Literature DB >> 33629202

Real world utilization of the myositis autoantibody panel.

Mithu Maheswaranathan1, Andrew Johannemann2, Jason J Weiner3, Ryan Jessee2, Amanda M Eudy4, Lisa Criscione-Schreiber4.   

Abstract

OBJECTIVE: Myositis autoantibody panel results can offer diagnostic and prognostic information in patients with concern for idiopathic inflammatory myopathy (IIM). However, there has been widespread utilization of myositis autoantibody testing clinically, often in situations where concern for an IIM is unclear. We sought to determine ordering practices and factors predicting positive results on ordered myositis antibody panels.
METHODS: We included all patients in the Duke University Health System who had a "myositis antibody panel" ordered from October 2014 through December 2016. Retrospective chart review was performed evaluating antibody positivity, provider specialty, ordering location, demographics, medical history, review of systems (ROS), physical examination (PE), and laboratory values. Fisher's exact and t test tests and backward multivariable regression analysis were performed for statistical analysis.
RESULTS: There were 642 unique tests obtained with 114 positive autoantibodies (17.7%) over the 26-month period. Myositis-specific autoantibodies (MSAs) were the most common and anti-Mi-2 was the most frequent (40% of MSAs). Pulmonology providers ordered the majority of tests (383; 59.6%). Adult Rheumatology had the highest antibody positivity rate (34.3%, p=0.0001) among specialties with at least 10 panels ordered. In backward multivariable regression analysis, factors independently associated with a positive myositis antibody panel were chronic corticosteroid use (OR: 2.10, 95% CI: 1.30-3.38) and sclerodermoid skin changes (OR: 6.89; 95% CI: 2.02-23.47).
CONCLUSION: The positivity rate of myositis antibody panel testing in this real-world clinical setting was 18%. Anti-Mi-2 antibody was the most frequent autoantibody present. Specific factors associated with positive results can be utilized to identify patients at higher risk for IIM. KEY POINTS: • Only eighteen percent of all myositis antibody panel tests ordered returned positive. • Anti-Mi-2 antibody was the most frequent autoantibody in our cohort. • Specific factors associated with positive results can help identify patients at higher risk for IIM, particularly for non-rheumatologists.
© 2021. International League of Associations for Rheumatology (ILAR).

Entities:  

Keywords:  Epidemiology; Idiopathic inflammatory myopathy; Myositis; Myositis antibody panel; Test utilization

Mesh:

Substances:

Year:  2021        PMID: 33629202     DOI: 10.1007/s10067-021-05658-y

Source DB:  PubMed          Journal:  Clin Rheumatol        ISSN: 0770-3198            Impact factor:   2.980


  23 in total

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Authors:  Minoru Satoh; Shin Tanaka; Angela Ceribelli; S John Calise; Edward K L Chan
Journal:  Clin Rev Allergy Immunol       Date:  2017-02       Impact factor: 8.667

Review 2.  Recent advances in dermatomyositis-specific autoantibodies.

Authors:  Manabu Fujimoto; Rei Watanabe; Yosuke Ishitsuka; Naoko Okiyama
Journal:  Curr Opin Rheumatol       Date:  2016-11       Impact factor: 5.006

Review 3.  Idiopathic inflammatory myopathies.

Authors:  Mazen M Dimachkie; Richard J Barohn; Anthony A Amato
Journal:  Neurol Clin       Date:  2014-08       Impact factor: 3.806

4.  The Prevalence of Individual Histopathologic Features Varies according to Autoantibody Status in Muscle Biopsies from Patients with Dermatomyositis.

Authors:  Iago Pinal-Fernandez; Livia A Casciola-Rosen; Lisa Christopher-Stine; Andrea M Corse; Andrew L Mammen
Journal:  J Rheumatol       Date:  2015-08       Impact factor: 4.666

Review 5.  The Clinical Features of Myositis-Associated Autoantibodies: a Review.

Authors:  Harsha Gunawardena
Journal:  Clin Rev Allergy Immunol       Date:  2017-02       Impact factor: 8.667

6.  Prognostic significance of anti-aminoacyl-tRNA synthetase antibodies in polymyositis/dermatomyositis-associated interstitial lung disease: a retrospective case control study.

Authors:  Hironao Hozumi; Noriyuki Enomoto; Masato Kono; Tomoyuki Fujisawa; Naoki Inui; Yutaro Nakamura; Hiromitsu Sumikawa; Takeshi Johkoh; Ran Nakashima; Yoshitaka Imura; Tsuneyo Mimori; Takafumi Suda
Journal:  PLoS One       Date:  2015-03-19       Impact factor: 3.240

7.  Identification of multiple cancer-associated myositis-specific autoantibodies in idiopathic inflammatory myopathies: a large longitudinal cohort study.

Authors:  Hanbo Yang; Qinglin Peng; Liguo Yin; Shanshan Li; Jingli Shi; Yamei Zhang; Xin Lu; Xiaoming Shu; Sigong Zhang; Guochun Wang
Journal:  Arthritis Res Ther       Date:  2017-11-25       Impact factor: 5.156

8.  Anti-MDA5 antibody as a potential diagnostic and prognostic biomarker in patients with dermatomyositis.

Authors:  Liubing Li; Qian Wang; Funing Yang; Chanyuan Wu; Si Chen; Xiaoting Wen; Chenxi Liu; Yongzhe Li
Journal:  Oncotarget       Date:  2017-04-18

9.  Dermatomyositis with Rapidly Progressive Interstitial Lung Disease Treated with Rituximab: A Report of 3 Cases in Japan.

Authors:  Kenichiro Tokunaga; Noboru Hagino
Journal:  Intern Med       Date:  2017-06-01       Impact factor: 1.271

Review 10.  Myositis-specific autoantibodies: an important tool to support diagnosis of myositis.

Authors:  Z Betteridge; N McHugh
Journal:  J Intern Med       Date:  2015-11-25       Impact factor: 8.989

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Authors:  Gianluca Sambataro; Chiara Alfia Ferrara; Carla Spadaro; Sebastiano Emanuele Torrisi; Giovanna Vignigni; Ada Vancheri; Giuseppe Muscato; Nicoletta Del Papa; Michele Colaci; Lorenzo Malatino; Stefano Palmucci; Lorenzo Cavagna; Giovanni Zanframundo; Francesco Ferro; Chiara Baldini; Domenico Sambataro; Carlo Vancheri
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