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VAMP-8 gene variant is associated with increased risk of early myocardial infarction

INTRODUCTION: Single nucleotide polymorphism in the 3’ untranslated region of the vesicle-associated membrane protein gene (VAMP-8) has been associated with increased risk of early-onset myocardial infarction (MI). In this study the risk of early onset MI conferred by VAMP-8 gene polymorphism was in...

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Detalles Bibliográficos
Autores principales: Gorący, Jarosław, Gorący, Iwona, Kaczmarczyk, Mariusz, Parczewski, Miłosz, Cyryłowski, Lech, Brykczyński, Mirosław, Peregud-Pogorzelska, Małgorzata, Ciechanowicz, Andrzej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3258745/
https://www.ncbi.nlm.nih.gov/pubmed/22295026
http://dx.doi.org/10.5114/aoms.2011.23409
Descripción
Sumario:INTRODUCTION: Single nucleotide polymorphism in the 3’ untranslated region of the vesicle-associated membrane protein gene (VAMP-8) has been associated with increased risk of early-onset myocardial infarction (MI). In this study the risk of early onset MI conferred by VAMP-8 gene polymorphism was investigated in a group of 171 male subjects. MATERIAL AND METHODS: Male patients with a history of MI who underwent coronary angiography were enrolled and divided into early (incident < 55 years of age) and late (incident ≥ 55 years of age) MI onset groups. Apart from the RFLP-PCR based analysis of the VAMP-8 variant, history of hypertension, lipid abnormalities, smoking and body mass index were recorded. In statistical analyses odds ratios and relative risk were used as a measure of genotype-MI association while logistic regression was implemented for evaluation of MI risk factor strength. RESULTS: VAMP-8 A allele frequency proved to be significantly higher in the early-onset MI group and conferred higher relative risk of early MI in the investigated cohort, when calculated for the individual A allele (p = 0.029). In logistic regression analyses no association between risk genotypes and traditional risk factors was observed. CONCLUSIONS: In this study VAMP-8 A variant was identified as a risk allele for early MI in male subjects.