No association of vascular endothelial growth factor A gene rs9369425 polymorphism with glucose metabolism in Chinese Han population.
- VernacularTitle:血管内皮生长因子A基因rs9369425变异与中国人糖代谢的相关性
- Author:
Rong ZHANG
1
;
Cheng HU
;
Cong-rong WANG
;
Jing XU
;
Xiao-jing MA
;
Kun-san XIANG
;
Wei-ping JIA
Author Information
- Publication Type:Journal Article
- MeSH: Alleles; Asian Continental Ancestry Group; ethnology; genetics; Blood Glucose; metabolism; Diabetes Mellitus, Type 2; genetics; Gene Frequency; Genetic Predisposition to Disease; Genotype; Glucose Tolerance Test; Humans; Insulin Resistance; genetics; Polymorphism, Genetic; Polymorphism, Single Nucleotide; genetics; Population Groups; genetics; Vascular Endothelial Growth Factor A; genetics
- From: Chinese Journal of Medical Genetics 2010;27(4):457-459
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the relationship between the vascular endothelial growth factor A gene (VEGFA) rs9369425 single nucleotide polymorphism (SNP) and type 2 diabetes in Chinese Han population.
METHODSOne thousand eight hundred and ninety two type 2 diabetes patients and 1808 controls with normal glucose were recruited in this study. Phenotypes including body mass index, waist, waist hip ratio, plasma glucose and serum insulin levels of blood obtained both at 0 and 120 minute during standard 75-gram glucose oral glucose tolerance tests, were analyzed. Insulin resistance and beta cell function were assessed by homeostasis model assessment (HOMA-IR and HOMA-B). Genotyping was performed by time-of-light mass spectrum using a Sequenom platform.
RESULTSThe frequencies of minor allele G in the diabetic patients and controls were 10.8% and 11.3% respectively. No significant difference of allele distribution was detected between the cases and controls (P=0.5086). No significant difference (P>0.05) was detected on the association between rs9369425 SNP and clinical phenotypes.
CONCLUSIONVEGFA rs9369425 was not associated with type 2 diabetes in Chinese Han population. Whether there is association in any other loci in this gene remained to be investigated.