Literature DB >> 28882953

SCARB1 Gene Polymorphisms and HDL Subfractions in Coronary Artery Disease.

Huseyin Ayhan1, Uzay Gormus2, Selim Isbir3, Seda Gulec Yilmaz1, Turgay Isbir4.   

Abstract

BACKGROUND/AIM: Cardiovascular diseases are a leading cause of mortality and morbidity worldwide. Polymorphisms in the SCARB1 gene are known to be related to plasma lipids. PATIENTS AND METHODS: Real time-polymerase chain reaction (RT-PCR) was used for identification of SCARB1 polymorphisms and the Lipoprint Quantimetrix System was employed in identification of HDL subfractions.
RESULTS: According to allelic distribution, in both groups SCARB1 AA genotype led to a two-fold decrease in the risk of developing cardiovascular disease (p=0.04), while the GA genotype increased the risk two-fold (p=0.03). According to the HDL subfraction analysis results, the AA genotype had higher levels of big-sized HDL subfraction (p=0.02).
CONCLUSION: The SCARB1AA genotype decreased cardiovascular risk and carrying GA genotype and G allele increased the risk of CAD. AA genotype carriers had higher levels of big-sized HDL subfraction. Copyright
© 2017, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Entities:  

Keywords:  Coronary artery disease; HDL subfractions; SCARB1; polymorphism

Mesh:

Substances:

Year:  2017        PMID: 28882953      PMCID: PMC5656860          DOI: 10.21873/invivo.11141

Source DB:  PubMed          Journal:  In Vivo        ISSN: 0258-851X            Impact factor:   2.155


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