Are serum C3 levels or kidney C3 deposits useful markers for predicting outcomes in patients with ANCA-associated vasculitis?
ANCA
Complement C3
Dialysis
Survival
Vasculitis
Journal
Journal of translational autoimmunity
ISSN: 2589-9090
Titre abrégé: J Transl Autoimmun
Pays: Netherlands
ID NLM: 101759413
Informations de publication
Date de publication:
Dec 2023
Dec 2023
Historique:
received:
11
07
2023
revised:
03
10
2023
accepted:
06
10
2023
medline:
25
10
2023
pubmed:
25
10
2023
entrez:
25
10
2023
Statut:
epublish
Résumé
Complement activation emerged as a key actor of anti-neutrophil cytoplasmic antibodies-associated vasculitis (AAV). Whether serum levels of C3 (sC3) or C3 kidney deposition may help to refine the prognosis of AAV remains elusive. Retrospective multicentric study that included 154 patients with a first flare of AAV and sC3 (n = 143) or C3 kidney staining (n = 95) available at diagnosis. Clinical presentations, kidney pathology, and survival of patients with normal or low sC3 were compared using univariate analyses, Kaplan-Maier curves with log-rank comparison, or multivariate Cox' model, as appropriate. 20 patients (14 %) had low sC3. sC3 (as bivariate low/normal or as a continuous variable) was associated with 5-year mortality but not with kidney survival. C3 kidney deposition (C3+) was identified in 23 patients who were characterized by more frequent chronic hypertension and lower eGFR at presentation (p = 0.04). C3+ correlated with IgG, IgM, C1q deposition (p = 0.07, p < 0.0001 and p = 0.003, respectively). Chronicity and activity scores were similar in C3+ and C3- patients. Among C3+ patients, those with C3 deposition ≥2+ had lower eGFR at presentation (p = 0.006) and were more frequently classified as sclerotic using the Berden classification (p = 0.04) and as 'high risk' using the Brix score (p = 0.03). However, eGFR improvement following induction regimen was similar between C3+ and C3- patients, and kidney survival at 5 years was similar. Correlation of sC3 with mortality confirms mechanistic links between complement pathways and AAV, but the lack of clear predictive sC3 cut-off and the similar kidney outcome irrespective of C3 deposition precludes their use as biomarkers of AAV outcomes and response to treatment.
Identifiants
pubmed: 37877133
doi: 10.1016/j.jtauto.2023.100217
pii: S2589-9090(23)00030-8
pmc: PMC10590832
doi:
Types de publication
Journal Article
Langues
eng
Pagination
100217Informations de copyright
© 2023 The Authors.
Déclaration de conflit d'intérêts
SF received consulting fees from Abionyx Pharma and Novartis SA, fees for Scientific advisory board or lecture fees by CSL-Vifor, Sanofi-Genzyme, Alexion-AstraZeneca and Baxter. Other authors reported no conflict of interests.
Références
Kidney Int. 2013 Jan;83(1):129-37
pubmed: 22913983
Clin Rheumatol. 2019 Oct;38(10):2819-2824
pubmed: 31222573
Atherosclerosis. 2018 Feb;269:204-210
pubmed: 29407595
Nephrol Dial Transplant. 2017 Aug 01;32(8):1302-1313
pubmed: 26275893
Front Immunol. 2018 Nov 20;9:2664
pubmed: 30515158
Front Immunol. 2021 Mar 25;12:625672
pubmed: 33841408
J Autoimmun. 2022 Dec;133:102924
pubmed: 36209693
J Nephrol. 2018 Apr;31(2):257-262
pubmed: 29027625
Arthritis Rheum. 1990 Aug;33(8):1068-73
pubmed: 2202306
Ann Rheum Dis. 2009 Dec;68(12):1827-32
pubmed: 19054820
N Engl J Med. 2010 Jul 15;363(3):211-20
pubmed: 20647198
J Am Soc Nephrol. 2014 Feb;25(2):225-31
pubmed: 24179165
Arthritis Rheum. 2013 Jan;65(1):1-11
pubmed: 23045170
Int J Mol Sci. 2021 Jun 19;22(12):
pubmed: 34205415
PLoS One. 2016 Jul 08;11(7):e0158871
pubmed: 27391243