Performance of the 2019 American College of Rheumatology/ European League Against Rheumatism Classification Criteria for IgG4-Related Disease in a Latin American Cohort
- Grupo Latino Americano de Estudio de la Enfermedad Relacionada a IgG4 (GLAER-IgG4),
- Eduardo Martín-Nares(Author),
- Gabriela Hernández-Molina(Author),
- Diego Federico Baenas(Author),
- Jesús Delgado de la Mora(Author),
- Francisco Caeiro(Author)
- Instituto Nacional de Ciencias Médicas y Nutrición,
- Hospital Privado Centro Medico de Cordoba,
- University of Chile's Clinical Hospital,
- ,
- ,
- Instituto Oftalmosalud
Publication Information
Output type
Original language
EnglishPages from-to (Number of pages)
Pages 52-57 (6 pages)Journal (Volume, Issue Number)
Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases (Volume 30, Issue 2)Publication milestones
- Published - 01/03/2024
Publication status
ISSN
1076-1608Publication IDs
- Scopus: 85185614359
- PubMed: 38206921
Abstract
Background/Objective: The 2019 American College of Rheumatology/ European League Against Rheumatism Classification Criteria (2019 AECC) for IgG4-related disease (IgG4-RD) is considered a significant advancement in the study of this condition. Most studies evaluating their performance have focused onWhite and Asian patients, leaving a knowledge gap regarding Latin American populations. Therefore, this study aimed to assess the performance of the 2019 AECC for IgG4-RD in a cohort of Latin American patients. Methods: Amulticenter medical records review study was conducted, involving centers from Argentina, Chile, Mexico, Peru, and Uruguay. Data on IgG4-RD patients and mimicker conditions were collected through a standardized online form. The criterion standard for diagnosing IgG4-RD was based on the fulfillment of the Comprehensive Diagnostic Criteria for IgG4-RD and/or the Consensus Statement on Pathology. The 2019 AECC was retrospectively applied. Results: We included 300 patients, with 180 (60%) having IgG4-RD and 120 (40%) having mimicker conditions. The 2019 AECC had a sensitivity of 66.7% and a specificity of 100%. Sensitivity increased to 73.3% when disease-specific autoantibody items were removed, without affecting specificity. The true-positive cases had more involved organs, a higher availability of biopsy results, and were more likely to belong to the Mikulicz/systemic and proliferative phenotypes. Conclusions: The use of the 2019 AECC for IgG4-RD in a Latin American population confirms its high specificity in excluding those without the disease. The presence of concomitant autoimmune diseases and clinically nonsignificant disease-specific autoantibodies excludes a significant number of patients from fulfilling the criteria.
