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Antineutrophil cytoplasmic antibody-associated vasculitis classification by cluster analysis based on clinical phenotypes: a single-center retrospective cohort study

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dc.contributor.author박용범-
dc.contributor.author송정식-
dc.contributor.author안성수-
dc.contributor.author이상원-
dc.contributor.author이은주-
dc.contributor.author표정윤-
dc.date.accessioned2024-03-22T06:23:45Z-
dc.date.available2024-03-22T06:23:45Z-
dc.date.issued2024-01-
dc.identifier.issn0770-3198-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/198541-
dc.description.abstractObjective Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) refers to a group of small vessel inflammatory disorders. Overlapping clinical phenotypes of AAV subgroups continually provoke controversies over their diagnostic and classification criteria. Methods Using the agglomerative hierarchical clustering method, we classified 210 Korean patients diagnosed with AAV into mutually exclusive clusters according to Birmingham Vasculitis Activity Score items, ANCA specificity, sex, and age. We analyzed the resulting clusters’ outcomes to investigate the clinical significance of the classification. We proposed a distance-based algorithm of patient assignment and explored its clinically relevant modification. Results In total, 116 patients (55%) had microscopic polyangiitis, 53 (25%) had granulomatosis with polyangiitis, and 42 (20%) had eosinophilic granulomatosis with polyangiitis. Our model grouped the patients into five clusters, namely, “limited proteinase 3 (PR3)-ANCA vasculitis,” “generalized PR3-ANCA vasculitis,” “ANCA-negative vasculitis,” “renal-limited vasculitis,” and “myeloperoxidase-ANCA vasculitis.” Patients clustered under “generalized PR3-ANCA vasculitis” had a higher relapse rate (hazard ratio [HR] = 2.12, P = 0.067). The incidence of end-stage renal disease was higher in patients belonging to the “renal-limited vasculitis” cluster (HR=1.50, P=0.03), and those in the “ANCA-negative vasculitis” cluster experienced a relatively milder clinical course of AAV (mortality = 0). Conclusion Because the clusters were naturally derived from their distinguished phenotypes and have different clinical courses, our clustering method may be a more clinically relevant classification system for AAV, revealing its phenotypic diversity. We also proposed a simple and intuitive distance-based assignment algorithm, which can be easily modified according to specific clinical needs.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherSpringer-
dc.relation.isPartOfCLINICAL RHEUMATOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAnti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis* / diagnosis-
dc.subject.MESHAntibodies, Antineutrophil Cytoplasmic-
dc.subject.MESHChurg-Strauss Syndrome*-
dc.subject.MESHCluster Analysis-
dc.subject.MESHGranulomatosis with Polyangiitis* / diagnosis-
dc.subject.MESHHumans-
dc.subject.MESHKidney Diseases*-
dc.subject.MESHMyeloblastin-
dc.subject.MESHPeroxidase-
dc.subject.MESHPhenotype-
dc.subject.MESHRetrospective Studies-
dc.titleAntineutrophil cytoplasmic antibody-associated vasculitis classification by cluster analysis based on clinical phenotypes: a single-center retrospective cohort study-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorLucy Eunju Lee-
dc.contributor.googleauthorJung Yoon Pyo-
dc.contributor.googleauthorSung Soo Ahn-
dc.contributor.googleauthorJason Jungsik Song-
dc.contributor.googleauthorYong-Beom Park-
dc.contributor.googleauthorSang-Won Lee-
dc.identifier.doi10.1007/s10067-023-06720-7-
dc.contributor.localIdA01579-
dc.contributor.localIdA02057-
dc.contributor.localIdA02233-
dc.contributor.localIdA02824-
dc.contributor.localIdA05935-
dc.contributor.localIdA04244-
dc.relation.journalcodeJ00612-
dc.identifier.eissn1434-9949-
dc.identifier.pmid37530864-
dc.identifier.urlhttps://link.springer.com/article/10.1007/s10067-023-06720-7-
dc.subject.keywordAntineutrophil cytoplasmic antibody-associated vasculitis-
dc.subject.keywordCluster analysis-
dc.subject.keywordEosinophilic granulomatosis with polyangiitis-
dc.subject.keywordGranulomatosis with polyangiitis-
dc.subject.keywordMicroscopic polyangiitis-
dc.contributor.alternativeNamePark, Yong Beom-
dc.contributor.affiliatedAuthor박용범-
dc.contributor.affiliatedAuthor송정식-
dc.contributor.affiliatedAuthor안성수-
dc.contributor.affiliatedAuthor이상원-
dc.contributor.affiliatedAuthor이은주-
dc.contributor.affiliatedAuthor표정윤-
dc.citation.volume43-
dc.citation.number1-
dc.citation.startPage367-
dc.citation.endPage376-
dc.identifier.bibliographicCitationCLINICAL RHEUMATOLOGY, Vol.43(1) : 367-376, 2024-01-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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