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子痫前期患者细胞间黏附分子-1基因K469E和血小板内皮细胞黏附分子-1基因C373G的多态性

[Polymorphisms of intercellular adhesion molecule-1 gene K469E and platelet endothelial cell adhesion molecule-1 gene C373G in patients with preeclampsia].

作者信息

He Yanhong, Wang Zhijian, Jin Jin, Zhu Xiaowen, Chen Yuying, Chen Shuying, Cao Yanwen

机构信息

Department of Obstetrics and Gynecology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.E-mail:

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2014 Apr;34(4):552-5, 559.

PMID:24752107
Abstract

OBJECTIVE

To investigate the distributions of genotypic and allelic frequencies of intercellular adhesion molecule-1 (ICAM-1) gene K469E and platelet endothelial cell adhesion molecule-1 (PECAM-1) gene C373G in patients with preeclampsia.

METHODS

Polymerase chain reaction-restriction fragment length polymorphism(PCR-RFLP) and DNA sequencing were used for detecting ICAM-1 gene K469E and PECAM-1 gene C373G genotypes in 110 women with preeclampsia and 110 normotensive pregnant women in comparison with their clinical characteristics.

ESULTS

The distributions of observed and expected genotype frequencies were consistent with Hardy-Weinberg equilibrium. No significant differences were found in the genotype and allele frequencies of ICAM-1 gene K469E between the two groups (P>0.05), but the CC and the CG genotype frequencies of PECAM-1 gene C373G were significantly different between them (P<0.05). The relative risk for preeclampsia of CG genotype was 1.959 folds of that in CC genotype carriers (OR=1.959, 95%CI: 1.090-3.520, P=0.024), and this association still existed after adjustment for age, gravidity, parity and BMI in logistic regression models. The C373G allele frequencies showed no significant difference between the two groups (P>0.05).

CONCLUSIONS

The CG genotype of PECAM-1 gene C373G genetically predispose the carriers to preeclampsia, while ICAM-1gene K469E polymorphisms is not associated with preeclampsia.

摘要

目的

探讨细胞间黏附分子-1(ICAM-1)基因K469E和血小板内皮细胞黏附分子-1(PECAM-1)基因C373G的基因型及等位基因频率在子痫前期患者中的分布情况。

方法

采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)及DNA测序技术,检测110例子痫前期患者和110例血压正常孕妇的ICAM-1基因K469E及PECAM-1基因C373G基因型,并分析其临床特征。

结果

观察到的基因型频率与预期基因型频率分布符合Hardy-Weinberg平衡。两组间ICAM-1基因K469E的基因型及等位基因频率差异无统计学意义(P>0.05),但PECAM-1基因C373G的CC和CG基因型频率在两组间差异有统计学意义(P<0.05)。CG基因型子痫前期的相对风险是CC基因型携带者的1.959倍(OR=1.959,95%CI:1.090-3.520,P=0.024),且在logistic回归模型中校正年龄、孕周、产次及BMI后该关联仍然存在。两组间C373G等位基因频率差异无统计学意义(P>0.05)。

结论

PECAM-1基因C373G的CG基因型使携带者具有子痫前期的遗传易感性,而ICAM-1基因K469E多态性与子痫前期无关。

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