Key result
Heterozygous mutation in Factor V Leiden and homozygous DD alleles of the ACE gene were significantly higher in hypertensive patients and their first-degree relatives compared to controls (p<0.05).
Why the study?
Are Factor V Leiden, MTHFR, and ACE gene mutations associated with essential hypertension in a Turkish population?
Case-Control (n=299)
Yes
Are Factor V Leiden, MTHFR, and ACE gene mutations associated with essential hypertension in a Turkish population?
ACE DD alleles and mutated alleles of FV Leiden and MTHFR genes are associated with essential hypertension in the Turkish population.
BACKGROUND: Hypertension is one of the leading causes of mortality and morbidity in the world, which is influenced by environmental and genetic factors. The methylenetetrahydrofolate reductase (MTHFR) and angiotensin-converting enzymes (ACE) are possible candidate genes that may influence both body fatness and blood pressure (BP). The purpose of this study was to examine the carriage of gene combinations of the ACE (insertion/deletion [I/D]), MTHFR 677T and 1298C, and lipid profiles in patients with essential hypertension (EH) in Turkey. METHODS: A total of 150 adult individuals (50 hypertensive, 50 first-degree relatives, and 50 healthy controls) from Sivas/Turkey with the same age and gender were assessed for body composition, lipid profiles, resting BP, and gene profiles. Additionally, 149 individuals (99 hypertensive, 50 controls) from Canakkale/Turkey had been investigated for ACE I/D polymorphism. Peripheral blood samples were genotyped using strip assay reverse-hybridization multiplex polymerase chain reaction tests for target genes. RESULTS: Heterozygous mutation in FV Leiden was found to be higher in the hypertensive and first-degree relatives when compared with the control group (p<0.05). Homozygous DD alleles of the ACE gene were also higher than the ACE I/D and control groups (p<0.05). The high rates of cholesterol and low-density lipoprotein and low rates of high-density lipoprotein were found in patients with EH when compared with the control. CONCLUSION: Results show that ACE with DD alleles and mutated alleles of FV Leiden and MTHFR genes were significantly different between genotypes and have a combined effect on EH in Turkish population. Further studies are needed to investigate the genetics of obesity, EH, and BP phenotypes in the current adult population.
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Demirel et al. (2011) conducted a case-control in Essential hypertension (n=299). Factor V Leiden, MTHFR, and ACE (I/D) gene mutations vs. Healthy controls was evaluated on Carriage of gene combinations (FV Leiden, ACE I/D, MTHFR) and lipid profiles (p=<0.05). Heterozygous mutation in Factor V Leiden and homozygous DD alleles of the ACE gene were significantly higher in hypertensive patients and their first-degree relatives compared to controls (p<0.05).
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