The idiopathic inflammatory myopathies module of the Rheumatic Diseases Portuguese Register

Eduardo Dourado1, Ana Teresa Melo1, Raquel Campanilho-Marques1

  • 1Centro Hospitalar Universitário Lisboa Norte, Centro Académico de Medicina de Lisboa.

ARP Rheumatology
|September 20, 2023
PubMed
Abstract

Insights

The Reuma.pt/myositis registry effectively characterizes idiopathic inflammatory myopathies (IIM) patients, revealing a diverse cohort with common muscle, joint, skin, and lung involvement. This study highlights the registry's utility in understanding IIM patient populations.

Area of Science:

  • Rheumatology
  • Clinical Research
  • Patient Registries

Background:

  • Idiopathic inflammatory myopathies (IIM) represent a group of rare autoimmune diseases affecting muscles.
  • Understanding the characteristics and clinical course of IIM patients is crucial for effective management.
  • The Rheumatic Diseases Portuguese Register (Reuma.pt) established a specific module (Reuma.pt/myositis) to capture comprehensive data on IIM.

Purpose of the Study:

  • To characterize the idiopathic inflammatory myopathies (IIM) module within the Reuma.pt registry.
  • To describe the demographic, clinical, immunological, and treatment features of patients in the Reuma.pt/myositis cohort.

Main Methods:

  • A multicentre open cohort study utilizing the Reuma.pt/myositis web-based registry.
  • Inclusion of patients registered up to January 2022, with data on diagnosis, clinical manifestations, immunological markers, and disease activity.
  • Analysis of 280 patients classified according to 2017 EULAR/ACR criteria.

Main Results:

  • The cohort comprised 71.4% females, predominantly Caucasian, with a median age at diagnosis of 48.9 years.
  • Dermatomyositis (43.6%) was the most common subtype, followed by polymyositis (21.1%).
  • Frequent manifestations included proximal muscle weakness (83.7%), lung involvement (33.9%), and presence of myositis-specific antibodies (65.3%).
  • Glucocorticoids (71.8%) and methotrexate (41.8%) were the most common treatments.

Conclusions:

  • The Reuma.pt/myositis registry successfully captures key characteristics of IIM patients.
  • The study depicts a heterogeneous IIM population with significant involvement of muscles, joints, skin, and lungs.
  • This initial report underscores the value of the registry for epidemiological and clinical research in IIM.

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