Steroid-sensitive nephrotic syndrome and vascular endothelial growth factor gene polymorphisms

被引:14
作者
Holt, RCL
Ralph, SA
Webb, NJA
Watson, CJ
Clark, AGB
Mathieson, PW
Brenchley, PEC
机构
[1] Manchester Royal Infirm, Manchester Inst Nephrol & Transplantat, Manchester M13 9WL, Lancs, England
[2] Royal Manchester Childrens Hosp, Dept Nephrol, Manchester M27 1HA, Lancs, England
[3] Guys Hosp, Paediat Renal Unit, London SE1 9RT, England
[4] Southmead Gen Hosp, Acad Renal Unit, Bristol, Avon, England
来源
EUROPEAN JOURNAL OF IMMUNOGENETICS | 2003年 / 30卷 / 01期
关键词
D O I
10.1046/j.1365-2370.2003.00360.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genetic polymorphisms have been recognized as important determinants of gene expression. Three common single nucleotide polymorphisms have been identified in the promoter and 5' untranslated region of the vascular endothelial growth factor (VEGF) gene: -460 C --> T, -141 A --> C and +405 G --> C. As VEGF has been postulated to play a role in the pathogenesis of childhood steroid-sensitive nephrotic syndrome (SSNS), this study tested the hypothesis that VEGF genotype may be associated with susceptibility to SSNS. We examined the genotype frequencies of these polymorphisms in a total of 116 children with SSNS and 150 control subjects, using polymerase chain reaction-restriction fragment length polymorphism analysis (PCR-RFLP). There were no statistically significant differences in any of the genotype frequencies between SSNS patients and controls. We conclude that VEGF -460, -141 and +405 genotypes are not associated with susceptibility to childhood SSNS.
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页码:1 / 3
页数:3
相关论文
共 15 条
[2]   Vascular endothelial growth factor mRNA expression in minimal change, membranous, and diabetic nephropathy demonstrated by non-isotopic in situ hybridisation [J].
Bailey, E ;
Bottomley, MJ ;
Westwell, S ;
Pringle, JH ;
Furness, PN ;
Feehally, J ;
Brenchley, PEC ;
Harper, SJ .
JOURNAL OF CLINICAL PATHOLOGY, 1999, 52 (10) :735-738
[3]  
CAMPBELL MJ, 1996, STAT SQUARE ONE, P45
[4]  
Cheong HI, 2001, J NEPHROL, V14, P263
[5]  
Clark AG, 1999, PEDIATR NEPHROL, P731
[6]   GENES ENCODING THE BETA-CHAINS OF HLA-DR7 AND HLA-DQW2 DEFINE MAJOR SUSCEPTIBILITY DETERMINANTS FOR IDIOPATHIC NEPHROTIC SYNDROME [J].
CLARK, AGB ;
VAUGHAN, RW ;
STEPHENS, HAF ;
CHANTLER, C ;
WILLIAMS, DG ;
WELSH, KI .
CLINICAL SCIENCE, 1990, 78 (04) :391-397
[7]   THE FMS-LIKE TYROSINE KINASE, A RECEPTOR FOR VASCULAR ENDOTHELIAL GROWTH-FACTOR [J].
DEVRIES, C ;
ESCOBEDO, JA ;
UENO, H ;
HOUCK, K ;
FERRARA, N ;
WILLIAMS, LT .
SCIENCE, 1992, 255 (5047) :989-991
[8]   Molecular and biological properties of vascular endothelial growth factor [J].
Ferrara, N .
JOURNAL OF MOLECULAR MEDICINE-JMM, 1999, 77 (07) :527-543
[9]  
FREEMAN MR, 1995, CANCER RES, V55, P4140
[10]   Dinucleotide repeat polymorphisms within the Flt-1 gene in minimal change nephropathy [J].
Parry, RG ;
Gillespie, KM ;
Clark, AGB ;
Mathieson, PW .
EUROPEAN JOURNAL OF IMMUNOGENETICS, 1999, 26 (05) :321-323