Vladeanu Maria-Cristina, Bojan Iris Bararu, Bojan Andrei, Iliescu Dan, Badescu Minerva Codruta, Badulescu Oana Viola, Badescu Magda, Georgescu Catalina Arsenescu, Ciocoiu Manuela
Department of Physiopathology, 'Grigore T. Popa' University of Medicine and Pharmacy, 700115 Iasi, Romania.
Department of Surgical Sciences, 'Grigore T. Popa' University of Medicine and Pharmacy, 700115 Iasi, Romania.
Exp Ther Med. 2020 Oct;20(4):3407-3411. doi: 10.3892/etm.2020.8978. Epub 2020 Jul 8.
Coronary artery disease (CAD) is the first cause of morbidity and mortality worldwide. An important goal is to diagnose patients in early stages, in order to reduce acute cardiovascular events. The angiotensin-converting enzyme (ACE) is an important element for the cardiovascular system, through its actions on hydro-salin balance and vascular tone. ACE polymorphism consists of insertions (I)/deletions (D) and there are 3 genotypes: II, ID, DD. It is speculated that the DD genotype may be a genetic basis for severe CAD, while the II genotype may have a protective effect on the coronary arteries. The present study included 154 patients with acute coronary syndroms admitted to the Institute for Cardiovascular Disease 'George I.M. Georgescu', Iasi. The patients underwent coronary angiography in order to assess the severity of the lesions and the ACE genotypes were determined for each patient. The genotypes were correlated with the severity of the vessel-disease and the exposure to classic risk factors. It was concluded that the D-allele is associated with a greater risk for acute coronary events and severe coronary stenosis, especially when risk genotype and risk phenotype interact.
冠状动脉疾病(CAD)是全球发病和死亡的首要原因。一个重要目标是在早期阶段诊断患者,以减少急性心血管事件。血管紧张素转换酶(ACE)通过其对水盐平衡和血管张力的作用,是心血管系统的一个重要因素。ACE基因多态性由插入(I)/缺失(D)组成,有3种基因型:II、ID、DD。据推测,DD基因型可能是严重CAD的遗传基础,而II基因型可能对冠状动脉有保护作用。本研究纳入了154例入住雅西“乔治一世·M·乔治斯库”心血管疾病研究所的急性冠状动脉综合征患者。患者接受冠状动脉造影以评估病变的严重程度,并为每位患者确定ACE基因型。这些基因型与血管疾病的严重程度以及经典危险因素的暴露情况相关。得出的结论是,D等位基因与急性冠状动脉事件和严重冠状动脉狭窄的更大风险相关,尤其是当风险基因型和风险表型相互作用时。