Glucose-6-phosphate dehydrogenase deficiency and sickle cell disease in Burkina Faso

Pakistan Journal of Biological Sciences

Volumn 10, Issue 3, 2007, Pages 409-414

  Simpore, Jacques ^a,b,c   Ilboudo, Denise ^b   Damintoti, Karou ^b   Sawadogo, Luc ^b   Maria, Esposito ^d   Binet, Scott ^e   Nitiema, Henri ^f   Ouedraogo, Paul ^f   Pignatelli, Salvatore ^a   Nikiema, Jean Baptiste ^b  

^a Medical Center Saint Camille   (Burkina Faso)

^b UNIVERSITÉ DE OUAGADOUGOU   (Burkina Faso)

^c UNIVERSITY OF ROME TOR VERGATA   (Italy)

^d UNIVERSITY OF MESSINA   (Italy)

^e Camillian Task Force   (Italy)

^f CATHOLIC UNIVERSITY   (Italy)

Author keywords

Burkina Faso; G 6 PD; HbS; Hemoglobinuria; Malaria; Sickle cell disease

Indexed keywords

EID: 33847043147     PISSN: 10288880     EISSN: 18125735     Source Type: Journal    
DOI: 10.3923/pjbs.2007.409.414     Document Type: Article

References (41)

1. Akoglu, T., F.L. Ozer and E. Akoglu, 1986. The coincidence of glucose-6-phosphate dehydrogenase deficiency and hemoglobin S gene in Cukurova Province, Turkey. Am. J. Epidemiol., 123: 677-680.
2. Ali, N., M. Anwar, M. Ayyub, F.A., Bhatti, M. Nadeem and A. Nadeem, 2005. Frequency of glucose-6-phosphate dehydrogenase deficiency in some ethnic groups of Pakistan. J. Coll. Phys. Surg. Pak., 15: 137-341.
3. Allison, A.C., 1954. The Distribution of the Sickle-Cell trait in east Africa and elsewhere and its apparent relationship to the incidence of subtertian malaria. trans. Royal. Soc. Trop. Med. Hyg., 48: 312-318.
4. Balgir, R.S., 2005. The spectrum of haemoglobin variants in two scheduled tribes of Sundargarh district in northwestern Orissa, India. Ann. Hum. Biol., 32: 560-573.
5. Bienzle, U., O. Sodeinde, C.E. Effiong and L. Luzzatto, 1975. Glucose 6-phosphate dehydrogenase deficiency and sickle cell anemia: frequency and features of the association in an African community. Blood, 46: 591-597.
6. Bouanga, J.C., R. Mouele, C. Prehu, H. Wajcman, J. Feingold and F. Galacteros, 1998. Glucose-6-phosphate dehydrogenase deficiency and homozygous sickle cell disease in Congo. Hum Hered., 48: 192-197.
7. Ciftci, M., 2005. Effects of some drugs on the activity of glucose 6-phosphate dehydro-genase from rainbow trout erythrocytes in vitro. J. Enzyme Inhib. Med. Chem., 20: 485-489.
8. Diallo, D., A.K. Traore, M. Baby, A.A. Rhaly, G. Bellis and A. Chaventre, 1994. Haemoglobinopathies C and S in the Dogons. Nouv Rev. Fr Hematol., 35: 551-554.
9. Diop, S., D. Thiam, A. Sene, M. Cisse, K. Fall and A.O. Toure-all et al., 2000. Association drepanocytose-deficit en G-6-PD: prévalence et influence sur le profil évolutif, Médecine d'Afrique Noire., 47: 7.
10. Diop, S., A. Sene, M. Cisse, A.O. Toure, O. Sow and D. Thiam et al., 2005. Prevalence and morbidity of G6PD deficiency in sickle cell disease in the homozygote. Dakar Med., 50: 56-60.
11. El-Hazmi, M.A. and A.S. Warsy, 1986. Glucose-6-phosphate dehydrogenase polymorphism in the Saudi population. Hum. Hered., 36: 24-30.
