The relationship between glutathione S-transferase M1 genotypes and lipid peroxidation in asbestos workers.
- Author:
Lei YAN
1
;
Qien WANG
;
Yanling YIN
;
Xiaohong ZHAO
;
Gangzhu LIU
;
Fei YU
;
Yuejin WANG
;
Shijie LIU
Author Information
- Publication Type:Journal Article
- MeSH: Asbestos; adverse effects; Genotype; Glutathione Transferase; genetics; Humans; Lipid Peroxidation; Malondialdehyde; analysis; Occupational Exposure
- From: Chinese Journal of Industrial Hygiene and Occupational Diseases 2002;20(2):97-99
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo study the relationship between glutathione S-transferase M1 (GSTM1) genotypes and lipid peroxidation of asbestos workers.
METHODS94 asbestos workers and 51 controls were selected as subjects. The general information, occupational history and individual habits were collected by questionnaires in all participants. The venous blood was sampled and the plasma was separated for the detection of malondialdehyde (MDA) level and lymphocytes for DNA isolation and GSTM1 genotyping.
RESULTSMDA level was significantly higher in asbestos workers [(0.283 +/- 0.054) nmol/L] than that in controls [(0.163 +/- 0.053) nmol/L, P < 0.01], however, neither duration of exposure nor accumulated asbestos exposure dose was related to MDA levels; MDA levels in control workers with GSTM1 +/- genotype [(0.190 +/- 0.034) nmol/L] were significantly higher than that in control workers with GSTM1 +/+ genotype [(0.138 +/- 0.055) nmol/L, P < 0.01]. Among asbestos workers, the same trend could be found, but the differences was not significant(P > 0.05). When the workers were stratified by duration of exposure or accumulated asbestos exposure dose, MDA levels in individuals with GSTM1 -/- genotype were also higher than those with GSTM1 +/+ genotype, but the differences were also not significant(P > 0.05).
CONCLUSIONBoth exposure to asbestos and deficiency of GSTM1 genotype were related to lipid peroxidation in workers, but the role of the former may be more important than that of the latter.