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Development and validation of a composite disease activity score for measurement of muscle and skin involvement in juvenile dermatomyositis

  • Silvia Rosina
  • , Alessandro Consolaro
  • , Pieter van Dijkhuizen
  • , Angela Pistorio
  • , Giulia Camilla Varnier
  • , Francesca Bovis
  • , Kiran Nistala
  • , Susan Maillard
  • , Adele Civino
  • , Elena Tsitsami
  • , Jaime de Inocencio
  • , Marija Jelusic
  • , Jelena Vojinovic
  • , Graciela Espada
  • , Balahan Makay
  • , Maria Martha Katsicas
  • , Polixeni Pratsidou-Gertsi
  • , Dragana Lazarevic
  • , Anand Prahalad Rao
  • , Denise Pires Marafon
  • Alberto Martini, Clarissa Pilkington, Nicolino Ruperto, Angelo Ravelli*
*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Objective. To develop a composite DAS for JDM and provide preliminary evidence of its validity. Methods. The Juvenile DermatoMyositis Activity Index (JDMAI) is composed of four items: physician's global assessment of overall disease activity; parent's/child's global assessment of child's wellbeing; measurement of muscle strength; and assessment of skin disease activity. The score of the JDMAI is the arithmetic sum of the scores of each individual component. Six versions of the JDMAI were tested, which differed in the tools used to assess the third and fourth items. Validation procedures were conducted using three large multinational patient samples including a total of 627 patients. Results. The JDMAI was found to possess face and content validity, good construct validity, satisfactory internal consistency (Cronbach's alpha = 0.58-0.89), fair responsiveness to clinically important change (standardized response mean = 0.82-3.12 among patients improved) and strong capacity to discriminate patients judged as being in the state of inactive disease or low, moderate or high disease activity by the physician (P<0.001) or whose parents were satisfied or not satisfied with the course of their child's illness (P<0.001). Overall, the six versions of the JDMAI showed similar metrological performances in validation analyses. Conclusion. The JDMAI was found to possess good measurement properties in a large population of patients with a wide range of disease activity, and is, therefore, suitable for use in both clinical and research settings. The final version of the JDMAI will be selected after its prospective validation.

Original languageEnglish
Pages (from-to)1196-1205
Number of pages10
JournalRheumatology (Oxford, England)
Volume58
Issue number7
DOIs
Publication statusPublished - 1 Jul 2019
Externally publishedYes

Keywords

  • Composite disease activity scores
  • Disease activity assessment
  • Idiopathic inflammatory myositis
  • JDM
  • Muscle strength assessment
  • Outcome measures
  • Paediatric rheumatology

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