scholarly journals Lack of association between the connexin 37 C1019T gene polymorphism and coronary artery disease in a Chinese population: Meta-analysis of 2,206 subjects

2013 ◽  
Vol 1 (3) ◽  
pp. 464-468 ◽  
Author(s):  
YAN-YAN LI ◽  
YUN QIAN ◽  
CHUAN-WEI ZHOU
2020 ◽  
Author(s):  
Hongyan Zhao ◽  
Shan Hu ◽  
Jidong Rong

AbstractObjectiveTo explore the association between the variant M235 locus of angiotensinogen (AGT) gene, 584C/T locus of Endothelial lipase (EL) gene, and coronary artery disease (CAD) by meta-analysis.MethodsThe case-control studies on the association between AGT/EL gene polymorphism and CAD were collected through searching PubMed, EMbase, Web of Science, CNKI and Wanfang database up to March 1, 2020. Stata 15.0 software was used for analysis.ResultsA total of 29 articles met the inclusion criteria. After analyzing, it was found that the M235T polymorphism of AGT gene was associated with the occurrence of CAD. In the allele model (T vs. M), OR=1.38 (P < 0.05). In other heredity, there was also statistically significant. Subgroup analysis indicated that except the heterozygous genetic model of the Chinese population, other genetic models of the Caucasian and Chinese population were also statistically significant. The 584C/T polymorphism of EL gene was associated with the occurrence of CAD, with OR=0.83 (P < 0.05) in the allele model (T vs. C) and OR=0.80 (P < 0.05) in the dominant gene model. Also, in the allele model of Caucasian subgroup, OR=0.83 (P < 0.05), while in Asian subgroup, there was no statistically significant genetic model.ConclusionAGT M235 and EL 584C/T polymorphisms are associated with CAD susceptibility. The genotype TT, TC or allele T of AGT M235T and genotype CC or allele C of EL 584C/T might be the genetic risk factors for the development of CAD.


2020 ◽  
Vol 40 (7) ◽  
Author(s):  
Hongyan Zhao ◽  
Ranzun Zhao ◽  
Shan Hu ◽  
Jidong Rong

Abstract Objective: To explore the association between the variant M235T locus of angiotensinogen (AGT) gene, 584C/T locus of Endothelial lipase (EL) gene, and coronary artery disease (CAD) by meta-analysis. Methods: The case–control studies on the association between AGT/EL gene polymorphism and CAD were collected through searching PubMed, Excerpta Medica Database (EMBASE), Web of Science, China National Knowledge Infrastructure (CNKI), and Wanfang databases up to 1 March 2020. Stata 15.0 software was used for analysis. Results: A total of 29 articles met the inclusion criteria. After analyzing, it was found that the M235T polymorphism of AGT gene was associated with the occurrence of CAD. In the allele model (T vs. M), OR = 1.38 (P&lt;v0.05). In other heredity, there was also statistical significance. Subgroup analysis indicated that except the heterozygous genetic model of the Chinese population, other genetic models of the Caucasian and Chinese population were also statistically significant. The 584C/T polymorphism of EL gene was associated with the occurrence of CAD, with OR = 0.83 (P&lt;0.05) in the allele model (T vs. C) and OR = 0.80 (P&lt;0.05) in the dominant gene model. Also, in the allele model of Caucasian subgroup, OR = 0.83 (P&lt;0.05), while in Asian subgroup, there was no statistically significant genetic model. Conclusion: AGT M235T and EL 584C/T polymorphisms are associated with CAD susceptibility. The genotype TT, TC or allele T of AGT M235T and genotype CC or allele C of EL 584C/T might be the genetic risk factors for the development of CAD.


PLoS ONE ◽  
2013 ◽  
Vol 8 (9) ◽  
pp. e70885 ◽  
Author(s):  
Zhijun Wu ◽  
Yuqing Lou ◽  
Wei Jin ◽  
Yan Liu ◽  
Lin Lu ◽  
...  

2007 ◽  
Vol 118 (2) ◽  
pp. 189-196 ◽  
Author(s):  
Argirios E. Tsantes ◽  
Georgios K. Nikolopoulos ◽  
Pantelis G. Bagos ◽  
Georgios Vaiopoulos ◽  
Anthi Travlou

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