Francisco J. Blanco-García

Universidade da Coruña
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Articles (11)

Background: Delay in diagnosis and therapy in patients with arthritis commonly leads to progressive articular damage. The study aimed to investigate the immunohistochemical reactivity of synovial cytokines associated with inflammation and the bone erosives/neoformatives processes among individuals diagnosed with psoriatic arthritis (PsA), rheumatoid arthritis (RA), osteoarthritis (OA), and radiographic axial spondyloarthritis (r-axSpA), with the intention of identifying potential biomarkers. Methods: Specimens were collected from the inflamed knee joints of patients referred for arthroscopic procedures, and the synovial tissue (ST) was prepared for quantifying protein expression through immunohistochemical analysis (% expressed in Ratio_Area-Intensity) for TGF-β1, IL-17A, Dkk1, BMP2, BMP4, and Wnt5b. The collected data underwent thorough analysis and examination of their predictive capabilities utilising receiver operating characteristic (ROC) curves. Results: Valid synovial tissue samples were acquired from 40 patients for IHC quantification analysis. Initially, these patients had not undergone treatment with biologics. However, after 5 years, 4 out of 13 patients diagnosed with PsA and two out of nine patients diagnosed with RA had commenced biologic treatments. Individuals with early PsA who received subsequent biologic treatment exhibited significantly elevated IHC reactivity in ST for TGF-β1 (p = 0.015). Additionally, patients with both PsA and RA who underwent biologic therapy displayed increased IHC reactivity for IL-17A (p = 0.016), TGF-β1 (p = 0.009), and Dkk1 (p = 0.042). ROC curve analysis of IHC reactivity for TGF-β1, Dkk1, and IL-17A in the synovial seems to predict future treatment with biologics in the next 5 years with the area under the curve (AUC) of a combined sum of the three values: AUC: 0.828 (95% CI: 0.689–0.968; p 0.005) S 75% E 84.4%. Conclusions: Higher synovial immunohistochemistry reactivity of IL-17A, Dkk1, and TGF-β1 in patients with early psoriatic arthritis and rheumatoid arthritis may serve as potential indicators for predicting the necessity of utilising biologic treatments.

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2024

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2023

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2023

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2023

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2023

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2023

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2022

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2022

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2022

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2022

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2021

Collaborators (11)

Antonio Fernandez-Nebro

Profesor titular acreditado como catedrático (Reader)

University of Malaga

SPAIN
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John Loughlin

Professor

Newcastle University

UNITED KINGDOM
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Antonio Julià Cano

Lab head

Vall d'Hebron Institut de Recerca

SPAIN
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Margreet Kloppenburg

Full Professor

Leiden University Medical Center

NETHERLANDS
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Noelia Flórez-Fernández

Universidade de Vigo

SPAIN
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Beatriz Carames

Head of Cartilage Biology group, Miguel Servet Type II-A Senior Scientist

-

SPAIN
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Silvia María Díaz-Prado

Universidade da Coruña

SPAIN
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Rosa Meijide-Failde

Full Professor

Universidade da Coruña

SPAIN
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Fernando Perez-Ruiz

Associate Professor

Universidad del País Vasco Facultad de Farmacia

SPAIN
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Herminia Dominguez

Universidade de Vigo

SPAIN
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Peter Nash

Professor

Griffith University

AUSTRALIA
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