Lack of association between the platelet glycoprotein Ia C807T gene polymorphism and coronary artery disease: A meta-analysis

2007 ◽  
Vol 118 (2) ◽  
pp. 189-196 ◽  
Author(s):  
Argirios E. Tsantes ◽  
Georgios K. Nikolopoulos ◽  
Pantelis G. Bagos ◽  
Georgios Vaiopoulos ◽  
Anthi Travlou
Platelets ◽  
2014 ◽  
Vol 26 (6) ◽  
pp. 530-535 ◽  
Author(s):  
Monica Verdoia ◽  
Ettore Cassetti ◽  
Alon Schaffer ◽  
Gabriella Di Giovine ◽  
Giuseppe De Luca

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

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.


Cytokine ◽  
2021 ◽  
Vol 139 ◽  
pp. 155403
Author(s):  
Marzieh Ghalandari ◽  
Khadijeh Jamialahmadi ◽  
Maryam Mardan Nik ◽  
Maryam Pirhoushiaran ◽  
Seyed Reza Mirhafez ◽  
...  

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