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Frequency of Duffy, Kidd, Lewis, and Rh Blood Group Antigens and Phenotypes Among Donors in the Al-Ahsa Region, Saudi Arabia.

Authors :
Kuriri, Fahd A.
Ahmed, Abdulrahman
Alhumud, Fahad
Alanazi, Fehaid
Abdalhabib, Ezeldine K.
Source :
Clinical Laboratory; 2024, Vol. 70 Issue 7, p1316-1322, 7p
Publication Year :
2024

Abstract

In Al-Ahsa, Saudi Arabia, the high consanguinity rates contribute to the prevalence of inherited hemoglobinopathies such as sickle cell disease and thalassemia, which frequently require blood transfusions. These transfusions carry the risk of alloimmunization, necessitating a precise blood component matching to mitigate health risks. Local antigen frequency data is vital for optimizing transfusion practices and enhancing the safety of these medical procedures for the Al-Ahsa population. Methods: This study investigated the distribution of Duffy, Kidd, Lewis, and Rh blood group antigens in 1,549 individuals from the region; comparing the frequencies with global data. Results: Serological analyses revealed a high prevalence of the Fy(a+b-) and Jk(a+b+) phenotypes in the Duffy and Kidd blood groups, respectively, with Jk(a-b-) being notably scarce. The Lewis blood group exhibited a significant presence of Le(a-b+) and Le(a+b-) phenotypes, whereas Le(a+b+) was less common. In the Rh system, the D antigen was most prevalent, with other antigens following in descending order of frequency. Conclusions: The study underscores the regional variation in antigen frequencies, emphasizing the need for local blood banks to adapt their screening and matching practices to mitigate the risk of alloimmunization and enhance transfusion safety. These findings are pivotal for refining transfusion strategies and understanding the immunohematology landscape in Al-Ahsa. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14336510
Volume :
70
Issue :
7
Database :
Complementary Index
Journal :
Clinical Laboratory
Publication Type :
Academic Journal
Accession number :
178448458
Full Text :
https://doi.org/10.7754/Clin.Lab.2024.240104