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血清血管生成素-1、血管生成素-2 及其受体 Tie-2 和 PAI-1 基因 4G/5G 变异体在子痫前期发病机制中的作用如何?

Do serum angiopoietin-1, angiopoietin-2, and their receptor Tie-2 and 4G/5G variant of PAI-1 gene have a role in the pathogenesis of preeclampsia?

机构信息

Department of Clinical and Chemical Pathology, Cairo University, Cairo, Egypt.

出版信息

J Investig Med. 2011 Oct;59(7):1147-50. doi: 10.2310/JIM.0b013e31822c5bdf.

Abstract

OBJECTIVE

To evaluate whether serum angiogenesis markers such as angiopoietins (Ang-1, Ang-2) and their receptor (Tie-2) are altered in women with preeclampsia. We also performed genotyping to determine if the 4G/5G genotypes of -675 PAI-1 gene may play a role in the pathogenesis of preeclampsia.

MATERIALS AND METHODS

Sixty-eight pregnant women with preeclampsia were compared to 35 normotensive pregnant women and 24 normotensive nonpregnant women in a cross-sectional study. Using enzyme-linked immunosorbent assay, levels of serum Ang-1 and Ang-2, and Tie-2 were measured. A single base pair insertion/deletion 4G/5G polymorphism of the PAI-1 gene was determined by polymerase chain reaction.

RESULTS

Serum levels of Ang-1 and Tie-2 were significantly different among the study groups (P = 0.001 and P = 0.025, respectively) being lower in the preeclamptic group. Positive significant correlation was found between Ang-2 and Tie-2, (r = 0.26, P = 0.024). The frequency of the genotypes (4G/5G, 4G/4G, and 5G/5G) differed among the groups (P = 0.001). Also, the mean of systolic and diastolic blood pressures differed significantly according to the PAI-1 genotype being higher in those bearing the 4G allele; P = 0.04 and P = 0.023, respectively.

CONCLUSION

Sera Ang-1 and Ang-2, and Tie-2 as well as variants of 4G/5G of PAI-1 polymorphism have positive implications in the pathogenesis of preeclampsia.

摘要

目的

评估血管生成标志物(如血管生成素 1、2 和其受体 Tie-2)在子痫前期妇女中是否发生改变。我们还进行了基因分型,以确定 PAI-1 基因 -675 位 4G/5G 基因型是否在子痫前期发病机制中起作用。

材料与方法

在一项横断面研究中,我们将 68 例子痫前期孕妇与 35 例正常血压孕妇和 24 例正常血压未孕妇女进行比较。采用酶联免疫吸附法测定血清 Ang-1 和 Ang-2、Tie-2 水平。采用聚合酶链反应测定 PAI-1 基因单碱基插入/缺失 4G/5G 多态性。

结果

研究组之间血清 Ang-1 和 Tie-2 水平差异有统计学意义(P=0.001 和 P=0.025),子痫前期组水平较低。Ang-2 和 Tie-2 之间存在正相关(r=0.26,P=0.024)。各组间基因型(4G/5G、4G/4G 和 5G/5G)频率不同(P=0.001)。此外,根据 PAI-1 基因型,收缩压和舒张压的平均值也有显著差异,携带 4G 等位基因的患者更高;P=0.04 和 P=0.023。

结论

血清 Ang-1、Ang-2 和 Tie-2 以及 PAI-1 多态性 4G/5G 变异与子痫前期的发病机制有关。

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