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Cut-Offs for Disease Activity States in Axial Spondyloarthritis With Ankylosing Spondylitis Disease Activity Score (ASDAS) Based on C-Reactive Protein and ASDAS Based on Erythrocyte Sedimentation Rate: Are They Interchangeable?
Georgiadis, Stylianos; Ørnbjerg, Lykke Midtbøll; Michelsen, Brigitte; Kvien, Tore K; Di Giuseppe, Daniela; Wallman, Johan K; Závada, Jakub; Provan, Sella A; Kristianslund, Eirik Klami; Rodrigues, Ana Maria; Santos, Maria José; Rotar, Ziga; Pirkmajer, Katja Perdan; Nordström, Dan; Macfarlane, Gary J; Jones, Gareth T; van der Horst-Bruinsma, Irene; Hellamand, Pasoon; Østergaard, Mikkel; Hetland, Merete Lund.
Afiliação
  • Georgiadis S; S. Georgiadis, PhD, L.M. Ørnbjerg, MD, PhD, Copenhagen Center for Arthritis Research (COPECARE), Center for Rheumatology and Spine Diseases, Centre for Head and Orthopaedics, Rigshospitalet, Glostrup, Denmark; stylianos.georgiadis@regionh.dk.
  • Ørnbjerg LM; S. Georgiadis, PhD, L.M. Ørnbjerg, MD, PhD, Copenhagen Center for Arthritis Research (COPECARE), Center for Rheumatology and Spine Diseases, Centre for Head and Orthopaedics, Rigshospitalet, Glostrup, Denmark.
  • Michelsen B; B. Michelsen, MD, PhD, Center for Treatment of Rheumatic and Musculoskeletal Diseases (REMEDY), Diakonhjemmet Hospital, Oslo, and Research Unit, Sørlandet Hospital, Kristiansand, Norway, and Copenhagen Center for Arthritis Research (COPECARE), Center for Rheumatology and Spine Diseases, Centre for H
  • Kvien TK; T.K. Kvien, MD, PhD, E.K. Kristianslund, MD, PhD, Center for Treatment of Rheumatic and Musculoskeletal Diseases (REMEDY), Diakonhjemmet Hospital, Oslo, Norway.
  • Di Giuseppe D; D. Di Giuseppe, PhD, Clinical Epidemiology Division, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
  • Wallman JK; J.K. Wallman, MD, PhD, Department of Clinical Sciences Lund, Rheumatology, Skåne University Hospital, Lund University, Lund, Sweden.
  • Závada J; J. Závada, MD, PhD, Institute of Rheumatology, Prague, Czech Republic and Department of Rheumatology, First Faculty of Medicine, Charles University, Prague, Czech Republic.
  • Provan SA; S.A. Provan, MD, PhD, Center for Treatment of Rheumatic and Musculoskeletal Diseases (REMEDY), Diakonhjemmet Hospital, Oslo, and Public Health Section, Inland Norway University of Applied Sciences, Elverum, Norway.
  • Kristianslund EK; T.K. Kvien, MD, PhD, E.K. Kristianslund, MD, PhD, Center for Treatment of Rheumatic and Musculoskeletal Diseases (REMEDY), Diakonhjemmet Hospital, Oslo, Norway.
  • Rodrigues AM; A.M. Rodrigues, MD, PhD, EpiDoC Unit, CEDOC, Nova Medical School, and Rheumatology Unit, Hospital dos Lusíadas, Lisbon, Portugal.
  • Santos MJ; M.J. Santos, MD, PhD, Department of Rheumatology, Hospital Garcia de Orta, Almada, and Instituto Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Centro Académico de Medicina de Lisboa, Lisbon, Portugal.
  • Rotar Z; Z. Rotar, MD, PhD, K. Perdan Pirkmajer, MD, Department of Rheumatology, University Medical Centre Ljubljana, and Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
  • Pirkmajer KP; Z. Rotar, MD, PhD, K. Perdan Pirkmajer, MD, Department of Rheumatology, University Medical Centre Ljubljana, and Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
  • Nordström D; D. Nordström, MD, PhD, Departments of Medicine and Rheumatology, Helsinki University Hospital, Helsinki, Finland.
  • Macfarlane GJ; G.J. Macfarlane, MD, PhD, G.T. Jones, PhD, Aberdeen Centre for Arthritis and Musculoskeletal Health (Epidemiology Group), University of Aberdeen, Aberdeen, UK.
  • Jones GT; G.J. Macfarlane, MD, PhD, G.T. Jones, PhD, Aberdeen Centre for Arthritis and Musculoskeletal Health (Epidemiology Group), University of Aberdeen, Aberdeen, UK.
  • van der Horst-Bruinsma I; I. van der Horst-Bruinsma, MD, PhD, Rheumatology, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Hellamand P; P. Hellamand, MD, Department of Rheumatology and Clinical Immunology, Amsterdam University Medical Center, Amsterdam, Netherlands and Amsterdam Rheumatology Immunology Center, Reade, and Amsterdam UMC, Amsterdam, the Netherlands.
  • Østergaard M; M. Østergaard, MD, PhD, DMSc, M.L. Hetland, MD, PhD, DMSc, Copenhagen Center for Arthritis Research (COPECARE), Center for Rheumatology and Spine Diseases, Centre for Head and Orthopaedics, Rigshospitalet, Glostrup, and Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Hetland ML; M. Østergaard, MD, PhD, DMSc, M.L. Hetland, MD, PhD, DMSc, Copenhagen Center for Arthritis Research (COPECARE), Center for Rheumatology and Spine Diseases, Centre for Head and Orthopaedics, Rigshospitalet, Glostrup, and Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
J Rheumatol ; 51(7): 673-677, 2024 Jul 01.
Article em En | MEDLINE | ID: mdl-38621792
ABSTRACT

