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Abstract Number: 2211

A Two-year Comparison of Back Pain and Morning Stiffness in Axial Spondyloarthritis and Non-axial Spondyloarthritis Chronic Back Pain Patients in the Spondyloarthritis Caught Early (SPACE) Cohort

Ana Bento da Silva1, Miranda Van Lunteren2, Mary Lucy marques3, Karen Fagerli4, Sofia Ramiro5, Désirée van der Heijde5 and Floris Van Gaalen2, 1Leiden University Medical Center, Leiden, Netherlands, 2Leiden University Medical Center, Department of Rheumatology, Leiden, Netherlands, 3Leiden University Medical Center; Centro Hospitalar e Universitário de Coimbra (Department of Rheumatology), Coimbra, Portugal, 4Diakonhjemmet Hospital, Oslo, Norway, 5Department of Rheumatology, Leiden University Medical Center, Leiden, Netherlands

Meeting: ACR Convergence 2023

Keywords: Back pain, Morning Stiffness, Patient reported outcomes, spondyloarthritis

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Session Information

Date: Tuesday, November 14, 2023

Title: (2195–2226) Spondyloarthritis Including Psoriatic Arthritis – Diagnosis, Manifestations, & Outcomes Poster III: SpA

Session Type: Poster Session C

Session Time: 9:00AM-11:00AM

Background/Purpose: Treatment of axial spondyloarthritis (axSpA) has been shown to improve symptoms of the disease such as back pain (BP) and morning stiffness (MS). As a result, early referral of patients suspected of having axSpA is strongly recommended. However, little data is available on the disease course of early axSpA in clinical practice, and particularly in comparison to referred patients who have chronic BP (CBP) but not axSpA. We set out to compare spinal symptoms at baseline and after 2 years (2y) in early axSpA and non-axSpA CBP patients in clinical practice.

Methods: The population consisted of adults (≥16 years) with CBP of unknown origin lasting more than 3 months and less than 2y, starting before 45 years, included in the SPondyloArthritis Caught Early (SPACE) cohort. Patients had a diagnosis of axSpA or non-axSpA at 2y with a high level of confidence by the treating rheumatologist (Marques ML, Ann Rheum Dis 2023;82:3-4). Patients reported the severity of BP (total and at night) and MS in the previous week on a numeric rating scale (NRS) ranging from 0 (no symptom) to 10 (unbearable symptom), both at baseline and 2y. For MS duration, a NRS ranging from 0 (0 hours) to 10 (≥2 hours) was used. For the assessment of each outcome, only patients with data at both timepoints were included. Wilcoxon signed-rank tests (for not normally distributed data) were used to compare baseline and 2y results within groups. For the comparison between groups, linear regression models were built, adjusting for the baseline value of the respective outcome, gender, age and use of NSAID.

Results: A total of 434 patients (303 axSpA; 131 non-axSpA) had undergone baseline and 2y visits. Data was available for both timepoints on at least one of the four questions related to BP and MS in 266 (88%) axSpA and 110 (84%) non-axSpA patients. Compared to non-axSpA, axSpA patients were more frequently male (52% vs 25%) and had more SpA features (mean (SD): 5 (2) vs 3 (1)), including HLA-B27 positivity (73% vs 29%). Age (mean (SD): 29 (8) vs 31 (8) years) and symptom duration (mean (SD): 13 (7) vs 13 (7) months) were similar between groups.

Overall, lower levels of BP and MS were observed in axSpA (vs non-axSpA) patients at baseline and 2y (Table 1). After 2y, BP (total and at night) and MS severity and duration significantly improved in both groups (all p≤0.001), even though symptoms persisted in a considerable number of patients (mainly in the non-axSpA group). A mean improvement ranging from 1.4 to 1.6 points for axSpA patients and 1.0 to 1.9 points for non-axSpA patients was reported for each outcome. In adjusted multivariate analysis, axSpA (vs non-axSpA) was an independent predictor of a lower BP at night at 2y (Table 2, adjusted coefficient = -0.8, 95% CI (-1.5; -0.2); p=0.012), with no significant differences found for total BP or MS severity and duration.

Conclusion: Over 2y, BP and MS significantly improve in early axSpA. Although a similar improvement is seen in non-axSpA patients, at 2y most patients have persisting symptoms. AxSpA (vs non-axSpA) is an independent predictor of larger improvement in BP at night but not of the observed improvements in total BP and MS.

Supporting image 1

Table 1. Baseline and two-years back pain and morning stiffness in early axSpA and non-axSpA chronic back pain patients.

Supporting image 2

Table 2. Comparison of two-year outcomes of axSpA (vs non-axSpA) chronic back pain patients.


Disclosures: A. Bento da Silva: None; M. Van Lunteren: None; M. marques: None; K. Fagerli: None; S. Ramiro: AbbVie, 2, 5, Eli Lilly, 2, Galapagos, 5, MSD, 2, 5, Novartis, 2, 5, Pfizer, 2, 5, Sanofi, 2, UCB Pharma, 2, 5; D. van der Heijde: AbbVie, 2, Bayer, 2, BMS, 2, Eli Lilly, 2, Galapagos, 2, Gilead, 2, GSK, 2, Imaging Rheumatology BV, 12, Director, Janssen, 2, Novartis, 2, Pfizer, 2, Takeda, 2, UCB Pharma, 2; F. Van Gaalen: AbbVie, 12, Personal fees, BMS, 12, Personal fees, Eli Lilly, 12, Personal fees, Jacobus Stichting, 5, MSD, 12, Personal fees, Novartis, 5, 12, Fees, Stichting ASAS, 5, Stichting Vrienden van Sole Mio, 5, UCB Pharma, 5.

To cite this abstract in AMA style:

Bento da Silva A, Van Lunteren M, marques M, Fagerli K, Ramiro S, van der Heijde D, Van Gaalen F. A Two-year Comparison of Back Pain and Morning Stiffness in Axial Spondyloarthritis and Non-axial Spondyloarthritis Chronic Back Pain Patients in the Spondyloarthritis Caught Early (SPACE) Cohort [abstract]. Arthritis Rheumatol. 2023; 75 (suppl 9). https://acrabstracts.org/abstract/a-two-year-comparison-of-back-pain-and-morning-stiffness-in-axial-spondyloarthritis-and-non-axial-spondyloarthritis-chronic-back-pain-patients-in-the-spondyloarthritis-caught-early-space-cohort/. Accessed .
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