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DOI 10.1016/j.reumae.2023.12.005

Медицинская библиотека · Reumatologia clinica · 2024

CXCL10 as a biomarker of interstitial lung disease in patients with rheumatoid arthritis.

Makarem Yasmine S, Ahmed Elzahraa A, Makboul Marwa, Farghaly Shimaa, Mostafa Naima, El Zohne Randa A, Goma Samar H

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Аннотация

INTRODUCTION

Pulmonary involvement is a frequent and serious rheumatoid arthritis (RA) manifestation that affects 60%-80% of patients. CXCL10 is an inflammatory chemokine that regulates different biological responses, such as chemotaxis, angiogenesis, and inflammation.

AIM: This study aimed to identify the role of CXCL10 as a peripheral blood marker of RA-ILD and its correlation with disease activity.

PATIENTS AND

METHODS

This cross-sectional study included 73 patients with RA (33 with ILD and 40 without ILD). Pulmonary function tests and high-resolution computed tomography were performed. Blood samples were taken for complete blood count and blood chemistry analysis, and human interferon-inducible protein 10 (IP-10/CXCL10) level. Statistical Package for the Social Sciences (version 22) was used for all statistical calculations.

RESULTS

The serum CXCL10 level and patient age (r=.393, p=.024), disease duration (r=.756, p<0.001), erythrocyte sedimentation rate (r=.516, p=.002), C-reactive protein (r=.539, p=.001), and rheumatoid factor (r=.663, p<.001) revealed a significant positive correlation. Furthermore, the Modified Health Assessment Questionnaire (r=-.418, p=.015) revealed a significant negative correlation. Patients with RA-ILD show significantly higher CXCL10 than those without ILD (p<.001).

CONCLUSION

CXCL10 is a useful RA disease activity biomarker and is an RA-ILD-sensitive biomarker, also CXCL10 is a significant predictor for development of RA-ILD.

Для цитирования: Makarem Yasmine S, Ahmed Elzahraa A, Makboul Marwa, Farghaly Shimaa, Mostafa Naima, El Zohne Randa A, Goma Samar H. CXCL10 as a biomarker of interstitial lung disease in patients with rheumatoid arthritis.. Reumatologia clinica. 2024. DOI: 10.1016/j.reumae.2023.12.005.

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