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MOV10 多态性及其表达水平与中国汉族人群子痫前期的相关性研究。

The association of MOV10 polymorphism and expression levels with preeclampsia in the Chinese Han population.

机构信息

Medical Genetic Department, the Affiliated Hospital of Qingdao University, Qingdao, China.

Prenatal Diagnosis Center, the Affiliated Hospital of Qingdao University, Qingdao, China.

出版信息

Mol Genet Genomic Med. 2021 Jan;9(1):e1564. doi: 10.1002/mgg3.1564. Epub 2020 Dec 2.

DOI:10.1002/mgg3.1564
PMID:33269545
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7963431/
Abstract

BACKGROUND

To assess the relationship between MOV10 rs2932538 polymorphism and susceptibility to preeclampsia (PE) in the Chinese Han population and to investigate whether the placental expression of MOV10 have association with PE.

METHODS

We enrolled 1021 pregnant women with PE and 1594 normotensive pregnant women to analyze genotyping of MOV10 rs2932538. Clinical data and related test results of all subjects were collected and analyzed. For volunteers providing placentas, real-time PCR, Western blot, and immunohistochemistry were applied to assess the expression level of MOV10.

RESULTS

There was significant statistical difference between preeclamptic patients and healthy subjects in genotype distributions and alleles. The frequencies of genotypes TT+CT were significantly associated with the increased risk of preeclampsia. Besides, T alleles were found to be related to a higher risk of PE. Significant statistical difference was also observed on distributions of genotype in PE without/with severe features group compared or early onset/late onset versus controls. The placental expression of MOV10 was lower in preeclamptic women, however, no relationship was found between MOV10 expression level and MOV10 rs2932538 genotypes.

CONCLUSION

This study suggests that MOV10 rs2932538 polymorphism may be associated with PE susceptibility in the Chinese Han population. The placental expression of MOV10 decrease in PE but have no relationship with rs2932538 polymorphism.

摘要

背景

评估 MOV10 rs2932538 多态性与中国汉族人群先兆子痫易感性的关系,并探讨胎盘 MOV10 的表达是否与先兆子痫有关。

方法

我们纳入了 1021 例先兆子痫孕妇和 1594 例正常血压孕妇进行 MOV10 rs2932538 基因分型分析。收集并分析所有受试者的临床资料和相关检测结果。对于提供胎盘的志愿者,应用实时 PCR、Western blot 和免疫组化法评估 MOV10 的表达水平。

结果

先兆子痫患者与健康受试者在基因型分布和等位基因上存在显著统计学差异。TT+CT 基因型的频率与先兆子痫的发病风险增加显著相关。此外,T 等位基因与 PE 的发病风险增加有关。在无/有严重特征的 PE 组与对照组、早发/晚发与对照组之间,基因型的分布也存在显著统计学差异。先兆子痫患者的胎盘 MOV10 表达降低,但 MOV10 表达水平与 MOV10 rs2932538 基因型之间无相关性。

结论

本研究提示 MOV10 rs2932538 多态性可能与中国汉族人群的先兆子痫易感性相关。PE 患者胎盘 MOV10 的表达降低,但与 rs2932538 多态性无相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e76/7963431/9941086e728a/MGG3-9-e1564-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e76/7963431/1df104e6ad19/MGG3-9-e1564-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e76/7963431/524965c5c7fb/MGG3-9-e1564-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e76/7963431/9941086e728a/MGG3-9-e1564-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e76/7963431/1df104e6ad19/MGG3-9-e1564-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e76/7963431/524965c5c7fb/MGG3-9-e1564-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e76/7963431/9941086e728a/MGG3-9-e1564-g004.jpg

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