4.2 Article

Clinical Characteristics and Prognostic Value of Ro52/SSA Antibodies in Idiopathic Inflammatory Myopathies

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JCR-JOURNAL OF CLINICAL RHEUMATOLOGY
卷 29, 期 7, 页码 347-353

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LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/RHU.0000000000002015

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anti-Ro52 antibodies; anti-SSA antibodies; idiopathic inflammatory myopathy (IIM); interstitial lung disease

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This study reviewed the frequency, significance, and clinical characteristics of Ro52/SSA antibodies in patients with idiopathic inflammatory myopathies (IIMs). The results showed that Ro52/SSA antibodies were present in nearly one-fourth of the patients and were strongly associated with antisynthetase syndrome, interstitial lung disease (ILD), and dysphagia. However, there was no significant difference in outcomes or severity of ILD between patients with and without these antibodies.
Background/Purpose Anti-Ro52 are myositis-associated antibodies found in idiopathic inflammatory myopathies (IIMs). This chart review aims to evaluate the frequency, significance, and associated clinical characteristics of Ro52/SSA positivity in IIM patients.Methods We performed a chart review of IIM patients diagnosed between January 2006 and December 2020. All patients met either the 1975 Bohan and Peter or the European League Against Rheumatism/American College of Rheumatology classification criteria for probable or definite myositis. Demographics, clinical and serologic parameters, treatments, and outcomes were compared in patients with anti-Ro52/SSA antibodies and patients without anti-Ro52/SSA antibodies.Results One hundred eighty-nine patients with IIM were tested for either Ro52 or SSA, with 45 positive for Ro52/SSA (23.8%). Patients with IIM and Ro52/SSA(+) were younger at age at onset of disease (44.8 vs. 51.2 years, p = 0.008). Ro52/SSA(+) was more common in antisynthetase syndrome (p < 0.001; odds ratio [OR], 4.44; 95% confidence interval [CI], 2.11-9.33) and not frequently identified in clinically amyopathic dermatomyositis (CADM) (p = 0.02; OR, 0.13; 95% CI, 0.02-0.96) or immune-mediated necrotizing myopathy (p = 0.003; OR, 0.14; 95% CI, 0.03-0.63). Of the extraskeletal muscle manifestations, interstitial lung disease (ILD) was strongly associated with Ro52/SSA(+) (p < 0.001; OR, 6.61; 95% CI, 3.15-13.86), as was dysphagia (p = 0.006; OR, 2.73; 95% CI, 1.31-5.71). Interstitial lung disease pattern and pulmonary function testing impairment did not differ based on antibody status. There was no significant difference in outcomes between groups.Conclusion In this myositis cohort, Ro52/SSA(+) was present in nearly one-fourth of the population and had a strong association with the antisynthetase syndrome subtype, ILD, and dysphagia. Although these disease manifestations are associated with significant morbidity, in our cohort, they were not associated with increased mortality or more severe ILD.

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