英文摘要 |
Objective: Myositis-specific antibodies are present in idiopathic inflammatory myopathies (IIM), and may have an association with prognosis of polymyositis (PM) and dermatomyositis (DM). To our knowledge, few studies have been conducted on anti-Mi-2 positivity in the Chinese population. The aim of this study was to investigate the prevalence of anti-Mi-2 antibody in PM/DM in the Taiwan Chinese population and explore the clinical characteristics among these patients. Methods: Eighty-nine patients with PM/DM followed up at the rheumatology outpatient clinics of Taichung Veterans General Hospital (TCVGH) were enrolled between Jan. 1st 2001 and Jan. 1st 2013. Anti-Mi-2 IgG antibodies were detected by enzyme fluoroimmunoassay. Demographic data, clinical features, and laboratory findings were analyzed. Results: Anti-Mi-2 antibodies were detected in six (6.7%) of 89 participants with IIM. The female-male ratio was 1:1. All six patients had an initial presentation of malar rash. Five had Gottron’s sign, V sign, or periungual erythema. Two patients had heliotrope rash or Shawl sign. Anti-Mi-2 antibody positivity was associated with a higher chance of developing malar rash and V sign, but not with malignancy or interstitial lung disease (ILD). Conclusion: The frequency of anti-Mi-2 antibodies in our PM/DM cohort was comparable with that in previous studies. Anti-Mi-2 positivity was not associated with ILD or malignancy. Long-term follow-up of a large cohort is needed to determine the true prevalence and prognostic value of anti-Mi2 antibodies in patients with PM/DM. |