dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorFaculdade de Medicina de São José do Rio Preto (FAMERP)
dc.contributorFaculdade SEAMA
dc.date.accessioned2014-05-27T11:23:32Z
dc.date.available2014-05-27T11:23:32Z
dc.date.created2014-05-27T11:23:32Z
dc.date.issued2008-04-22
dc.identifierGenetics and Molecular Research, v. 7, n. 1, p. 60-64, 2008.
dc.identifier1676-5680
dc.identifierhttp://hdl.handle.net/11449/70389
dc.identifier10.4238/vol7-1gmr408
dc.identifier2-s2.0-40749127614
dc.identifier2-s2.0-40749127614.pdf
dc.identifier3279428066176719
dc.identifier0000-0002-4603-9467
dc.description.abstractMalaria is an endemic parasitosis and its causitive agent, Plasmodium, has a metabolism linked to iron supply. HFE is a gene with the polymorphisms C282Y and H63D, which are associated with a progressive iron accumulation in the organism leading to a disease called hereditary hemochromatosis. The aim of the present study was to determine the allelic and genotypic frequencies of the HFE gene polymorphisms in malaria patients and blood donors from the Brazilian Amazon region. We screened 400 blood donors and 400 malaria patients for the HFE C282Y and H63D polymorphisms from four states of the Brazilian Amazon region by polymerase chain reaction and restriction fragment length polymorphism analysis. We did not find any C282Y homozygous individuals, and the only five heterozygous individuals detected were from Pará State. The most frequent genotype in the North region of Brazil was the H63D heterozygote, in both study groups. Our results contribute to the concept that the Brazilian Amazon region should not be regarded as a single entity in South America. These polymorphisms did not influence the symptoms of malaria in the population studied, as neither severe signs nor high parasitemia were observed. Therefore, different hereditary hemochromatosis diagnostic and control measures must be developed and applied within its diverse locations. Investigations are currently being carried out in our laboratory in order to determine the importance of the coexistence of hereditary hemochromatosis in patients affected by parasitic diseases, such as malaria. ©FUNPEC-RP.
dc.languageeng
dc.relationGenetics and Molecular Research
dc.relation0,439
dc.rightsAcesso aberto
dc.sourceScopus
dc.subjectBlood donors
dc.subjectBrazilian Amazon region
dc.subjectHFE gene polymorphisms
dc.subjectMalaria
dc.subjectaspartic acid
dc.subjectcysteine
dc.subjecthistidine
dc.subjectiron
dc.subjecttyrosine
dc.subjectadult
dc.subjectallele
dc.subjectblood donor
dc.subjectBrazil
dc.subjectfemale
dc.subjectgene
dc.subjectgene frequency
dc.subjectgenetic polymorphism
dc.subjecthemochromatosis
dc.subjectheterozygote
dc.subjectHFE gene
dc.subjecthuman
dc.subjectmajor clinical study
dc.subjectmalaria
dc.subjectmale
dc.subjectparasitemia
dc.subjectPlasmodium
dc.subjectpolymerase chain reaction
dc.subjectrestriction fragment length polymorphism
dc.subjectsymptom
dc.subjectanimal
dc.subjectblood
dc.subjectcase control study
dc.subjectcomparative study
dc.subjectendemic disease
dc.subjectgenetics
dc.subjectparasitology
dc.subjectPlasmodium falciparum
dc.subjectPlasmodium vivax
dc.subjectprevalence
dc.subjectAdult
dc.subjectAlleles
dc.subjectAnimals
dc.subjectBlood Donors
dc.subjectCase-Control Studies
dc.subjectEndemic Diseases
dc.subjectFemale
dc.subjectGene Frequency
dc.subjectHeterozygote
dc.subjectHumans
dc.subjectMale
dc.subjectPolymorphism, Genetic
dc.subjectPrevalence
dc.titleFrequency of the HFE C282Y and H63D polymorphisms in Brazilian malaria patients and blood donors from the Amazon region
dc.typeArtículos de revistas


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