Prevalence of glucose-6-phosphate dehydrogenase deficiency and sickle cell trait among blood donors in Riyadh
- PMID: 20376264
- PMCID: PMC2847342
- DOI: 10.4103/0973-6247.59389
Prevalence of glucose-6-phosphate dehydrogenase deficiency and sickle cell trait among blood donors in Riyadh
Abstract
Background and aims: Blood donation from glucose-6-phosphate dehydrogenase (G6PD)-deficient and sickle cell trait (SCT) donors might alter the quality of the donated blood during processing, storage or in the recipient's circulatory system. The aim of this study was to determine the prevalence of G6PD deficiency and SCT among blood donors coming to King Khalid University Hospital (KKUH) in Riyadh. It was also reviewed the benefits and risks of transfusing blood from these blood donors.
Materials and methods: This cross-sectional study was conducted on 1150 blood samples obtained from blood donors that presented to KKUH blood bank during the period April 2006 to May 2006. All samples were tested for Hb-S by solubility test, alkaline gel electrophoresis; and for G6PD deficiency, by fluorescent spot test.
Results: Out of the 1150 donors, 23 (2%) were diagnosed for SCT, 9 (0.78%) for G6PD deficiency and 4 (0.35%) for both conditions. Our prevalence of SCT and G6PD deficiency is higher than that of the general population of Riyadh.
Conclusion: We recommend to screen all units for G6PD deficiency and sickle cell trait and to defer donations from donors with either of these conditions, unless if needed for special blood group compatibility, platelet apheresis or if these are likely to affect the blood bank inventory. If such blood is to be used, special precautions need to be undertaken to avoid complications in high-risk recipients.
Keywords: Blood transfusion; glucose-6-phosphate dehydrogenase deficiency; sickle cell trait.
Conflict of interest statement
Similar articles
-
Significantly elevated foetal haemoglobin levels in individuals with glucose 6-phosphate dehydrogenase disease and/or sickle cell trait: a cross-sectional study in Cape Coast, Ghana.BMC Hematol. 2017 Sep 25;17:16. doi: 10.1186/s12878-017-0088-6. eCollection 2017. BMC Hematol. 2017. PMID: 29021902 Free PMC article.
-
Prevalence of G6PD deficiency in Thai blood donors, the characteristics of G6PD deficient blood, and the efficacy of fluorescent spot test to screen for G6PD deficiency in a hospital blood bank setting.Hematology. 2022 Dec;27(1):208-213. doi: 10.1080/16078454.2022.2027082. Hematology. 2022. PMID: 35134307
-
Glucose-6-Phosphate Dehydrogenase Deficiency and Sickle Cell Trait among Prospective Blood Donors: A Cross-Sectional Study in Berekum, Ghana.Adv Hematol. 2016;2016:7302912. doi: 10.1155/2016/7302912. Epub 2016 Sep 14. Adv Hematol. 2016. PMID: 27703480 Free PMC article.
-
Blood Donors with Thalassemic Trait, Glucose-6-Phosphate Dehydrogenase Deficiency Trait, and Sickle Cell Trait and Their Blood Products: Current Status and Future Perspective.Lab Med. 2023 Jan 5;54(1):6-12. doi: 10.1093/labmed/lmac061. Lab Med. 2023. PMID: 35943550 Review.
-
Glucose-6-phosphate dehydrogenase deficiency in transfusion medicine: the unknown risks.Vox Sang. 2013 Nov;105(4):271-82. doi: 10.1111/vox.12068. Epub 2013 Jul 2. Vox Sang. 2013. PMID: 23815264 Free PMC article. Review.
Cited by
-
Prevalence and molecular characterization of Glucose-6-Phosphate dehydrogenase deficient variants among the Kurdish population of Northern Iraq.BMC Blood Disord. 2010 Jul 5;10:6. doi: 10.1186/1471-2326-10-6. BMC Blood Disord. 2010. PMID: 20602793 Free PMC article.
-
Significantly elevated foetal haemoglobin levels in individuals with glucose 6-phosphate dehydrogenase disease and/or sickle cell trait: a cross-sectional study in Cape Coast, Ghana.BMC Hematol. 2017 Sep 25;17:16. doi: 10.1186/s12878-017-0088-6. eCollection 2017. BMC Hematol. 2017. PMID: 29021902 Free PMC article.
-
Seven novel glucose-6-phosphate dehydrogenase (G6PD) deficiency variants identified in the Qatari population.Hum Genomics. 2021 Oct 7;15(1):61. doi: 10.1186/s40246-021-00358-9. Hum Genomics. 2021. PMID: 34620237 Free PMC article.
-
Molecular characterization of glucose-6-phosphate dehydrogenase deficient variants in Baghdad city - Iraq.BMC Blood Disord. 2012 Mar 27;12:4. doi: 10.1186/1471-2326-12-4. BMC Blood Disord. 2012. PMID: 22452742 Free PMC article.
-
Analysis of G6PD enzyme deficiency in Saudi population.Bioinformation. 2012;8(25):1260-4. doi: 10.6026/97320630081260. Epub 2012 Dec 19. Bioinformation. 2012. PMID: 23275731 Free PMC article.
References
-
- El-Hazmi MA, Warsy AS. Appraisal of sickle-cell and thalassaemia genes in Saudi Arabia. East Mediterr Health J. 1999;5:1147–53. - PubMed
-
- El-Hazmi MA, Warsy AS, Al-Swailem AR, Al-Swailem AM, Bahakim HM. Sickle cell gene in the population of Saudi Arabia. Hemoglobin. 1996;20:187–98. - PubMed
-
- Alhamdan NA, Almazrou YY, Alswaidi FM, Choudhry AJ. Premarital screening for thalassemia and sickle cell disease in Saudi Arabia. Genet Med. 2007;9:372–7. - PubMed
-
- Warsy AS, El-Hazmi MA. G6PD deficiency, distribution and variants in Saudi Arabia: An overview. Ann Saudi Med. 2001;21:174–7. - PubMed
LinkOut - more resources
Full Text Sources
Miscellaneous