首页> 外文期刊>Egyptian Journal of Medical Human Genetics >Possible association of interleukin-1beta (-511C/T) and interleukin-6 (-174G/C) gene polymorphisms with atherosclerosis in end stage renal disease Egyptian patients on maintenance haemodialysis
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Possible association of interleukin-1beta (-511C/T) and interleukin-6 (-174G/C) gene polymorphisms with atherosclerosis in end stage renal disease Egyptian patients on maintenance haemodialysis

机译:终末期肾脏疾病埃及人维持血液透析的白细胞介素-1β(-511C / T)和白细胞介素6(-174G / C)基因多态性可能与动脉粥样硬化相关

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In end stage renal disease, inflammation is considered a critical regulator of atherosclerotic plaque formation and progression, to which many dialysis and non-dialysis-related factors may contribute. Since circulating inflammatory cytokine levels vary inter-individually, one may speculate that genetic factors, such as polymorphisms in genes encoding them, may be involved in determining the individual inflammatory reaction in response to a given insult. The present work aimed to study interleukin-1B (-511C/T), and interleukin-6 (-174G/C) gene polymorphisms and their possible association with atherosclerosis in Egyptian patients with end stage renal disease on maintenance haemodialysis. The present study was conducted on 100 Egyptian subjects, the control group ( n =30) and the patient group ( n =70) with end stage renal disease on maintenance haemodialysis which were further subdivided into two subgroups with ( n =33) and without atherosclerosis ( n =37) as evidenced by CIMT, ECG ischaemic changes, cerebrovascular insufficiency (CVI), and peripheral vascular insufficiency (PVI). All studied subjects were subjected to detailed history taking, routine laboratory investigations and molecular studies including detection of IL-1B (-511C/T) and IL-6 (-174G/C) gene polymorphisms using the Polymerase chain reaction/Restriction fragment length polymorphism (PCR/RFLP) technique. The genotype distribution and allele frequency of IL-1B (-511C/T) and IL-6 (-174G/C) showed no statistical significant difference among the studied groups. To conclude the development of atherosclerosis among Egyptian patients on maintenance haemodialysis cannot be attributed to these two gene polymorphisms.
机译:在终末期肾脏疾病中,炎症被认为是动脉粥样硬化斑块形成和发展的关键调节因子,许多透析和非透析相关因素都可能导致炎症。由于循环中炎性细胞因子的水平因人而异,因此人们可能推测遗传因素(例如编码它们的基因中的多态性)可能参与确定对特定伤害做出反应的个体炎症反应。本工作旨在研究埃及维持性血液透析终末期肾脏疾病患者的白介素-1B(-511C / T)和白介素-6(-174G / C)基因多态性及其与动脉粥样硬化的可能关系。本研究针对100名埃及受试者,对照组(n = 30)和患有终末期肾脏疾病的维持性血液透析患者组(n = 70)进行了进一步细分,将其分为两个亚组,分别为(n = 33)和不包括CIMT,ECG缺血性变化,脑血管功能不全(CVI)和周围血管功能不全(PVI)证明动脉粥样硬化(n = 37)。所有研究对象均接受了详细的历史记录,常规实验室研究和分子研究,包括使用聚合酶链反应/限制性片段长度多态性检测IL-1B(-511C / T)和IL-6(-174G / C)基因多态性(PCR / RFLP)技术。 IL-1B(-511C / T)和IL-6(-174G / C)的基因型分布和等位基因频率在研究组之间无统计学差异。可以得出结论,维持性血液透析的埃及患者中动脉粥样硬化的发展不能归因于这两个基因多态性。

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