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The haptoglobin 2-2 genotype is associated with a reduced incidence of Plasmodium falciparum malaria in children on the coast of Kenya

Abstract:
Background: Haptoglobin (Hp) genotype determines the efficiency of haemoglobin clearance after malaria-induced hemolysis and alters antioxidant and immune functions. The Hp² allele is thought to have spread under strong selection pressure, but it is unclear whether this is due to protection from malaria or other diseases. Methods: We monitored the incidence of febrile malaria and other childhood illnesses with regard to Hp genotypes in a prospective cohort of 312 Kenyan children during 558.3 child-years of follow-up. We also conducted 7 cross-sectional surveys to determine the prevalence of Plasmodium falciparum parasitemia. Results: The Hp ^2/2 genotype was associated with a 30% reduction in clincal malarial episodes (adjusted incidence rate ratio, 0.67; P = .008 for Hp^ 2/2 vs. Hp ^1/1 and Hp ^2/1 combined). Protection increased with age; there was no protection in the first 2 years of life, 30% protection at ≥2 years of age, and 50% protection from 4-10 years of age. Children with the Hp ^1/1 genotype had a significantly lower rate of nonmalarial fever (P= .001). Conclusions: Balancing selection pressures may have influenced the spread of the Hp gene. Our observations suggest that the Hp² allele may have spread as a result of protection from malaria, and the Hp¹ allele may be sustained by protection from other infections.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1086/511868

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Institution:
"KEMRI/Wellcome Trust Programme, Centre of Geographic Medicine Research, Kilifi District Hospital, Kenya", "London School of Hygiene and Tropical Medicine"
Department:
Medical Research Council International Nutrition Group,Nutrition and Public Health Intervention Research Unit
Role:
Author
More by this author
Institution:
"KEMRI/Wellcome Trust Programme, Centre of Geographic Medicine Research, Kilifi District Hospital, Kenya"
Role:
Author
More by this author
Institution:
"KEMRI/Wellcome Trust Programme, Centre of Geographic Medicine Research, Kilifi District Hospital, Kenya"
Role:
Author
More by this author
Institution:
"KEMRI/Wellcome Trust Programme, Centre of Geographic Medicine Research, Kilifi District Hospital, Kenya"
Role:
Author
More by this author
Institution:
"KEMRI/Wellcome Trust Programme, Centre of Geographic Medicine Research, Kilifi District Hospital, Kenya"
Role:
Author

Contributors

Institution:
"KEMRI/Wellcome Trust Programme, Centre of Geographic Medicine Research, Kilifi District Hospital, Kenya"


Publisher:
University of Chicago Press
Journal:
Clinical Infectious Diseases More from this journal
Volume:
44
Issue:
6
Pages:
802-809
Publication date:
2007-03-01
Edition:
Publisher's version
DOI:
ISSN:
1058-4838


Language:
English
Keywords:
Subjects:
UUID:
uuid:1b479370-72f1-4355-b83d-34b08c858862
Local pid:
ora:2965
Deposit date:
2009-09-15
ARK identifier:

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