Gene polymorphism of vascular endothelial growth factor in children with Henoch-Schonlein purpura nephritis.
- Author:
Hua-Song ZENG
1
;
Xiao-Yan XIONG
;
Yao-Yong CHEN
;
Xiao-Ping LUO
Author Information
- Publication Type:Journal Article
- MeSH: Child; Child, Preschool; Gene Frequency; Genotype; Humans; Nephritis; genetics; Polymorphism, Genetic; Purpura, Schoenlein-Henoch; genetics; Vascular Endothelial Growth Factor A; blood; genetics
- From: Chinese Journal of Contemporary Pediatrics 2009;11(6):417-421
- CountryChina
- Language:English
-
Abstract:
OBJECTIVETo study the relationship of -634G/C gene polymorphism of vascular endothelial growth factor (VEGF) with Henoch-Schonlein purpura nephritis (HSPN) in children.
METHODSOne hundred ethnic Han children with HSP, including 50 children with concurrent nephritis (HSPN group) and 50 children without nephritis (HSP without nephritis group), were enrolled. Fifty age-, sex-and ethnics-matched healthy children were used as the control group. VEGF-634G/C genotypes were determined by PCR-RFLP. Plasma VEGF levels were measured using ELISA.
RESULTSCC genotype distribution (32%) and C allele frequency (56%) in the HSPN group were significantly higher than those in the control group (10% and 35% respectively) and the HSP without nephritis group (10% and 33% respectively) (P<0.01). The incidence of nephritis in HSP patients with CC genotype increased significantly when compared with those with GG genotype (76% vs 31%; P<0.01). Plasma VEGF levels in patients with CC genotype (180.5+/- 40.7 pg/mL) were significantly higher than those in patients with CG (145.2+/- 48.3 pg/mL) and GG (101.5+/- 26.5 pg/mL) genotypes (P<0.05).
CONCLUSIONSVEGF-634G/C gene polymorphism may be associated with the development of HSPN. C allele may a susceptible gene of HSPN.
