J Rheum Dis.  2019 Jul;26(3):156-164. 10.4078/jrd.2019.26.3.156.

Classification of Antineutrophil Cytoplasmic Antibody-associated Vasculitis

Affiliations
  • 1Division of Rheumatology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea. sangwonlee@yuhs.ac

Abstract

Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a group of systemic vasculitides, that are characterized by inflammation in the small vessels, ranging from capillaries to arterioles or venules. AAV is divided into three variants based on the clinical manifestations and histological findings such as microscopic polyangiitis (MPA), granulomatosis with polyangiitis (GPA) and eosinophilic GPA (EGPA). MPA often induces rapid progressive necrotising glomerulonephritis, and occasionally induces diffuse alveolar hemorrhage. In contrast, GPA preferentially affects the respiratory tracts from the bronchus to the nasal cavity. GPA can also involve the kidneys, but the frequency of renal involvement is less than MPA. EGPA is based on allergic components such as asthma, peripheral eosinophilia, migratory eosinophilic pneumonia and eosinophil infiltration. Since 1982, when the association between ANCA and systemic vasculitis was first reported, several classification criteria for AAV have been proposed. This review describes the classification criteria for and nomenclature of AAV from the 1990 American College of Rheumatology (ACR) classification criteria to the 2012 revised Chapel Hill consensus conference (CHCC) nomenclature of Vasculitides. New classification trials for AAV such as AAV based on the ANCA-types (myeloperoxidase-ANCA vasculitis, proteinase 3-ANCA vasculitis and ANCA negative vasculitis) and the ACR/European League Against Rheumatism (EULAR) 2017 provisional classification criteria for GPA were also introduced. In addition, the histopathological classification of ANCA-associated glomerulonephritis and the revised 2017 international consensus on testing of ANCAs in GPA and MPA are also discussed.

Keyword

Antineutrophil cytoplasmic antibody; Vasculitis; Classification

MeSH Terms

Antibodies, Antineutrophil Cytoplasmic
Arterioles
Asthma
Bronchi
Capillaries
Classification*
Consensus
Cytoplasm*
Eosinophilia
Eosinophils
Glomerulonephritis
Granulomatosis with Polyangiitis
Hemorrhage
Inflammation
Kidney
Microscopic Polyangiitis
Nasal Cavity
Pulmonary Eosinophilia
Respiratory System
Rheumatic Diseases
Rheumatology
Systemic Vasculitis
Vasculitis*
Venules
Antibodies, Antineutrophil Cytoplasmic

Cited by  3 articles

Lipid Profiles in Anti-neutrophil Cytoplasmic Antibody-associated Vasculitis: A Cross-sectional Analysis
Sung Soo Ahn, Taejun Yoon, Jason Jungsik Song, Yong-Beom Park, Sang-Won Lee
J Rheum Dis. 2020;27(4):261-269.    doi: 10.4078/jrd.2020.27.4.261.

Acute coronary syndrome in antineutrophil cytoplasmic antibody-associated vasculitis: a Korean single-centre cohort study
Jin Seok Kim, Yong-Beom Park, Sang-Won Lee
J Rheum Dis. 2023;30(2):106-115.    doi: 10.4078/jrd.2023.0002.

The monocyte-to-high-density lipoprotein-cholesterol ratio at diagnosis is associated with cerebrovascular accident during follow-up in patients with antineutrophil cytoplasmic antibody-associated vasculitis
Jang Woo Ha, Sung Soo Ahn, Jason Jungsik Song, Yong-Beom Park, Sang-Won Lee
J Rheum Dis. 2024;31(3):151-159.    doi: 10.4078/jrd.2024.0001.

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