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Genetic and Environmental Dispositions for Cardiovascular Variability: A Pilot Study
Background: The aim of our study was to evaluate the degree of genetic homozygosity in the group of patients with coronary artery disease (CAD), as well as to evaluate morphogenetic variability in CAD patients regarding the presence of investigated risk factors (RF) compared to a control sample of i...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6162867/ https://www.ncbi.nlm.nih.gov/pubmed/30142875 http://dx.doi.org/10.3390/jcm7090232 |
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author | Karan, Radmila Cvjeticanin, Suzana Kovacevic-Kostic, Natasa Nikolic, Dejan Velinovic, Milos Milicevic, Vladimir Obrenovic-Kircanski, Biljana |
author_facet | Karan, Radmila Cvjeticanin, Suzana Kovacevic-Kostic, Natasa Nikolic, Dejan Velinovic, Milos Milicevic, Vladimir Obrenovic-Kircanski, Biljana |
author_sort | Karan, Radmila |
collection | PubMed |
description | Background: The aim of our study was to evaluate the degree of genetic homozygosity in the group of patients with coronary artery disease (CAD), as well as to evaluate morphogenetic variability in CAD patients regarding the presence of investigated risk factors (RF) compared to a control sample of individuals. Additionally, we aimed to evaluate the distribution of ABO blood type frequencies between tested samples of individuals. Methods: This study analyzed individual phenotype and morphogenetic variability of 17 homozygously-recessive characteristics (HRC), by using HRC test in a sample of 148 individuals in CAD patients group and 156 individuals in the control group. The following RF were analyzed: hypertension, diabetes mellitus, hyperlipidemia, and smoking. Results: The mean value of HRC in CAD patients is significantly higher, while variability decreases compared to the control sample (CAD patients: 4.24 ± 1.59, control sample: 3.75 ± 1.69; V(CAD-patients) = 37.50%, V(C) = 45.07%). There is a significant difference in individual variations of 17 HRC between control sample and CAD patients (χ(2) = 169.144; p < 0.01), which points out to different variability for tested genes. Mean values of HRC significantly differed in CAD patients in regard to the number of RF present. A blood type (OR = 1.75) is significant predictor for CAD, while O blood type (OR = 0.43) was significantly associated with controls. Conclusion: There is a higher degree of recessive homozygosity in CAD patients versus individuals in the control sample, and the presence of significant variations in the degree of recessive homozygosity as the number of tested RF increases. |
format | Online Article Text |
id | pubmed-6162867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61628672018-10-02 Genetic and Environmental Dispositions for Cardiovascular Variability: A Pilot Study Karan, Radmila Cvjeticanin, Suzana Kovacevic-Kostic, Natasa Nikolic, Dejan Velinovic, Milos Milicevic, Vladimir Obrenovic-Kircanski, Biljana J Clin Med Article Background: The aim of our study was to evaluate the degree of genetic homozygosity in the group of patients with coronary artery disease (CAD), as well as to evaluate morphogenetic variability in CAD patients regarding the presence of investigated risk factors (RF) compared to a control sample of individuals. Additionally, we aimed to evaluate the distribution of ABO blood type frequencies between tested samples of individuals. Methods: This study analyzed individual phenotype and morphogenetic variability of 17 homozygously-recessive characteristics (HRC), by using HRC test in a sample of 148 individuals in CAD patients group and 156 individuals in the control group. The following RF were analyzed: hypertension, diabetes mellitus, hyperlipidemia, and smoking. Results: The mean value of HRC in CAD patients is significantly higher, while variability decreases compared to the control sample (CAD patients: 4.24 ± 1.59, control sample: 3.75 ± 1.69; V(CAD-patients) = 37.50%, V(C) = 45.07%). There is a significant difference in individual variations of 17 HRC between control sample and CAD patients (χ(2) = 169.144; p < 0.01), which points out to different variability for tested genes. Mean values of HRC significantly differed in CAD patients in regard to the number of RF present. A blood type (OR = 1.75) is significant predictor for CAD, while O blood type (OR = 0.43) was significantly associated with controls. Conclusion: There is a higher degree of recessive homozygosity in CAD patients versus individuals in the control sample, and the presence of significant variations in the degree of recessive homozygosity as the number of tested RF increases. MDPI 2018-08-23 /pmc/articles/PMC6162867/ /pubmed/30142875 http://dx.doi.org/10.3390/jcm7090232 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Karan, Radmila Cvjeticanin, Suzana Kovacevic-Kostic, Natasa Nikolic, Dejan Velinovic, Milos Milicevic, Vladimir Obrenovic-Kircanski, Biljana Genetic and Environmental Dispositions for Cardiovascular Variability: A Pilot Study |
title | Genetic and Environmental Dispositions for Cardiovascular Variability: A Pilot Study |
title_full | Genetic and Environmental Dispositions for Cardiovascular Variability: A Pilot Study |
title_fullStr | Genetic and Environmental Dispositions for Cardiovascular Variability: A Pilot Study |
title_full_unstemmed | Genetic and Environmental Dispositions for Cardiovascular Variability: A Pilot Study |
title_short | Genetic and Environmental Dispositions for Cardiovascular Variability: A Pilot Study |
title_sort | genetic and environmental dispositions for cardiovascular variability: a pilot study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6162867/ https://www.ncbi.nlm.nih.gov/pubmed/30142875 http://dx.doi.org/10.3390/jcm7090232 |
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