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Abstract Number: 0818

Defining BASDAI Cut-offs for Disease Activity States in Axial Spondylarthritis – Results from the EuroSpA Collaboration

Stylianos Georgiadis1, Lykke Oernbjerg1, Brigitte Michelsen2, Tore K. Kvien3, Simon Horskjær Rasmussen4, Jakub Závada5, Kristýna Bubová6, Bente Glintborg7, Anne Gitte Loft8, Ana Maria Rodrigues9, Maria Jose Santos10, Adrian Ciurea11, Michael Nissen12, Laura Kuusalo13, Jarno Rutanen14, Ziga Rotar15, Katja Perdan-Pikmajer15, Bjorn Gudbjornsson16, Olafur Palsson17, Daniela DiGuiseppe18, Mikkel Ostergaard19 and Merete Hetland20, 1Rigshospitalet Glostrup, Glostrup, Hovedstaden, Denmark, 2Rigshospitalet Glostrup, Diakonhjemmet Hospital and Sørlandet Hospital, Copenhagen, Denmark, 3Center for treatment of Rheumatic and Musculoskeletal Diseases (REMEDY), Diakonhjemmet Hospital, Oslo, Norway and University of Oslo (UiO), Institute of Clinical Medicine, Oslo, Norway, Oslo, Norway, 4Rigshospitalet Glostrup, Glostrup, Denmark, 5Institute of Rheumatology and Charles University, Praha, Czech Republic, 6Institute of Rheumatology and Charles University, Prague, Czech Republic, 7DANBIO, Rigshospitalet Glostrup and University of Copenhagen, Virum, Denmark, 8Aarhus University Hospital and Aarhus University, Horsens, Denmark, 9Nova Medical School and Hospital dos Lusíadas, Lisbon, Portugal, 10Hospital Garcia de Orta and Centro Académico de Medicina de Lisboa, Lisboa, Portugal, 11University Hospital Zurich, Zürich, Switzerland, 12Geneva University Hospital, Geneva, Switzerland, 13University of Turku and Turku University Hospital, Turku, Finland, 14Tampere University Hospital, Tampere, Finland, 15University Medical Centre Ljubljana and University of Ljubljana, Ljubljana, Slovenia, 16Landspitali University Hospital and University of Iceland, Reykjavik, Iceland, 17University of Iceland and Skåne University Hospital, Reykjavik, Iceland, 18Karolinska Institutet, Stockholm, 19Department of Clinical Medicine, University of Copenhagen and Center for Rheumatology, Copenhagen Center for Arthritis Research, Glostrup, Denmark, 20Rigshospitalet Glostrup and University of Copenhagen, Glostrup, Denmark

Meeting: ACR Convergence 2024

Keywords: Disease Activity, Outcome measures, Patient reported outcomes

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Session Information

Date: Saturday, November 16, 2024

Title: Abstracts: SpA Including PsA – Diagnosis, Manifestations, & Outcomes I

Session Type: Abstract Session

Session Time: 1:00PM-2:30PM

Background/Purpose: While the Axial Spondyloarthritis Disease Activity Score based on C-reactive protein (ASDAS) is recommended for assessment of disease activity in patients with axial spondyloarthritis (axSpA), the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) is still widely used, particularly in settings where inflammatory laboratory markers are unavailable. BASDAI values of < 2, < 4 and >6 have been applied as cut-offs for remission, between low disease activity (LDA) and high disease activity (HDA) and for very high disease activity (VHDA), respectively, although these cut-offs remain unvalidated. We aimed to (i) determine BASDAI cut-offs for disease activity states against predefined external criteria, and (ii) assess the level of agreement between BASDAI and ASDAS disease activity states.

Methods: Prospectively collected real-world data from patients with axSpA initiating a first tumour necrosis factor inhibitor or an interleukin-17A inhibitor from registries participating in the European Spondyloarthritis (EuroSpA) collaboration were analyzed. We applied the same approach as previously used by Machado et al. [1] to define the endorsed ASDAS cut-offs for disease activity states against external criteria, i.e., ASAS partial remission, and patient and physician global assessments. Follow-up data at 6 months were used to select the cut-offs between BASDAI remission and LDA, and between LDA and HDA, while baseline data were used to select the cut-off for VHDA. Receiver operating characteristic analyses were performed to determine the optimal BASDAI cut-offs. The level of agreement between disease activity states based on BASDAI and ASDAS cut-offs was assessed using proportion of discordance and weighted kappa coefficient.

Results: We analyzed data from 2,791 patients from seven European registries with available data on BASDAI and the above-mentioned external criteria. Mean (standard deviation) BASDAI (on a 0-10 scale) and ASDAS were 6.1 (1.9) and 3.8 (0.9) at baseline, and 3.0 (2.3) and 2.0 (1.0) at 6-month follow-up, respectively. The optimal BASDAI cut-off values against external criteria were estimated to be < 1.4, < 2.8 and >5.9 (Table 1). Analyses on the level of agreement between BASDAI and ASDAS disease activity states demonstrated that the proportions of discordance decreased from 32.6% to 27.8% in baseline data and from 36.4% to 32.9% in follow-up data, when the estimated BASDAI cut-offs (< 1.4, < 2.8 and >5.9) were applied instead of the unvalidated BASDAI cut-offs (< 2, < 4 and >6) (Figure 1). The corresponding weighted kappa values increased slightly, but only a fair level of agreement was observed. The level of agreement between BASDAI and ASDAS disease activity states was superior at baseline compared to follow-up.

