Nickel Renate, Haider Assja, Sengler Claudia, Lau Susanne, Niggemann Bodo, Deichmann Klaus A, Wahn Ulrich, Heinzmann Andrea
Department of Pediatric Pneumonology and Immunology, Charité, Humboldt University, Berlin, Germany.
Pediatr Allergy Immunol. 2005 Sep;16(6):539-41. doi: 10.1111/j.1399-3038.2005.00307.x.
Glutathione S-Transferase P1 (GSTP1) is an important enzyme in the detoxification of products of oxidative stress. Several studies have shown an association of the amino acid variant Ile105Val with bronchial asthma and the reaction of the lung to inhalant pollutants. The aim of this study was to test the two known amino acid variants in GSTP1 for association with bronchial asthma and airway hyper-responsiveness in two German pediatric populations. We genotyped Ile105Val and Ala114Val in the Multicenter Allergy Study cohort (85 children with asthma, 123 controls) and asthmatic children from Freiburg (n = 178). We did not find association of either polymorphisms with bronchial asthma or airway hyper-responsiveness. We conclude from our data that polymorphisms within GSTP1 do not play a major role in the development of bronchial asthma in German children.
谷胱甘肽S-转移酶P1(GSTP1)是氧化应激产物解毒过程中的一种重要酶。多项研究表明,氨基酸变体Ile105Val与支气管哮喘以及肺部对吸入性污染物的反应有关。本研究的目的是在两个德国儿科人群中测试GSTP1中两种已知的氨基酸变体与支气管哮喘和气道高反应性的关联。我们对多中心过敏研究队列(85名哮喘儿童,123名对照)以及来自弗莱堡的哮喘儿童(n = 178)中的Ile105Val和Ala114Val进行了基因分型。我们未发现任何一种多态性与支气管哮喘或气道高反应性有关联。我们从数据中得出结论,GSTP1内的多态性在德国儿童支气管哮喘的发病中不发挥主要作用。