PHACTR1 Gene Polymorphism Is Associated with Increased Risk of Developing Premature Coronary Artery Disease in Mexican Population

Single-nucleotide polymorphisms (SNPs) in the protein phosphatase and actin regulator 1 gene (PHACTR1) have been associated with susceptibility to develop several diseases, including cardiovascular disease. The purpose of this study was to evaluate the role of two polymorphisms (rs2026458 and rs9349...

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Veröffentlicht in:International journal of environmental research and public health 2016-08, Vol.13 (8), p.1-1
Hauptverfasser: Pérez-Hernández, Nonanzit, Vargas-Alarcón, Gilberto, Posadas-Sánchez, Rosalinda, Martínez-Rodríguez, Nancy, Tovilla-Zárate, Carlos Alfonso, Rodríguez-Cortés, Adrián Asael, Pérez-Méndez, Oscar, Blachman-Braun, Ruben, Rodríguez-Pérez, José Manuel
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container_issue 8
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container_title International journal of environmental research and public health
container_volume 13
creator Pérez-Hernández, Nonanzit
Vargas-Alarcón, Gilberto
Posadas-Sánchez, Rosalinda
Martínez-Rodríguez, Nancy
Tovilla-Zárate, Carlos Alfonso
Rodríguez-Cortés, Adrián Asael
Pérez-Méndez, Oscar
Blachman-Braun, Ruben
Rodríguez-Pérez, José Manuel
description Single-nucleotide polymorphisms (SNPs) in the protein phosphatase and actin regulator 1 gene (PHACTR1) have been associated with susceptibility to develop several diseases, including cardiovascular disease. The purpose of this study was to evaluate the role of two polymorphisms (rs2026458 and rs9349379) of the PHACTR1 gene in the susceptibility to the risk of developing premature coronary artery disease (CAD) in the Mexican population. The genotype analysis was performed using 5'exonuclease TaqMan genotyping assays in a group of 994 patients with premature CAD and 703 controls. A similar genotype distribution of rs2026458 was observed in both groups; however, under an additive model adjusted by age, body mass index, type 2 diabetes mellitus, smoking, dyslipidemia, and hypertension, the rs9349379 G allele was associated with a higher risk for developing premature CAD (odds ratio (OR) = 1.22, 95% confidence interval (CI) = 1.03-1.46, p-value (p) = 0.024). The two PHACTR1 polymorphisms were not in linkage disequilibrium. In summary, our results suggest that the PHACTR1 rs9349379 polymorphism plays an important role in the risk of developing premature CAD in the Mexican population.
doi_str_mv 10.3390/ijerph13080803
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The purpose of this study was to evaluate the role of two polymorphisms (rs2026458 and rs9349379) of the PHACTR1 gene in the susceptibility to the risk of developing premature coronary artery disease (CAD) in the Mexican population. The genotype analysis was performed using 5'exonuclease TaqMan genotyping assays in a group of 994 patients with premature CAD and 703 controls. A similar genotype distribution of rs2026458 was observed in both groups; however, under an additive model adjusted by age, body mass index, type 2 diabetes mellitus, smoking, dyslipidemia, and hypertension, the rs9349379 G allele was associated with a higher risk for developing premature CAD (odds ratio (OR) = 1.22, 95% confidence interval (CI) = 1.03-1.46, p-value (p) = 0.024). The two PHACTR1 polymorphisms were not in linkage disequilibrium. 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subjects Adult
Age
Alcohol
Alleles
Atherosclerosis
Calcification
Cardiology
Cardiovascular disease
Coronary Artery Disease - epidemiology
Coronary Artery Disease - genetics
Coronary vessels
Data collection
Diabetes
Dyslipidemias - genetics
Family medical history
Female
Gene expression
Genealogy
Genetic Predisposition to Disease - genetics
Genotype
Haplotypes
Heart attacks
Humans
Hypertension
Hypertension - genetics
Male
Maximum likelihood method
Metabolism
Mexico
Microfilament Proteins - genetics
Middle Aged
Minority & ethnic groups
Odds Ratio
Phosphatase
Polymorphism
Polymorphism, Single Nucleotide - genetics
Population
Public health
Risk factors
Studies
title PHACTR1 Gene Polymorphism Is Associated with Increased Risk of Developing Premature Coronary Artery Disease in Mexican Population
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