scispace - formally typeset
Journal ArticleDOI

Myositis specific antibodies are associated with isolated anti-Ro-52 associated interstitial lung disease

Reads0
Chats0
TLDR
Wang et al. as discussed by the authors found that isolated anti-Ro-52 positivity with cytoplasmic ANA positivity was strongly associated with ASA+-ILD, while ANA negativity was associated with anti-MDA-5+-ILD.
Abstract
Objectives Anti-Ro-52 antibody positivity might be associated with the presence of interstitial lung disease (ILD) among patients with autoimmune features. However, the clinical significance of isolated anti-Ro-52 positivity (i.e., the presence of anti-Ro52 antibodies but the absence of anti-Ro60 antibodies; anti-Ro52+-Ro60-) in patients with ILD is not clear. Methods This is a prospective and observational study of Chinese ILD patients with isolated anti-Ro-52 positivity. According to their myositis-specific antibody (MSA) status, patients were split into groups, and their clinical and radiological features were compared. Results Of the 158 enrolled patients with ILD and isolated anti-Ro-52 positivity (isolated anti-Ro-52-ILD), there were 130 patients with a positive MSA status and 28 patients with a negative MSA status. Anti-synthetase antibodies (ASAs) were found in 61.5% of patients with MSA+ ILD, and anti-melanoma differentiated-associated protein 5 (MDA-5) antibodies were found in the remaining 38.5% of patients. The anti-nuclear antibody (ANA) pattern was associated with ASA and anti-MDA-5 positivity (χ2=70.7, P Conclusions Patients with isolated anti-Ro-52-ILD showed high positivity of MSA. Isolated anti-Ro-52 positivity with cytoplasmic ANA positivity was strongly associated with ASA+-ILD, while ANA negativity was associated with anti-MDA-5+-ILD.

read more

Citations
More filters
Journal ArticleDOI

Anti-Ro52-positive antisynthetase syndrome (ASS): a case report and review of the literature

TL;DR: In this paper , the authors diagnose and treat a patient with anti-Ro52-positive antisynthetase syndrome (ASS), investigate the association between antiRo52 antibodies and ASS, and determine its clinical significance.
Journal ArticleDOI

Risk Factors and Predictive Model for Dermatomyositis Associated with Rapidly Progressive Interstitial Lung Disease

TL;DR: Wang et al. as mentioned in this paper developed prediction models of Rapidly progressive interstitial lung disease (RP-ILD) by machine learning methods, namely least absolute shrinkage and selection operator (LASSO), random forest (RF), and extreme gradient boosting (XGBoost).
Journal ArticleDOI

Myositis interstitial lung disease and autoantibodies

TL;DR: In this article , the authors examined and evaluated published literature associated with idiopathic inflammatory myopathies and interstitial lung disease (ILD) based on myositis specific autoantibodies (MSA).
Journal ArticleDOI

Clinical, radiological and pathological features of anti-MDA5 antibody-associated interstitial lung disease

TL;DR: In this article , the clinical, radiographic and pathological features of interstitial lung disease (ILD) in patients with anti-melanoma differentiation-associated gene 5 antibody-positive dermatomyositis (anti-MDA5+DM) were investigated.
References
More filters
Journal ArticleDOI

American thoracic society/European respiratory society international multidisciplinary consensus classification of the idiopathic interstitial pneumonias

TL;DR: The Diagnostic Process Is Dynamic Clinical Evaluation Radiological Evaluation Role of Surgical Lung Biopsy Unclassifiable Interstitial Pneumonia Bronchoalveolar Lavage Fluid Evaluation Idiopathic Pulmonary Fibrosis.
Journal ArticleDOI

Autoantibody profiles in the sera of European patients with myositis

TL;DR: The data show that some sera may contain more than one type of MSA and confirm the strong association of anti-Ro52 with anti-Jo-1 reactivity, which may be explained by the use of multiple recombinant fragments spanning the complete antigen.
Journal ArticleDOI

Interstitial lung disease associated with the idiopathic inflammatory myopathies: what progress has been made in the past 35 years?

TL;DR: In the 35 years since the association between inflammatory myopathy and interstitial lung disease was initially described, there has been progress in diagnosing and treating this disorder, however, there remains much about pathogenesis and therapeutics to be learned.
Journal ArticleDOI

The clinical phenotype associated with myositis-specific and associated autoantibodies: A meta-analysis revisiting the so-called antisynthetase syndrome

TL;DR: The presence of anti-ARS autoantibodies delimits a heterogeneous subset of patients with a high prevalence of myositis, MH, arthralgia in anti-Jo1 patients, and RPh and fever in non-anti-Jo 1 patients, challenging the clinical delimitation of the antisynthetase syndrome.
Related Papers (5)