Hanna Mariam Onsy F, Shahin Rasha Mohamad Hosny, Meshaal Safa S, Kostandi Inas F
a Department of Clinical Pathology and.
b Department of Internal Medicine , Faculty of Medicine, Cairo University , Kasr Al Ainy , Cairo , Egypt.
J Recept Signal Transduct Res. 2015;35(5):381-5. doi: 10.3109/10799893.2014.956757. Epub 2014 Oct 15.
The role of the angiotensin II type 1 receptor (AT1R) gene polymorphism, A1166C, has been shown to be associated with end stage renal disease (ESRD) and its progression. There is also some evidence that HLA class II alleles are associated with ESRD independent of other factors.
To examine the association between AT1R gene polymorphism in the susceptibility and progression to ESRD in patients with chronic renal failure and to investigate if the AT1R genotypes and HLA-DR alleles predict the time to ESRD.
Genotyping was performed in 50 ESRD patients and 44 control subjects for the AT1R A1166C gene polymorphism using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). ESRD patients were examined for HLA-DRB1 alleles according to a reverse hybridization line probe assay.
Allele and genotype frequencies of the AT1R polymorphism did not differ significantly between ESRD patients and controls. Furthermore, there was no association between the AT1R gene polymorphism or HLA-DRB1 alleles with the time to the occurrence of end stage failure.
We concluded that the AT1R genotype does not contribute to the genetic susceptibility of ESRD and is not associated with progression of chronic kidney failure to ESRD.
血管紧张素II 1型受体(AT1R)基因多态性A1166C已被证明与终末期肾病(ESRD)及其进展相关。也有一些证据表明,人类白细胞抗原II类等位基因独立于其他因素与ESRD相关。
研究慢性肾衰竭患者中AT1R基因多态性与ESRD易感性及进展之间的关联,并调查AT1R基因型和人类白细胞抗原-DR(HLA-DR)等位基因是否能预测ESRD发生时间。
采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术,对50例ESRD患者和44例对照者进行AT1R A1166C基因多态性基因分型。根据反向杂交线探针分析法对ESRD患者检测HLA-DRB1等位基因。
ESRD患者与对照者之间,AT1R多态性的等位基因和基因型频率无显著差异。此外,AT1R基因多态性或HLA-DRB1等位基因与终末期肾衰竭发生时间之间无关联。
我们得出结论,AT1R基因型对ESRD的遗传易感性无影响,且与慢性肾衰竭进展至ESRD无关。