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Predictive Features and Clinical Presentation of Interstitial Lung Disease in Inflammatory Myositis

Interstitial lung disease (ILD) represents one of the most severe extra-muscular features of idiopathic inflammatory myositis (IIM). We aimed to identify any clinical and serological predictors of ILD in a monocentric cohort of 165 IIM patients. ILD+ patients were defined as having restrictive impai...

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Autores principales: Vojinovic, Tamara, Cavazzana, Ilaria, Ceruti, Paolo, Fredi, Micaela, Modina, Denise, Berlendis, Marialma, Franceschini, Franco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7819919/
https://www.ncbi.nlm.nih.gov/pubmed/33141387
http://dx.doi.org/10.1007/s12016-020-08814-5
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author Vojinovic, Tamara
Cavazzana, Ilaria
Ceruti, Paolo
Fredi, Micaela
Modina, Denise
Berlendis, Marialma
Franceschini, Franco
author_facet Vojinovic, Tamara
Cavazzana, Ilaria
Ceruti, Paolo
Fredi, Micaela
Modina, Denise
Berlendis, Marialma
Franceschini, Franco
author_sort Vojinovic, Tamara
collection PubMed
description Interstitial lung disease (ILD) represents one of the most severe extra-muscular features of idiopathic inflammatory myositis (IIM). We aimed to identify any clinical and serological predictors of ILD in a monocentric cohort of 165 IIM patients. ILD+ patients were defined as having restrictive impairment in lung function tests and signs of ILD at chest high-resolution computed tomography (HRCT). Available HRCT images were centralized and classified in different ILD patterns: non-specific interstitial pneumonia (NSIP), organizing pneumonia (OP), usual interstitial pneumonia-like (UIP), indeterminate for UIP, and interstitial lung abnormalities (ILA). Lung function test data were recorded at onset, at 1 and 5 years after ILD diagnosis. ILD was found in 52 IIM patients (31.5%): 46.2% was affected by anti-synthetase syndrome (ARS), 21% by polymyositis (PM), 19% by dermatomyositis (DM), and 13.5% by overlap myositis. Most of ILD+ showed NSIP (31.9%), OP (19%), indeterminate for UIP (19%), and UIP (12.8%) patterns. At multivariate analysis, ILD was predicted by anti-Ro52 (p: 0.0026) and dyspnea (p: 0.015) at IIM onset. Most of ILD onset within is 12 months after IIM. In five cases, ILD occurs after 12 months since IIM diagnosis: these patients more frequently show dry cough and anti-Ku antibodies. Anti-Ro52 + ILD patients showed a significant increase of DLCO at 1 and 5 years of follow-up, compared with anti-Ro52 negative cases. ILD occurs in about one third of IIM and was predicted by dyspnea at onset and anti-Ro52 antibodies. Anti-Ro52 defines a subgroup of ILD showing a significant improvement of DLCO during follow-up. This retrospective study has been approved by local ethic committee (ASST-Spedali Civili of Brescia, Italy); protocol number: NP3511 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12016-020-08814-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-78199192021-01-28 Predictive Features and Clinical Presentation of Interstitial Lung Disease in Inflammatory Myositis Vojinovic, Tamara Cavazzana, Ilaria Ceruti, Paolo Fredi, Micaela Modina, Denise Berlendis, Marialma Franceschini, Franco Clin Rev Allergy Immunol Article Interstitial lung disease (ILD) represents one of the most severe extra-muscular features of idiopathic inflammatory myositis (IIM). We aimed to identify any clinical and serological predictors of ILD in a monocentric cohort of 165 IIM patients. ILD+ patients were defined as having restrictive impairment in lung function tests and signs of ILD at chest high-resolution computed tomography (HRCT). Available HRCT images were centralized and classified in different ILD patterns: non-specific interstitial pneumonia (NSIP), organizing pneumonia (OP), usual interstitial pneumonia-like (UIP), indeterminate for UIP, and interstitial lung abnormalities (ILA). Lung function test data were recorded at onset, at 1 and 5 years after ILD diagnosis. ILD was found in 52 IIM patients (31.5%): 46.2% was affected by anti-synthetase syndrome (ARS), 21% by polymyositis (PM), 19% by dermatomyositis (DM), and 13.5% by overlap myositis. Most of ILD+ showed NSIP (31.9%), OP (19%), indeterminate for UIP (19%), and UIP (12.8%) patterns. At multivariate analysis, ILD was predicted by anti-Ro52 (p: 0.0026) and dyspnea (p: 0.015) at IIM onset. Most of ILD onset within is 12 months after IIM. In five cases, ILD occurs after 12 months since IIM diagnosis: these patients more frequently show dry cough and anti-Ku antibodies. Anti-Ro52 + ILD patients showed a significant increase of DLCO at 1 and 5 years of follow-up, compared with anti-Ro52 negative cases. ILD occurs in about one third of IIM and was predicted by dyspnea at onset and anti-Ro52 antibodies. Anti-Ro52 defines a subgroup of ILD showing a significant improvement of DLCO during follow-up. This retrospective study has been approved by local ethic committee (ASST-Spedali Civili of Brescia, Italy); protocol number: NP3511 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12016-020-08814-5) contains supplementary material, which is available to authorized users. Springer US 2020-11-03 2021 /pmc/articles/PMC7819919/ /pubmed/33141387 http://dx.doi.org/10.1007/s12016-020-08814-5 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Vojinovic, Tamara
Cavazzana, Ilaria
Ceruti, Paolo
Fredi, Micaela
Modina, Denise
Berlendis, Marialma
Franceschini, Franco
Predictive Features and Clinical Presentation of Interstitial Lung Disease in Inflammatory Myositis
title Predictive Features and Clinical Presentation of Interstitial Lung Disease in Inflammatory Myositis
title_full Predictive Features and Clinical Presentation of Interstitial Lung Disease in Inflammatory Myositis
title_fullStr Predictive Features and Clinical Presentation of Interstitial Lung Disease in Inflammatory Myositis
title_full_unstemmed Predictive Features and Clinical Presentation of Interstitial Lung Disease in Inflammatory Myositis
title_short Predictive Features and Clinical Presentation of Interstitial Lung Disease in Inflammatory Myositis
title_sort predictive features and clinical presentation of interstitial lung disease in inflammatory myositis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7819919/
https://www.ncbi.nlm.nih.gov/pubmed/33141387
http://dx.doi.org/10.1007/s12016-020-08814-5
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