Literature DB >> 31694813

First external validation of sensitivity and specificity of the European League Against Rheumatism (EULAR)/American College of Rheumatology (ACR) classification criteria for idiopathic inflammatory myopathies with a Japanese cohort.

Masatoshi Jinnin1, Akiko Ohta2, Shoichiro Ishihara3, Hirofumi Amano4, Tatsuya Atsumi5, Manabu Fujimoto6, Takashi Kanda7, Yasushi Kawaguchi8, Atsushi Kawakami9, Akio Mimori10, Tsuneyo Mimori11, Toshihide Mimura12, Yoshinao Muro13, Hajime Sano14, Jun Shimizu15, Tsutomu Takeuchi16, Yoshiya Tanaka17, Kazuhiko Yamamoto18, Takayuki Sumida19, Hitoshi Kohsaka20.   

Abstract

OBJECTIVE: To externally validate the performance of the new European League Against Rheumatism (EULAR)/American College of Rheumatology (ACR) classification criteria set for idiopathic inflammatory myopathies (IIM) with a Japanese cohort.
METHODS: This study included 420 IIM and 402 non-IIM cases. Probability of having IIM in each patient was calculated using the collected data set. The cut-off probability was set at 55%, as recommended by EULAR/ACR. Patients classified as IIM by the criteria were further subclassified with classification trees.
RESULTS: When the probability cut-off was set at 55%, the sensitivity/specificity of the new criteria to diagnose IIM were 89.3%/91.0% in the total cohort, 88.1%/95.1% without muscle biopsy data and 90.4%/65.5% with biopsy data. The cohort included 12 overlap syndrome patients with biopsy data, who were included as non-IIM cases in accordance with traditional Japanese methods. When they were included in the IIM cases, the specificity in patients with biopsy increased to 74.4%. The sensitivity/specificity of the new criteria to diagnose polymyositis/dermatomyositis (PM/DM) plus juvenile and amyopathic DM in the Japanese cohort was 87.4%/92.4%, which were greater than those of the Tanimoto's criteria revised to enable classification of amyopathic DM (ADM) (71.2%/87.8%) and were comparable with those of Bohan & Peter's criteria to diagnose those diseases except for ADM (88.4%/88.3%).
CONCLUSIONS: Our study externally validated high specificity of the new criteria for the first time, although with several limitations, including low percentage of child patients. The new criteria have higher sensitivity and/or specificity in classification of PM/DM than the previously reported criteria, demonstrating its usefulness for interethnic patients. © Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  autoimmune diseases; dermatomyositis; polymyositis

Mesh:

Year:  2019        PMID: 31694813     DOI: 10.1136/annrheumdis-2019-215488

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN: 0003-4967            Impact factor:   19.103


  3 in total

1.  The balance between clinical convenience and the new concepts of the 2017 European League Against Rheumatism/American College of Rheumatology classification criteria for adult and juvenile idiopathic inflammatory myopathies.

Authors:  Hyun-Sook Kim
Journal:  Korean J Intern Med       Date:  2021-02-25       Impact factor: 2.884

2.  Clinically amyopathic dermatomyositis associated with anti-nuclear matrix protein 2 antibody.

Authors:  Saori Abe; Hiroto Tsuboi; Hirofumi Toko; Fumika Honda; Mizuki Yagishita; Shinya Hagiwara; Yuya Kondo; Risa Konishi; Mari Okune; Yuki Ichimura; Naoko Okiyama; Isao Matsumoto
Journal:  Rheumatol Adv Pract       Date:  2021-12-20

3.  Juvenile Dermatomyositis: New Clues to Diagnosis and Therapy.

Authors:  Lauren M Pachman; Brian E Nolan; Deidre DeRanieri; Amer M Khojah
Journal:  Curr Treatm Opt Rheumatol       Date:  2021-02-06
  3 in total

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