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BVAS version 3 and BVAS/GPA: standing on the same line?

Authors
 Sung Soo Ahn  ;  Jang Woo Ha  ;  Yong-Beom Park  ;  Sang-Won Lee 
Citation
 CLINICAL RHEUMATOLOGY, Vol.41(11) : 3429-3437, 2022-11 
Journal Title
CLINICAL RHEUMATOLOGY
ISSN
 0770-3198 
Issue Date
2022-11
MeSH
Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis* / drug therapy ; Antibodies, Antineutrophil Cytoplasmic ; Granulomatosis with Polyangiitis* ; Humans ; Microscopic Polyangiitis* ; Proportional Hazards Models ; Retrospective Studies
Keywords
Anti-neutrophil cytoplasmic antibody ; Birmingham vasculitis activity score ; Granulomatosis with polyangiitis ; Microscopic polyangiitis ; Vasculitis
Abstract
Introduction/objectives: Birmingham vasculitis activity score (BVAS) version 3 (BVAS 3.0) and BVAS/granulomatosis with polyangiitis (BVAS/GPA) are used as indicators of disease activity in anti-neutrophil cytoplasmic antibody-associated vasculitis. We evaluated the association between these indices and the significance in patients with GPA and microscopic polyangiitis (GPA/MPA).

Methods: We retrospectively reviewed the records of 203 patients with GPA/MPA in our hospital. The correlation between BVAS 3.0 and BVAS/GPA with the five-factor score (FFS) and laboratory data was investigated. The episodes of all-cause mortality, end-stage renal disease, and disease relapse were counted as adverse clinical outcomes. Multivariate Cox hazard analyses were performed to assess the relationships between both indices and patient outcomes.

Results: Sixty-five (32.0%) and 138 (68.0%) patients with GPA and MPA were included. The median BVAS 3.0 was significantly higher in patients with MPA than in those with GPA (13.0 vs. 11.0, p = 0.015), whereas BVAS/GPA was higher in patients with GPA (4.0 vs. 3.0, p = 0.001). BVAS 3.0 and BVAS/GPA correlated significantly (r = 0.670, p < 0.001); both BVAS 3.0 and BVAS/GPA were shown to be associated with the outcomes investigated in separate Cox models. However, the correlation between BVAS 3.0 and BVAS/GPA was especially higher in a subgroup of patients with MPA than in those with GPA (MPA: r = 0.817, p < 0.001 vs. GPA: r = 0.570, p < 0.001) and with renal involvement (r = 0.676, p < 0.001).

Conclusions: Although both BVAS 3.0 and BVAS/GPA significantly correlated and predicted outcomes well in those with GPA/MPA, a discord was observed based on disease subtypes and organ involvement. Key Points • BVAS 3.0 and BVAS/GPA significantly correlated and predicted outcomes in those with GPA/MPA. • A discordance was also observed based on disease subtypes and organ involvement.
Full Text
https://link.springer.com/article/10.1007/s10067-022-06267-z
DOI
10.1007/s10067-022-06267-z
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Park, Yong Beom(박용범)
Ahn, Sung Soo(안성수) ORCID logo https://orcid.org/0000-0002-9002-9880
Lee, Sang-Won(이상원) ORCID logo https://orcid.org/0000-0002-8038-3341
Ha, Jang Woo(하장우)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/192303
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