首页> 美国卫生研究院文献>International Journal of Molecular and Cellular Medicine >Vascular Endothelial Growth Factor (VEGF) Gene Promoter Polymorphisms and Disease Progression in North Indian Cohort with Autosomal Dominant Polycystic Kidney Disease
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Vascular Endothelial Growth Factor (VEGF) Gene Promoter Polymorphisms and Disease Progression in North Indian Cohort with Autosomal Dominant Polycystic Kidney Disease

机译:北印度人常染色体显性多囊肾疾病人群的血管内皮生长因子(VEGF)基因启动子多态性和疾病进展。

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摘要

Autosomal dominant polycystic kidney disease (ADPKD) is characterized by a significant phenotypic variability in progression of the disease. Vascular endothelial growth factor (VEGF) has been reported to play a major role in renal pathophysiology. The aim of the present case-control study was to evaluate the association of two promoter polymorphisms (-2578C>A and-1154G>A) of VEGF gene and ADPKD. Genotyping was carried out in 123 ADPKD patients and 100 healthy controls, using a polymerase chain reaction-restriction fragment length polymorphism technique (PCR-RFLP). The genotype, allele and haplotype frequencies of these two polymorphisms in ADPKD patients were compared with those in controls, as well as in patients with early and advanced chronic kidney disease (CKD) stages, using Chi-square (χ2) test. The distribution frequency of CC, CA and AA genotypes of -2578C>A polymorphism differed significantly between patients and controls (0.31, 0.63 and 0.06 vs 0.37, 0.44 and 0.19, respectively (P=0.003)), but no significantly different genotype distribution was observed for the-1154G>A polymorphism. The A allele of -2578C>A and G allele of -1154G>A, were significantly more present in the controls as compared to the patients, and may provide protection for CKD under recessive (OR, 3.73; 95% CI, 1.45-9.62; P=0.0042), and dominant (OR, 0.55; 95%CI, 0.31-0.98; P=0.041) models. The [A;G] haplotype was more frequently present in controls (18%) than in cases (8%), (OR 0.398; 95% CI 0.22-0.71; P=0.002). These results suggest that the two promoter polymorphisms of VEGF may modify the disease risk in ADPKD patients from North India.
机译:常染色体显性遗传性多囊肾病(ADPKD)的特征是疾病进展过程中存在明显的表型变异性。据报道,血管内皮生长因子(VEGF)在肾脏病理生理中起着重要作用。本病例对照研究的目的是评估VEGF基因和ADPKD的两个启动子多态性(-2578C> A和-1154G> A)的关联。使用聚合酶链反应-限制性片段长度多态性技术(PCR-RFLP)在123位ADPKD患者和100位健康对照中进行了基因分型。使用卡方(χ2)检验比较ADPKD患者中这两个多态性的基因型,等位基因和单倍型频率与对照组以及早期和晚期慢性肾脏病(CKD)期患者的基因型,等位基因和单倍型频率。患者和对照组之间-2578C> A多态性的CC,CA和AA基因型的分布频率存在显着差异(分别为0.31、0.63和0.06,分别为0.37、0.44和0.19(P = 0.003)),但基因型分布没有显着差异观察到-1154G> A多态性。与患者相比,对照组中-2578C> A的A等位基因和-1154G> A的G等位基因显着更多,并且可以在隐性条件下为CKD提供保护(OR,3.73; 95%CI,1.45-9.62 ; P = 0.0042)和显性(OR,0.55; 95%CI,0.31-0.98; P = 0.041)模型。 [A; G]单倍型在对照组(18%)中比在病例(8%)中更常见(OR 0.398; 95%CI 0.22-0.71; P = 0.002)。这些结果表明,VEGF的两个启动子多态性可以改变北印度ADPKD患者的疾病风险。

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