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Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1997 Oct;34(10):874–875. doi: 10.1136/jmg.34.10.874

Mutation in the 3' region of the alpha-1-antitrypsin gene and chronic obstructive pulmonary disease.

A J Sandford 1, J J Spinelli 1, T D Weir 1, P D Paré 1
PMCID: PMC1051102  PMID: 9350828

Abstract

A mutation in the 3' flanking region of the alpha-1-antitrypsin gene has been reported to be associated with chronic obstructive pulmonary disease (COPD). We have investigated the prevalence of this mutation in a group of 185 patients with airway obstruction and in 69 non-obstructed controls. The subjects were selected on the basis of their development of lung cancer and therefore had similar exposure to cigarette smoke, the major risk factor for COPD. In the majority of subjects, the level of airway inflammation and loss of elastic recoil was known, and therefore we were able to test whether the mutation was associated with one of these pathological mechanisms. The prevalence of heterozygotes for the mutation was 10% in both the obstructed group and controls. The mutation was not associated with increased airway inflammation or loss of elastic recoil. This result indicates that the 3' mutation is not a significant risk factor for COPD in this population, and suggests heterogeneity in the pathogenesis of the disease.

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Selected References

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  1. Kalsheker N. A., Watkins G. L., Hill S., Morgan K., Stockley R. A., Fick R. B. Independent mutations in the flanking sequence of the alpha-1-antitrypsin gene are associated with chronic obstructive airways disease. Dis Markers. 1990 May-Jun;8(3):151–157. [PubMed] [Google Scholar]
  2. Morgan K., Scobie G., Kalsheker N. A. Point mutation in a 3' flanking sequence of the alpha-1-antitrypsin gene associated with chronic respiratory disease occurs in a regulatory sequence. Hum Mol Genet. 1993 Mar;2(3):253–257. doi: 10.1093/hmg/2.3.253. [DOI] [PubMed] [Google Scholar]
  3. Ohhara M., Kurosu Y., Esumi M. Direct PCR of whole blood and hair shafts by microwave treatment. Biotechniques. 1994 Oct;17(4):726–728. [PubMed] [Google Scholar]
  4. Poller W., Meisen C., Olek K. DNA polymorphisms of the alpha 1-antitrypsin gene region in patients with chronic obstructive pulmonary disease. Eur J Clin Invest. 1990 Feb;20(1):1–7. doi: 10.1111/j.1365-2362.1990.tb01769.x. [DOI] [PubMed] [Google Scholar]
  5. Redline S., Tishler P. V., Rosner B., Lewitter F. I., Vandenburgh M., Weiss S. T., Speizer F. E. Genotypic and phenotypic similarities in pulmonary function among family members of adult monozygotic and dizygotic twins. Am J Epidemiol. 1989 Apr;129(4):827–836. doi: 10.1093/oxfordjournals.aje.a115197. [DOI] [PubMed] [Google Scholar]
  6. Snider G. L. Chronic obstructive pulmonary disease: risk factors, pathophysiology and pathogenesis. Annu Rev Med. 1989;40:411–429. doi: 10.1146/annurev.me.40.020189.002211. [DOI] [PubMed] [Google Scholar]

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