Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/194742
Type: Artigo de periódico
Title: C282y Mutation In The Hla-h Gene Is Not A Risk Factor For Patients With Myocardial Infarction.
Author: Annichino-Bizzacchi, J M
Saad, S T
Arruda, V R
Ramires, J A
Siqueira, L H
Chiaparini, L C
Mansur, A P
Abstract: Iron is suspected to play a role in the development of atherosclerosis and in the progression of the disease, and consequently in myocardial infarction. Authors of a recent study identified a mutation in HLA-H gene, C282Y, that is an excellent marker for hemochromatosis, which is the most common cause of iron overload. There is a high prevalence of carriers of heterozygous hemochromatosis, most of whom are asymptomatic even with abnormalities of iron metabolism. To study C282Y mutation in the HLA-H gene of 173 survivors of myocardial infarction matched with 172 controls by age, race, and sex, and 119 patients upon diagnosis of acute myocardial infarction. Identification of the mutation was performed by PCR amplification of the DNA fragment followed by Rsal digestion. The prevalence of heterozygotes for the mutated allele both among patients and among controls was 1.74%. None of the 119 patients studied upon diagnosis was a carrier of the mutation. Our data suggested that the most common cause of iron overload is not associated with myocardial infarction.
Subject: Adult
Aged
Base Sequence
Case-control Studies
Cohort Studies
Confidence Intervals
Cross-sectional Studies
Female
Hla Antigens
Hemochromatosis
Heterozygote
Histocompatibility Antigens Class I
Humans
Male
Middle Aged
Molecular Sequence Data
Mutation
Myocardial Infarction
Odds Ratio
Polymerase Chain Reaction
Prevalence
Risk Factors
Sensitivity And Specificity
Rights: fechado
Identifier DOI: 
Address: http://www.ncbi.nlm.nih.gov/pubmed/10785872
Date Issue: 2000
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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