Identification of clinical parameters associated with serum oxidative stress in patients with rheumatoid arthritis

Abstract Objectives. Reactive oxygen species (ROS) are considered to be involved in the pathobiology of rheumatoid arthritis (RA); however, their association with disease activity has not been elucidated. In this study, we measured reactive oxygen metabolites (ROM) in patients with RA using a new Fr...

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Veröffentlicht in:Modern rheumatology 2014-11, Vol.24 (6), p.926-930
Hauptverfasser: Nakajima, Arata, Aoki, Yasuchika, Shibata, Yoshifumi, Sonobe, Masato, Terajima, Fumiaki, Takahashi, Hiroshi, Saito, Masahiko, Taniguchi, Shinji, Yamada, Manabu, Nakagawa, Koichi
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Sprache:eng
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Zusammenfassung:Abstract Objectives. Reactive oxygen species (ROS) are considered to be involved in the pathobiology of rheumatoid arthritis (RA); however, their association with disease activity has not been elucidated. In this study, we measured reactive oxygen metabolites (ROM) in patients with RA using a new Free Radical Analytical System and determined clinical parameters associated with ROM. Methods. One hundred and fifty-two patients with RA and 80 patients with diabetes mellitus (DM) were included in this observational study. To measure ROM, the d-ROM test was performed on blood samples drawn from all subjects. The correlation between ROM and biomarkers, disease activity, doses of methotrexate (MTX), and prednisolone (PSL) were investigated. Results. There were significant, positive correlations between ROM and CRP, matrix metalloproteinase 3 (MMP3), Disease Activity Score 28-erythrocyte sedimentation rate (DAS28-ESR), Clinical Disease Activity Index (CDAI), and the Simplified Disease Activity Index (SDAI). Multiple regression analysis revealed that CRP and DAS28-ESR were correlated with ROM. Conclusions. The serum level of ROM was associated with CRP and DAS28-ESR, suggesting that ROM, in conjunction with CRP and MMP3, may be able to be used as a new biological disease marker to evaluate the disease activity of RA.
ISSN:1439-7595
1439-7609
DOI:10.3109/14397595.2014.891495