Thorax, 2000-02, Vol.55 (2), p.121-125
2000
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- Autor(en) / Beteiligte
- Titel
- Genetic susceptibility to chronic obstructive pulmonary disease in Koreans: combined analysis of polymorphic genotypes for microsomal epoxide hydrolase and glutathione S-transferase M1 and T1
- Ist Teil von
- Thorax, 2000-02, Vol.55 (2), p.121-125
- Ort / Verlag
- London: BMJ Publishing Group Ltd and British Thoracic Society
- Erscheinungsjahr
- 2000
- Quelle
- Free E-Journal (出版社公開部分のみ）
- Beschreibungen/Notizen
- BACKGROUND Although smoking is the major causal factor in the development of chronic obstructive pulmonary disease (COPD), only 10–20% of chronic heavy cigarette smokers develop symptomatic COPD which suggests the presence of genetic susceptibility. This genetic susceptibility to COPD might depend on variations in enzyme activities that detoxify cigarette smoke products such as microsomal epoxide hydrolase (mEPHX) and glutathione-S transferase (GST). As there is increasing evidence that several genes influence the development of COPD, multiple gene polymorphisms should be investigated to find out the genetic susceptibility to COPD. METHODS The genotypes of 83 patients with COPD and 76 healthy smoking control subjects were determined by polymerase chain reaction (PCR) followed by restriction fragment length polymorphism (PCR-RFLP) for the mEPHX gene, and multiplex PCR for GST M1 and GST T1 genes. The frequencies of polymorphic genotypes of mEPHX, GST M1, and GST T1 genes were compared both individually and in combination in patients with COPD and healthy smokers. RESULTS No differences were observed in the frequency of polymorphic genotypes in exons 3 and 4 of mEPHX, GST M1, and GST T1 genes between patients with COPD and healthy smokers. The frequencies of any combination of these genotypes also showed no differences between the COPD group and the control group. CONCLUSIONS Genetic polymorphisms in mEPHX, GST M1, and GST T1 genes are not associated with the development of COPD in Koreans.
- Sprache
- Englisch
- Identifikatoren
- ISSN: 0040-6376eISSN: 1468-3296DOI: 10.1136/thorax.55.2.121Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1745681
- Format
- –
- Schlagworte
- Adult, Aged, Aged, 80 and over, Biological and medical sciences, Cancer, Chronic obstructive pulmonary disease, Chronic obstructive pulmonary disease, asthma, Enzymes, Epoxide Hydrolases - blood, Epoxide Hydrolases - genetics, Female, Forced Expiratory Volume - physiology, Gene amplification, Genetic Predisposition to Disease - genetics, genetics, Genotype & phenotype, Glutathione Transferase - blood, Glutathione Transferase - genetics, glutathione-S transferase, Humans, Korea - ethnology, Lung Diseases, Obstructive - blood, Lung Diseases, Obstructive - ethnology, Lung Diseases, Obstructive - genetics, Male, Medical sciences, microsomal epoxide hydrolase, Microsomes, Middle Aged, Original, Pathogenesis, Pneumology, Polymerase Chain Reaction, Polymorphism, Polymorphism, Genetic, Polymorphism, Restriction Fragment Length, Smoking, Smoking - ethnology, Smoking - genetics, Tropical medicine, Vital Capacity - physiology