The presence of a geographical pattern in the distribution of the sickle cell gene (S gene) and its association with malaria is well documented. To study the distribution of the S gene among various ethnic and linguistic groups in the Sudan we analyzed a hospital-based sample of 189 sickle cell anemia (SCA) patients who reported to the Khartoum Teaching Hospital between June 1996 and March 2000 and 118 controls with other complaints, against their ethnic and linguistic affiliations and geographic origin. Electrophoresis for hemoglobin S and sickling tests were carried out on all patients and controls as a prerequisite for inclusion. The majority of patients (93.7%) belonged to families of single ethnic descent, indicating the high degree of within-group marriages and thus the higher risk of augmenting the gene. SCA was found to be predominant among the Afro-Asiatic-speaking groups (68.4%) including nomadic groups of Arab and non- Arab descent that migrated to the Sudan in various historical epochs. Those patients clustered in western Sudan (Kordofan and Darfur) from where 73% of all cases originate. The proportion of patients reporting from other geographic areas like the south (3.1%), which is primarily inhabited by Nilo-Saharan-speaking groups (19% of the whole sample) who populated the country in previous times, is disproportionate to their total population in the country (χ2 = 71.6; p = 0.0001). Analysis of the haplotypes associated with the S gene indicated that the most abundant haplotypes are the Cameroon, Benin, Bantu and Senegal haplotypes, respectively. No relationship was seen between haplotypes and the various hematological parameters in the sub-sample analyzed for such association. These results provide an insight into the distribution of the sickle cell gene in the Sudan, and highlight the strong link of the middle Nile Valley with West Africa through the open plateau of the Sahel and the nomadic cattle herders and also probably the relatively young age of the S gene.

1.
Lanclos KD, Oner C, Dimovski AJ, Gu YC, Huisman TH: Sequence variations in the 5′ flanking and IVS-II regions of the G gamma- and A gamma-globin genes of βS chromosomes with five different haplotypes. Blood 1991;77:2488–2496.
2.
Oner C, Dimovki A, Olivieri N, Schiliro G, Codrington J, Fattoum S, et al: βs haplotypes in various world populations. Hum Genet 1992;89:99–104.
3.
Goncalves MS, Nechtman JF, Figueiredo MS, Kerbauy J, Arruda VR, Sonati MF, Saad SO, Costa FF, Stoming TA: Sickle cell disease in Brazilian population: a study of bs haplotypes. Hum Hered 1994;44:322–327.
4.
Vivenes De Lugo M, Rodriguez-Larralde A, Castro De Guerra D: Beta-globin gene cluster haplotypes as evidence of African gene flow to the northeastern coast of Venezuela. Am J Hum Biol 2003;15:29–37.
5.
Lehmann H: Distribution of the sickle cell gene. A new light on the origin of the East Africans. Eugen Rev 1954;46:101–121.
6.
Lehmann H: Origin of the sickle cell. S Afr J Sci 1954;50:140–141.
7.
Gelpi AP: Migrant populations and the diffusion of the sickle-cell gene. Ann Intern Med 1973;79:258–264.
8.
Kurnit DM: Evolution of sickle variant gene. Lancet 1979;i:104.
9.
Pagnier J, Mears JG, Dunda-Belkhodja O, Schaefer-Rego KE, Beldjord C, Nagel RL, Labie D: Evidence for the multicentric origin of the sickle cell hemoglobin gene in Africa. Proc Natl Acad Sci USA 1984;81:1771.
10.
Grimes BF (ed): Ethnologue: Languages of the World, ed 13. Dallas, Summer Institute of Linguistics, 1996.
11.
Greenberg JH: Studies in African Linguistic Classification. Bradford, Compass Publishing, 1955.
12.
Konotey-Ahulu FID: The sickle cell disease patient. Watford, Tetteh-A’Domenco, 1996.
13.
Government of the Sudan: 1997 Census.
14.
