# Incidence and clinical features of ANCA-associated vasculitis before and during the COVID-19 pandemic: experience from a single-center in Northern Spain

**Authors:** Ligia Gabrie, Fabricio Benavides-Villanueva, Héctor Miguel Ulloa-Alvarado, Vanesa Calvo-Río, Iván Ferraz-Amaro, Santos Castañeda, Marcos López-Hoyos, Ricardo Blanco

PMC · DOI: 10.3389/fmed.2026.1766518 · Frontiers in Medicine · 2026-02-06

## TL;DR

This study found a temporary increase in a type of vasculitis during the early years of the COVID-19 pandemic in Northern Spain.

## Contribution

The study reports a significant rise in ANCA-associated vasculitis cases during the pandemic and links it to recent SARS-CoV-2 infection or vaccination.

## Key findings

- AAV incidence increased from 22.4 to 37.9 cases per million between 2019 and 2021.
- About 40% of AAV cases during the pandemic were linked to recent SARS-CoV-2 infection or vaccination.
- MPO-ANCA remained the most common subtype despite a rise in PR3-ANCA cases.

## Abstract

A transient increase in anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) incidence was observed during the coronavirus disease 2019 (COVID-19) pandemic. This study aimed to assess new AAV diagnoses during the COVID-19 pandemic in a single-center cohort.

We conducted a retrospective observational study of patients newly diagnosed with AAV at a tertiary care university hospital in Northern Spain between January 2019 and December 2022. Cases were classified according to the 2022 American College of Rheumatology/European Alliance of Associations for Rheumatology (ACR/EULAR) criteria. Clinical and serologic data were collected, including antibody specificity for proteinase 3 (PR3-ANCA) and myeloperoxidase (MPO-ANCA), as well as the temporal relationship to SARS-CoV-2 infection or COVID-19 vaccination.

A significant increase in AAV incidence was observed during the pandemic, rising from 22.4 cases per million in 2019 to 37.9 cases per million in 2021 (p = 0.031). Approximately 40% of patients diagnosed during this period had a recent SARS-CoV-2 infection or had been vaccinated against COVID-19 in the preceding 3 months. By 2022, AAV incidence returned to pre-pandemic levels. Contrary to initial trends, demographic and clinical characteristics remained stable; no significant differences were observed in age, gender distribution, disease severity, or organ involvement between the pre-pandemic and pandemic periods. While a numerical increase in PR3-ANCA cases was noted during the pandemic, MPO-ANCA remained the predominant subtype.

The temporary but significant rise in AAV incidence suggests a possible temporal association with COVID-19 infection or vaccination. These findings underscore the need to conduct larger, multicentre studies to confirm these observations, investigate potential pathophysiological mechanisms, and improve clinical management approaches.

## Linked entities

- **Diseases:** ANCA-associated vasculitis (MONDO:0012105), coronavirus disease 2019 (MONDO:0100096)

## Full-text entities

- **Genes:** MPO (myeloperoxidase) [NCBI Gene 4353], CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, PRTN3 (proteinase 3) [NCBI Gene 5657] {aka ACPA, AGP7, C-ANCA, CANCA, MBN, MBT}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, RNF130 (ring finger protein 130) [NCBI Gene 55819] {aka G1RP, G1RZFP, GOLIATH, GP}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}
- **Diseases:** ANCA-associated vasculitis (MESH:D056648), anorexia (MESH:D000855), AAV (MESH:D014657), respiratory tract infection (MESH:D012141), inflammation (MESH:D007249), systemic autoimmune diseases (MESH:D020274), necrotising vasculitis (MESH:D019283), Fever (MESH:D005334), hematologic malignancies (MESH:D019337), systemic lupus erythematosus (MESH:D008180), autoimmune diseases (MESH:D001327), adnexal tumor (MESH:D000292), COVID (MESH:D000086382), infection (MESH:D007239), weight loss (MESH:D015431), rheumatoid arthritis (MESH:D001172), vascular epilepsy (MESH:D004827), dysphagia (MESH:D003680), MPA (MESH:D055953), EGPA (MESH:D014890), death (MESH:D003643), asthenia (MESH:D001247), cognitive impairment (MESH:D003072), inflammatory bowel disease (MESH:D015212), infectious endocarditis (MESH:D004696), bronchial aspiration (MESH:D011015), interstitial lung disease (MESH:D017563)
- **Chemicals:** cyclophosphamide (MESH:D003520), cocaine (MESH:D003042), Rituximab (MESH:D000069283)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12920425/full.md

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Source: https://tomesphere.com/paper/PMC12920425