Evidence map›Paper›PMID 38396719›Full record

ArticleInternational journal of molecular sciences2024

Overexpression of Human sFLT1 in the Spongiotrophoblast Is Sufficient to Induce Placental Dysfunction and Fetal Growth Restriction in Transgenic Mice.

Rebekka Vogtmann, Alina Riedel, Ivanka Sassmannshausen, Sarah Langer, Elisabeth Kühnel-Terjung, Rainer Kimmig, Hubert Schorle, Elke Winterhager, Alexandra Gellhaus

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
3.5field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
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  5. 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

9 authors at 2 institutions in 1 country.

Rebekka VogtmannDepartment of Gynecology and Obstetrics, University Hospital, 45147 Essen, Germany.
Alina RiedelDepartment of Gynecology and Obstetrics, University Hospital, 45147 Essen, Germany.ORCID 0009-0000-3404-2573
Ivanka SassmannshausenDepartment of Gynecology and Obstetrics, University Hospital, 45147 Essen, Germany.
Sarah LangerDepartment of Gynecology and Obstetrics, University Hospital, 45147 Essen, Germany.
Elisabeth Kühnel-TerjungDepartment of Gynecology and Obstetrics, University Hospital, 45147 Essen, Germany.
Rainer KimmigDepartment of Gynecology and Obstetrics, University Hospital, 45147 Essen, Germany.
Hubert SchorleDepartment of Developmental Pathology, Institute of Pathology, University Hospital Bonn, 53127 Bonn, Germany.ORCID 0000-0001-8272-0076
Elke WinterhagerEM Unit, Imaging Center Essen, University Hospital, 45147 Essen, Germany.
Alexandra GellhausDepartment of Gynecology and Obstetrics, University Hospital, 45147 Essen, Germany.ORCID 0000-0001-9506-4581
Essen University Hospital · DEUniversity Hospital Bonn · DE

Funding

Deutsche Forschungsgemeinschaft 491780329Deutsche Forschungsgemeinschaft Scho 503/27-1Mercator Research Center Ruhr An-2015-0009University of Duisburg-Essen D/107-81240University of Duisburg-Essen Open Acess Fund
6 · The paper itself

Abstract

Preeclampsia (PE) is characterized by maternal hypertension and placental dysfunction, often leading to fetal growth restriction (FGR). It is associated with an overexpression of the anti-angiogenic sFLT1 protein, which originates from the placenta and serves as a clinical biomarker to predict PE. To analyze the impact of sFLT1 on placental function and fetal growth, we generated transgenic mice with placenta-specific human sFLT1 (hsFLT1) overexpression. Immunohistochemical, morphometrical, and molecular analyses of the placentas on 14.5 dpc and 18.5 dpc were performed with a focus on angiogenesis, nutrient transport, and inflammation. Additionally, fetal development upon placental hsFLT1 overexpression was investigated. Dams exhibited a mild increase in serum hsFLT1 levels upon placental hsFLT1 expression and revealed growth restriction of the fetuses in a sex-specific manner. Male FGR fetuses expressed higher amounts of placental

Indexed as

Fetal Growth RetardationPre-EclampsiaAnimalsFemaleHumansInflammationMaleMiceMice, TransgenicPlacentaPregnancyVascular Endothelial Growth Factor Receptor-1FLT1 protein, humanVascular Endothelial Growth Factor Receptor-1angiogenesisfetal growth restrictionplacentapreeclampsiapregnancysFLT1spongiotrophoblasttransgenic mouse model

Identifiers

PMID38396719
PMCPMC10888837
OpenAlexW4391598196

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.