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Arch Bronconeumol. 2013 Dec;49(12):507-12. doi: 10.1016/j.arbres.2013.04.002. Epub 2013 Jul 1.

Frequency of polymorphism -262 c/t in catalase gene and oxidative damage in Slovak children with bronchial asthma.

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1
Department of Medical Biochemistry, Jessenius Faculty of Medicine, Comenius University de Bratislava, Martin, República Eslovaca. Electronic address: babusikova@jfmed.uniba.sk.

Abstract

INTRODUCTION:

Bronchial asthma is a complex disease in which genetic factors, environmental factors and oxidative damage are responsible for the initiation and modulation of disease progression. If antioxidant mechanisms fail, reactive oxygen species damage the biomolecules followed by progression of the disease. Catalase is one of the most important endogenous enzymatic antioxidants. In the present study, we examined the hypothesis that increased oxidative damage and polymorphism in the CAT gene (-262 promoter region, C/T) are associated with childhood bronchial asthma.

PATIENTS AND METHODS:

Genotyping of the polymorphisms in the CAT gene in healthy (249) and asthmatic children (248) was performed using polymerase chain reaction-restriction fragment length polymorphism. Markers of oxidative damage: content of sulfhydryl groups and thiobarbituric acid-reactive substances were determined by spectrophotometry in children.

RESULTS:

The TT genotype of catalase was more frequent among the asthmatic patients (22.6%) than in healthy children (4.8%) (odds ratio=5.63; 95% confidence interval=2.93-10.81, P<.001). The amount of sulfhydryl groups decreased significantly and conversely, the content of thiobarbituric acid-reactive substances increased significantly in bronchial asthma and in catalase TT genotype compared to other catalase genotypes of this gene.

CONCLUSIONS:

These results suggest that catalase polymorphism might participate in development of bronchial asthma and in enhanced oxidative damage in asthmatic children. Genetic variation of enzymatic antioxidants may modulate disease risk.

KEYWORDS:

Asma bronquial; Bronchial asthma; Catalasa; Catalase; Children; Gene polymorphism; Lesión oxidativa; Niños; Oxidative damage; Polimorfismo genético

PMID:
23827365
DOI:
10.1016/j.arbres.2013.04.002
[Indexed for MEDLINE]
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