Hewitt R, Krause A, Goldman A, Campbell G, Jenkins T: Beta-globin haplotype analysis suggests that a major source of Malagasy ancestry is derived from Bantu-speaking Negroids. Am J Hum Genet 1996;58:1303–1308.
15.
Elhassan AM, Godber MG, Kopec AC, Mourant AE, Tills D, Lehmann H: The inherited blood factors of the Beja of the Sudan. Man 1968;3:272.
16.
Ibrahim SA, Dafalla AA, Lauder JR: A search for abnormal hemoglobin and thalassaemia in the Beni Amer tribe. Sudan Med J 1970;8:88–92.
17.
Aspinalli PJ, Dyson SM, Anionwu EN: The feasibility of using ethnicity as a primary tool for antenatal selective screening for sickle cell disorders: pointers from the research evidence. Soc Sci Med 2003;56:285–297.
18.
Ahmed S, Saleem M, Modell B, Petrou M: Screening extended families for genetic hemoglobin disorders in Pakistan. N Engl J Med 2002;347:1162–1168.
19.
Archibald RG: A case of sickle cell anemia in Sudan. Trans R Soc Trop Med Hyg 1926;19:389–393.
20.
Vella F: Hemoglobin S and sickling in Khartoum province. Trans R Soc Trop Med Hyg 1966;60:48–52.
21.
Launden RJ, Ibrahim SA: Sickling in South West Kordufan. Sud Med J 1970;8:207–217.
22.
Vella F: Sickling in the Western Sudan. Sudan Med J 1964;3:16–17.
23.
Ahmed HA, Baker EA: Sickling in the Sudan. Results of surveys in the Blue Nile Province. East Afr Med J 1986;63:395–399.
24.
Foy H, Kondi A, Brass W: The variability of sickle-cell rates in the tribes of Kenya and the southern Sudan. Br Med J 1954;4857:294–297.
25.
Ojwang PJ, Ogada T, Gonzaleez-Redondo JM, Kutlar A, Kutlar F, Huisman TH: Beta S-haplotypes and alpha-thalassemia along the coastal belt of Kenya. East Afr Med J 1989;66:377–380.
26.
Cruciani F, Santolamazza P, Shen P, Macaulay V, Moral P, Olckers A, Modiano D, Holmes S, Destro-Bisol G, Coia V, Wallace DC, Oefner PJ, Torroni A, Cavalli-Sforza LL, Scozzari R, Underhill PA: A back migration from Asia to sub-Saharan Africa is supported by high-resolution analysis of human Y-chromosome haplotypes. Am J Hum Genet 2003;70:1197–1214.
27.
Balamoan GA: People and Economics in the Sudan, 1884–1956 (A Study in migration policies and economics). London, White Friars Press, 1976.
28.
Encyclopedia Britannica (Chicago), 1994, vol 28, pp 256.
29.
Achtman M: Microevolution during epidemic spread of Neisseria meningitides. Electrophoresis 1998;19:593–596.
30.
Bayoumi RA, Taha TS: A study of some genetic characteristics of the Fur and Baggara tribes of the Sudan. Am J Phys Anthropol 1985;67:363–370.
31.
Bayoumi RA, Saha N: Some blood genetic markers of the Nuba and Hawazma tribes of western Sudan. Am J Phys Anthropol 1987;73:379–388.
32.
Volkman SK, Barry AE, Lyons EJ, Nielsen KM, Thomas SM, Choi M, Thakore SS, Day KP, Wirth DF, Hartl DL: Recent origin of Plasmodium falciparum from a single progenitor. Science 2001;293:482–483.
33.
Tishkoff SA, Varkonyl R, Cahinhinan N, Abbes S, Argyropoulos G, Destro-Bisol G, Drousiotou A, Dangerfield B, Lefranc G, Loiselet J, Piro A, Stoneking M, Tagarelli A, Tagarelli G, Touma EH, Williams SM, Clark AG: Haplotype diversity and linkage disequilibrium at human G6PD: Recent origin of alleles that confer malaria resistance. Science 2001;293:455–462.
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