Low serum complement 3 level is associated with severe ANCA-associated vasculitis at diagnosis.
Antineutrophil cytoplasmic antibody-associated vasculitis
Complement 3
Renal outcome
Severity
Journal
Clinical and experimental nephrology
ISSN: 1437-7799
Titre abrégé: Clin Exp Nephrol
Pays: Japan
ID NLM: 9709923
Informations de publication
Date de publication:
Feb 2019
Feb 2019
Historique:
received:
07
07
2018
accepted:
14
08
2018
pubmed:
1
9
2018
medline:
18
6
2019
entrez:
1
9
2018
Statut:
ppublish
Résumé
We investigated whether low serum C3 level can cross-sectionally estimate severe antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) in immunosuppressive drug-naïve patients at diagnosis. We retrospectively reviewed the medical records of 139 patients with AAV, who were first classified as AAV at Severance Hospital. We obtained clinical and laboratory data including serum complement 3 (C3) level and calculated Birmingham vasculitis activity score (BVAS) at diagnosis. We stratified AAV patients into three groups according to the tertile of BVAS and defined the lower limit of the highest tertile as the cutoff for severe AAV (BVAS at diagnosis ≥ 16) at diagnosis. Low serum C3 level was defined as C3 < 90 mg/dL. The odds ratio (OR) was assessed using the multivariable logistic regression. The mean age at diagnosis was 56.3 years and 41 patients were men (29.5%). The mean initial BVAS was 12.8. The mean serum C3 and C4 levels were 110.6 and 26.8 mg/dL. Thirty-one patients (22.3%) exhibited low serum C3 level at diagnosis. In the multivariable analysis, serum C3 level at diagnosis < 90 mg/dL (OR 2.963) exhibited the significant association with severe AAV at diagnosis. Patients with low serum C3 level exhibited a significantly high relative risk (RR) for severe AAV at diagnosis compared to those without (RR 3.600). Patients with low serum C3 level at diagnosis exhibited poor renal prognosis than those without. Low serum C3 level can estimate severe AAV and predict poor renal outcome in immunosuppressive drug-naïve patients at diagnosis.
Identifiants
pubmed: 30168048
doi: 10.1007/s10157-018-1634-7
pii: 10.1007/s10157-018-1634-7
doi:
Substances chimiques
Biomarkers
0
C3 protein, human
0
Complement C3
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
223-230Subventions
Organisme : Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education
ID : 2017R1D1A1B03029050
Organisme : a grant from the Korea Health Technology R&D Project through the Korea Health Industry Development Institute, funded by the Ministry of Health and Welfare, Republic of Korea
ID : HI14C1324
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