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Anti-tRNA synthetase syndrome interstitial lung disease: A single center experience
Journal article

Anti-tRNA synthetase syndrome interstitial lung disease: A single center experience

E.M. Wilfong, J.J. Young-Glazer, B.K. Sohn, G. Schroeder, N. Annapureddy, E.A. Gillaspie, A. Barnado, L.J. Crofford and R.B. Dudenhofer
Respiratory Medicine, Vol.191
2022

Abstract

Anti-tRNA synthetase syndrome Connective tissue disease related interstitial lung disease Idiopathic inflammatory myopathies Systemic sclerosis Usual interstitial pneumonia Amino Acyl-tRNA Synthetases Autoantibodies Dermatomyositis Humans Lung Diseases, Interstitial Myositis Retrospective Studies amino acid transfer RNA ligase antinuclear antibody autoantibody creatine kinase cyclic citrullinated peptide antibody docking protein EJ antibody interferon induced helicase C domain containing protein 1 Jo 1 antibody nuclear receptor coactivator 2 NXP2 protein PL 12 antibody PL 7 antibody rheumatoid factor ro52 antibody Ro60 antibody SAE1 antibody Scl 100 antibody U2RNP protein U3RNP antibody unclassified drug amino acid transfer RNA ligase autoantibody adult analysis of variance antisynthetase syndrome Article bronchiectasis cohort analysis connective tissue disease controlled study dermatomyositis disease severity assessment dysphagia echocardiography extracorporeal oxygenation female fibrosing alveolitis Fisher exact test forced vital capacity ground glass opacity human interstitial lung disease interstitial pneumonia lung artery pressure major clinical study middle aged muscle weakness myositis observational study phenotype polymyositis pulmonary hypertension radiography rank sum test Raynaud phenomenon retrospective study rheumatoid arthritis rheumatology serology systemic sclerosis thorax radiography complication dermatomyositis myositis
Background: Recognition of Anti-tRNA synthetase (ARS) related interstitial lung disease (ILD) is key to ensuring patients have prompt access to immunosuppressive therapies. The purpose of this retrospective cohort study was to identify factors that may delay recognition of ARS-ILD. Methods: Patients seen at Vanderbilt University Medical Center between 9/17/2017-10/31/2018 were included in this observational cohort. Clinical and laboratory features were obtained via chart abstraction. Kruskal-Wallis ANOVA, Mann-Whitney U, and Fisher's exact t tests were utilized to determine statistical significance. Results: Patients with ARS were found to have ILD in 51.9% of cases, which was comparable to the frequency of ILD in systemic sclerosis (59.5%). The severity of FVC reduction in ARS (53.2%) was comparable to diffuse cutaneous systemic sclerosis (56.8%, p = 0.48) and greater than dermatomyositis (66.9%, p = 0.005) or limited cutaneous systemic sclerosis (71.8%, p = 0.005). Frank honeycombing was seen with ARS antibodies but not other myositis autoantibodies. ARS patients were more likely to first present to a pulmonary provider in a tertiary care setting (53.6%), likely due to fewer extrapulmonary manifestations. Only 33% of ARS-ILD were anti-nuclear antibody, rheumatoid factor, or anti-cyclic citrullinated peptide positive. Patients with ARS-ILD had a two-fold longer median time to diagnosis compared to other myositis-ILD patients (11.0 months, IQR 8.5–43 months vs. 5.0 months, IQR 3.0–9.0 months, p = 0.003). Conclusions: ARS patients without prominent extra-pulmonary manifestations are at high risk for not being recognized as having a connective tissue disease related ILD and miscategorized as usual interstitial pneumonia/idiopathic pulmonary fibrosis without comprehensive serologies. © 2021 The Author(s)
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https://www.scopus.com/inward/record.uri?eid=2-s2.0-85105781829&doi=10.1016%2fj.rmed.2021.106432&partnerID=40&md5=6b4a27a8712f03e8bb0b8b26ae4806d5View

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