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Oxidative stress parameters in different systemic rheumatic diseases
Omidreza Firuzi1, Leos Fuksa, Chiara Spadaro
1Dipartimento di Fisiologia Umana e Farmacologia "Vittorio Erspamer", Università di Roma "La Sapienza", Italy.
Oxidative stress markers are elevated in systemic sclerosis, psoriatic arthritis, and rheumatoid arthritis, indicating free radical damage. Antioxidant therapies may help manage these rheumatic diseases.
Area of Science:
- Rheumatology
- Biochemistry
- Pathophysiology
Background:
- Oxidative stress is implicated in rheumatic disease pathogenesis but lacks robust experimental verification.
- Systemic sclerosis (SSc), psoriatic arthritis (PsA), and rheumatoid arthritis (RA) are chronic inflammatory conditions affecting joints and connective tissues.
Purpose of the Study:
- To experimentally investigate the role of oxidative stress in SSc, PsA, and RA.
- To quantify specific plasmatic oxidative stress biomarkers in patients with these rheumatic disorders compared to healthy controls.
Main Methods:
- Analysis of four plasmatic oxidative stress parameters: total antioxidant capacity (TAC), hydroperoxides, sulfhydryl groups, and carbonyl groups.
- Utilized spectrophotometric assays including ferric reducing antioxidant power (FRAP) for TAC and ferrous ion oxidation in presence of xylenol orange (FOX) for hydroperoxides.
- Compared biomarker levels in patients with SSc (n=17), PsA (n=10), RA (n=9) against a control group (n=22).
Main Results:
- Significantly elevated hydroperoxide levels were observed in SSc, PsA, and RA patients compared to controls (P < 0.05).
- Sulfhydryl groups were significantly reduced in all three disease groups versus controls (P < 0.05).
- Carbonyl groups were significantly higher in RA patients than in controls (P < 0.05), while TAC showed no significant differences.
Conclusions:
- The findings demonstrate increased free radical-mediated injury in SSc, PsA, and RA.
- These results suggest a potential therapeutic role for antioxidants in the prevention and treatment of these rheumatic diseases.
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