Etanercept reduces the oxidative stress marker levels in patients with rheumatoid arthritis
Autor: | Masaaki Takahashi, Akira Nagano, Tetsuyuki Nagafusa, Yasunori Kageyama, Eiji Torikai |
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Rok vydání: | 2007 |
Předmět: |
musculoskeletal diseases
Glycation End Products Advanced Male medicine.medical_specialty Urinary system Immunology Urology Arthritis Enzyme-Linked Immunosorbent Assay medicine.disease_cause Arginine Receptors Tumor Necrosis Factor Etanercept Lipid peroxidation Arthritis Rheumatoid chemistry.chemical_compound Rheumatology Internal medicine medicine Immunology and Allergy Humans Pentosidine skin and connective tissue diseases Chromatography High Pressure Liquid Aged Retrospective Studies business.industry Lysine Deoxyguanosine Middle Aged medicine.disease Oxidative Stress Cross-Linking Reagents Treatment Outcome chemistry 8-Hydroxy-2'-Deoxyguanosine Rheumatoid arthritis Antirheumatic Agents Case-Control Studies Immunoglobulin G Female business Oxidative stress Biomarkers medicine.drug |
Zdroj: | Rheumatology international. 28(3) |
ISSN: | 1437-160X |
Popis: | This study was performed to evaluate the effects of the TNF-alpha inhibitor etanercept on oxidation stress markers representing DNA damage, lipid peroxidation, and protein glycosylation. Twenty-two rheumatoid arthritis (RA) patients underwent etanercept treatment. The levels of serum total, urinary total, and urinary free pentosidine, which is an advanced glycation end-product (AGE), of urinary N(epsilon)-hexanoyl lysine (N(epsilon)-HEL), and of 8-hydroxy-deoxy guanosine (8-OHdG) were measured at baseline and at 3 and 6 months after the initial treatment with etanercept. Serum total and urinary total pentosidine levels were reduced at 6 months after the initial treatment with etanercept, and urinary free pentosidine levels were reduced at 3 and 6 months. Urinary N(epsilon)-HEL levels were also reduced at 3 and 6 months, and urinary 8-OHdG levels were reduced at 6 months. Serum total and urinary total pentosidine levels in RA patients correlated with the number of swelling joints and tender joints, and urinary total pentosidine levels correlated with the Disease Activity Score using 28 joints (DAS28). This study demonstrated that etanercept acts as a regulator against pentosidine formation, oxidative DNA damage, and lipid peroxidation in RA patients. |
Databáze: | OpenAIRE |
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