SCARB1 gene polymorphisms and HDL subfractions in coronary artery disease
Yükleniyor...
Dosyalar
Tarih
2017
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Int Inst Anticancer Research
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
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.
Açıklama
Anahtar Kelimeler
Coronary Artery Disease, Hdl Subfractions, Scarb1, Polymorphism
Kaynak
In Vivo
WoS Q Değeri
Q4
Scopus Q Değeri
Q2
Cilt
31
Sayı
5
Künye
Ayhan, H., Gormus, U., Isbir, S., Yilmaz, S. G., & Isbir, T. (2017). SCARB1 gene polymorphisms and HDL subfractions in coronary artery disease. In Vivo, 31(5), 873–876. https://doi.org/10.21873/invivo.11141
