» Articles » PMID: 23591685

The Distribution of Haemoglobin C and Its Prevalence in Newborns in Africa

Overview
Journal Sci Rep
Specialty Science
Date 2013 Apr 18
PMID 23591685
Citations 54
Authors
Affiliations
Soon will be listed here.
Abstract

Haemoglobin C (HbC) is one of the commonest structural haemoglobin variants in human populations. Although HbC causes mild clinical complications, its diagnosis and genetic counselling are important to prevent inheritance with other haemoglobinopathies. Little is known about its contemporary distribution and the number of newborns affected. We assembled a global database of population surveys. We then used a Bayesian geostatistical model to create maps of HbC frequency across Africa and paired our predictions with high-resolution demographics to calculate heterozygous (AC) and homozygous (CC) newborn estimates and their associated uncertainty. Data were too sparse outside Africa for this methodology to be applied. The highest frequencies were found in West Africa but HbC was commonly found in other parts of the continent. The expected annual numbers of AC and CC newborns in Africa were 672,117 (interquartile range (IQR): 642,116-705,163) and 28,703 (IQR: 26,027-31,958), respectively. These numbers are about two times previous estimates.

Citing Articles

Sickle cell retinopathy among Ghanaian high school students: a school-based screening.

Sedhom J, Ahmed A, DesLauriers A, Ahmed E, Baah C, Ackah P BMJ Glob Health. 2025; 9(12).

PMID: 39937756 PMC: 11664335. DOI: 10.1136/bmjgh-2024-016896.


Screening for sickle cell anemia in two populations of eastern Gabon using alkaline electrophoresis and hemoglobin level combined with leukocyte count.

Mombo L, Moreau B, Bisseye C, Mikelet Boussoukou I, Mongo Delis A, Lendamba R Int J Hematol. 2025; .

PMID: 39907907 DOI: 10.1007/s12185-025-03934-0.


Epidemiologic profile of hemoglobinopathies in Benin.

Gomez S, Amoussa A, Dedjinou E, Kakpo M, Gbedji P, Amossou Soule N Hematol Transfus Cell Ther. 2024; 46 Suppl 6:S257-S262.

PMID: 39426879 PMC: 11726114. DOI: 10.1016/j.htct.2024.07.008.


Prevalence and Regional Distribution of Beta-Hemoglobin Variants in Saudi Arabia: Insights from the National Premarital Screening Program".

Aljabry M, Sulimani S, Alotaibi G, Aljabri H, Alomary S, Aljabri O J Epidemiol Glob Health. 2024; 14(3):1242-1248.

PMID: 39073533 PMC: 11442792. DOI: 10.1007/s44197-024-00281-x.


Association between fetal hemoglobin, lactate dehydrogenase, and disease severity in patients with sickle cell disease at Bugando Medical Centre, Mwanza, Tanzania.

Kahema S, Mbulwa C, Nkubi Bagenda C, Niyonzima N, Muwanguzi E, Mcharo T PLoS One. 2024; 19(7):e0286891.

PMID: 39008448 PMC: 11249230. DOI: 10.1371/journal.pone.0286891.


References
1.
Patel D, Patel S, Mashon R, Dash P, Mukherjee M . Diverse phenotypic expression of sickle cell hemoglobin C disease in an Indian family. Ann Hematol. 2010; 90(3):357-8. DOI: 10.1007/s00277-010-1014-1. View

2.
Kan Y, DOZY A . Evolution of the hemoglobin S and C genes in world populations. Science. 1980; 209(4454):388-91. DOI: 10.1126/science.7384810. View

3.
Hill A, Allsopp C, Kwiatkowski D, Anstey N, Twumasi P, Rowe P . Common west African HLA antigens are associated with protection from severe malaria. Nature. 1991; 352(6336):595-600. DOI: 10.1038/352595a0. View

4.
Flint J, Harding R, Boyce A, Clegg J . The population genetics of the haemoglobinopathies. Baillieres Clin Haematol. 1993; 6(1):215-62. DOI: 10.1016/s0950-3536(05)80071-x. View

5.
Gulbis B, Cotton F, Ferster A, Ketelslegers O, Dresse M, Ronge-Collard E . Neonatal haemoglobinopathy screening in Belgium. J Clin Pathol. 2008; 62(1):49-52. DOI: 10.1136/jcp.2008.060517. View