Author:
Qian Yue,Ding Li,Cao Liou,Yu Zanzhe,Shao Xinghua,Wang Ling,Zhang Minfang,Wang Qin,Che Xiajing,Jiang Na,Yan Hao,Fang Wei,Jin Yan,Huang Jiaying,Gu Aiping,Ni Zhaohui
Abstract
Abstract
Background
Peritoneal dialysis (PD) is an effective and successful renal replacement therapy. The baseline peritoneal solute transfer rate (PSTR) is related to local membrane inflammation and may be partially genetically determined. Herein, we focused on vascular endothelial growth factor (VEGF) and its receptor, kinase insert domain containing receptor (KDR).
Methods
This study recruited 200 PD patients from Renji Hospital in Shanghai, China. We analysed the association between the polymorphisms of VEGF and KDR and the 4-hour dialysate-to-plasma ratio for creatinine (4 h D/P Cr), which was measured between one and three months after initiating PD.
Results
The CC genotype in VEGF rs3025039 and the AA genotype in KDR rs2071559 were both positively associated with a fast baseline PSTR (VEGF rs3025039 CC vs. TT + TC: 0.65 ± 0.12 vs. 0.61 ± 0.11; P = 0.029; KDR rs2071559 AA vs. GA + GG: 0.65 ± 0.12 vs. 0.62 ± 0.12; P = 0.039).
Conclusion
Baseline PSTR was partly determined by VEGF and KDR gene polymorphisms.
Funder
National Natural Science Foundation of China
Shanghai Municipal Health Bureau
School of Medicine, Shanghai Jiao Tong University
Publisher
Springer Science and Business Media LLC
Cited by
3 articles.
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