Evidence map›Paper›PMID 40617587›Full record

ArticleRMD open2025

Incidence and prevalence of ANCA-associated vasculitis in Oslo, Norway, applying different criteria-based case definitions: a population-based cohort study.

Karin R Kilian, Cathrine Brunborg, Sigrun Skaar Holme, Garen Torhild, Ragnar Gunnarsson, Øyvind Molberg

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Article in RMD open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Karin R KilianDepartment of Rheumatology, Oslo University Hospital, Oslo, Norway karin.kilian@medisin.uio.no.ORCID 0009-0003-3692-0458
Cathrine BrunborgBiostatistics, Epidemiology and Health Economics, Oslo University Hospital, Oslo, Norway.
Sigrun Skaar HolmeDepartment of Teleradiology, Unilabs Røntgen Majorstuen, Oslo, Norway.
Garen TorhildDepartment of Rheumatology, Oslo University Hospital, Oslo, Norway.
Ragnar GunnarssonDepartment of Rheumatology, Oslo University Hospital, Oslo, Norway.
Øyvind MolbergDepartment of Rheumatology, Oslo University Hospital, Oslo, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo provide complete data on the incidence and prevalence of antineutrophil cytoplasmic antibody-associated vasculitides (AAV) over the years 2000-2016 in the Oslo area, Norway, with 528 924 adults (aged 18+) in 2016.

methodsFrom administrative databases, we identified all cases with International Classification of Disease, 10th Revision (ICD-10) codes indicative of necrotising small vessel vasculitis during 2000-2016 in the Oslo area. We manually chart reviewed every case identified through the ICD-10 search to confirm (or reject) a clinical AAV diagnosis. Cases with confirmed clinical AAV were classified by the European Medicine Agency (EMA) algorithm and the 2022 American College of Rheumatology/European Alliance of Associations for Rheumatology (ACR/EULAR 2022) classification criteria.

resultsAmong 469 cases with an ICD-10 code indicative of small vessel vasculitis, chart review confirmed AAV in 133 cases with 97 having new onset during the study. Of these 97 incident cases, 57 (60%) were classified as granulomatosis with polyangiitis (GPA), 29 (31%) as microscopic polyangiitis (MPA) and 9 (9%) as eosinophilic granulomatosis with polyangiitis (EGPA) per ACR/EULAR 2022 criteria, while 2 remained unclassified. There was an 11% discordance in AAV case classification between the 2022 criteria and the EMA algorithm. The mean annual incidence of AAV in adults was 12.2 per million (7.3 for GPA, 3.7 for MPA and 1.2 for EGPA). Across the study period, incidence rates increased numerically, and prevalence peaked at 143.7 AAV cases/million adults in 2016.

conclusionThis population-based study adds new evidence that AAV increases in Europe and indicates that using the ACR/EULAR 2022 criteria shifts cases from GPA to MPA relative to the EMA algorithm, affecting epidemiology estimates.

Indexed as

Anti-Neutrophil Cytoplasmic Antibody-Associated VasculitisAdolescentAdultAgedAged, 80 and overAlgorithmsCohort StudiesFemaleGranulomatosis with PolyangiitisHumansIncidenceMaleMiddle AgedNorwayPrevalenceYoung AdultClassificationEpidemiologyIncidencePrevalenceSystemic vasculitis

Identifiers

PMID40617587
PMCPMC12228444

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.