The association of ITGB3 gene and NOS3 gene with the severity of coronary artery disease with and without type 2 diabetes

Type 2 diabetes (T2DM) is one of the key predictors of coronary artery disease (CAD) and its complications. Currently, along with metabolic risk factors for CAD, much attention has been given to the study candidate genes, including platelet fibrinogen receptor gene ITGB3 and the gene NOS3 of endothe...

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Autores principales: Elvira F. Muslimova, Tatyana Y. Rebrova, Sergey A. Afanasiev, Tatyana N. Sergienko, Aleksey N. Repin
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Publicado: Endocrinology Research Centre 2016
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spelling oai:doaj.org-article:184f097173fe444d889977c08b86320f2021-11-14T09:00:20ZThe association of ITGB3 gene and NOS3 gene with the severity of coronary artery disease with and without type 2 diabetes2072-03512072-037810.14341/DM7875https://doaj.org/article/184f097173fe444d889977c08b86320f2016-11-01T00:00:00Zhttps://www.dia-endojournals.ru/jour/article/view/7875https://doaj.org/toc/2072-0351https://doaj.org/toc/2072-0378Type 2 diabetes (T2DM) is one of the key predictors of coronary artery disease (CAD) and its complications. Currently, along with metabolic risk factors for CAD, much attention has been given to the study candidate genes, including platelet fibrinogen receptor gene ITGB3 and the gene NOS3 of endothelial NO-synthase type 3.Aim. To estimate the associations of T1565C ITGB3 and T-786C NOS3 polymorphisms with the clinical condition of russian patients from West Siberian region with concomitant development of coronary artery disease and type 2 diabetes.Materials and methods. The study included 237 CAD patients; 78 (32.9%) of them had T2DM. The genotyping was performed by allele-specific polymerase chain reaction. Comparison of quantitative variables between groups with different genotypes was done by Mann-Whitney U test or Kruskal-Wallis test. Comparison of discrete parameters was done by Pearson χ2 test or Fisher's exact test.Results. Genotype 786CC (NOS3) (p=0,039) and allele 1565C (ITGB3) (p=0,045) were less common in the group CAD+T2DM than in the group CAD without T2DM. But in the group CAD+T2DM the frequency of obesity was higher among carriers of 1565C allele than in homozygotes 1565TT (p=0,039), and carriers of 786C allele have the highest concentration of glucose compared to homozygous 786TT (p=0,018). Furthermore, 786C allele is associated with obesity in the group of patients without T2DM detected (p = 0,015).Conclusion. Carriage of 1565C (ITGB3) allele and 786C (NOS3) allele can be considered as predictors of adverse course of the disease at concomitant development of CAD and T2DM.Elvira F. MuslimovaTatyana Y. RebrovaSergey A. AfanasievTatyana N. SergienkoAleksey N. RepinEndocrinology Research Centrearticlepolymorphismsitgb3nos3diabetes mellituscadNutritional diseases. Deficiency diseasesRC620-627ENRUСахарный диабет, Vol 19, Iss 4, Pp 302-308 (2016)
institution DOAJ
collection DOAJ
language EN
RU
topic polymorphisms
itgb3
nos3
diabetes mellitus
cad
Nutritional diseases. Deficiency diseases
RC620-627
spellingShingle polymorphisms
itgb3
nos3
diabetes mellitus
cad
Nutritional diseases. Deficiency diseases
RC620-627
Elvira F. Muslimova
Tatyana Y. Rebrova
Sergey A. Afanasiev
Tatyana N. Sergienko
Aleksey N. Repin
The association of ITGB3 gene and NOS3 gene with the severity of coronary artery disease with and without type 2 diabetes
description Type 2 diabetes (T2DM) is one of the key predictors of coronary artery disease (CAD) and its complications. Currently, along with metabolic risk factors for CAD, much attention has been given to the study candidate genes, including platelet fibrinogen receptor gene ITGB3 and the gene NOS3 of endothelial NO-synthase type 3.Aim. To estimate the associations of T1565C ITGB3 and T-786C NOS3 polymorphisms with the clinical condition of russian patients from West Siberian region with concomitant development of coronary artery disease and type 2 diabetes.Materials and methods. The study included 237 CAD patients; 78 (32.9%) of them had T2DM. The genotyping was performed by allele-specific polymerase chain reaction. Comparison of quantitative variables between groups with different genotypes was done by Mann-Whitney U test or Kruskal-Wallis test. Comparison of discrete parameters was done by Pearson χ2 test or Fisher's exact test.Results. Genotype 786CC (NOS3) (p=0,039) and allele 1565C (ITGB3) (p=0,045) were less common in the group CAD+T2DM than in the group CAD without T2DM. But in the group CAD+T2DM the frequency of obesity was higher among carriers of 1565C allele than in homozygotes 1565TT (p=0,039), and carriers of 786C allele have the highest concentration of glucose compared to homozygous 786TT (p=0,018). Furthermore, 786C allele is associated with obesity in the group of patients without T2DM detected (p = 0,015).Conclusion. Carriage of 1565C (ITGB3) allele and 786C (NOS3) allele can be considered as predictors of adverse course of the disease at concomitant development of CAD and T2DM.
format article
author Elvira F. Muslimova
Tatyana Y. Rebrova
Sergey A. Afanasiev
Tatyana N. Sergienko
Aleksey N. Repin
author_facet Elvira F. Muslimova
Tatyana Y. Rebrova
Sergey A. Afanasiev
Tatyana N. Sergienko
Aleksey N. Repin
author_sort Elvira F. Muslimova
title The association of ITGB3 gene and NOS3 gene with the severity of coronary artery disease with and without type 2 diabetes
title_short The association of ITGB3 gene and NOS3 gene with the severity of coronary artery disease with and without type 2 diabetes
title_full The association of ITGB3 gene and NOS3 gene with the severity of coronary artery disease with and without type 2 diabetes
title_fullStr The association of ITGB3 gene and NOS3 gene with the severity of coronary artery disease with and without type 2 diabetes
title_full_unstemmed The association of ITGB3 gene and NOS3 gene with the severity of coronary artery disease with and without type 2 diabetes
title_sort association of itgb3 gene and nos3 gene with the severity of coronary artery disease with and without type 2 diabetes
publisher Endocrinology Research Centre
publishDate 2016
url https://doaj.org/article/184f097173fe444d889977c08b86320f
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