Evidence map›Paper›PMID 41928308›Full record

ArticleBMC rheumatology2026

Serum ICAM-1 and VCAM-1 as markers of endothelial activation in ankylosing spondylitis and psoriatic arthritis: a cross-sectional study.

Miroslav Markov, Maria Dimova, Simona Bogdanova, Trifon Chervenkov, Tsvetoslav Georgiev

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Article in BMC rheumatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Miroslav MarkovDepartment of Propaedeutics of Internal Medicine, Faculty of Medicine, Medical University of Varna, Varna, 9002, Bulgaria.
Maria DimovaDepartment of Propaedeutics of Internal Medicine, Faculty of Medicine, Medical University of Varna, Varna, 9002, Bulgaria.
Simona BogdanovaFirst Department of Internal Medicine, Faculty of Medicine, Medical University of Varna, Varna, 9002, Bulgaria.
Trifon ChervenkovDepartment of Medical Genetics, Faculty of Medicine, Medical University of Varna, Varna, 9002, Bulgaria.
Tsvetoslav GeorgievFirst Department of Internal Medicine, Faculty of Medicine, Medical University of Varna, Varna, 9002, Bulgaria. tsetso@medfaculty.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients with ankylosing spondylitis (AS) and psoriatic arthritis (PsA) have increased cardiovascular risk beyond traditional factors. Endothelial activation is an early and potentially reversible stage of atherogenesis, and circulating adhesion molecules such as intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) have been proposed as markers of vascular involvement in inflammatory diseases. This study aimed to compare serum ICAM-1 and VCAM-1 levels in patients with ankylosing spondylitis and psoriatic arthritis versus controls, and to examine their associations with disease activity, systemic inflammatory burden, cardiovascular risk profile, and treatment status.

methodsThis cross-sectional study included 154 participants recruited between 2023 and 2024, including 83 patients with AS, 40 with PsA, and 31 controls. Disease activity was assessed using ASDAS-CRP (AS) and DAS28-CRP (PsA). Inflammatory markers, lipid profile, cardiovascular risk scores, and treatment history were recorded. Serum ICAM-1 and VCAM-1 concentrations were measured by enzyme-linked immunosorbent assay. Group comparisons used Kruskal-Wallis and Mann-Whitney U tests; correlations used Spearman or Pearson coefficients as appropriate. Multivariable linear regression was applied to identify independent predictors of VCAM-1.

resultsSerum VCAM-1 and ICAM-1 levels did not differ significantly between AS, PsA, and controls. VCAM-1 showed positive correlations with C-reactive protein (ρ = 0.247, p = 0.002) and erythrocyte sedimentation rate (ρ = 0.163, p = 0.044), whereas ICAM-1 showed no significant associations with inflammatory, metabolic, or vascular parameters. In multivariable analysis, body mass index was the only independent predictor of VCAM-1 (β = 0.198, p = 0.027). In AS, higher disease activity defined by ASDAS-CRP > 2.1 was associated with higher CRP (p = 0.002), ESR (p = 0.04), and VCAM-1 concentrations (p = 0.002). Biologic-naïve patients had higher VCAM-1 levels than treated patients (p = 0.046), while those receiving Janus kinase inhibitors had lower VCAM-1 compared with biologic-naïve individuals (p = 0.014).

conclusionsAlthough ICAM-1 and VCAM-1 levels were comparable between patients and controls, VCAM-1 reflected inflammatory activity and treatment status, particularly in AS. VCAM-1 may represent a more sensitive marker of endothelial activation than ICAM-1 in treated spondyloarthritis.

Indexed as

Ankylosing spondylitisCardiovascular riskEndothelial dysfunctionICAM-1InflammationPsoriatic arthritisVCAM-1

Identifiers

PMID41928308
PMCPMC13162378

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