Association study between 834+7G/A and +1332C/T polymorphisms in the growth arrest specific 6 gene and risk of severe preeclampsia in Chinese population.
- Author:
Liyan YE
1
;
Linbo GUAN
;
Ping FAN
;
Xinghui LIU
;
Rui LIU
;
Jinxin CHEN
;
Yue ZHU
;
Xin WEI
;
Yu LIU
;
Huai BAI
Author Information
- Publication Type:Journal Article
- MeSH: Adult; Alleles; Asian Continental Ancestry Group; genetics; China; Female; Gene Frequency; Genetic Predisposition to Disease; ethnology; genetics; Genotype; Humans; Intercellular Signaling Peptides and Proteins; genetics; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Pre-Eclampsia; ethnology; genetics; pathology; Pregnancy; Risk Factors; Severity of Illness Index; Young Adult
- From: Chinese Journal of Medical Genetics 2017;34(1):45-49
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the relationship between polymorphisms of the growth arrest specific 6 (GAS6) gene and severe preeclampsia in a South West Han Chinese population.
METHODSBlood samples from 167 patients with severe preeclampsia and 312 normal pregnant women as controls from Han Chinese in Chengdu area were analyzed by polymerase chain reaction-restriction fragment length polymorphisms.
RESULTSC and T allele frequencies for +1332C/T site were 85.63% and 14.37% in the patient group, respectively, and 78.04% and 21.96% in control group, respectively. The TT genotype and variant T allelic frequencies of the +1332C/T polymorphism were significantly lower in patients with severe preeclampsia than in the control group (both P<0.05), and the odds ratio for the risk of severe preeclampsia was 0.602 (95%CI: 0.401-0.904) in carriers for the variant T allele (χ=6.045, P=0.014). G and A allele frequencies for 834+7G/A site were 72.75% and 27.25% in case group, respectively, and 74.36% and 25.64% in control group, respectively. The genotype and allele frequencies of the 834+7G/A polymorphism in patients with severe preeclampsia and controls showed no significant differences (both P>0.05). In addition, there was no significant association between the polymorphisms and blood pressure levels in the patient or control groups.
CONCLUSIONThe variant GAS6+1332 T allele is associated with a decreased risk for severe preeclampsia in a South West Han Chinese population. On the other hand, the 834+7G/A polymorphism has no effect on the severe preeclampsia.