PMID- 35452854 OWN - NLM STAT- MEDLINE DCOM- 20220524 LR - 20220524 IS - 1873-0183 (Electronic) IS - 1568-9972 (Linking) VI - 21 IP - 6 DP - 2022 Jun TI - Performance of MPO-ANCA and PR3-ANCA immunoassays for the stratification of specific ANCA-associated vasculitis: A systematic review and meta-analysis. PG - 103100 LID - S1568-9972(22)00070-2 [pii] LID - 10.1016/j.autrev.2022.103100 [doi] AB - OBJECTIVE: To determine the impact of myeloperoxidase (MPO) and proteinase 3 (PR3) antigen-specific immunoassays in the stratification of patients at-risk for anti-neutrophil cytoplasmic antibodies (ANCA)-associated vasculitides (AAV) at diagnosis. METHODS: A Medline search was conducted to identify diagnostic accuracy studies using PR3-ANCA or MPO-ANCA for the evaluation of granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), and eosinophilic granulomatosis with polyangiitis (EGPA). Studies estimates were pooled using the bivariate method. RESULTS: Diagnostic accuracy varied by analyte and AAV subtype. PR3-ANCA had greater sensitivity than MPO-ANCA for GPA (74% vs 11%, p < 0.001) and MPO-ANCA greater sensitivity for MPA (73% vs 7%, p < 0.001). Specificities of both MPO-ANCA and PR3-ANCA were consistently high (mean 97%, range: 93-99%) for both AAV subtypes. There was insufficient data to perform meta-analysis for the diagnostic accuracy of EPGA. CONCLUSION: These results validate the use of high quality MPO-ANCA and PR3-ANCA immunoassays to screen patients at-risk for AAV as well as to categorize disease as GPA or MPA subtype. However, caution must be exercised in doing so, since some assays may not have optimal performance. Each laboratory should validate appropriate algorithms based on the tests used and testing population. CI - Copyright (c) 2022 Elsevier B.V. All rights reserved. FAU - Walker, Brandon S AU - Walker BS AD - ARUP Laboratories, Salt Lake City, UT, United States of America. FAU - Peterson, Lisa K AU - Peterson LK AD - ARUP Laboratories, Salt Lake City, UT, United States of America; Department of Pathology, University of Utah, Salt Lake City, UT, United States of America. FAU - Koening, Curry AU - Koening C AD - Department of Internal Medicine, Division of Rheumatology, University of Utah, Salt Lake City, UT, United States of America. FAU - White, Sandra K AU - White SK AD - Department of Pathology, University of Utah, Salt Lake City, UT, United States of America. FAU - Schmidt, Robert L AU - Schmidt RL AD - ARUP Laboratories, Salt Lake City, UT, United States of America; Department of Pathology, University of Utah, Salt Lake City, UT, United States of America. FAU - Tebo, Anne E AU - Tebo AE AD - ARUP Laboratories, Salt Lake City, UT, United States of America; Department of Pathology, University of Utah, Salt Lake City, UT, United States of America. Electronic address: tebo.anne@mayo.edu. LA - eng PT - Journal Article PT - Meta-Analysis PT - Review PT - Systematic Review DEP - 20220419 PL - Netherlands TA - Autoimmun Rev JT - Autoimmunity reviews JID - 101128967 RN - 0 (Antibodies, Antineutrophil Cytoplasmic) RN - EC 1.11.1.7 (Peroxidase) RN - EC 3.4.21.76 (Myeloblastin) SB - IM MH - *Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis/diagnosis MH - Antibodies, Antineutrophil Cytoplasmic MH - *Churg-Strauss Syndrome/diagnosis MH - *Granulomatosis with Polyangiitis/diagnosis MH - Humans MH - Immunoassay MH - *Microscopic Polyangiitis MH - Myeloblastin MH - Peroxidase OTO - NOTNLM OT - ANCA-associated vasculitis OT - Anti-neutrophil cytoplasmic antibodies OT - Diagnostic performance OT - Immunoassay OT - Myeloperoxidase OT - Proteinase 3 OT - Sensitivity OT - Specificity EDAT- 2022/04/23 06:00 MHDA- 2022/05/25 06:00 CRDT- 2022/04/22 20:10 PHST- 2022/03/26 00:00 [received] PHST- 2022/04/18 00:00 [accepted] PHST- 2022/04/23 06:00 [pubmed] PHST- 2022/05/25 06:00 [medline] PHST- 2022/04/22 20:10 [entrez] AID - S1568-9972(22)00070-2 [pii] AID - 10.1016/j.autrev.2022.103100 [doi] PST - ppublish SO - Autoimmun Rev. 2022 Jun;21(6):103100. doi: 10.1016/j.autrev.2022.103100. Epub 2022 Apr 19.