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Evaluation of glutathione peroxidase and superoxide dismutase enzyme polymorphisms in celiac disease patients. | LitMetric

Evaluation of glutathione peroxidase and superoxide dismutase enzyme polymorphisms in celiac disease patients.

Genet Mol Res

Department of Clinical Biochemistry, Faculty of Medicine, University of Gaziosmanpasa, Tokat, Turkey.

Published: February 2014

AI Article Synopsis

  • Celiac disease (CD) is an inflammatory disorder of the small intestine caused by the consumption of gluten-containing grains, leading to nutrient malabsorption and oxidative stress.
  • This study investigated genetic variations (polymorphisms) in the enzymes superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) in 265 individuals, focusing on their potential link to common mutations associated with CD.
  • Results indicated that most CD patients with known mutations also had SOD and GSH-Px polymorphisms; however, while SOD variations were more prevalent, the overall statistical significance of these findings was not established.

Article Abstract

Celiac disease (CD) is a multifactorial, inflammatory small bowel disorder characterized by nutrient malabsorption resulting from mucosal damage, the latter induced by cereal products like barley, oat, and wheat. Oxidative stress has previously been reported to play an important role in the pathogenesis of CD. In the present study, we aimed to evaluate the frequency of polymorphisms that affects the structure of the enzymes superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px), with levels being dependent on the amount of oxidative stress and whether or not there is an association with the mutations DQA1*0501, DQB1*0201, and DRB1*04 that are frequently reported for CD. SOD and GSH-Px polymorphisms were investigated by real-time quantitative polymerase chain reaction in 265 cases. Of the 117 cases that had at least one of DQA1*0501, DQB1*0201, or DRB1*04, 98 (83.75%) also had SOD enzyme polymorphisms and 68 (58.12%) also had GSH-Px polymorphisms. In conclusion, although the etiology of CD is not yet entirely clear, many mechanisms have been suggested. This study supports the notion that SOD and GSH-Px polymorphisms are involved in CD development, even though our findings were not statistically significant, and, furthermore, are influenced at various levels. SOD polymorphisms and activities were more frequently identified than those of GSH-Px.

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Source
http://dx.doi.org/10.4238/2014.February.20.4DOI Listing

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