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Significance of anti-neutrophil cytoplasmic antibodies in systemic sclerosis

BACKGROUND: Up to 12% of patients with systemic sclerosis (SSc) have anti-neutrophil cytoplasmic antibodies (ANCA). However, the majority of these patients do not manifest ANCA-associated vasculitis (AAV) and the significance of ANCA in these patients is unclear. The aim of this study is to determin...

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Autores principales: Moxey, Jayne, Huq, Molla, Proudman, Susanna, Sahhar, Joanne, Ngian, Gene-Siew, Walker, Jenny, Strickland, Gemma, Wilson, Michelle, Ross, Laura, Major, Gabor, Roddy, Janet, Stevens, Wendy, Nikpour, Mandana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376778/
https://www.ncbi.nlm.nih.gov/pubmed/30764870
http://dx.doi.org/10.1186/s13075-019-1839-5
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author Moxey, Jayne
Huq, Molla
Proudman, Susanna
Sahhar, Joanne
Ngian, Gene-Siew
Walker, Jenny
Strickland, Gemma
Wilson, Michelle
Ross, Laura
Major, Gabor
Roddy, Janet
Stevens, Wendy
Nikpour, Mandana
author_facet Moxey, Jayne
Huq, Molla
Proudman, Susanna
Sahhar, Joanne
Ngian, Gene-Siew
Walker, Jenny
Strickland, Gemma
Wilson, Michelle
Ross, Laura
Major, Gabor
Roddy, Janet
Stevens, Wendy
Nikpour, Mandana
author_sort Moxey, Jayne
collection PubMed
description BACKGROUND: Up to 12% of patients with systemic sclerosis (SSc) have anti-neutrophil cytoplasmic antibodies (ANCA). However, the majority of these patients do not manifest ANCA-associated vasculitis (AAV) and the significance of ANCA in these patients is unclear. The aim of this study is to determine the prevalence of ANCA in a well-characterised SSc cohort and to examine the association between ANCA and SSc clinical characteristics, other autoantibodies, treatments and mortality. METHODS: Clinical data were obtained from 5 centres in the Australian Scleroderma Cohort Study (ASCS). ANCA positive was defined as the presence of any one or combination of cytoplasmic ANCA (c-ANCA), perinuclear ANCA (p-ANCA), atypical ANCA, anti-myeloperoxidase (anti-MPO) or anti-proteinase-3 (anti-PR3). Associations of demographic and clinical features with ANCA were investigated by logistic or linear regression. Survival analysis was performed using Kaplan-Meyer curves and Cox regression models. RESULTS: Of 1303 patients, 116 (8.9%) were ANCA positive. Anti-PR3 was more common than anti-MPO (13.8% and 11.2% of ANCA-positive patients, respectively). Only 3 ANCA-positive patients had AAV. Anti-Scl-70 was more common in ANCA positive vs ANCA negative (25% vs 12.8%, p < 0.001), anti-MPO positive vs anti-MPO negative (38.5% vs 13.6%, p = 0.006) and anti-PR3 positive vs anti-PR3 negative patients (44.4% vs 13.4%, p < 0.001). A higher prevalence of interstitial lung disease (ILD) was found in the ANCA positive (44.8% vs 21.8%, p < 0.001) and the anti-PR3 positive groups (50.0% vs 23.4%, p = 0.009). In multivariable analysis, ANCA-positive status remained associated with ILD after adjusting for anti-Scl-70 antibodies. Pulmonary embolism (PE) was more common in ANCA-positive patients (8.6% vs 3.0%, p = 0.002) and anti-PR3-positive patients (16.7% vs 3.3%, p = 0.022). ANCA-positive status remained associated with PE in a multivariable analysis adjusting for anti-phospholipid antibodies. Kaplan-Meier analysis revealed increased mortality in ANCA-positive patients (p = 0.006). In Cox regression analysis, ANCA was associated with increased mortality, after adjusting for age and sex. CONCLUSIONS: ANCA is associated with increased prevalence of ILD and PE in SSc. ANCA should be tested in SSc, as it identifies individuals with worse prognosis who require close monitoring for adverse outcomes.
