Immunological biomarkers in patients with radiographic axial spondyloarthritis, an exploratory longitudinal Swedish study
(2025) In Modern Rheumatology 35(1). p.134-143- Abstract
Objectives: There is a need for more specific biomarkers to diagnose and predict disease course in patients with axial spondyloarthritis (axSpA). This study aimed to study immunological plasma biomarkers at different time-points in radiographic (r)-axSpA patients overall and stratified by sex and compare these biomarker patterns in r-axSpA patients concerning disease phenotypes and disease activity. Methods: Plasma samples were analysed from r-axSpA patients at and prior (Pre-Backbone) inclusion in the Backbone study. Interferon gamma, interleukin-10, -17A, -17F, -22, -23, -6, MCP-1, TNF-α, VEGF-A, MIF, IgA anti-CD74, zonulin, ESR, hsCRP, white blood cell count, and blood lipids were measured. Results: Biomarker pattern discriminated... (More)
Objectives: There is a need for more specific biomarkers to diagnose and predict disease course in patients with axial spondyloarthritis (axSpA). This study aimed to study immunological plasma biomarkers at different time-points in radiographic (r)-axSpA patients overall and stratified by sex and compare these biomarker patterns in r-axSpA patients concerning disease phenotypes and disease activity. Methods: Plasma samples were analysed from r-axSpA patients at and prior (Pre-Backbone) inclusion in the Backbone study. Interferon gamma, interleukin-10, -17A, -17F, -22, -23, -6, MCP-1, TNF-α, VEGF-A, MIF, IgA anti-CD74, zonulin, ESR, hsCRP, white blood cell count, and blood lipids were measured. Results: Biomarker pattern discriminated significantly between r-axSpA patients in Backbone and Pre-Backbone compared with controls. When stratifying by sex, it was possible to discriminate between male and female r-axSpA patients in Backbone vs controls and between male r-axSpA patients in pre-Backbone and controls. In Backbone, markers with high discriminative capacity were MIF, IgA anti-CD74, and MCP-1. In Pre-Backbone, IL-6, TNF-α, MIF, triglycerides, cholesterol, IL-10, and zonulin displayed high discriminative capacity. Conclusion: Based on their temporal pattern and mutual relationship, we suggest studying MIF, IgA anti-CD74, and MCP-1 in depth, at more time points, to further elucidate disease-driving mechanisms in this complex disease.
(Less)
- author
- Hellman, Urban ; Lejon, Kristina ; Do, Lan ; Geijer, Mats LU ; Baraliakos, Xenofon ; Witte, Torsten and Forsblad-D’Elia, Helena
- organization
- publishing date
- 2025
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Ankylosing spondylitis, biomarkers, longitudinal observational study, Northern Sweden Health and Disease Study, radiographic axial spondyloarthritis
- in
- Modern Rheumatology
- volume
- 35
- issue
- 1
- pages
- 10 pages
- publisher
- Oxford University Press
- external identifiers
-
- pmid:38706167
- scopus:85214054667
- ISSN
- 1439-7595
- DOI
- 10.1093/mr/roae039
- language
- English
- LU publication?
- yes
- id
- 296ce96c-11aa-4320-8007-ef478177ad9e
- date added to LUP
- 2025-02-24 12:29:54
- date last changed
- 2025-07-29 00:49:19
@article{296ce96c-11aa-4320-8007-ef478177ad9e, abstract = {{<p>Objectives: There is a need for more specific biomarkers to diagnose and predict disease course in patients with axial spondyloarthritis (axSpA). This study aimed to study immunological plasma biomarkers at different time-points in radiographic (r)-axSpA patients overall and stratified by sex and compare these biomarker patterns in r-axSpA patients concerning disease phenotypes and disease activity. Methods: Plasma samples were analysed from r-axSpA patients at and prior (Pre-Backbone) inclusion in the Backbone study. Interferon gamma, interleukin-10, -17A, -17F, -22, -23, -6, MCP-1, TNF-α, VEGF-A, MIF, IgA anti-CD74, zonulin, ESR, hsCRP, white blood cell count, and blood lipids were measured. Results: Biomarker pattern discriminated significantly between r-axSpA patients in Backbone and Pre-Backbone compared with controls. When stratifying by sex, it was possible to discriminate between male and female r-axSpA patients in Backbone vs controls and between male r-axSpA patients in pre-Backbone and controls. In Backbone, markers with high discriminative capacity were MIF, IgA anti-CD74, and MCP-1. In Pre-Backbone, IL-6, TNF-α, MIF, triglycerides, cholesterol, IL-10, and zonulin displayed high discriminative capacity. Conclusion: Based on their temporal pattern and mutual relationship, we suggest studying MIF, IgA anti-CD74, and MCP-1 in depth, at more time points, to further elucidate disease-driving mechanisms in this complex disease.</p>}}, author = {{Hellman, Urban and Lejon, Kristina and Do, Lan and Geijer, Mats and Baraliakos, Xenofon and Witte, Torsten and Forsblad-D’Elia, Helena}}, issn = {{1439-7595}}, keywords = {{Ankylosing spondylitis; biomarkers; longitudinal observational study; Northern Sweden Health and Disease Study; radiographic axial spondyloarthritis}}, language = {{eng}}, number = {{1}}, pages = {{134--143}}, publisher = {{Oxford University Press}}, series = {{Modern Rheumatology}}, title = {{Immunological biomarkers in patients with radiographic axial spondyloarthritis, an exploratory longitudinal Swedish study}}, url = {{http://dx.doi.org/10.1093/mr/roae039}}, doi = {{10.1093/mr/roae039}}, volume = {{35}}, year = {{2025}}, }