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Frequency of the HFE C282Y and H63D polymorphisms in Brazilian malaria patients and blood donors from the Amazon region
- Source :
- Scopus, Repositório Institucional da UNESP, Universidade Estadual Paulista (UNESP), instacron:UNESP, ResearcherID, Scopus-Elsevier
- Publication Year :
- 2008
-
Abstract
- Submitted by Vitor Silverio Rodrigues (vitorsrodrigues@reitoria.unesp.br) on 2014-05-27T11:23:32Z No. of bitstreams: 0Bitstream added on 2014-05-27T14:33:20Z : No. of bitstreams: 1 2-s2.0-40749127614.pdf: 356366 bytes, checksum: b0281b66c4d7c1c0d48d2d87c07e88cd (MD5) Made available in DSpace on 2014-05-27T11:23:32Z (GMT). No. of bitstreams: 0 Previous issue date: 2008-04-22 Malaria 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. Laboratório de Hemoglobinas e Genética Das Doenças Hematológicas Departamento de Biologia Instituto de Biociencias, Letras e Ciencias Exatas (IBILCE-UNESP), São José do Rio Preto, SP Departamento de Doenças Dermatológicas, Infecciosas e Parasitárias Centro de Investigação de Microrganismos Faculdade de Medicina de São José do Rio Preto, São José do Rio Preto, SP Faculdade SEAMA, Macapá, AP Laboratório de Hemoglobinas e Genética Das Doenças Hematológicas Departamento de Biologia Instituto de Biociencias, Letras e Ciencias Exatas (IBILCE-UNESP), São José do Rio Preto, SP
- Subjects :
- Male
Plasmodium
Endemic Diseases
parasitology
polymerase chain reaction
Hfe gene
Blood Donors
iron
Gene Frequency
Prevalence
genetic polymorphism
animal
genetics
parasitemia
cysteine
restriction fragment length polymorphism
comparative study
Endemic disease
Amazon rainforest
adult
allele
General Medicine
symptom
Blood donor
female
Female
HFE gene polymorphisms
HFE gene
Brazil
Adult
medicine.medical_specialty
Heterozygote
Plasmodium falciparum
malaria
Biology
Brazilian Amazon region
hemochromatosis
blood
Genetics
medicine
Animals
Humans
human
blood donor
gene
Molecular Biology
endemic disease
Alleles
Gynecology
Polymorphism, Genetic
histidine
case control study
medicine.disease
major clinical study
Malaria
Case-Control Studies
Immunology
aspartic acid
Endemic diseases
Plasmodium vivax
tyrosine
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Scopus, Repositório Institucional da UNESP, Universidade Estadual Paulista (UNESP), instacron:UNESP, ResearcherID, Scopus-Elsevier
- Accession number :
- edsair.doi.dedup.....c746127e8be8827779799292390056eb