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Apolipoprotein E gene polymorphisms as risk factors for carotid atherosclerosis

机译:载脂蛋白E基因多态性为颈动脉粥样硬化的危险因素

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Background/Aim. Atherosclerosis is still the leading cause of death in Western world. Development of atherosclerotic plaque involves accumulation of inflammatory cells, lipids, smooth muscle cells and extracellular matrix proteins in the intima of the vascular wall. Apolipoprotein E participates in the transport of exogenous cholesterol, endogenouly synthesized lipids and triglycerides in the organism. Apolipoprotein E gene has been identified as one of the candidate genes for atherosclerosis. Previous studies in different populations have clearly implicated apolipoprotein E genetic variation (ε polymorphisms) as a major modulator of low density lipoprotein cholesterol levels. Data considering apolipoprotein E polymorphisms in relation to carotid atherosclerosis gave results that are not in full compliance. The aim of present study was to investigate the apolipoprotein E polymorphisms in association with carotid plaque presence, apolipoprotein E and lipid serum levels in patients with carotid atherosclerosis from Serbia. Methods. The study group enrolled 495 participants: 285 controls and 210 consecutive patients with carotid atherosclerosis who underwent carotid endarterectomy. Genotyping of apolipoprotein E polymorphisms were done using polymerase chain reaction and restriction fragment length polymorphism methods. Results. Patients had significantly decreased frequency of the ε2 allele compared to controls. Patients who carry at least one ε2 allele had a significantly higher level of serum apolipoprotein E and significantly lower low density lipoprotein cholesterol levels compared to those who do not carry this allele. Conclusion. Our results suggest protective effect of apolipoprotein E ε2 allele on susceptibility for carotid plaque presence as well as low density lipoprotein cholesterol lowering effect in Serbian patients with carotid atherosclerosis. Further research of multiple gene and environmental factors that contribute to the appearance and the progression of atherosclerosis should be continued with respect to different populations. [Projekat Ministarstva nauke Republike Srbije, br. OI175085 i br. II I41028]
机译:背景/目标。动脉粥样硬化仍然是西方世界死亡的主要原因。动脉粥样硬化斑块的形成涉及血管壁内膜中炎症细胞,脂质,平滑肌细胞和细胞外基质蛋白的积累。载脂蛋白E参与生物体内外源胆固醇,内源性合成脂质和甘油三酸酯的运输。载脂蛋白E基因已被鉴定为动脉粥样硬化的候选基因之一。先前在不同人群中进行的研究清楚地表明,载脂蛋白E的遗传变异(ε多态性)是低密度脂蛋白胆固醇水平的主要调节剂。考虑载脂蛋白E多态性与颈动脉粥样硬化相关的数据得出的结果并不完全符合。本研究的目的是调查来自塞尔维亚的颈动脉粥样硬化患者的载脂蛋白E多态性与颈动脉斑块的存在,载脂蛋白E和脂质血清水平的关系。方法。该研究组招募了495名参与者:285名对照和210名连续接受颈动脉内膜切除术的颈动脉粥样硬化患者。使用聚合酶链反应和限制性片段长度多态性方法对载脂蛋白E多态性进行基因分型。结果。与对照组相比,患者的ε2等位基因频率明显降低。携带至少一个ε2等位基因的患者与不携带该等位基因的患者相比,血清载脂蛋白E水平明显升高,低密度脂蛋白胆固醇水平明显降低。结论。我们的结果表明,载脂蛋白Eε2等位基因对塞尔维亚颈动脉粥样硬化患者的颈动脉斑块敏感性以及低密度脂蛋白胆固醇降低作用具有保护作用。对于不同人群,应继续研究有助于动脉粥样硬化的出现和发展的多种基因和环境因素。 [Projekat Ministarstva nauke Republike Srbije,br。 OI175085 i br。 II I41028]

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