Renal relapse in antineutrophil cytoplasmic autoantibody-associated vasculitis: unpredictable, but predictive of renal outcome.


Journal

Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501

Informations de publication

Date de publication:
01 01 2019
Historique:
received: 07 02 2018
entrez: 15 12 2018
pubmed: 15 12 2018
medline: 24 10 2019
Statut: ppublish

Résumé

To determine predictors of renal relapse and end-stage renal failure (ESRF) in patients with ANCA-associated vasculitis. Data from four European Vasculitis Society randomized controlled trials, conducted roughly simultaneously between 15 March 1995 and 30 September 2002, was pooled to determine predictors of long-term renal outcome. The respective trial inclusion criteria covered the entire spectrum of disease severity. Baseline predictors of time to first renal relapse and time to ESRF were assessed by competing events analysis and Cox proportional hazards regression. The effect of renal relapse on time to ESRF was assessed by adding renal relapses to the competing events analysis as a time-varying covariate. The number of patients participating was 535; mean serum creatinine (±s.d.) at entry was 341 ± 321 µmol/l and 19.7% developed ESRF. One or more renal relapse(s) was experienced by 101 patients. Multivariable regression analysis demonstrated that, in addition to impaired baseline renal function, developing ⩾1 renal relapse was an independent risk factor for ESRF (subhazard ratio 9; 95% CI 4, 19; P < 0.001). No predictive factors for renal relapse were found. In addition to baseline renal function, the occurrence of renal relapses is an important determinant of ESRF in patients with ANCA-associated vasculitis. We did not find any clinical predictors for renal relapse itself, including disease activity elsewhere. In light of the silent nature of renal relapse in ANCA-associated vasculitis, we stress the need for long-term vigilant monitoring for early signs of renal relapse and propose performing 3-monthly urinalysis. This will enable timely treatment and help further improve renal outcome.

Identifiants

pubmed: 30551161
pii: 5078552
doi: 10.1093/rheumatology/key260
doi:

Substances chimiques

Immunosuppressive Agents 0
Creatinine AYI8EX34EU

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

103-109

Auteurs

Maria A C Wester Trejo (MAC)

Department of Pathology, Leiden University Medical Center, Leiden, The Netherlands.

Oliver Floßmann (O)

Renal Department, Royal Berkshire Hospital, Reading, UK.

Kerstin W Westman (KW)

Department of Clinical Sciences, Skane University Hospital, Lund, Sweden.
Department of Nephrology, Skane University Hospital, Lund, Sweden.

Peter Höglund (P)

Department of Laboratory Medicine, Skane University Hospital, Lund, Sweden.
Department of Clinical Chemistry and Pharmacology, Skane University Hospital, Lund, Sweden.

E Christiaan Hagen (EC)

Department of Internal Medicine, Meander Medical Center, Amersfoort, The Netherlands.

Michael Walsh (M)

Department of Medicine, McMaster University, Hamilton, Canada.
Department of Clinical Epidemiology and Biostatistics, McMaster University, Hamilton, Canada.

Jan A Bruijn (JA)

Department of Pathology, Leiden University Medical Center, Leiden, The Netherlands.

David R W Jayne (DRW)

Renal Unit, Addenbrooke's Hospital, Cambridge, UK.

Ingeborg M Bajema (IM)

Department of Pathology, Leiden University Medical Center, Leiden, The Netherlands.

Annelies E Berden (AE)

Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.

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Classifications MeSH