Literature DB >> 29079590

2017 European League Against Rheumatism/American College of Rheumatology classification criteria for adult and juvenile idiopathic inflammatory myopathies and their major subgroups.

Ingrid E Lundberg1, Anna Tjärnlund1, Matteo Bottai2, Victoria P Werth3, Clarissa Pilkington4, Marianne de Visser5, Lars Alfredsson2, Anthony A Amato6, Richard J Barohn7, Matthew H Liang8, Jasvinder A Singh9,10, Rohit Aggarwal11, Snjolaug Arnardottir12, Hector Chinoy13, Robert G Cooper14, Katalin Dankó15, Mazen M Dimachkie7, Brian M Feldman16, Ignacio Garcia-De La Torre17, Patrick Gordon18, Taichi Hayashi19, James D Katz20, Hitoshi Kohsaka21, Peter A Lachenbruch22, Bianca A Lang23, Yuhui Li24, Chester V Oddis11, Marzena Olesinska25, Ann M Reed26, Lidia Rutkowska-Sak27, Helga Sanner28, Albert Selva-O'Callaghan29, Yeong-Wook Song30, Jiri Vencovsky31, Steven R Ytterberg32, Frederick W Miller33, Lisa G Rider33.   

Abstract

OBJECTIVE: To develop and validate new classification criteria for adult and juvenile idiopathic inflammatory myopathies (IIM) and their major subgroups.
METHODS: Candidate variables were assembled from published criteria and expert opinion using consensus methodology. Data were collected from 47 rheumatology, dermatology, neurology and paediatric clinics worldwide. Several statistical methods were used to derive the classification criteria.
RESULTS: Based on data from 976 IIM patients (74% adults; 26% children) and 624 non-IIM patients with mimicking conditions (82% adults; 18% children), new criteria were derived. Each item is assigned a weighted score. The total score corresponds to a probability of having IIM. Subclassification is performed using a classification tree. A probability cut-off of 55%, corresponding to a score of 5.5 (6.7 with muscle biopsy) 'probable IIM', had best sensitivity/specificity (87%/82% without biopsies, 93%/88% with biopsies) and is recommended as a minimum to classify a patient as having IIM. A probability of ≥90%, corresponding to a score of ≥7.5 (≥8.7 with muscle biopsy), corresponds to 'definite IIM'. A probability of <50%, corresponding to a score of <5.3 (<6.5 with muscle biopsy), rules out IIM, leaving a probability of ≥50 to <55% as 'possible IIM'.
CONCLUSIONS: The European League Against Rheumatism/American College of Rheumatology (EULAR/ACR) classification criteria for IIM have been endorsed by international rheumatology, dermatology, neurology and paediatric groups. They employ easily accessible and operationally defined elements, and have been partially validated. They allow classification of 'definite', 'probable' and 'possible' IIM, in addition to the major subgroups of IIM, including juvenile IIM. They generally perform better than existing criteria. © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

Entities:  

Keywords:  autoimmune diseases; dermatomyositis; polymyositis

Mesh:

Year:  2017        PMID: 29079590      PMCID: PMC5736307          DOI: 10.1136/annrheumdis-2017-211468

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


  32 in total

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Authors:  Marinos C Dalakas; Reinhard Hohlfeld
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Journal:  Neurology       Date:  2003-08-12       Impact factor: 9.910

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