Hmimech Wiam, Diakite Brehima, Idrissi Hind Hassani, Hamzi Khalil, Korchi Farah, Baghdadi Dalila, Habbal Rachida, Nadifi Sellama
Laboratory of Genetics and Molecular Pathology, Medical School, University Hassan II, Casablanca 22000, Morocco.
Department of Cardiology, University Hospital Center Ibn Rochd, Casablanca 22000, Morocco.
Biomed Rep. 2016 Nov;5(5):618-622. doi: 10.3892/br.2016.768. Epub 2016 Sep 30.
Coagulation factor Leiden mutation has been described as a common genetic risk factor for venous thrombosis; however, this mutation was reported to be practically absent in an African population. Recently, a novel non-sense mutation in the gene encoding factor V has been associated with the risk of occurrence of cardio-cerebrovascular diseases such as stroke and venous thrombosis. The aim of the present study was to investigate whether the factor V Leiden (FVL) and C2491T non-sense mutations are associated with the risk of developing myocardial infarction. Genotyping of FVL and C2491T FV was performed using the polymerase chain reaction restriction fragment length polymorphism method on a sample of 100 patients with myocardial infarction as well as 211 controls. In the study population, the frequency of the FVL mutation was practically zero. However, with regard to the C2491T mutation, the TT genotype was associated with an increased risk of myocardial infarction [odds ratio (OR)=3.16, 95% confidence interval (CI): 1.29-7.71, P=0.03]. A significant association between the C2491T FV mutation and the risk of myocardial infarction was identified using recessive (OR=2.74, 95% CI: 1.14-6.58, P=0.04), dominant (OR=1.85, 95% CI: 1.13-3.04, P=0.02) and additive (OR=1.88, 95% CI: 1.25-2.80, P=0.004) models. Furthermore, a positive correlation was found between the presence of the C2491T FV mutation and hypertension (P=0.02), which is associated with myocardial infarction. In conclusion, the results of the present study suggested that the C2491T non-sense mutation of the FV gene may be a risk factor for myocardial infarction in a Moroccan population.
凝血因子莱顿突变已被描述为静脉血栓形成的常见遗传风险因素;然而,据报道这种突变在非洲人群中几乎不存在。最近,编码因子V的基因中一种新的无义突变与中风和静脉血栓形成等心脑血管疾病的发生风险相关。本研究的目的是调查因子V莱顿(FVL)和C2491T无义突变是否与心肌梗死的发生风险相关。采用聚合酶链反应-限制性片段长度多态性方法对100例心肌梗死患者和211例对照样本进行FVL和C2491T FV基因分型。在研究人群中,FVL突变的频率几乎为零。然而,关于C2491T突变,TT基因型与心肌梗死风险增加相关[比值比(OR)=3.16,95%置信区间(CI):1.29-7.71,P=0.03]。使用隐性(OR=2.74,95%CI:1.14-6.58,P=0.04)、显性(OR=1.85,95%CI:1.13-3.04,P=0.02)和加性(OR=1.88,95%CI:1.25-2.80,P=0.004)模型确定了C2491T FV突变与心肌梗死风险之间的显著关联。此外,发现C2491T FV突变的存在与高血压之间存在正相关(P=0.02),而高血压与心肌梗死相关。总之,本研究结果表明,FV基因的C2491T无义突变可能是摩洛哥人群中心肌梗死的一个风险因素。