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The oxidative protection analysis measures the body´s antioxidant capacity and helps detect oxidative stress at an early stage, supporting targeted prevention and therapy.
The oxidative protection analysis measures the body´s antioxidant capacity and helps detect oxidative stress at an early stage, supporting targeted prevention and therapy.
The oxidative protection analysis is a diagnostic procedure that assesses the antioxidant defence capacity of the human body. It examines the balance between free radicals – reactive oxygen species generated during normal metabolism – and the antioxidants provided by the body itself or through nutrition. When free radicals outnumber antioxidants, a state known as oxidative stress occurs, which has been linked to a wide range of chronic diseases.
Free radicals are naturally produced as by-products of cellular metabolism, but their production is also accelerated by external factors such as UV radiation, tobacco smoke, environmental toxins, alcohol consumption, and inflammatory processes. These highly reactive molecules can damage cell membranes, proteins, and DNA. The body defends itself through an elaborate antioxidant system that includes enzymatic mechanisms (e.g., superoxide dismutase, catalase, glutathione peroxidase) and non-enzymatic antioxidants such as vitamin C, vitamin E, beta-carotene, selenium, and zinc.
This analysis is commonly used in preventive medicine, functional medicine, and nutritional medicine. Typical indications include:
The oxidative protection analysis is typically performed on a blood sample (serum or whole blood). Several laboratory methods are used to evaluate different aspects of antioxidant capacity:
Specific micronutrients and protective compounds are quantified, including vitamin C, vitamin E (tocopherol), beta-carotene, selenium, zinc, coenzyme Q10, and glutathione.
Tests such as the FRAP assay (Ferric Reducing Ability of Plasma) and the ORAC assay (Oxygen Radical Absorbance Capacity) measure the overall ability of blood plasma to neutralise free radicals, providing a summary of total antioxidant potential.
Complementary markers of oxidative damage can also be assessed, including 8-hydroxy-2-deoxyguanosine (8-OHdG) as an indicator of DNA oxidation, malondialdehyde (MDA) as a marker of lipid peroxidation, and oxidised LDL cholesterol.
The results of an oxidative protection analysis provide an individualised picture of a patient´s antioxidant defence status. Low levels of individual antioxidants or a reduced total antioxidant capacity may indicate insufficient dietary intake or increased consumption due to elevated oxidative stress. Results are always interpreted in the context of the clinical presentation, dietary habits, and lifestyle of the individual.
Based on the findings, targeted interventions may be recommended, including:
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