Literature DB >> 23647352

Hemoglobinopathy carrier prevalence in the United Arab Emirates: first analysis of the Dubai Health Authority premarital screening program results.

Khawla M Belhoul1, Mahera Abdulrahman, Rafeeiah F Alraei.   

Abstract

The aim of this study was to determine the prevalence of hemoglobinopathy carriers in United Arab Emirates (UAE) nationals subjected to mandatory premarital screening in Dubai over a 4-year period. Data from UAE nationals who underwent premarital screening by the Dubai Health Authority between January 2007 and December 2010 were collected and analyzed. Premarital screening in Dubai is based on complete blood counts (CBC) and hemoglobin (Hb) high performance liquid chromatography (HPLC). Among the 6,420 UAE nationals screened, 8.5% (n = 545) were suspected to be carriers. The following carrier frequencies were observed: β-thalassemia (β-thal), 4.56% (n = 293); Hb S [β6(A3)Glu→Val, GAG>GTG; HBB: c.20A>T], 2.9% (n = 186); Hb D-Punjab [β121(GH4)Glu→Gln, GAA>CAA; HBB: c.364G>C], 0.78% (n = 50); Hb Lepore (δβ hybrid gene) with an undetermined molecular genotype, 0.17% (n = 11); Hb E [β26(B8)Glu→Lys, GAG>AAG; HBB: c.79G>A], 0.03% (n = 2); and hereditary persistence of fetal Hb (HPFH), 0.016% (n = 1). Hb E-Hb S and Hb E-β-thal also occurred at a rate of 0.016% (n = 1) each; and 0.87% (n = 56) subjects were suspected of carrying silent β-thal. The prevalence of β-thal trait was consistent with the prevalence published by others in the region. Silent β-thal is challenging for screening programs, and is expected to arise in populations with a high prevalence of β-thal carriers. The prevalence of Hb S trait observed in this study was lower than that in other reports for the region. New cases of β-thal major (β-TM) still arise because many fertile couples got married before the screening programs were implemented, and pregnancy termination is not widely practiced in the UAE due to religious restraints. Moreover, some couples choose not to have prenatal diagnosis (PND) or pre implantation genetic diagnosis (PGD), even if they are aware of their risk status. The prevalence of β-thal trait in the UAE is high. This justifies efforts to control the disease by holding regular community awareness and screening programs, performing premarital screening and genetic counseling, and making PND and PGD available to couples who request it.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23647352     DOI: 10.3109/03630269.2013.791627

Source DB:  PubMed          Journal:  Hemoglobin        ISSN: 0363-0269            Impact factor:   0.849


  10 in total

1.  Productivity Loss and Associated Costs Among Patients with Transfusion-Dependent Thalassemia in Dubai, United Arab Emirates.

Authors:  Shaikha Alshamsi; Samer Hamidi; Hacer Ozgen Narci
Journal:  Clinicoecon Outcomes Res       Date:  2021-09-29

2.  Red cell parameters in infant and children from the Arabian Peninsula.

Authors:  Lolowa A Al Mekaini; Srdjan Denic; Omar N Al Jabri; Hassib Narchi; Abdul-Kader Souid; Suleiman Al-Hammadi
Journal:  Am J Blood Res       Date:  2015-12-25

3.  Analysis of blood donor pre-donation deferral in Dubai: characteristics and reasons.

Authors:  Laila Al Shaer; Ranjita Sharma; Mahera AbdulRahman
Journal:  J Blood Med       Date:  2017-05-25

4.  Thalassemia in the United Arab Emirates: Why it can be prevented but not eradicated.

Authors:  Sehjeong Kim; Abdessamad Tridane
Journal:  PLoS One       Date:  2017-01-30       Impact factor: 3.240

5.  Evolution of family medicine residency training program in Dubai Health Authority: A 24-year review, challenges, and outcomes.

Authors:  Wadeia Mohammad AlSharief; Mahera Abdulrahman; Hamda Hassan Khansaheb; Shaima Amin Abdulghafoor; Ashraf Ahmed
Journal:  J Family Med Prim Care       Date:  2018 Mar-Apr

6.  Healthcare resource utilization and direct costs of transfusion-dependent thalassemia patients in Dubai, United Arab Emirates: a retrospective cost-of-illness study.

Authors:  Shaikha Alshamsi; Samer Hamidi; Hacer Ozgen Narci
Journal:  BMC Health Serv Res       Date:  2022-03-05       Impact factor: 2.655

Review 7.  Genetic testing and genomic analysis: a debate on ethical, social and legal issues in the Arab world with a focus on Qatar.

Authors:  Hatem El Shanti; Lotfi Chouchane; Ramin Badii; Imed Eddine Gallouzi; Paolo Gasparini
Journal:  J Transl Med       Date:  2015-11-14       Impact factor: 5.531

8.  Epidemiology of Thalassemia in Gulf Cooperation Council Countries: A Systematic Review.

Authors:  Amani Abu-Shaheen; Humariya Heena; Abdullah Nofal; Doaa A Abdelmoety; Abdulrahman Almatary; Mohammed Alsheef; Isamme AlFayyad
Journal:  Biomed Res Int       Date:  2020-10-28       Impact factor: 3.411

Review 9.  Current Updates on Expanded Carrier Screening: New Insights in the Omics Era.

Authors:  Iolanda Veneruso; Chiara Di Resta; Rossella Tomaiuolo; Valeria D'Argenio
Journal:  Medicina (Kaunas)       Date:  2022-03-21       Impact factor: 2.430

10.  Social and cultural influences on genetic screening programme acceptability: A mixed-methods study of the views of adults, carriers, and family members living with thalassemia in the UK.

Authors:  Felicity K Boardman; Corinna Clark; Elsita Jungkurth; Philip J Young
Journal:  J Genet Couns       Date:  2020-03-01       Impact factor: 2.717

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.