Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/33146
Title: Hemojuvelin and Hepcidin Genes Sequencing in Brazilian Patients with Primary Iron Overload
Authors: Junior de Lima Santos, Paulo Caleb
Pereira, Alexandre C.
Cancado, Rodolfo D.
Schettert, Isolmar T.
Hirata, Rosario D. C.
Hirata, Mario H.
Figueiredo, Maria Stella [UNIFESP]
Chiattone, Carlos S.
Krieger, Jose E.
Guerra-Shinohara, Elvira M.
Universidade de São Paulo (USP)
Santa Casa Blood Ctr São Paulo
Novo Atibaia Hosp
Universidade Federal de São Paulo (UNIFESP)
Issue Date: 1-Dec-2010
Publisher: Mary Ann Liebert, Inc
Citation: Genetic Testing and Molecular Biomarkers. New Rochelle: Mary Ann Liebert, Inc, v. 14, n. 6, p. 803-806, 2010.
Abstract: Background: Most hereditary hemochromatosis (HH) patients are homozygous for the p. C282Y mutation in the HFE gene. Some studies reported that HH phenotypic expression could be modulated by genetic factors such as HJV and HAMP gene mutations. Aims: the aims of this study were to identify HJV and HAMP mutations and to analyze their impact on HH phenotype in non-p. C282Y homozygous individuals. Methods: Twenty-four Brazilian patients with primary iron overload and non-p. C282Y homozygous genotype (transferrin saturation >50% in women and >60% in men and absence of secondary causes) were selected. Subsequent bidirectional sequencing of the HJV and HAMP exons was performed. Results: Sequencing revealed a substitution in heterozygosis, c. 929C>G, which corresponds to p.A310G polymorphism in HJV exon 4 (rs7540883). in the same gene, in another individual, an IVS1-36C>G intronic variant was detected in heterozygosis. in the HAMP gene, an IVS3 + 42G>A intronic variant was identified. There were six (25.0%) patients carrying a heterozygous genotype for the HFE p. C282Y and nine (37.5%) patients carrying a heterozygous genotype for the HFE p. H63D. Conclusion: HJV p.A310G polymorphism and two intronic variants were found, but none of these alterations were associated with digenic inheritance with the HFE gene. Our data indicate that HJV and HAMP functional mutations are not frequent in these patients.
URI: http://repositorio.unifesp.br/handle/11600/33146
ISSN: 1945-0265
Other Identifiers: http://dx.doi.org/10.1089/gtmb.2010.0056
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