Title of article :
The Relationship Between Coronary Artery Disease and Genetic Polymorphisms of Melanoma Inhibitory Activity 3
Author/Authors :
Zaimkohan ، Hooshang Department of Medical Genetics - Faculty of Medicine - Tehran University of Medical Sciences , Keramatipour ، Mohammad Department of Medical Genetics - Faculty of Medicine - Tehran University of Medical Sciences , Mirhafez ، Reza Metabolic Syndrome Research Center, School of Medicine - Mashhad University of Medical Sciences , Tavakkoly-Bazzaz ، Javad Department of Medical Genetics - Faculty of Medicine - Tehran University of Medical Sciences , Tahooni ، Azadeh Department of Internal Medicine - School of Medicine - Iran University of Medical Sciences , Piryaei ، Mohammad Department of Medical Genetics - School of Medicine - Shahid Beheshti University of Medical Sciences , Ghayour-Mobarhan ، Majid Metabolic Syndrome Research Center, School of Medicine - Mashhad University of Medical Sciences , Ghaderian ، Mohammad Hossein Department of Medical Genetics - School of Medicine - Shahid Beheshti University of Medical Sciences
Abstract :
Background: Melanoma Inhibitory Activity 3 regulates the plasma level of LDL cholesterol. The c.3169 + 315G A single-nucleotide polymorphism of the MIA3 gene has been reported to be associated with serum coronary artery disease (CAD). However, there have been no studies analyzing the association of this polymorphism with CAD in Iranian individuals with CAD. Objectives: Therefore, in the present studywehave investigated the potential protective effect of the rs3008621 MIA3polymorphism in 188 subjects with and without CAD. Materials and Methods: Genotyping of the MIA3 gene was undertaken using TaqMan real-time PCR in all subjects. Anthropometric and biochemical features, including HDL, LDL, and TG were assessed in all subjects. Results: The CAD patients had significantly (P 0.05) higher BMI and significantly higher levels of TG, LDL, SBP, and DBP, while the level of HDL was lower compared to that of the control group. the MIA3 gene polymorphism was not associated with CAD in our population sample. Conclusions: The MIA3 polymorphism is unlikely to play an important role in CAD in the Iranian population. However, further studies are needed in a larger population to confirm this.
Keywords :
Proprotein Convertase Subtilisin , Kexin Type 9 , Polymorphism , Coronary Artery Disease
Journal title :
Iranian Red Crescent Medical Journal
Journal title :
Iranian Red Crescent Medical Journal