Literature DB >> 32293565

Anti-Mi-2 antibodies characterize a distinct clinical subset of dermatomyositis with favourable prognosis.

Lin Liang1, Ya-Mei Zhang2, He Chen2, Li-Fang Ye2, Shan-Shan Li2, Xin Lu2, Guo-Chun Wang1, Qing-Lin Peng2.   

Abstract

BACKGROUND: Anti-Mi-2 antibody is a type of myositis-specific autoantibody found in idiopathic inflammatory myopathy patients.
OBJECTIVES: To investigate the clinical features and long-term outcomes in anti-Mi-2-positive dermatomyositis (DM) patients.
MATERIALS AND METHODS: Serum anti-Mi-2β antibodies were detected in 357 DM patients by enzyme-linked immunosorbent assays, and possible associated clinical features were investigated based on cross-sectional and longitudinal studies.
RESULTS: Of the DM patients, 40/357 (11.2%) were positive for anti-Mi-2β antibodies and found to have a significantly higher frequency of V sign (72.5% vs 45.7%; p = 0.001), shawl sign (60.0% vs 35.6%; p = 0.003), and muscle weakness (77.5% vs 57.1%; p = 0.013), but a lower incidence of interstitial lung disease (ILD) (37.5% vs 60.9%; p = 0.005) and malignancy (0% vs 12.0%; p = 0.041) than anti-Mi-2β-negative patients. Anti-Mi-2β antibody levels positively correlated with disease activity. After a median follow-up period of 44 months, 97.0% of patients showed clinical remission. Twenty-six anti-Mi-2β-positive patients had a disease course longer than two years, and 16/26 (61.5%) were monocyclic without relapse. Moreover, five patients (15.1%) were drug-free with complete remission for more than three months. Kaplan-Meier survival curves showed that DM patients with positive anti-Mi-2β had a significantly lower mortality rate compared to anti-Mi-2β-negative patients (log-rank; p = 0.035). Interestingly, anti-Mi-2β antibodies did not disappear in all patients over time.
CONCLUSION: Anti-Mi-2β antibodies were associated with a subgroup of DM with a low frequency of ILD and malignancy, good treatment response, and favourable outcome. Moreover, anti-Mi-2β levels correlated with disease activity.

Entities:  

Keywords:  Mi-2; antibody; clinical significance; dermatomyositis; outcome

Year:  2020        PMID: 32293565     DOI: 10.1684/ejd.2020.3750

Source DB:  PubMed          Journal:  Eur J Dermatol        ISSN: 1167-1122            Impact factor:   3.328


  4 in total

1.  A Man With Recurrent Pneumonitis: A Rare Case of Interstitial Lung Disease Associated With Anti-Mi-2 Beta-Specific Dermatomyositis.

Authors:  Anam Ahmad; Yeswanth Attoti; Keith A Bernstein
Journal:  Cureus       Date:  2021-12-10

2.  Anti-Mi2 Antibody Positive Dermatomyositis With Hyper-Elevated Creatine Kinase: A Case Report.

Authors:  Ryuichi Ohta; Naho Yoshioka; Fumiko Yamane; Maika Hayashi; Chiaki Sano
Journal:  Cureus       Date:  2022-09-07

3.  The Association of Myositis Specific Antibodies in Patients with Inflammatory Myositis: Preliminary Data in Indian Patients.

Authors:  Natasha Vijay Negalur; Gayatri G Ekbote; Dhiren N Raval; Dhaval V Tanna; Wasim S Kazi; Muzaffar A Bindroo; Durgarao J Yadavalli; Rajiva Gupta
Journal:  Ann Indian Acad Neurol       Date:  2021-05-21       Impact factor: 1.383

4.  NanoString technology distinguishes anti-TIF-1γ+ from anti-Mi-2+ dermatomyositis patients.

Authors:  Corinna Preusse; Pascale Eede; Lucie Heinzeling; Kiara Freitag; Randi Koll; Waltraud Froehlich; Udo Schneider; Yves Allenbach; Olivier Benveniste; Anne Schänzer; Hans-Hilmar Goebel; Werner Stenzel; Josefine Radke
Journal:  Brain Pathol       Date:  2021-05       Impact factor: 6.508

  4 in total

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