Comparative analysis of complement C3 and C4 serum levels for outcome prediction in ANCA-associated renal vasculitis.
ANCA-associated vasculitis
Complement C3
Complement C4
Journal
Journal of nephrology
ISSN: 1724-6059
Titre abrégé: J Nephrol
Pays: Italy
ID NLM: 9012268
Informations de publication
Date de publication:
01 2023
01 2023
Historique:
received:
17
05
2022
accepted:
19
07
2022
pubmed:
14
8
2022
medline:
7
2
2023
entrez:
13
8
2022
Statut:
ppublish
Résumé
The activation of the complement system contributes essentially to the pathogenesis of anti-neutrophil cytoplasmic antibody (ANCA)-associated renal vasculitis. We here aimed to directly compare levels of C3 and C4 for outcome prediction in ANCA-associated renal vasculitis. Serum levels of complement components C3 and C4 were directly compared in association with clinical and outcome data in a retrospective cohort of ANCA-associated renal vasculitis. As compared to poor outcome prediction by low levels of complement C3 (p = 0.0093), low levels of complement C4 did not associate with early requirement of kidney replacement therapy (KRT) or death (p = 0.2396). In the subgroup that experienced KRT or death, low C3 levels identified 11/14 (78.6%, p = 0.0071) and C4 levels 9/14 (64.3%, p = 0.1786) cases. Interestingly, 2/14 (14.3%) patients that experienced KRT or death had isolated C4 lowering, and combining low C3 and/or C4 levels identified 13/14 (92.3%, p < 0.0001) cases in this subgroup. Non-superiority to predict poor outcome by low C3 and/or C4 as compared to C3 alone in the total cohort was attributed to 4/24 (16.7%) patients with isolated C4 lowering in the subgroup that did not experience KRT or death. While low levels of complement C3 were superior in predicting poor outcome in ANCA-associated renal vasculitis, a minor fraction with poor outcome had isolated C4 lowering not captured by serum C3 measurements. Therefore, detailed knowledge of distinct complement components contributing to kidney injury could be of relevance to improve current strategies targeting the complement system in ANCA-associated renal vasculitis.
Sections du résumé
BACKGROUND
The activation of the complement system contributes essentially to the pathogenesis of anti-neutrophil cytoplasmic antibody (ANCA)-associated renal vasculitis. We here aimed to directly compare levels of C3 and C4 for outcome prediction in ANCA-associated renal vasculitis.
METHODS
Serum levels of complement components C3 and C4 were directly compared in association with clinical and outcome data in a retrospective cohort of ANCA-associated renal vasculitis.
RESULTS
As compared to poor outcome prediction by low levels of complement C3 (p = 0.0093), low levels of complement C4 did not associate with early requirement of kidney replacement therapy (KRT) or death (p = 0.2396). In the subgroup that experienced KRT or death, low C3 levels identified 11/14 (78.6%, p = 0.0071) and C4 levels 9/14 (64.3%, p = 0.1786) cases. Interestingly, 2/14 (14.3%) patients that experienced KRT or death had isolated C4 lowering, and combining low C3 and/or C4 levels identified 13/14 (92.3%, p < 0.0001) cases in this subgroup. Non-superiority to predict poor outcome by low C3 and/or C4 as compared to C3 alone in the total cohort was attributed to 4/24 (16.7%) patients with isolated C4 lowering in the subgroup that did not experience KRT or death.
CONCLUSION
While low levels of complement C3 were superior in predicting poor outcome in ANCA-associated renal vasculitis, a minor fraction with poor outcome had isolated C4 lowering not captured by serum C3 measurements. Therefore, detailed knowledge of distinct complement components contributing to kidney injury could be of relevance to improve current strategies targeting the complement system in ANCA-associated renal vasculitis.
Identifiants
pubmed: 35962865
doi: 10.1007/s40620-022-01414-w
pii: 10.1007/s40620-022-01414-w
pmc: PMC9894999
doi:
Substances chimiques
Antibodies, Antineutrophil Cytoplasmic
0
Complement C3
0
Complement C4
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
125-132Subventions
Organisme : Research program, University Medical Center, University of Göttingen
ID : 1403720
Organisme : Else Kröner-Fresenius-Stiftung
ID : 7-67-1840876
Informations de copyright
© 2022. The Author(s).
Références
Front Immunol. 2021 Jan 21;11:624547
pubmed: 33552089
Kidney Int. 2018 Dec;94(6):1177-1188
pubmed: 30385041
Front Immunol. 2018 Nov 20;9:2664
pubmed: 30515158
Kidney Int Rep. 2021 Sep 07;6(11):2930
pubmed: 34805645
Kidney Int Rep. 2021 Sep 07;6(11):2931-2933
pubmed: 34805646
Kidney Int Rep. 2021 Jun 12;6(9):2425-2435
pubmed: 34514203
J Clin Med. 2021 Apr 06;10(7):
pubmed: 33917561
Nephrol Ther. 2019 Nov;15(6):409-412
pubmed: 31631015
Ann Intern Med. 2009 May 5;150(9):604-12
pubmed: 19414839
Kidney Int Rep. 2016 Aug 31;2(1):66-75
pubmed: 29142942
Front Med (Lausanne). 2021 Feb 09;7:622028
pubmed: 33634143
Kidney Int Rep. 2022 Jan 15;7(3):660-661
pubmed: 35257082
J Clin Med. 2021 Mar 16;10(6):
pubmed: 33809645
J Am Soc Nephrol. 2010 Oct;21(10):1628-36
pubmed: 20616173
J Nephrol. 2018 Apr;31(2):257-262
pubmed: 29027625
Ann Rheum Dis. 2009 Dec;68(12):1827-32
pubmed: 19054820
Int J Mol Sci. 2021 Jun 19;22(12):
pubmed: 34205415
PLoS One. 2016 Jul 08;11(7):e0158871
pubmed: 27391243