12. El-Hazmi M.A. and A.S. Warsy, 1987. Interaction between glucose-6-phosphate dehydrogenase deficiency and sickle cell gene in Saudi Arabia. Trop. Geogr. Med., 39: 32-5.
13. Enevold, A., L.S. Vestergaard, J. Lusingu, C.J. Drakeley, M.M. Lemnge and T.G. Theander et al., 2005. Rapid screening for glu-cose-6-phosphate dehydrogenase deficiency and haemoglobin polymorphisms in Africa by a simple high-throughput SSOP-ELISA method. Malar. J., 15: 4: 61.
14. Fleming, A.F., J. Storey, L. Molineaux, E.A. Iroko and E.D. Attai, 1979. Abnormal haemoglobins in the Sudan savanna of Nigeria. I. Prevalence of haemoglobins and relationships between sickle cell trait, malaria and survival. Ann. Trop. Med. Parasitol., 73: 161-172.
15. Gbadoe, A.D. K.Atsou, O.A. Agbodjan-Djossou, E. Tsolenyanu, M. Nyadanu and A.D. Dogba et al., 2001. Ambulatory management of sickle cell disease: evaluation of the first year follow up of patients in the pediatric department of Lome, Togo. Bull. Soc. Pathol. Exot., 94: 101-105.
16. Ghani, R., M.A. Manji and N. Ahmed, 2002. Hemoglobinopathies among five major ethnic groups in Karachi, Pakistan. Southeast Asian J. Trop. Med. Public Health., 33: 855-861.
17. Gupte, S.C., P.U. Patel and J.M. Ranat, 2005. G6PD deficiency in Vataliya Prajapati community settled in Surat. Ind. J. Med. Sci., 59: 51-56.
18. Jacob, E., J.E. Beyer, C. Miaskowski, M. Savedra, M. Treadwell and L. Styles, 2005. Are there phases to the vasoocclusive painful episode in sickle cell disease? J. Pain Symptom Manage., 29: 392-400.
19. Kaplan, M., M. Muraca, H.J. Vreman, C. Hammerman, M.T. Vilei and F.F. Rubaltelli et al., 2005. Neonatal bilirubin production-conjugation imbalance: Effect of glucose-6-phosphate dehydrogenase deficiency and borderline prematurity. Arch Dis Child Fetal Neonatal Ed. 90: F123-F127.
20. Labie, D., C. Richin, J. Pagnier, M. Gentilini and R.L. Nagel, 1984. Hemoglobin S and C in Upper Volta. Hum. Genet., 65: 300-302.
21. Laosombat, V., B. Sattayasevana, T. Chotsampancharoen and M. Wongchanchailert, 2006. Glu-cose-6-phosphate dehydrogenase variants associated with favism in Thai children. Intl. J. Hematol., 83: 139-143.
22. Lewis, R.A., R.W. Kay and M. Harthorn, 1966. Sickle cell disease and glucose-6-phosphate dehydrogenase. Acta Haematol (Basel)., 36: 399-411.
23. Lewis, R.A., 1973. Glucose-6-phosphate dehydrogenase electrophoresis in Ghanaians with AA and SS haemoglobin. Acta Haematol., 50: 105-111.
24. Luzzatto, L. and N.C. Allan, 1968. Relationship between the genes for glucose-6-phosphate dehy-drogenase and for haemoglobin in a Nigerian population. Nature, 7;219: 1041-1042.
25. Mockenhaupt, P.P., B. Rong, M. Gunther, S. Beck, H. Till and E. Kohne et al., 2000. Anaemia in pregnant Ghanaian women: importance of malaria, iron deficiency and haemoglobinopathies. Trans. R Soc. Trop. Med. Hyg., 94: 477-483.
26. Modiano, D., G. Luoni, B.S. Sirima, J. Simpore, F. Verra and A. Konate et al., 2001a. Haemoglobin C protects against clinical Plasmodium falciparum malaria. Nature, 15;414: 305-308.
