Previous evidence supports the important role that oxidative stress (OxS) plays in metabolic syndrome (MetS)-related manifestations. We determined the relationship between the number of MetS components and the degree of OxS in MetS patients. In this comparative cross-sectional study from the LIPGENE cohort, a total of 91 MetS patients (43 men and 48 women; aged between 45 and 68 years) were divided into four groups based on the number of MetS components: subjects with 2, 3, 4 and 5 MetS components (n=20, 31, 28 and 12, respectively). We measured ischemic reactive hyperemia (IRH), plasma levels of soluble vascular cell adhesion molecule-1 (sVCAM-1), total nitrite, lipid peroxidation products (LPO), hydrogen peroxide (H2O2), superoxide dismutase (SOD) and glutathione peroxidase (GPx) plasma activities. sVCAM-1, H2O2 and LPO levels were lower in subjects with 2 or 3 MetS components than subjects with 4 or 5 MetS components. IRH and total nitrite levels were higher in subjects with 2 or 3 MetS components than subjects with 4 or 5 MetS components. SOD and GPx activities were lower in subjects with 2 MetS components than subjects with 4 or 5 MetS components. Waist circumference, weight, age, homeostatic model assessment-β, triglycerides (TGs), high-density lipoprotein and sVCAM-1 levels were significantly correlated with SOD activity. MetS subjects with more MetS components may have a higher OxS level. Furthermore, association between SOD activity and MetS components may indicate that this variable could be the most relevant OxS biomarker in patients suffering from MetS and could be used as a predictive tool to determine the degree of the underlying OxS in MetS. An exploration of the disruptions associated with metabolic syndrome yields potentially useful indicators for assessing physiological damage. Metabolic syndrome encompasses different combinations of symptoms, including obesity and elevated cholesterol levels, but it is generally associated with risk of diabetes, cardiovascular disease and kidney disease. Research has also associated metabolic syndrome with cellular damage from a process called oxidative stress. Jose Lopez-Miranda's team at Spain's University of Cordoba examined these manifestations in a cohort of patients. They grouped their subjects based on their number of metabolic syndrome symptoms, and observed that patients with severe disease produced the greatest amount of molecules that cause oxidative stress. These patients also produced higher levels of superoxide dismutase, an enzyme that clears those molecules, revealing a potentially useful biomarker for tracking oxidative stress and examining its effects in metabolic syndrome.
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Yubero‐Serrano et al. (2013) studied this question.
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