Journal of Natural Science, Biology and Medicine

REVIEW ARTICLE
Year
: 2019  |  Volume : 10  |  Issue : 1  |  Page : 97--102

The frequency and spectrum of HBB gene mutation in β-Thalassemia patients in Saudi Arabia


Raniah S Alotibi1, Eman Alharbi1, Bushra Aljuhani1, Bdoor Alamri1, Mohieldin Elsayid1, Naif M Alhawiti1, Fazal Hussain2, Fahad Almohareb2, Cherry Colcol2, Shoeb Qureshi3 
1 Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia
2 King Faisal Specialists Hospital and Research Center, Riyadh, Saudi Arabia
3 Department of Research Methodology, College of Applied Medical Sciences, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia

Correspondence Address:
Shoeb Qureshi
Department of Research Methodology, College of Applied Medical Sciences, King Saud Bin Abdulaziz University for Health Sciences, Riyadh
Saudi Arabia

Background: β-thalassemia is an autosomal disorder of the blood caused by mutations in HBB gene responsible for the production of β-globin. The HBB mutations reduce the synthesis of β-globin which results in severe anemia. A high frequency of β-thalassemia is reported in Saudi Arabia, and hence this study assessed the most frequent β-thalassemia mutations in Saudi Arabia. Materials and Methods: Data of preimplantation genetic diagnosis and gene sequencing for 59 β-thalassemia patients and carriers were collected from the electronic medical record system at KFSH and RC and were analyzed using SPSS version 19. Results: Twelve mutations were confirmed in the five regions investigated in this study. Cd39 was identified as the most frequent mutation with a frequency of 22.7%, with high prevalence in the central parts of Saudi Arabia. IVS-II-1 G > A was the second frequent mutation observed with a frequency of 21.2%, while IVS-I-1 (G-A) and IVS I-130G>C mutations were observed to be least frequent in the study. Of the 12 gene mutations, 85% were frequently observed in Saudi Arabia, while 15% were less frequent. The regional distribution of HBB gene mutations varied considerably. Conclusion: The population diversity in Saudi Arabia contributes to the variability in the prevalence rates of HBB gene mutations. Nevertheless, this study identifies Cd39 and IVS-II-1 G > A as the predominant mutations in HBB gene in Saudi Arabia.


How to cite this article:
Alotibi RS, Alharbi E, Aljuhani B, Alamri B, Elsayid M, Alhawiti NM, Hussain F, Almohareb F, Colcol C, Qureshi S. The frequency and spectrum of HBB gene mutation in β-Thalassemia patients in Saudi Arabia.J Nat Sc Biol Med 2019;10:97-102


How to cite this URL:
Alotibi RS, Alharbi E, Aljuhani B, Alamri B, Elsayid M, Alhawiti NM, Hussain F, Almohareb F, Colcol C, Qureshi S. The frequency and spectrum of HBB gene mutation in β-Thalassemia patients in Saudi Arabia. J Nat Sc Biol Med [serial online] 2019 [cited 2020 Feb 25 ];10:97-102
Available from: http://www.jnsbm.org/article.asp?issn=0976-9668;year=2019;volume=10;issue=1;spage=97;epage=102;aulast=Alotibi;type=0