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Abstract Number: 0758

Association Between Baseline IL-6 Levels and the Clinical Phenotype of Giant Cell Arteritis

Raquel Ugena-García1, Clara Churtichaga Domenech2, Judith Vidal-Ripoll2, Francina salabert-Carreras2, Cristina Calomarde-Gómez1, Cristina Rocamora-Gisbert3, Irene Peralta-García4, Niccolo Viveros2, Anne Riveros Frutos3, Ivette Casafont-Solé1 and Judit Font-Urgelles1, 1Hospital Universitari Germans Trias i Pujol, Badalona, Spain, 2Hospital Germans Trias i Pujol, Barcelona, 3Hospital Germans Trias i Pujol, Barcelona, Spain, 4Karolinska Institutet, Clinical Epidemiology Division, Department of Medicine Solna. Karolinska University Hospital, Medical Unit of Gastroenterology, Dermatology, Rheumatology. Theme Inflammation and Ageing, Stockholm, Sweden

Meeting: ACR Convergence 2025

Keywords: Biologicals, Biomarkers, Interleukins, Vasculitis

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Session Information

Date: Sunday, October 26, 2025

Title: (0731–0764) Vasculitis – Non-ANCA-Associated & Related Disorders Poster I

Session Type: Poster Session A

Session Time: 10:30AM-12:30PM

Background/Purpose: Giant cell arteritis (GCA) is the most common form of vasculitis in patients over the age of 50. Interleukin-6 (IL-6) has been shown to play a potential role in the pathogenesis and prognosis of GCA, becoming a key therapeutic target. Moreover, some studies have suggested a potential prognostic value. This study explores the association between baseline IL-6 concentrations and the clinical phenotype of the disease, with the aim of identifying patients who may benefit from anti–IL-6 therapies.

Methods: We conducted a cross-sectional study of a cohort of patients diagnosed with GCA between 2020 and 2024 in a tertiary care hospital. Patients were classified into two groups: those with exclusively cranial involvement (cranial GCA) and those with extracranial fluorodeoxyglucose (FDG) uptake at a PET-CT scan with or without cranial involvement (extracranial/mixed GCA).A multiple linear regression model was used to evaluate the association between IL-6 levels and the clinical phenotype of GCA, adjusting for potential confounding and interaction variables (age, BMI, smoking status, type 2 diabetes mellitus, and prior corticosteroid therapy).Regression coefficients (β), 95% confidence intervals (95% CI), and p-values were calculated, using a significance threshold of p < 0.05.Model fit was assessed using the adjusted R-squared (adjusted R²) and the F-test.

Results: A total of 39 patients were included. Epidemiological, clinical and diagnostic variables are detailed in Table 1. In the multiple regression analysis, no significant association was found between IL-6 levels and clinical phenotype (p = 0.673).A significant negative association was observed between IL-6 levels and age (β = -1.059, 95% CI: -1.741 to -0.376, p = 0.003), as well as between IL-6 le levels and prior corticosteroid therapy (β = -16.398, 95% CI: -26.709 to -6.086, p = 0.003).A significant positive correlation was found between IL-6 and CRP (r = 0.4546, p = 0.0032) and between IL-6 and ESR (r = 0.3754, p = 0.0185).Other clinical and diagnostic variables did not reach statistical significance.

Conclusion: In our cohort, no significant association was found between IL-6 levels and the clinical phenotype of GCA. Patients with constitutional symptoms and PMR tended to have higher IL-6 levels, which may suggest a greater inflammatory burden—an observation that should be confirmed in studies with larger sample sizes. Notably, IL-6 levels were inversely associated with age, a finding that contrasts with current literature and may open new avenues for research.This study reinforces the importance of further exploring the role of IL-6 to identify patients who may benefit most from targeted therapy against this molecule.*The first two authors contributed equally to this abstract.

Supporting image 1Table 1. Patient’s epidemiological, clinical, and diagnostic characteristics.


Disclosures: R. Ugena-García: None; C. Churtichaga Domenech: None; J. Vidal-Ripoll: None; F. salabert-Carreras: None; C. Calomarde-Gómez: None; C. Rocamora-Gisbert: None; I. Peralta-García: Johnson & Johnson, 5; N. Viveros: None; A. Riveros Frutos: None; I. Casafont-Solé: None; J. Font-Urgelles: None.

To cite this abstract in AMA style:

Ugena-García R, Churtichaga Domenech C, Vidal-Ripoll J, salabert-Carreras F, Calomarde-Gómez C, Rocamora-Gisbert C, Peralta-García I, Viveros N, Riveros Frutos A, Casafont-Solé I, Font-Urgelles J. Association Between Baseline IL-6 Levels and the Clinical Phenotype of Giant Cell Arteritis [abstract]. Arthritis Rheumatol. 2025; 77 (suppl 9). https://acrabstracts.org/abstract/association-between-baseline-il-6-levels-and-the-clinical-phenotype-of-giant-cell-arteritis/. Accessed .
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All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

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