Chen C, Arjomandi M, Tager I B, Holland N, Balmes J R
School of Public Health, University of California, San Francisco, CA 94143-0843, USA.
Eur Respir J. 2007 Oct;30(4):677-83. doi: 10.1183/09031936.00160806. Epub 2007 Jul 25.
Chronic exposure to ozone (O(3)) can cause changes in lung function that may reflect remodelling of small airways. It is likely that antioxidant enzyme function affects susceptibility to O(3). The aim of the present study was to determine whether polymorphisms in antioxidant enzyme (GSTM1, GSTP1 and NQO1) genes affect the risk of lung function changes related to chronic exposure to O(3). In total, 210 young adults who participated in a previous study, which showed a relationship between lifetime exposure to O(3) and decreased lung function, were genotyped. Multivariable linear regression was used to model sex-specific associations between genotypes and O(3)-related lung function changes, adjusting for height, weight, lifetime exposure to nitrogen dioxide and particles with a 50% cut-off aerodynamic diameter of 10 mum, and self-identified race/ethnicity. The GSTM1-null/NQO1 Pro187Pro-combination genotype was significantly associated with increased risk of an O(3)-related decrease in mean forced expiratory flow between 25-75% of forced vital capacity in females (parameter estimate+/-se -75+/-35 mL.s(-1)), while the GSTP1 Val105 variant genotypes were significantly associated with greater risk of an O(3)-related decrease in mean forced expiratory flow at 75% of forced vital capacity in males (-81+/-31 mL.s(-1)). GSTM1-null status was not significantly associated with any O(3)-related changes in lung function in either sex. The current authors conclude that the effects of antioxidant enzyme gene polymorphisms on the risk of decreased lung function related to chronic exposure to ozone may be modified by sex-specific factors.
长期暴露于臭氧(O₃)可导致肺功能改变,这可能反映了小气道的重塑。抗氧化酶功能可能会影响对O₃的易感性。本研究的目的是确定抗氧化酶(GSTM1、GSTP1和NQO1)基因多态性是否会影响与长期暴露于O₃相关的肺功能改变风险。共有210名参与过先前一项研究的年轻人进行了基因分型,该研究表明终生暴露于O₃与肺功能下降之间存在关联。采用多变量线性回归模型来分析基因型与O₃相关肺功能改变之间的性别特异性关联,并对身高、体重、终生二氧化氮暴露量、空气动力学直径50%截断值为10微米的颗粒物暴露量以及自我认定的种族/民族进行了校正。GSTM1缺失/NQO1 Pro187Pro组合基因型与女性用力肺活量25%至75%之间平均用力呼气流量因O₃相关而降低的风险增加显著相关(参数估计值±标准误为-75±35 mL·s⁻¹),而GSTP1 Val105变异基因型与男性用力肺活量75%时平均用力呼气流量因O₃相关而降低的风险增加显著相关(-81±31 mL·s⁻¹)。GSTM1缺失状态与任何性别中与O₃相关的肺功能改变均无显著关联。作者得出结论,抗氧化酶基因多态性对与长期暴露于臭氧相关的肺功能下降风险的影响可能受性别特异性因素的影响。