Key result
The VAMP-8 A allele was significantly associated with an increased risk of early-onset myocardial infarction (<55 years) in male subjects compared to late-onset MI (OR 1.65).
Why the study?
Does the VAMP-8 A allele increase the risk of early-onset myocardial infarction in male patients?
Observational (n=171)
No
Does the VAMP-8 A allele increase the risk of early-onset myocardial infarction in male patients?
The VAMP-8 A allele is associated with an increased risk of early-onset myocardial infarction in Polish men, suggesting a potential genetic marker for premature coronary artery disease.
Answers are grounded in this paper and cite their sources.
VAMP-8 A allele may flag higher premature MI risk in men; leaves open validation in prospective cohorts before any clinical use.
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.
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Gorący et al. (2011) conducted an observational in Myocardial infarction (n=171). VAMP-8 A allele (rs1010 polymorphism) vs. VAMP-8 G allele was evaluated on Early-onset myocardial infarction (< 55 years of age) (OR 1.65, 95% CI 1.03-2.65, p=0.029). The VAMP-8 A allele was significantly associated with an increased risk of early-onset myocardial infarction (<55 years) in male subjects compared to late-onset MI (OR 1.65).
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