HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS		QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

This Article Full Text Full Text (PDF) Supplementary tables Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via ISI Web of Science (1) Citing Articles via Google Scholar Google Scholar Articles by Chen, C. Articles by Balmes, J. R. Search for Related Content PubMed PubMed Citation Articles by Chen, C. Articles by Balmes, J. R.

Effects of antioxidant enzyme polymorphisms on ozone-induced lung function changes

¹ School of Public Health, University of California, Berkeley, and ² Lung Biology Center, Dept of Medicine, University of California, San Francisco, CA, USA, ³ These authors contributed equally to the present study.

CORRESPONDENCE: J. R. Balmes, University of California, Box 0843, San Francisco, CA 94143-0843, USA. Fax: 1 4152068949. E-mail: john.balmes{at}ucsf.edu

Keywords: Antioxidant enzymes, lung function, oxidative injury, ozone

Received: December 8, 2006
Accepted June 29, 2007

Chronic exposure to ozone (O₃) can cause changes in lung function that may reflect remodelling of small airways. It is likely that antioxidant enzyme function affects susceptibility to O₃. 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 O₃.

In total, 210 young adults who participated in a previous study, which showed a relationship between lifetime exposure to O₃ and decreased lung function, were genotyped. Multivariable linear regression was used to model sex-specific associations between genotypes and O₃-related lung function changes, adjusting for height, weight, lifetime exposure to nitrogen dioxide and particles with a 50% cut-off aerodynamic diameter of 10 µm, and self-identified race/ethnicity.

The GSTM1-null/NQO1 Pro187Pro-combination genotype was significantly associated with increased risk of an O₃-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 O₃-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 O₃-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.