Measurement of the total antioxidant response using a novel automated method in subjects with nonalcoholic steatohepatitis

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Abstract

Background: Oxidative stress, an increase in oxidants and/or a decrease in antioxidant capacity, is one of the potential biochemical mechanisms involved in the pathogenesis of nonalcoholic steatohepatitis. We aimed to investigate the total antioxidant response using a novel automated method in nonalcoholic steatohepatitis subjects. As a reciprocal measure, we also aimed to determine total peroxide level in the same plasma samples. Methods: Twenty-two subjects with biopsy proven nonalcoholic steatohepatitis and 22 healthy controls were enrolled. Total antioxidant response and total peroxide level measurements were done in all participants. The ratio percentage of total peroxide level to total antioxidant response was regarded as oxidative stress index. Results: Total antioxidant response of subjects with nonalcoholic steatohepatitis was significantly lower than controls (p<0.05), while mean total peroxide level and mean oxidative stress index were higher (all p <0.05). In subjects with nonalcoholic steatohepatitis, fibrosis score was significantly correlated with total peroxide level, total antioxidant response and oxidative stress index (p<0.05, r = 0.607; p<0.05, r = -0.506; p<0.05, r = 0.728, respectively). However, no correlation was observed between necroimflamatory grade and those oxidative status parameters (all p >0.05). Conclusion: Nonalcoholic steatohepatitis is associated with increased oxidant capacity, especially in the presence of liver fibrosis. The novel automated assay is a reliable and easily applicable method for total plasma antioxidant response measurement in nonalcoholic steatohepatitis. © 2005 Horoz et al., licensee BioMed Central Ltd.

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Horoz, M., Bolukbas, C., Bolukbas, F. F., Sabuncu, T., Aslan, M., Sarifakiogullari, S., … Erel, O. (2005). Measurement of the total antioxidant response using a novel automated method in subjects with nonalcoholic steatohepatitis. BMC Gastroenterology, 5. https://doi.org/10.1186/1471-230X-5-35

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