Three single nucleotide polymorphisms of the vascular endothelial growth factor (VEGF) gene and glioma risk in a Chinese population

Objective To investigate the association between three single nucleotide polymorphisms (SNPs) of the vascular endothelial growth factor (VEGF) gene and the risk of glioma in a Han Chinese population. Methods This hospital-based case–control study used polymerase chain reaction–restriction fragment l...

Full description

Saved in:
Bibliographic Details
Published inJournal of international medical research Vol. 41; no. 5; pp. 1484 - 1494
Main Authors Jiang, Haitao, Lian, Minxue, Xie, Jiangtao, Li, Jinzheng, Wang, Maode
Format Journal Article
LanguageEnglish
Published London, England SAGE Publications 01.10.2013
Sage Publications
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Objective To investigate the association between three single nucleotide polymorphisms (SNPs) of the vascular endothelial growth factor (VEGF) gene and the risk of glioma in a Han Chinese population. Methods This hospital-based case–control study used polymerase chain reaction–restriction fragment length polymorphism analysis to detect three SNPs (−634 G/C, +936 C/T and +1612 G/A) of the VEGF gene in patients with glioma compared with healthy control subjects. Results The study investigated 880 patients with gliomas and 880 age- and sex-matched healthy control subjects. Patients with gliomas had a significantly higher frequency of the −634 CC genotype (odds ratio [OR] 1.35, 95% confidence interval [CI] 1.05, 1.75) and the +936 TT (OR 1.73, 95% CI 1.20, 2.48) genotype compared with the control subjects. Patients with glioblastomas had a significantly higher frequency of the −634 CC and +936 TT genotypes. Patients with grade IV gliomas had a significantly higher frequency of the −634 CC and +936 TT genotypes. The +1612 G/A polymorphisms were not associated with glioma risk. Conclusion The VEGF − 634 CC and +936 TT genotypes were associated with a higher risk of glioma in a Han Chinese population.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0300-0605
1473-2300
1473-2300
DOI:10.1177/0300060513498667