Oxidative stress and genetic and epidemiologic determinants of oxidant injury in childhood asthma

被引:121
作者
Ercan, Hulya
Birben, Esra
Dizdar, Evrim A.
Keskin, Ozlem
Karaaslan, Cagatay
Soyer, Ozge U.
Dut, Raziye
Sackesen, Cansin
Besler, Tanju
Kalayci, Omer [1 ]
机构
[1] Hacettepe Univ, Sch Med, Pediat Allergy & Asthma Unit, TR-06100 Ankara, Turkey
[2] Hacettepe Univ, Fac Sci, Dept Biol Mol, TR-06100 Ankara, Turkey
[3] Hacettepe Univ, Dept Dietet, Sch Hlth Technol, TR-06100 Ankara, Turkey
关键词
asthma; genotype; glutathione; glutathione S transferase; malondialdehyde; oxidation; severity;
D O I
10.1016/j.jaci.2006.08.012
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: The factors contributing to the oxidant! antioxidant imbalance in asthma are incompletely understood. Objective: To determine the factors associated with oxidative stress including asthma severity and the genotype of the antioxidant enzymes. Methods: A total of 196 children with mild asthma, 116 children with moderate-severe asthma, and 2 healthy control groups (187 and 68 children) were included in the study. Plasma levels of malondialdehyde were measured as the indicator of oxidative stress, and reduced glutathione levels as the indicator of antioxidant defense. Children were genotyped for null variants of glutathione S transferase (GST) T1 and GSTMl, and ile105val variant of GSTP1. Risk factors were analyzed with multivariate logistic regression. Results: Systemic levels of malondialdehyde increased and reduced glutathione levels decreased significantly from healthy controls to patients with mild asthma and then to patients with moderate-severe asthma (P <.001 for each). Multivariate logistic regression identified asthma and asthma severity as independent factors associated with oxidative stress (odds ratio between 17 and 56; P <.001). Children with asthma with GSTP1 val/val genotype had higher malondialdehyde and lower glutathione levels compared with other genotypes (P =.023 and P =.014, respectively). GSTPI vaUval genotype was independently associated with asthma severity (odds ratio, 4.210; 95% CI, 1.581-11.214; P =.004). Conclusion: Our study indicates the presence of a strong oxidative stress in children with asthma that increases with the severity of the disease. In this population, val/val genotype at GSTPI ile105vaI locus may be an important factor in determining the degree of oxidant injury. Clinical implications: Children with asthma with val/val genotype at GSTPI ile105val locus may be good candidates for supplemental antioxidant therapy.
引用
收藏
页码:1097 / 1104
页数:8
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