Saudi Journal of Gastroenterology
Home About us Instructions Submission Subscribe Advertise Contact Login    Print this page  Email this page Small font sizeDefault font sizeIncrease font size 
Users Online: 1149 
Year : 2011  |  Volume : 17  |  Issue : 4  |  Page : 256-260

Prevalence of α-1-Antitrypsin gene mutations in Saudi Arabia

1 Department of Medicine, Gastroenterology Division, Qassim University, Saudi Arabia
2 Research Center, Qassim University, Saudi Arabia
3 Research Center, Qassim University; Department of Pediatrics, College of Medicine, Qassim University, Saudi Arabia

Correspondence Address:
Badr Aljarallah
Department of Medicine, King Fahad Specialist Hospital, Faculty of Medicine, Qassim University, Maledia-51452
Saudi Arabia
Login to access the Email id

Source of Support: 1st author received grant from Qassim University, Conflict of Interest: None

DOI: 10.4103/1319-3767.82580

Rights and Permissions

Background/Aim: α-1 antitrypsin (AAT) deficiency results from mutations of the protease inhibitor (PI). The AAT gene is mapped on chromosome 14 and has been associated with chronic liver disease and chronic obstructive pulmonary disease (COPD). Objective: To determine the frequency of AAT mutations on S and Z carrier alleles in healthy Saudi individuals from Qassim Province in Saudi Arabia. Patients and Methods : A total of 158 healthy, unrelated participants from Qassim Province were recruited. They were genotyped for the two AAT-deficiency alleles, PI*S and PI*Z, using polymerase chain reaction, with primers designed throughout to mediate site-directed mutagenesis. Results: Of the 158 subjects, 11.39% were carriers for the S mutation (i.e., had the MS genotype), whereas 2.53% were carriers for the Z mutation (i.e., had the MZ genotype). The SZ genotype was present in 3.8% of subjects, while the homozygous genotype SS was present in 1.9% of subjects. No subjects showed the ZZ mutant genotype. Accordingly, frequency of the mutant S and Z alleles of AAT gene was 9.49% and 3.19%, respectively. Conclusion: The results obtained showed a high prevalence of the AAT deficiency allele in the Saudi population. This probably warrants adoption of a screening program for at-risk individuals, so that they might initiate adequate prophylactic measures.

Print this article     Email this article
 Next article
 Previous article
 Table of Contents

 Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
 Citation Manager
 Access Statistics
 Reader Comments
 Email Alert *
 Add to My List *
 * Requires registration (Free)

 Article Access Statistics
    PDF Downloaded410    
    Comments [Add]    
    Cited by others 5    

Recommend this journal