Potential Impact of MicroRNA-423 Gene Variability in Coronary Artery Disease

被引:24
作者
Jha, Chandan K. [1 ]
Mir, Rashid [2 ]
Elfaki, Imadeldin [3 ]
Khullar, Naina [4 ]
Rehman, Suriya [5 ]
Javid, Jamsheed [2 ]
Banu, Shaheena [6 ]
Chahal, Sukh Mohinder Singh [1 ]
机构
[1] Punjabi Univ, Dept Human Genet, Patiala, Punjab, India
[2] Univ Tabuk, Fac Appl Med Sci, Dept Med Lab Technol, Tabuk, Saudi Arabia
[3] Univ Tabuk, Fac Sci, Dept Biochem, Tabuk, Saudi Arabia
[4] Mata Guri Coll, Dept Zool, Fatehgarh Sahib, Punjab, India
[5] Imam Abdulrahman Bin Faisal Univ, Inst Res & Med Consultat, Dammam, Saudi Arabia
[6] Sri Jayadeva Inst Cardiovasc Sci & Res, Bangalore, Karnataka, India
关键词
MicroRNA-423; coronary artery disease (CAD); congenital heart disease (CHD); cerebrovascular disease; Amplification refractory mutation system PCR method (ARMS-PCR); polymorphism; genotype; O-GLCNAC TRANSFERASE; NF-KAPPA-B; TRANSLATIONAL REPRESSION; ATHEROSCLEROSIS; RISK; POLYMORPHISMS; PATHOGENESIS; MIR-423-5P; RS6505162; SURVIVAL;
D O I
10.2174/1871530318666181005095724
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim: Studies have evaluated the association of miRNA-423 C>A genotyping with the susceptibility to various diseases such cancers, atherosclerosis and inflammatory bowel disease but the results were contradictory. However, no studies have reported the association between miRNA-423 rs6505162 C>A polymorphism and susceptibility of coronary artery disease. MicroRNAs regulate expression of multiple genes involved in atherogenesis. Therefore, we investigated the association of microRNA-423C>T gene variations with susceptibility to coronary artery disease. Methodology: This study was conducted on 100 coronary artery disease patients and 117 matched healthy controls. The genotyping of the microRNA-423 rs6505162C>A was performed by using Amplification refractory mutation system PCR method (ARMS-PCR). Results: A significant difference was observed in the genotype distribution among the coronary artery disease cases and sex-matched healthy controls (P=0.048). The frequencies of all three genotypes CC, CA, AA reported in the patient's samples were 55%, 41% and 4% and in the healthy controls samples were 55%, 41% and 4% respectively. Our findings showed that the microRNA-423 C>A variant was associated with an increased risk of coronary artery disease in codominant model (OR = 1.96, 95 % CI, 1.12-3.42; RR 1.35(1.05-1.75, p=0.017) of microRNA-423CA genotype and significant association in dominant model (OR 1.97, 95% CI (1.14-3.39), (CA+AA vs CC) and non-significant association for recessive model (OR=1.42, 95%CI=0.42-4.83, P=0.56, AA vs CC+CA).While, the A allele significantly increased the risk of coronary artery disease (OR =1.56, 95 % CI, 1.03-2.37; p=0.035) compared to C allele. Therefore, it was observed that more than 1.96, 1.97 and 1.56 fold increased risk of developing coronary artery disease. Conclusion: Our findings indicated that microRNA-423 CA genotype and A allele are associated with an increased susceptibility to Coronary artery disease.
引用
收藏
页码:67 / 74
页数:8
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