scholarly journals Association between Apolipoprotein E Gene Polymorphism and the Risk of Coronary Artery Disease in Chinese Population: Evidence from a Meta-Analysis of 40 Studies

PLoS ONE ◽  
2013 ◽  
Vol 8 (6) ◽  
pp. e66924 ◽  
Author(s):  
Yan-Wei Yin ◽  
Qian-Qian Sun ◽  
Bei-Bei Zhang ◽  
Ai-Min Hu ◽  
Hong-Li Liu ◽  
...  
2012 ◽  
Vol 11 (1) ◽  
pp. 36 ◽  
Author(s):  
Rajesh Chaudhary ◽  
Atip Likidlilid ◽  
Thavatchai Peerapatdit ◽  
Damras Tresukosol ◽  
Sorachai Srisuma ◽  
...  

2010 ◽  
Vol 10 (3) ◽  
pp. 202-208 ◽  
Author(s):  
F. Demet Arslan Ince ◽  
Aysenur Atay ◽  
Mehmet Koseoglu ◽  
Murat Yesil ◽  
Erdal Deveci

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.


Sign in / Sign up

Export Citation Format

Share Document