Evidence map›Paper›PMID 33269545›Full record

ArticleMolecular genetics & genomic medicine2021

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

Qian Tang, Ling Wang, Renmei Cai, Lu Zhang, Xiaoxiao Zhang, Xuemei Liu, Shiguo Liu

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics & genomic medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 34% of its field
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Unwinding the roles of RNA helicase MOV10.Wiley interdisciplinary reviews. RNA · 2022
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Qian TangMedical Genetic Department, the Affiliated Hospital of Qingdao University, Qingdao, China.ORCID 0000-0001-8221-005X
Ling WangDepartment of Nephrology, the Affiliated Hospital of Qingdao University, Qingdao, China.
Renmei CaiPrenatal Diagnosis Center, Qingdao Municipal Hospital, Qingdao, China.
Lu ZhangMedical Genetic Department, the Affiliated Hospital of Qingdao University, Qingdao, China.
Xiaoxiao ZhangDepartment of Nephrology, the Affiliated Hospital of Qingdao University, Qingdao, China.
Xuemei LiuDepartment of Nephrology, the Affiliated Hospital of Qingdao University, Qingdao, China.
Shiguo LiuMedical Genetic Department, the Affiliated Hospital of Qingdao University, Qingdao, China.
Qingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo 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.

methodsWe 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.

resultsThere 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.

conclusionThis 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.

Indexed as

Polymorphism, Single NucleotideAdultChinaFemaleHumansPlacentaPre-EclampsiaPregnancyRNA HelicasesMov10 protein, humanRNA HelicasesexpressionMoloney leukemia virus 10placentapolymorphismpreeclampsia

Identifiers

PMID33269545
PMCPMC7963431
OpenAlexW3110325868

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.