samoreau (C)

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.

Assia Djema (A)

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

Nicolas Henry (N)

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

Viviane Gnemmi (V)

Service d'anatomopathologie, Centre Hospitalier Universitaire de Lille, Lille, France.

Marie-Christine Copin (MC)

Univ Angers, Nantes Université, Inserm, CNRS, CRCI2NA, SFR ICAT, Angers, France.
Département de pathologie cellulaire et tissulaire, Université d'Angers, CHU Angers, Angers, France.

Giorgina Barbara Piccoli (GB)

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

Cyrille Vandenbussche (C)

Nephrology and Internal Medicine Department, Hospital of Valenciennes, Valenciennes, France.

Jean-François Augusto (JF)

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

Benoit Brilland (B)

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

Classifications MeSH