Conclusion: We estimated BASDAI cut-offs for the disease activity states against predefined external criteria to be < 1.4, < 2.8 and >5.9 in a large European observational cohort of patients with axSpA. Moderate agreement between disease activity states according to BASDAI and ASDAS was observed, which reflects that the underlying domains of BASDAI and ASDAS are not identical.

References:

1. Machado et al. (2011). Ann Rheum Dis, 70(1), 47-53.

Supporting image 1

Table 1. BASDAI cut-offs for disease activity states against external criteria

Supporting image 2

Figure 1. Stacked bar charts of BASDAI states according to estimated cut-offs dependent on ASDAS states according to A. unvalidated cut-offs (<2, <4 and >6), and B. estimated cut-offs: <1.4, <2.8 and >5.9. ASDAS states: ID (ASDAS<1.3), LDA (1.3≤ASDAS<2.1), HDA (2.1≤ASDAS≤3.5) and VHDA (ASDAS>3.5). ASDAS: Ankylosing Spondylitis Disease Activity Score based on C-Reactive Protein; BASDAI: Bath Ankylosing Spondylitis Disease Activity Index; Disc: proportion of discordance; HDA: high disease activity; ID: inactive disease; LDA: low disease activity; VHDA: very high disease activity; kappa: weighted kappa coefficient.


Disclosures: S. Georgiadis: Novartis, 5, UCB, 5; L. Oernbjerg: Novartis, 5, UCB, 5; B. Michelsen: Novartis, 5, 6; T. Kvien: AbbVie/Abbott, 1, 2, 5, Bristol-Myers Squibb(BMS), 5, Galapagos, 5, Gilead, 2, Grünenthal, 6, Janssen, 2, 6, Novartis, 2, 5, Pfizer, 2, 5, Sandoz, 2, 6, UCB, 2, 5; S. Rasmussen: Novartis, 5; J. Závada: AbbVie/Abbott, 1, AstraZeneca, 6, Eli Lilly, 6, Sanofi, 6, Sobi, 6, UCB, 6; K. Bubová: None; B. Glintborg: AbbVie/Abbott, 5, Bristol-Myers Squibb(BMS), 5, Pfizer, 5, Sandoz, 5; A. Loft: AbbVie/Abbott, 2, 6, Eli Lilly, 2, 6, Janssen, 2, 6, Novartis, 2, 5, 6, Pfizer, 2, 6, UCB, 2, 6; A. Rodrigues: AbbVie/Abbott, 5, Amgen, 5, AstraZeneca, 5, Boehringer-Ingelheim, 5, Eli Lilly, 5, Merck/MSD, 5, Novartis, 5, Pfizer, 5; M. Santos: None; A. Ciurea: None; M. Nissen: AbbVie/Abbott, 2, 6, Amgen, 2, 6, Janssen, 2, 6, 12, Support for conference participation, Novartis, 2, 2, 5, 6, 6, Pfizer, 2, 6, UCB, 2, 6, 12, Support for conference participation; L. Kuusalo: None; J. Rutanen: None; Z. Rotar: None; K. Perdan-Pikmajer: None; B. Gudbjornsson: None; O. Palsson: None; D. DiGuiseppe: None; M. Ostergaard: Abbott, 2, 5, 6, BMS, 6, Centocor, 5, Merck, 2, 6, Mundipharma, 6, Pfizer, 2, 5, 6, Roche, 2, UCB Pharma, 2, 6; M. Hetland: AbbVie/Abbott, 5, 12, Paid to my institution, no personal fee, Bristol-Myers Squibb(BMS), 5, 12, Paid to my institution, no personal fee, Eli Lilly, 5, 12, Paid to my institution, no personal fee, Medac, 6, 12, Paid to my institution, no personal fee, Merck/MSD, 5, 12, Paid to my institution, no personal fee, Novartis, 5, 6, Pfizer, 5, 6, 12, Paid to my institution, no personal fee, Sandoz, 5, 6, 12, Paid to my institution, no personal fee, UCB, 6, 12, Paid to my institution, no personal fee.

To cite this abstract in AMA style:

Georgiadis S, Oernbjerg L, Michelsen B, Kvien T, Rasmussen S, Závada J, Bubová K, Glintborg B, Loft A, Rodrigues A, Santos M, Ciurea A, Nissen M, Kuusalo L, Rutanen J, Rotar Z, Perdan-Pikmajer K, Gudbjornsson B, Palsson O, DiGuiseppe D, Ostergaard M, Hetland M. Defining BASDAI Cut-offs for Disease Activity States in Axial Spondylarthritis – Results from the EuroSpA Collaboration [abstract]. Arthritis Rheumatol. 2024; 76 (suppl 9). https://acrabstracts.org/abstract/defining-basdai-cut-offs-for-disease-activity-states-in-axial-spondylarthritis-results-from-the-eurospa-collaboration/. Accessed .
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