Association of Endothelial NO Synthase Gene Glu298Asp Polymorphism with Acute Myocardial Infarction

2001 ◽  
Vol 31 (10) ◽  
pp. 973 ◽  
Author(s):  
Chang Jin Choi ◽  
Kang Sook Lee ◽  
Sang Hong Baek ◽  
Ki Bae Seung ◽  
Wook Sung Chung ◽  
...  
2014 ◽  
Vol 18 (1 (69)) ◽  
Author(s):  
J. V. Ursuliak ◽  
L. P. Sydorchuk

Changes in the platelet-vascular hemostasis influenced by basic treatment of 102 patients with acute myocardial infarction (AMI) depending on allelic variants of genes angiotensin-converting enzyme (ACE, I/D) and endothelial NO-synthase (eNOS, 894G> T) have been analyzed. The dependence of the treatment efficacy on genotypes and haplotypes of the analyzed genes in relation to hemostasis key-chains has been established.


1998 ◽  
Vol 5 ◽  
pp. 9
Author(s):  
A.A. Moibenko ◽  
N.P. Maxyutina ◽  
N.A. Mochort ◽  
A.N. Parchomenko ◽  
A.V. Kotzuruba ◽  
...  

2019 ◽  
Vol 40 (Supplement_1) ◽  
Author(s):  
O Petyunina ◽  
M P Kopytsya ◽  
A E Berezin ◽  
A A Berezin

Abstract Introduction Endothelial NO-synthase (eNOS) is constitutive enzyme, which is expressed in mature endothelial cells and promotes direct vascular dilatation. Single nucleotide polymorphism (SNP) of T786C in eNOS gene may influence on adverse cardiac remodeling after ST-elevation myocardial infarction (STEMI). Purpose To investigate possible associations between SNP T786C in eNOS gene and adverse cardiac remodeling after STEMI Methods 177 acute STEMI patients treated with primary and facilitate percutaneous coronary intervention that were admitted to intensive care unit of a Therapy National Institute were enrolled in the study. Anthropometry, cardiovascular risk assay, coronary angiography, echocardiography and biomarkers' measure were performed at baseline. The DNA extraction was performed with a commercial kit using real-time polymerase chain reaction PCR. All procedures performed in the study involving human participants were in accordance with the ethical standards and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards and approved by the local ethics committee (Protocol No. 8, 29.08.2016). Written informed consent was obtained from each patient. Results There were correlations between 786CC polymorphism in eNOs gene and adverse cardiac remodeling (r=0.48; p=0.001), LDL cholesterol (r=0.32; p=0.012), type 2 diabetes mellitus (r=0.30; p=0.042), diastolic BP (r=−0.26; p=0.048), unstable angina prior to STEMI (r=0.25; p=0.047) and total quantity of complicated STEMI (r=0.23; p=0.042). Additionally, there were not significant relations between 786CC polymorphism in eNOs gene and multiple coronary vessel injury, STEMI localization, levels of circulating biomarkers of myocardial injury, and amount of damaged coronary arteries. Using univariate and multivariate regressive logistic analysis we found that 786CC genotype of eNOS was independent predictor for late adverse LV remodeling (β-coefficient = 1.57342; odds ratio = 4.8231; 95% confidence interval = 1.5349–15.1552; p=0.0071). Conclusions The polymorphism 786CC in eNOs gene was found as an independent predictor for late adverse cardiac remodeling after STEMI. Acknowledgement/Funding None


2017 ◽  
Vol 162 (5) ◽  
pp. 615-618
Author(s):  
N. S. Fattakhov ◽  
D. A. Skuratovskaya ◽  
M. A. Vasilenko ◽  
E. V. Kirienkova ◽  
P. A. Zatolokin ◽  
...  

2000 ◽  
Vol 18 (12) ◽  
pp. 1767-1773 ◽  
Author(s):  
Markus P. Schneider ◽  
Jeanette Erdmann ◽  
Christian Delles ◽  
Eckart Fleck ◽  
Vera Regitz-Zagrosek ◽  
...  

Author(s):  
Masahiro Ono ◽  
Kaoru Aihara ◽  
Gompachi Yajima

The pathogenesis of the arteriosclerosis in the acute myocardial infarction is the matter of the extensive survey with the transmission electron microscopy in experimental and clinical materials. In the previous communication,the authors have clarified that the two types of the coronary vascular changes could exist. The first category is the case in which we had failed to observe no occlusive changes of the coronary vessels which eventually form the myocardial infarction. The next category is the case in which occlusive -thrombotic changes are observed in which the myocardial infarction will be taken placed as the final event. The authors incline to designate the former category as the non-occlusive-non thrombotic lesions. The most important findings in both cases are the “mechanical destruction of the vascular wall and imbibition of the serous component” which are most frequently observed at the proximal portion of the coronary main trunk.


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