Hemoglobin C and resistance to severe malaria in Ghanaian children

被引:57
作者
Mockenhaupt, FP
Ehrhardt, S
Cramer, JP
Otchwemah, RN
Anemana, SD
Goltz, K
Mylius, F
Dietz, E
Eggelte, TA
Bienzle, U
机构
[1] Humboldt Univ, Fac Med Charite, Inst Trop Med, D-14050 Berlin, Germany
[2] Free Univ Berlin, Inst Int Hlth, D-1000 Berlin, Germany
[3] Reg Hlth Adm, Takoradi, Ghana
[4] Univ Dev Studies, Sch Med & Hlth Sci, Tamale, Ghana
[5] Univ Amsterdam, Acad Med Ctr, Div Infect Dis Trop Med & AIDS, NL-1105 AZ Amsterdam, Netherlands
关键词
D O I
10.1086/422847
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Hemoglobin (Hb) C has been reported to protect against severe malaria. It is unclear whether relative resistance affects infection, disease, or both. Its extent may vary between regions and with disease pattern. We conducted a case-control study of children with severe malaria, asymptomatic parasitemic children, and healthy children in Ghana. HbAC did not prevent infection but reduced the odds of developing severe malaria and severe anemia. Protection was stronger with HbAS. The frequencies of HbCC and HbSC decreased, from healthy children to asymptomatic parasitemic children to children with severe malaria. These data support the notion that natural selection of HbC occurs because of the relative resistance it confers against severe malaria but argue against the notion that HbC offers resistance to infection.
引用
收藏
页码:1006 / 1009
页数:4
相关论文
共 16 条
[1]   Hemoglobin C associated with protection from severe malaria in the Dogon of Mali, a West African population with a low prevalence of hemoglobin S [J].
Agarwal, A ;
Guindo, A ;
Cissoko, Y ;
Taylor, JG ;
Coulibaly, D ;
Koné, A ;
Kayentao, K ;
Djimde, A ;
Plowe, CV ;
Doumbo, O ;
Wellems, TE ;
Diallo, D .
BLOOD, 2000, 96 (07) :2358-2363
[2]   Protective effects of the sickle cell gene against malaria morbidity and mortality [J].
Aidoo, M ;
Terlouw, DJ ;
Kolczak, M ;
McElroy, PD ;
ter Kuile, FO ;
Kariuki, S ;
Nahlen, BL ;
Lal, AA ;
Udhayakumar, V .
LANCET, 2002, 359 (9314) :1311-1312
[3]  
Beales PF, 2000, T ROY SOC TROP MED H, V94, pS1
[4]  
BOHNING D, IN PRESS STAT METHOD
[5]   Early phagocytosis of glucose-6-phosphate dehydrogenase (G6PD)-deficient erythrocytes parasitized by plasmodium falciparum may explain malaria protection in G6PD deficiency [J].
Cappadoro, M ;
Giribaldi, G ;
O'Brien, E ;
Turrini, F ;
Mannu, F ;
Ulliers, D ;
Simula, G ;
Luzzatto, L ;
Arese, P .
BLOOD, 1998, 92 (07) :2527-2534
[6]  
Djimdé A, 2001, NEW ENGL J MED, V344, P257, DOI 10.1056/NEJM200101253440403
[7]  
DUFLO B, 1985, B SOC PATHOL EXOT, V78, P393
[8]   RELATIONSHIP BETWEEN HAEMOGLOBIN-C AND HAEMOGLOBIN-S AND MALARIA IN GHANA [J].
EDINGTON, GM ;
LAING, WN .
BMJ-BRITISH MEDICAL JOURNAL, 1957, 2 (JUL20) :143-145
[9]   Aberrant development of Plasmodium falciparum in hemoglobin CC red cells:: implications for the malaria protective effect of the homozygous state [J].
Fairhurst, RM ;
Fujioka, H ;
Hayton, K ;
Collins, KF ;
Wellems, TE .
BLOOD, 2003, 101 (08) :3309-3315
[10]   ROLE OF HEMOGLOBINS C, S, AND NBALT IN THE INHIBITION OF MALARIA PARASITE DEVELOPMENT INVITRO [J].
FRIEDMAN, MJ ;
ROTH, EF ;
NAGEL, RL ;
TRAGER, W .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1979, 28 (05) :777-780