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Individual regression modelling of spinal mobility measurements in long-term ankylosing spondylitis: In-depth analyses with comparison to norm data
Umeå University, Faculty of Medicine, Department of Public Health and Clinical Medicine, Section of Medicine.ORCID iD: 0000-0002-4750-6055
Umeå University, Faculty of Medicine, Department of Public Health and Clinical Medicine, Section of Medicine. Center for Rheumatology, Academic Specialist Center, Stockholm Health Services, Stockholm, Sweden.ORCID iD: 0000-0001-8999-0925
Umeå University, Faculty of Medicine, Wallenberg Centre for Molecular Medicine at Umeå University (WCMM). Umeå University, Faculty of Medicine, Department of Public Health and Clinical Medicine, Section of Medicine.ORCID iD: 0000-0002-7436-7900
Umeå University, Faculty of Medicine, Department of Public Health and Clinical Medicine, Section of Medicine. Centre for Research and Development, Uppsala University/Region Gävleborg, Sweden.ORCID iD: 0000-0001-7226-0969
2023 (English)In: Arthritis care & research, ISSN 2151-464X, E-ISSN 2151-4658, Vol. 75, no 4, p. 793-800Article in journal (Refereed) Published
Abstract [en]

Objectives: Normal age-related decline and temporary restrictions in mobility complicate the understanding of spinal mobility deterioration over time in patients with ankylosing spondylitis (AS). In this study, we aimed to determine whether spinal mobility deterioration occurred linearly in patients with AS. We also aimed to compare patterns of change with corresponding age-related normal values and analyze variations in temporary fluctuations in mobility measurements over time.

Methods: We included 111 men and 30 women (median age 20.9 years at symptom onset), who were followed for median 34 years since symptom onset. This resulted in 9 697 spinal mobility measurements for analysis. Individual linear regression models for development of lateral spinal flexion (LSF), 10 cm Schober test (ST10), chest expansion (CE), and cervical rotation (CR) were analyzed and compared with normal age-related decline over time.

Results: The median values for the constants of all measurements were significantly lower than the norm data. However, LSF, ST10, and CE followed a yearly linear decline comparable to the norm data, whereas CR declined about twice as fast as expected from the norm data (beta median [25th-75th percentile]: -0.62° [-1.16°, -0.22°] and -0.35° [-0.35°, -0.35°]), respectively. Temporary fluctuations in LSF and CE were significantly higher during the early phase of the disease, with decreasing residuals over time.

Conclusion: Based on median constants of our data, mobility restrictions related to AS seem to mainly occur during the first years of disease, indicating a narrow window of opportunity for prevention.

Place, publisher, year, edition, pages
John Wiley & Sons, 2023. Vol. 75, no 4, p. 793-800
National Category
Clinical Medicine
Identifiers
URN: urn:nbn:se:umu:diva-201631DOI: 10.1002/acr.24895ISI: 000889287800001PubMedID: 35412031Scopus ID: 2-s2.0-85143234618OAI: oai:DiVA.org:umu-201631DiVA, id: diva2:1718901
Available from: 2022-12-14 Created: 2022-12-14 Last updated: 2025-02-18Bibliographically approved

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Hörnberg, KristinaLjung, LottaSödergren, AnnaSundström, Björn

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