Pregled bibliografske jedinice broj: 994790
Hereditary hemochromatosis gene mutations in patients with myocardial infarction
Hereditary hemochromatosis gene mutations in patients with myocardial infarction // Molecular and Experimental Biology in Medicine, 2 (2019), 1; 24-28 doi:0.33602/mebm.2019 (2).1.4 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 994790 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Hereditary hemochromatosis gene mutations in
patients with myocardial infarction
Autori
Škrlec, Ivana ; Florijancic, Mirela ; Steiner, Robert ; Wagner Kostadinovic , Jasenka
Izvornik
Molecular and Experimental Biology in Medicine (2584-671X) 2
(2019), 1;
24-28
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
HFE ; hereditary hemochromatosis ; myocardialinfarction ; real-time PCR
Sažetak
Hereditary hemochromatosis (HH) is a disorder of iron accumulation in tissues, which is related to coronary heart diseases. Free radicals and reactive oxygen species, created because of iron deposition, promote oxidation of LDL cholesterol and could lead to the development of atherosclerosis. Studies have shown that HFEgene mutation carriers might be at higher risk of developing cardiovascular diseases compared with non-carriers.This study aimed to determine the frequency of HFE gene mutations in patientswith myocardial infarction compared to a healthy group in eastern Slavonia.A retrospective case- control study was carried out on a population of 400 participants. In the first group there were 200 patients (114 males and 86 females) with myocardial infarction. The second group consisted of 200 controls (103 males and 97 females) without a history of cardiovascular diseases. All patients were genotyped for the three most common mutations of the HH in the HFE gene: C282Y, H63D, and S65C, by real-time PCR. The difference in the frequency of carriers of these mutations between the patients and the controls was not significant (C282Y: 4.5 vs. 8.1% ; H63D: 19 vs. 24.5% ; S65C: 3.5 versus 4%), and neither was the frequency and distribution of possible HFEgene genotypes and compound heterozygotes. There were no statistically significant associations of cardiovascular risk factors and HFEgene mutations in patients with myocardial infarction.In this study, no association was found between the HFEgene mutation for HH and myocardial infarction in the population of eastern Slavonia.
Izvorni jezik
Engleski
Znanstvena područja
Biologija, Temeljne medicinske znanosti, Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Klinički bolnički centar Osijek,
Medicinski fakultet, Osijek,
Fakultet za dentalnu medicinu i zdravstvo, Osijek