OBJECTIVE:

Ankylosing Spondylitis Disease Activity Score based on C-reactive protein (ASDAS-CRP) is recommended over ASDAS based on erythrocyte sedimentation rate (ASDAS-ESR) to assess disease activity in axial spondyloarthritis (axSpA). Although ASDAS-CRP and ASDAS-ESR are not interchangeable, the same disease activity cut-offs are used for both. We aimed to estimate optimal ASDAS-ESR values corresponding to the established ASDAS-CRP cut-offs (1.3, 2.1, and 3.5) and investigate the potential improvement of level of agreement between ASDAS-ESR and ASDAS-CRP disease activity states when applying these estimated cut-offs.

METHODS:

We used data from patients with axSpA from 9 European registries initiating a tumor necrosis factor inhibitor. ASDAS-ESR cut-offs were estimated using the Youden index. The level of agreement between ASDAS-ESR and ASDAS-CRP disease activity states was compared against each other.

RESULTS:

In 3664 patients, mean ASDAS-CRP was higher than ASDAS-ESR at both baseline (3.6 and 3.4, respectively) and aggregated follow-up at 6, 12, or 24 months (1.9 and 1.8, respectively). The estimated ASDAS-ESR values corresponding to the established ASDAS-CRP cut-offs were 1.4, 1.9, and 3.3. By applying these cut-offs, the proportion of discordance between disease activity states according to ASDAS-ESR and ASDAS-CRP decreased from 22.93% to 19.81% in baseline data but increased from 27.17% to 28.94% in follow-up data.

CONCLUSION:

We estimated the optimal ASDAS-ESR values corresponding to the established ASDAS-CRP cut-off values. However, applying the estimated cut-offs did not increase the level of agreement between ASDAS-ESR and ASDAS-CRP disease activity states to a relevant degree. Our findings did not provide evidence to reject the established cut-off values for ASDAS-ESR.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Espondilite Anquilosante / Índice de Gravidade de Doença / Sedimentação Sanguínea / Proteína C-Reativa / Espondiloartrite Axial Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Espondilite Anquilosante / Índice de Gravidade de Doença / Sedimentação Sanguínea / Proteína C-Reativa / Espondiloartrite Axial Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article