Literature DB >> 36227529

Coexistence of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) and IgA nephropathy.

Yong Zhong1,2, Xiangcheng Xiao3,4, Qi Xiong5,6, Wei Lin7, Chanjuan Shen8, Ting Meng5, Rong Tang5, Joshua D Ooi5,9, Peter J Eggenhuizen9, Jinbiao Chen10, Wannian Nie5, Xia Li5, Qiaoling Zhou5, Ping Xiao5.   

Abstract

Co-occurrence of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) and IgA nephropathy (IgAN) is extremely uncommon. To date, only a few case reports have described such patients. Here, we describe the clinical presentation, pathologic features, treatment response, and outcome data of five patients with the rare form of co-existing AAV and IgAN and compared the characteristics of these patients to AAV patients with pauci-immune glomerulonephritis (n = 10) and IgAN patients (n = 10) that were selected as controls by stratified random sampling. In addition, we summarize all the previously reported cases of AAV and IgAN. In total, including the current study, 16 AAV/IgAN overlap cases were reported. Our five patients with the coexistence of AAV and IgAN were younger than the ten AAV patients with pauci-immune glomerulonephritis (22.6 ± 8.2 years versus 48.9 ± 15.7 years, respectively, P = 0.004). Histologically, they had a significantly lower percentage of glomeruli with fibrous crescents compared with AAV patients (0.0% versus 4.0%, P = 0.038). Compared with ten IgAN patients, our five AAV/IgAN patients had higher levels of ESR (P = 0.032) and CRP (P = 0.031). After accepting treatment with a combination of steroid and immunosuppressants, all patients showed a positive response to therapy, except for one patient in our cohort and another previously reported patient. We described the clinical presentation, pathologic features, treatment response, and outcome data of five patients with overlapping AAV and IgAN. They had mild glomerular pathological lesions and a positive response to aggressive immunosuppressive therapy. They were quite similar to pauci-immune AAV patients in clinical features, except for younger age. They had a lower percentage of glomeruli with fibrous crescents compared with AAV patients. In contrast to IgAN patients, they had higher levels of ESR and CRP. The mechanism of the coexistence of IgAN and AAV needs further study.
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Antineutrophil cytoplasmic antibody; Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV); Autoimmune disease; Glomerular disease; IgA nephropathy

Year:  2022        PMID: 36227529     DOI: 10.1007/s12026-022-09322-8

Source DB:  PubMed          Journal:  Immunol Res        ISSN: 0257-277X            Impact factor:   4.505


  25 in total

1.  Simultaneous IgA nephropathy and Wegener's granulomatosis--overlap or coincidence (the role of renal biopsy).

Authors:  F Vrtovsnik; G Queffeulou; H Skhiri; D Nochy; F Walker; G Hayem; F Mignon
Journal:  Nephrol Dial Transplant       Date:  1999-05       Impact factor: 5.992

2.  Rapidly progressive IgA nephropathy with anti-myeloperoxidase antibodies benefits from immunosuppression.

Authors:  E Allmaras; R Nowack; K Andrassy; R Waldherr; F van der Woude; E Ritz
Journal:  Clin Nephrol       Date:  1997-11       Impact factor: 0.975

3.  Clinical value of systemic symptoms in IgA nephropathy with ANCA positivity.

Authors:  Lijiao Xie; Jianghua He; Xing Liu; Sha Tang; Weili Wang; Furong Li; Ying Zhang; Jun Zhang; Yunjian Huang; Jinghong Zhao; Yafei Li; Jingbo Zhang
Journal:  Clin Rheumatol       Date:  2017-12-04       Impact factor: 2.980

4.  Epidemiology of IgA Nephropathy: A Global Perspective.

Authors:  Francesco Paolo Schena; Ionut Nistor
Journal:  Semin Nephrol       Date:  2018-09       Impact factor: 5.299

5.  Antineutrophil cytoplasmic antibodies in IgA nephropathy and Henoch-Schönlein purpura.

Authors:  D J O'Donoghue; P Nusbaum; L H Noel; L Halbwachs-Mecarelli; P Lesavre
Journal:  Nephrol Dial Transplant       Date:  1992       Impact factor: 5.992

Review 6.  ANCA-associated vasculitis.

Authors:  A Richard Kitching; Hans-Joachim Anders; Neil Basu; Elisabeth Brouwer; Jennifer Gordon; David R Jayne; Joyce Kullman; Paul A Lyons; Peter A Merkel; Caroline O S Savage; Ulrich Specks; Renate Kain
Journal:  Nat Rev Dis Primers       Date:  2020-08-27       Impact factor: 52.329

7.  The Clinicopathologic Characteristics and Complement Activation of Antineutrophil Cytoplasmic Antibody-associated Vasculitides With Glomerular IgA Deposition.

Authors:  Yanhong Ma; Liangliang Chen; Ying Xu; Quan Han; Binfeng Yu; Jie Zhao; Zhou Hua; Yi Yang; Jianghua Chen; Fei Han
Journal:  Appl Immunohistochem Mol Morphol       Date:  2020 Nov/Dec

8.  Is presence of ANCA in crescentic IgA nephropathy a coincidence or novel clinical entity? A case series.

Authors:  Christos Bantis; Maria Stangou; Christoph Schlaugat; Efstathios Alexopoulos; Aphroditi Pantzaki; Dimitrios Memmos; Katrin Ivens; Peter J Heering
Journal:  Am J Kidney Dis       Date:  2009-12-30       Impact factor: 8.860

Review 9.  IgA nephropathy with serum ANCA positivity: case series and literature review.

Authors:  Gabriel Ștefan; George Terinte-Balcan; Simona Stancu; Adrian Zugravu; Mihaela Gherghiceanu; Gabriel Mircescu
Journal:  Rheumatol Int       Date:  2021-05-17       Impact factor: 2.631

10.  Clinical features of IgA nephropathy with serum ANCA positivity: a retrospective case-control study.

Authors:  Ya-Zi Yang; Su-Fang Shi; Yu-Qing Chen; Min Chen; Yi-He Yang; Xin-Fang Xie; Rong Zou; Ji-Cheng Lv; Li-Jun Liu; Hong Zhang
Journal:  Clin Kidney J       Date:  2015-08-30
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