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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...

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Detalles Bibliográficos
Autores principales: Geramizadeh, Bita, Jowkar, Zahra, Karami, Leila, Masoumpour, Masoum, Mehrabi, Samrad, Ghayoumi, Mohammad-Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2013
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
Descripción
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.