Literature DB >> 31366272

Elevated levels of inflammatory markers in women with rheumatoid arthritis.

Camila Medeiros Costa1, Matheus Augusto Teixeira Dos Santos1, Andrei Pereira Pernambuco1,2.   

Abstract

Rheumatoid arthritis (RA) is an autoimmune and progressive disease. Evidence indicates that inflammatory mediators may contribute to the genesis and/or evolution of this clinical condition. Thus, the objective was to evaluate and compare the plasma levels of Interleukin-17 (IL-17), Tumor Necrosis Factor-Alpha (TNF-α) and Complement 3 (C3) in women with RA and healthy controls (HC), as well as to evaluate the association them with the disease activity. 25 women with RA and 15 HC were recruited. Plasma levels of biomarkers were measured by ELISA. All statistical analyzes were performed with a significance level set at α = 0.05. In the women with RA, the median age was 55 and, in the HC, was 50 years. The median value of DAS-28 was 3.79. The plasma levels of IL-17 (p = .03), TNF-α (p ≤ 0.01) and C3 (p ≤ 0.01) were higher in women with RA. The ROC curve showed that TNF- α has a higher discriminating ability than IL-17 and C3. DAS-28 score correlated significantly with C3 levels in women with RA (r = 0.91; p < .01). These findings reaffirm the participation of the immune system in pathophysiology of RA, suggest that TNF-α levels may be a good biomarker and that elevated C3 levels contribute to the worsening of the disease.

Entities:  

Keywords:  Arthritis; complement system proteins; cytokines; inflammation mediators; inteleukin-17; rheumatoid; tumor necrosis factor-alpha

Mesh:

Substances:

Year:  2019        PMID: 31366272     DOI: 10.1080/15321819.2019.1649695

Source DB:  PubMed          Journal:  J Immunoassay Immunochem        ISSN: 1532-1819


  3 in total

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Journal:  Rheumatol Int       Date:  2022-01-13       Impact factor: 2.631

Review 2.  A Role of IL-17 in Rheumatoid Arthritis Patients Complicated With Atherosclerosis.

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Review 3.  Interleukin-17A Interweaves the Skeletal and Immune Systems.

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Journal:  Front Immunol       Date:  2021-02-04       Impact factor: 7.561

  3 in total

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