TY - JOUR
T1 - Hematological and molecular analyses of the HbS allele among the Sudanese population
AU - Khalafallah, Tariq Osman
AU - Ajab Eldoor, Ahmed Abdalla
AU - Babker, Asaad M.A.
AU - Bin Shaya, Abdulkarim S.
AU - Alfahed, Abdulaziz
AU - Alharithi, Nahed S.
AU - Aloraini, Ghfren S.
AU - Waggiallah, Hisham Ali
N1 - Publisher Copyright:
© The Author(s) 2022.
PY - 2022/9
Y1 - 2022/9
N2 - Objective: The purpose of this study was to perform hematological and molecular analyses of the HbS allele of the hemoglobin subunit beta gene in the Sudanese population. Methods: This was a descriptive cross-sectional study. Hematological parameters and fetal hemoglobin (HbF) levels were assessed in all participants. Data were gathered through the use of questionnaires and laboratory investigations. The βS-globin haplotypes, S allele distributions, and hematological parameters with HbF levels were investigated using PCR-restriction fragment length polymorphism, gel electrophoresis, and a Sysmex hematology analyzer, respectively. Results: According to our findings, the Bantu (BA) haplotype was found in 10.8% of participants with homozygous uncontested haplotypes, followed by Benin (BA) and Sudan (SU), each in 9.8% of participants. This Sudanese group from Northern Kordofan lacked the Arab-Indian haplotype. Two heterozygous versions of undisputed haplotypes were found in 17.3% of participants: SU/BA in 10.8% and CA/BE in 6.5%. Conclusion: As a result of sickle cell anemia, this investigation found changes in hematological parameters. In the Sudanese population, a new haplotype of the S gene was discovered.
AB - Objective: The purpose of this study was to perform hematological and molecular analyses of the HbS allele of the hemoglobin subunit beta gene in the Sudanese population. Methods: This was a descriptive cross-sectional study. Hematological parameters and fetal hemoglobin (HbF) levels were assessed in all participants. Data were gathered through the use of questionnaires and laboratory investigations. The βS-globin haplotypes, S allele distributions, and hematological parameters with HbF levels were investigated using PCR-restriction fragment length polymorphism, gel electrophoresis, and a Sysmex hematology analyzer, respectively. Results: According to our findings, the Bantu (BA) haplotype was found in 10.8% of participants with homozygous uncontested haplotypes, followed by Benin (BA) and Sudan (SU), each in 9.8% of participants. This Sudanese group from Northern Kordofan lacked the Arab-Indian haplotype. Two heterozygous versions of undisputed haplotypes were found in 17.3% of participants: SU/BA in 10.8% and CA/BE in 6.5%. Conclusion: As a result of sickle cell anemia, this investigation found changes in hematological parameters. In the Sudanese population, a new haplotype of the S gene was discovered.
KW - HbS allele
KW - hematological analysis
KW - hemoglobin subunit beta
KW - molecular analysis
KW - Sickle cell anemia
KW - Sudan
UR - http://www.scopus.com/inward/record.url?scp=85138268772&partnerID=8YFLogxK
U2 - 10.1177/03000605221125050
DO - 10.1177/03000605221125050
M3 - Article
C2 - 36134571
AN - SCOPUS:85138268772
SN - 0300-0605
VL - 50
JO - Journal of International Medical Research
JF - Journal of International Medical Research
IS - 9
ER -