FEATURES OF THE CLINICAL SIGNIFICANCE OF POLYMORPHIC VARIANTS OF ENOS AND AGTR2 GENES IN PATIENTS WITH CAD
Coronary heart disease (CHD) is a major cause of mortality. Morphological substrate of CHD in most cases is atherosclerosis, which is based on structural genes polymorphism eNOS and AGTR2. The aim of the study was to study the prevalence of eNOS and AGTR2 genes in patients with coronary artery disea...
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doaj-08921629dd5143edac7fbcd13fcc56302021-07-29T08:11:34ZrusSINAPS LLCArhivʺ Vnutrennej Mediciny2226-67042411-65642016-06-0163535810.20514/2226-6704-2016-6-3-53-58523FEATURES OF THE CLINICAL SIGNIFICANCE OF POLYMORPHIC VARIANTS OF ENOS AND AGTR2 GENES IN PATIENTS WITH CADA. L. Khokhlov0N. O. Pozdnyakov1A. E. Miroshnikov2I. N. Tzareva3S. O. Pozdnyakov4Yaroslavl medical state universityYaroslavl medical state universityYaroslavl medical state universityRailway clinical hospitalYaroslavl medical state universityCoronary heart disease (CHD) is a major cause of mortality. Morphological substrate of CHD in most cases is atherosclerosis, which is based on structural genes polymorphism eNOS and AGTR2. The aim of the study was to study the prevalence of eNOS and AGTR2 genes in patients with coronary artery disease and the association of these genes with coronary heart disease. The study involved 187 patients aged 36 to 86 years (62,2±11,2) with different forms of CHD: stable and unstable angina, myocardial infarction and 45 people without CHD. Determination of gene polymorphisms was performed by real-time PCR analyzer of nucleic acids IQ 5 Bio-Rad. Statistical analysis was performed using Statistica 10.0. The study revealed a significant difference between the incidence of homozygous AA allelic variant gene AGTR2 group of patients with myocardial infarction and the comparison group; polymorphic variant AA AGTR2 gene is associated with earlier onset of coronary artery disease; It found that carriers of the polymorphic variant gene GA AGTR2 beginning statistically CHD occurred significantly later than in carriers of alleles GG and AA; age CHD debut TT allele carriers of the eNOS gene is associated with an earlier onset of the disease and statistically significantly different from the age of first CHD in carriers of alleles of polymorphic variants of GG and GT; revealed a positive correlation between the polymorphic allele AGTR2 gene with the presence of arterial hypertension in patients with coronary artery disease; It determined that the T allele carriers of the polymorphic gene eNOS is associated more early onset of hypertension, found the association of the polymorphic allele gene AGTR2 the need to use higher doses of ACE inhibitor — perindopril.https://www.medarhive.ru/jour/article/view/534coronary heart diseasegene polymorphismenosagtr2 |
collection |
DOAJ |
language |
Russian |
format |
Article |
sources |
DOAJ |
author |
A. L. Khokhlov N. O. Pozdnyakov A. E. Miroshnikov I. N. Tzareva S. O. Pozdnyakov |
spellingShingle |
A. L. Khokhlov N. O. Pozdnyakov A. E. Miroshnikov I. N. Tzareva S. O. Pozdnyakov FEATURES OF THE CLINICAL SIGNIFICANCE OF POLYMORPHIC VARIANTS OF ENOS AND AGTR2 GENES IN PATIENTS WITH CAD Arhivʺ Vnutrennej Mediciny coronary heart disease gene polymorphism enos agtr2 |
author_facet |
A. L. Khokhlov N. O. Pozdnyakov A. E. Miroshnikov I. N. Tzareva S. O. Pozdnyakov |
author_sort |
A. L. Khokhlov |
title |
FEATURES OF THE CLINICAL SIGNIFICANCE OF POLYMORPHIC VARIANTS OF ENOS AND AGTR2 GENES IN PATIENTS WITH CAD |
title_short |
FEATURES OF THE CLINICAL SIGNIFICANCE OF POLYMORPHIC VARIANTS OF ENOS AND AGTR2 GENES IN PATIENTS WITH CAD |
title_full |
FEATURES OF THE CLINICAL SIGNIFICANCE OF POLYMORPHIC VARIANTS OF ENOS AND AGTR2 GENES IN PATIENTS WITH CAD |
title_fullStr |
FEATURES OF THE CLINICAL SIGNIFICANCE OF POLYMORPHIC VARIANTS OF ENOS AND AGTR2 GENES IN PATIENTS WITH CAD |
title_full_unstemmed |
FEATURES OF THE CLINICAL SIGNIFICANCE OF POLYMORPHIC VARIANTS OF ENOS AND AGTR2 GENES IN PATIENTS WITH CAD |
title_sort |
features of the clinical significance of polymorphic variants of enos and agtr2 genes in patients with cad |
publisher |
SINAPS LLC |
series |
Arhivʺ Vnutrennej Mediciny |
issn |
2226-6704 2411-6564 |
publishDate |
2016-06-01 |
description |
Coronary heart disease (CHD) is a major cause of mortality. Morphological substrate of CHD in most cases is atherosclerosis, which is based on structural genes polymorphism eNOS and AGTR2. The aim of the study was to study the prevalence of eNOS and AGTR2 genes in patients with coronary artery disease and the association of these genes with coronary heart disease. The study involved 187 patients aged 36 to 86 years (62,2±11,2) with different forms of CHD: stable and unstable angina, myocardial infarction and 45 people without CHD. Determination of gene polymorphisms was performed by real-time PCR analyzer of nucleic acids IQ 5 Bio-Rad. Statistical analysis was performed using Statistica 10.0. The study revealed a significant difference between the incidence of homozygous AA allelic variant gene AGTR2 group of patients with myocardial infarction and the comparison group; polymorphic variant AA AGTR2 gene is associated with earlier onset of coronary artery disease; It found that carriers of the polymorphic variant gene GA AGTR2 beginning statistically CHD occurred significantly later than in carriers of alleles GG and AA; age CHD debut TT allele carriers of the eNOS gene is associated with an earlier onset of the disease and statistically significantly different from the age of first CHD in carriers of alleles of polymorphic variants of GG and GT; revealed a positive correlation between the polymorphic allele AGTR2 gene with the presence of arterial hypertension in patients with coronary artery disease; It determined that the T allele carriers of the polymorphic gene eNOS is associated more early onset of hypertension, found the association of the polymorphic allele gene AGTR2 the need to use higher doses of ACE inhibitor — perindopril. |
topic |
coronary heart disease gene polymorphism enos agtr2 |
url |
https://www.medarhive.ru/jour/article/view/534 |
work_keys_str_mv |
AT alkhokhlov featuresoftheclinicalsignificanceofpolymorphicvariantsofenosandagtr2genesinpatientswithcad AT nopozdnyakov featuresoftheclinicalsignificanceofpolymorphicvariantsofenosandagtr2genesinpatientswithcad AT aemiroshnikov featuresoftheclinicalsignificanceofpolymorphicvariantsofenosandagtr2genesinpatientswithcad AT intzareva featuresoftheclinicalsignificanceofpolymorphicvariantsofenosandagtr2genesinpatientswithcad AT sopozdnyakov featuresoftheclinicalsignificanceofpolymorphicvariantsofenosandagtr2genesinpatientswithcad |
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1721257199922053120 |