27. Modiano, D., G. Luoni, B.S. Sirima, A. Lanfrancotti, V. Petrarca, F. Cruciani and J. Simpore et al., 2001b. The lower susceptibility to Plasmodium falciparum malaria of Fulani of Burkina Faso (West Africa) is associated with low frequencies of classic malaria-resistance genes. Trans. R Soc. Trop. Med. Hyg., 95: 149-152.
28. Muzaffer, M.A., 2005. Neonatal screening of glucose-6-phosphate dehydrogenase deficiency in Yanbu, Saudi Arabia. J. Med. Screen, 12: 170-171.
29. Ozmen, I. and O.I. Kufrevioglu, 2004. Effects of antiemetic drugs on glucose 6-phosphate dehy-drogenase and some antioxidant enzymes. Pharmacol. Res., 50: 499-504.
30. Rattazzi, M.C., L.M. Corash, G.E. van Zanen, E.R. Jaffe and S. Piomelli, 1971. G6PD deficiency and chronic hemolysis: four new mutants - relationships between clinical syndrome and enzyme kinetics. Blood. 38: 205-218.
31. Rogers, Z.R., 2005. Priapism in sickle cell disease. Hematol. Oncol. Clin. North Am., 19: 917-928.
32. Saad, S.T. and F.F. Costa, 1992. Glucose-6-phosphate dehydrogenase deficiency and sickle cell dis-ease in Brazil. Hum. Hered., 42: 125-128.
33. Samuel, A.P.W., N. Saha, J.K. Acquaye, A. Omer, K. Gameshagura and E. Hassounh, 1986. Association of red cell glucose-6-phosphate dehydrogenase with haemoglobinopathies. Hum. Hered., 36: 107-112.
34. Shimizu, H., M. Tamam, A. Soemantri and T. Ishida, 2005. Glucose-6-phosphate dehydrogenase deficiency and Southeast Asian ovalocytosis in asymptomatic Plasmodium carriers in Sumba island, Indonesia. J. Hum. Genet., 50: 420-424.
35. Simpore, J., S. Pignatelli, S. Barlati and S. Musumeci, 2002. Biological and clinical presentation of patients with hemoglobinopathies attending an urban hospital in Ouagadougou: Confirmation of the modification of the balance between HbS and HbC in Burkina Faso Hemoglobin, 26: 121-127.
36. Singh, S., D.K. Singh, R. Gupta, S. Nigam and T. Singh, 2006. Persistent splenomegaly in an adult female with homozygous sickle cell anemia. Hematology, 11: 63-65.
37. Steinberg, M.H. and B.J. Dreiling, 1974. Glucose-6-phosphate dehydrogenase deficiency in Sickle-cell anemia. A study in adults. Ann. Intl. Med., 80: 217-220.
38. Storey, J., A.F. Fleming, R. Cornille-Brogger, L. Molineaux, T. Matsushima and I. Kagan, 1979. Abnormal haemoglobins in the Sudan savanna of Nigeria. IV. Malaria, immunoglobulins and antimalarial antibodies in haemoglobin AC individuals. Ann. Trop. Med. Parasitol., 73: 311-315.
39. Trabuchet, G., J. Elion, O. Dunda, C. Lapoumeroulie, R. Ducrocq and S. Nadifi et al., 1991. Nucleotide sequence evidence of the unicentric origin of the beta C mutation in Africa. Hum. Genet., 87: 597-601.
40. Williams, T.N., T.W. Mwangi, S. Wambua, N.D. Alexander, M. Kortok and R.W. Snow et al., 2005. Sickle cell trait and the risk of Plasmodium falciparum malaria and other childhood diseases. J. Infect. Dis., 1: 178-186.
41. Znaidi, R., R. Hafsia, A. M'Rad, R. Kastally and A. Hafsia, 1995. Association of heterozygote dre-panocytosis and G6PD deficiency: apropos of a case. Tunis Med., 73: 415-417.