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spelling pubmed-63767782019-02-27 Significance of anti-neutrophil cytoplasmic antibodies in systemic sclerosis Moxey, Jayne Huq, Molla Proudman, Susanna Sahhar, Joanne Ngian, Gene-Siew Walker, Jenny Strickland, Gemma Wilson, Michelle Ross, Laura Major, Gabor Roddy, Janet Stevens, Wendy Nikpour, Mandana Arthritis Res Ther Research Article BACKGROUND: Up to 12% of patients with systemic sclerosis (SSc) have anti-neutrophil cytoplasmic antibodies (ANCA). However, the majority of these patients do not manifest ANCA-associated vasculitis (AAV) and the significance of ANCA in these patients is unclear. The aim of this study is to determine the prevalence of ANCA in a well-characterised SSc cohort and to examine the association between ANCA and SSc clinical characteristics, other autoantibodies, treatments and mortality. METHODS: Clinical data were obtained from 5 centres in the Australian Scleroderma Cohort Study (ASCS). ANCA positive was defined as the presence of any one or combination of cytoplasmic ANCA (c-ANCA), perinuclear ANCA (p-ANCA), atypical ANCA, anti-myeloperoxidase (anti-MPO) or anti-proteinase-3 (anti-PR3). Associations of demographic and clinical features with ANCA were investigated by logistic or linear regression. Survival analysis was performed using Kaplan-Meyer curves and Cox regression models. RESULTS: Of 1303 patients, 116 (8.9%) were ANCA positive. Anti-PR3 was more common than anti-MPO (13.8% and 11.2% of ANCA-positive patients, respectively). Only 3 ANCA-positive patients had AAV. Anti-Scl-70 was more common in ANCA positive vs ANCA negative (25% vs 12.8%, p < 0.001), anti-MPO positive vs anti-MPO negative (38.5% vs 13.6%, p = 0.006) and anti-PR3 positive vs anti-PR3 negative patients (44.4% vs 13.4%, p < 0.001). A higher prevalence of interstitial lung disease (ILD) was found in the ANCA positive (44.8% vs 21.8%, p < 0.001) and the anti-PR3 positive groups (50.0% vs 23.4%, p = 0.009). In multivariable analysis, ANCA-positive status remained associated with ILD after adjusting for anti-Scl-70 antibodies. Pulmonary embolism (PE) was more common in ANCA-positive patients (8.6% vs 3.0%, p = 0.002) and anti-PR3-positive patients (16.7% vs 3.3%, p = 0.022). ANCA-positive status remained associated with PE in a multivariable analysis adjusting for anti-phospholipid antibodies. Kaplan-Meier analysis revealed increased mortality in ANCA-positive patients (p = 0.006). In Cox regression analysis, ANCA was associated with increased mortality, after adjusting for age and sex. CONCLUSIONS: ANCA is associated with increased prevalence of ILD and PE in SSc. ANCA should be tested in SSc, as it identifies individuals with worse prognosis who require close monitoring for adverse outcomes. BioMed Central 2019-02-14 2019 /pmc/articles/PMC6376778/ /pubmed/30764870 http://dx.doi.org/10.1186/s13075-019-1839-5 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Moxey, Jayne
Huq, Molla
Proudman, Susanna
Sahhar, Joanne
Ngian, Gene-Siew
Walker, Jenny
Strickland, Gemma
Wilson, Michelle
Ross, Laura
Major, Gabor
Roddy, Janet
Stevens, Wendy
Nikpour, Mandana
Significance of anti-neutrophil cytoplasmic antibodies in systemic sclerosis
title Significance of anti-neutrophil cytoplasmic antibodies in systemic sclerosis
title_full Significance of anti-neutrophil cytoplasmic antibodies in systemic sclerosis
title_fullStr Significance of anti-neutrophil cytoplasmic antibodies in systemic sclerosis
title_full_unstemmed Significance of anti-neutrophil cytoplasmic antibodies in systemic sclerosis
title_short Significance of anti-neutrophil cytoplasmic antibodies in systemic sclerosis
title_sort significance of anti-neutrophil cytoplasmic antibodies in systemic sclerosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376778/
https://www.ncbi.nlm.nih.gov/pubmed/30764870
http://dx.doi.org/10.1186/s13075-019-1839-5
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