血管紧张素转换酶基因型在埃及原发性肾病和终末期肾病患者中的流行

F. Zahran, S.Hamed, A.T.Keshta, M.Hussien
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引用次数: 0

摘要

肾素-血管紧张素系统(RAS)是血压和肾脏功能及其相互作用的关键调节因子。在这种情况下,RAS不同组成部分基因的遗传变异性可能导致其在肾病患者中的异质性关联。血管紧张素转换酶-1 (ACE-1)是ras的重要组成部分,它决定血管活性肽血管紧张素- ii。本研究对来自埃及曼苏拉市的103例终末期肾病(ESRD)、104例原发性肾病(pn)患者和102例正常健康对照者进行了调查,以推断ACE基因多态性与ESRD、pn之间的关系。选取的样本采用特异性侧边引物进行基于(PCR)的dna扩增,对face I/D进行基因分型。结果显示,DD基因型在ESRD组和对照组之间存在显著性分布(p < 1),导致ESRD的风险增加。ESRD组与对照组ID基因型差异有统计学意义(p<0.05),无发病风险(OR <1)。基于这些观察,我们得出结论,ACE DD基因型在埃及人的肾损害中可能起着重要作用。该研究将有助于预先确定ESRD患者的治疗时间、类型和剂量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Angiotensin converting enzyme genotype prevalence among Egyptian primary nephrotic and end stage renal diseases patients
The Renin-Angiotensin system (RAS) is a key regulator of both blood pressure and kidney functions and their interaction. In such a situation, genetic variability in the genes of different components of RAS is likely to contribute for its heterogeneous association in the renal disease patients. Angiotensin converting enzyme-1 (ACE-1) is an important component of RASwhich determines the vasoactive peptideAngiotensin-II. In the present study,we have investigated 103 end stage renal diseases (ESRD), 104 primary nephrotic (P.N) patients and 102 normal healthy controls from Mansoura city in Egypt to deduce the association between ACE gene polymorphism and ESRD, P.N. The selected sampleswere assayed for genotyping ofACE I/D by (PCR) based DNAamplification using specific flanking primers. The results revealed that there was a significance distribution in DD genotype between ESRD and control group (p 1) which resulting in increasing the risk for ESRD. Therewas significance distribution in ID genotype between ESRD and control group (p<0.05), without disease risk (OR <1). Based on these observations we conclude that ACE DD genotype implicate a strong possible role in the in renal damage among Egyptians. The studywill help in predetermining the timing, type and doses of therapy for ESRD patients.
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