alpha-۱ antitrypsin deficiency in iranian patients with chronic obstructive pulmonary disease

Authors

bita geramizadeh department of pathology, transplant research center, shiraz university of medical sciences, shiraz, ir iran; transplant research center, shiraz university of medical sciences, shiraz, ir iran; department of pathology, transplant research center, shiraz university of medical sciences, shiraz, ir iran. tel: +98-7116474331, fax: +98-7116474331

zahra jowkar department of pathology, transplant research center, shiraz university of medical sciences, shiraz, ir iran

leila karami department of pathology, transplant research center, shiraz university of medical sciences, shiraz, ir iran

masoum masoumpour department of internal medicine, shiraz university of medical sciences, shiraz, ir iran

abstract

background alpha-1 antitrypsin deficiency is a genetic disease which affects both lung and liver. this disease is a recognized factor for chronic obstructive pulmonary disease (copd). however its importance as the cause of copd in a country such as iran is unclear. objectives this study was conducted to find out the role of α-1 antitrypsin deficiency as a cause of copd in iranian patients. materials and methods the serum concentration of α-1 antitrypsin was determined and the genotype of α-1 antitrypsin was also evaluated by pcr-rflp in 130 patients with copd and 50 normal healthy blood donors. results no α-1 antitrypsin deficient case was found in normal healthy people and copd patients. conclusions our results clarify that deficiency of α-antitrypsin is not a major cause of copd in iranian patients.

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Journal title:
iranian red crescent medical journal

جلد ۱۵، شماره ۱۱، صفحات ۰-۰

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