Kamberi Bajram, Kamberi Farije, Spiroski Mirko
Neurological Department, Clinical Hospital, Tetovo, Republic of Macedonia.
School Medical Centre, "Nikolla Shtejn" Tetovo, Republic of Macedonia.
Open Access Maced J Med Sci. 2016 Dec 15;4(4):556-564. doi: 10.3889/oamjms.2016.114. Epub 2016 Oct 1.
Acute first-ever ischemic stroke (FIS) is a heterogeneous, polygenic disorder. The contribution of vascular genetic variants as inherited causes of ischemic stroke has remained controversial.
To examine the association of genetic variants in vascular factors with the occurrence of FIS.
The current research was performed in a group of 39 patients with FIS (study group) and 102 healthy volunteers (control group). We analyzed the prevalence of vascular genetic variants in following genes: and .
It was found that heterozygous and were significantly more frequent in patients with FIS than in control group (p = 0.036 and p = 0.017, respectively). The frequency of was significantly lower in patients with FIS than in control group (p = 0.020). Other frequencies of vascular gene variants in patients with FIS and in control group were not significantly different.
This is the first comprehensive study to present data indicating that polymorphism of vascular genes in the prevalence of acute FIS exists in the Albanian population from the Republic of Macedonia. Variations in these genes have been detected in patients with acute FIS, suggesting that their combination might act in a susceptible or protective manner in this Albanian population.
首次发生的急性缺血性卒中(FIS)是一种异质性多基因疾病。血管遗传变异作为缺血性卒中的遗传病因所起的作用一直存在争议。
研究血管因素中的基因变异与首次发生的急性缺血性卒中的发生之间的关联。
本研究纳入39例首次发生的急性缺血性卒中患者(研究组)和102名健康志愿者(对照组)。我们分析了以下基因中血管遗传变异的发生率: 和 。
发现杂合子 和 在首次发生的急性缺血性卒中患者中的出现频率显著高于对照组(分别为p = 0.036和p = 0.017)。首次发生的急性缺血性卒中患者中 的频率显著低于对照组(p = 0.020)。首次发生的急性缺血性卒中患者和对照组中其他血管基因变异的频率无显著差异。
这是第一项全面研究,提供的数据表明,来自马其顿共和国的阿尔巴尼亚人群中存在急性首次发生的缺血性卒中患病率方面的血管基因多态性。在急性首次发生的缺血性卒中患者中检测到了这些基因的变异,表明它们的组合可能在该阿尔巴尼亚人群中以易感或保护的方式起作用。