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Eligibility criteria for biologic disease-modifying antirheumatic drugs in axial spondyloarthritis: going beyond BASDAI.
Marona, Jose; Sepriano, Alexandre; Rodrigues-Manica, Santiago; Pimentel-Santos, Fernando; Mourão, Ana Filipa; Gouveia, Nélia; Branco, Jaime Cunha; Santos, Helena; Vieira-Sousa, Elsa; Vinagre, Filipe; Tavares-Costa, João; Rovisco, João; Bernardes, Miguel; Madeira, Nathalie; Cruz-Machado, Rita; Roque, Raquel; Silva, Joana Leite; Marques, Mary Lucy; Ferreira, Raquel Miriam; Ramiro, Sofia.
Afiliação
  • Marona J; Rheumatology, Hospital Egas Moniz, Centro Hospitalar de Lisboa Ocidental EPE, Lisboa, Portugal.
  • Sepriano A; CEDOC - NOVA Medical School | Faculdade de Ciências Médicas (FCM), Universidade Nova de Lisboa, Lisboa, Portugal.
  • Rodrigues-Manica S; CEDOC - NOVA Medical School | Faculdade de Ciências Médicas (FCM), Universidade Nova de Lisboa, Lisboa, Portugal.
  • Pimentel-Santos F; Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.
  • Mourão AF; Rheumatology, Hospital Egas Moniz, Centro Hospitalar de Lisboa Ocidental EPE, Lisboa, Portugal.
  • Gouveia N; CEDOC - NOVA Medical School | Faculdade de Ciências Médicas (FCM), Universidade Nova de Lisboa, Lisboa, Portugal.
  • Branco JC; Rheumatology, Hospital Egas Moniz, Centro Hospitalar de Lisboa Ocidental EPE, Lisboa, Portugal.
  • Santos H; CEDOC - NOVA Medical School | Faculdade de Ciências Médicas (FCM), Universidade Nova de Lisboa, Lisboa, Portugal.
  • Vieira-Sousa E; Rheumatology, Hospital Egas Moniz, Centro Hospitalar de Lisboa Ocidental EPE, Lisboa, Portugal.
  • Vinagre F; CEDOC - NOVA Medical School | Faculdade de Ciências Médicas (FCM), Universidade Nova de Lisboa, Lisboa, Portugal.
  • Tavares-Costa J; CEDOC - NOVA Medical School | Faculdade de Ciências Médicas (FCM), Universidade Nova de Lisboa, Lisboa, Portugal.
  • Rovisco J; Rheumatology, Hospital Egas Moniz, Centro Hospitalar de Lisboa Ocidental EPE, Lisboa, Portugal.
  • Bernardes M; CEDOC - NOVA Medical School | Faculdade de Ciências Médicas (FCM), Universidade Nova de Lisboa, Lisboa, Portugal.
  • Madeira N; Rheumatology, Instituto Português de Reumatologia, Lisboa, Portugal.
  • Cruz-Machado R; Rheumatology and Metabolic Bone Diseases Department, Hospital de Santa Maria, Centro Hospitalar Lisboa Norte EPE, Lisboa, Portugal.
  • Roque R; Rheumatology Research Unit, Instituto de Medicina Molecular, Faculty of Medicine, Universidade de Lisboa, Lisboa, Portugal.
  • Silva JL; Rheumatology, Hospital Garcia de Orta EPE, Almada, Portugal.
  • Marques ML; Rheumatology, Unidade Local de Saude do Alto Minho EPE, Viana do Castelo, Portugal.
  • Ferreira RM; Rheumatology, Centro Hospitalar e Universitario de Coimbra EPE, Coimbra, Portugal.
  • Ramiro S; Clínica Universitária de Reumatologia, Faculdade de Medicina, Universidade de Coimbra, Coimbra, Portugal.
RMD Open ; 6(1)2020 01.
Article em En | MEDLINE | ID: mdl-32144137
ABSTRACT

OBJECTIVES:

To compare definitions of high disease activity of the Ankylosing Spondylitis Disease Activity Score (ASDAS) and Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) in selecting patients for treatment with biologic disease-modifying antirheumatic drugs (bDMARDs).

METHODS:

Patients from Rheumatic Diseases Portuguese Register (Reuma.pt) with a clinical diagnosis of axial spondyloarthritis (axSpA) were included. Four subgroups (cross-tabulation between ASDAS (≥2.1) and BASDAI (≥4) definitions of high disease activity) were compared regarding baseline characteristics and response to bDMARDs at 3 and 6 months estimated in multivariable regression models.

RESULTS:

Of the 594 patients included, the majority (82%) had both BASDAI≥4 and ASDAS ≥2.1. The frequency of ASDAS ≥2.1, if BASDAI<4 was much larger than the opposite (ie, ASDAS <2.1, if BASDAI≥4) 62% vs 0.8%. Compared to patients fulfilling both definitions, those with ASDAS ≥2.1 only were more likely to be male (77% vs 51%), human leucocyte antigen B27 positive (79% vs 65%) and have a higher C reactive protein (2.9 (SD 3.5) vs 2.1 (2.9)). Among bDMARD-treated patients (n=359), responses across subgroups were globally overlapping, except for the most 'stringent' outcomes. Patients captured only by ASDAS responded better compared to patients fulfilling both definitions (eg, ASDAS inactive disease at 3 months 61% vs 25% and at 6 months 42% vs 25%).

CONCLUSION:

The ASDAS definition of high disease activity is more inclusive than the BASDAI definition in selecting patients with axSpA for bDMARD treatment. The additionally 'captured' patients respond better and have higher likelihood of predictors thereof. These results support using ASDAS≥2.1 as a criterion for treatment decisions.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Espondilite Anquilosante / Índice de Gravidade de Doença / Seleção de Pacientes / Antirreumáticos / Inibidores do Fator de Necrose Tumoral Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: RMD Open Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Portugal

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Espondilite Anquilosante / Índice de Gravidade de Doença / Seleção de Pacientes / Antirreumáticos / Inibidores do Fator de Necrose Tumoral Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: RMD Open Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Portugal