The Gender Impact on Morphogenetic Variability in Coronary Artery Disease: A Preliminary Study
Autor: | Biljana Obrenovic-Kircanski, Vladimir Milicevic, Dejan Nikolic, Natasa Kovacevic-Kostic, Radmila Karan, Milica Vranes-Stoimirov, Suzana Cvjeticanin, Milos Velinovic |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
medicine.medical_specialty homozygous recessive characteristics lcsh:Medicine 030204 cardiovascular system & hematology Article Coronary artery disease 03 medical and health sciences 0302 clinical medicine Internal medicine Diabetes mellitus gender medicine Genetic predisposition cardiovascular diseases 10. No inequality variability business.industry lcsh:R Significant difference General Medicine coronary artery disease medicine.disease 030104 developmental biology Healthy individuals Cardiology business |
Zdroj: | Journal of Clinical Medicine; Volume 7; Issue 5; Pages: 103 Journal of Clinical Medicine, Vol 7, Iss 5, p 103 (2018) Journal of Clinical Medicine |
ISSN: | 2077-0383 |
DOI: | 10.3390/jcm7050103 |
Popis: | We analyzed morphogenetic variability and degree of genetic homozygosity in male and female individuals with coronary artery disease (CAD) versus unaffected controls. We have tested 235 CAD patients; 109 were diagnosed also with diabetes mellitus (DM) and 126 with hypertension (HTN). We additionally evaluated 152 healthy individuals without manifested CAD. For the evaluation of the degree of recessive homozygosity, we have performed the homozygously recessive characteristics (HRC) test and tested 19 HRCs. In controls, the frequency of HRC for males was 2.88 ± 1.89, while for females, it was 3.65 ± 1.60. In the CAD group, the frequency of HRC for males was 4.21 ± 1.47, while for females, it was 4.73 ± 1.60. There is significant difference in HRC frequencies between controls and CAD separately for males (p < 0.001) and females (p < 0.001). The same applies between controls and CAD with DM (males: p < 0.001 and females: p = 0.004), and controls and CAD with HTN (males: p < 0.001 and females: p < 0.001). There is no significant difference in HRC frequencies between the group of CAD with DM and the group of CAD with HTN (males: p = 0.952 and females: p = 0.529). Our findings point to the increased degree of recessive homozygosity and decreased variability in both genders of CAD patients versus controls, indicating the potential genetic predisposition for CAD. |
Databáze: | OpenAIRE |
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