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Alpha-1 Antitrypsin Deficiency in Iranian Patients with Chronic Obstructive Pulmonary Disease
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 conduc...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Kowsar
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3971777/ https://www.ncbi.nlm.nih.gov/pubmed/24719685 http://dx.doi.org/10.5812/ircmj.7508 |
Sumario: | 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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