Evidence map›Paper›PMID 31530576›Full record

ArticleJournal of lipid research2019

Metabolism of cholesterol and progesterone is differentially regulated in primary trophoblastic subtypes and might be disturbed in recurrent miscarriages.

Sigrid Vondra, Victoria Kunihs, Tanja Eberhart, Karin Eigner, Raimund Bauer, Peter Haslinger, Sandra Haider, Karin Windsperger, Günter Klambauer, Birgit Schütz and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
8.2field-weighted citation impact, top 2% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

  1. Pooled it
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  8. Article
  9. Review
  10. Exposure to Extreme Heat Increases Preterm Birth Risk: Hypothetical Pathophysiological Mechanisms.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  11. Article
  12. Article
  13. The multifaceted roles of the transcriptional coactivator TAZ in extravillous trophoblast development of the human placenta.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  14. Review
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  16. Evidence for hypoxia-induced dysregulated cholesterol homeostasis in preeclampsia: Insights into the mechanisms from human placental cells and tissues.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
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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

19 authors at 4 institutions in 2 countries.

Sigrid VondraDepartment of Obstetrics and Gynecology, Reproductive Biology Unit, Center for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria.
Victoria KunihsDepartment of Obstetrics and Gynecology, Reproductive Biology Unit, Center for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria.
Tanja EberhartDepartments of Medical Chemistry Center for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-3621-5594
Karin EignerDepartments of Medical Chemistry Center for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria.
Raimund BauerDepartments of Medical Chemistry Center for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria.
Peter HaslingerDepartment of Obstetrics and Gynecology, Reproductive Biology Unit, Center for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria.
Sandra HaiderDepartment of Obstetrics and Gynecology, Reproductive Biology Unit, Center for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria.
Karin WindspergerDepartment of Obstetrics and Gynecology, Reproductive Biology Unit, Center for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria.
Günter KlambauerInstitute of Machine Learning, Johannes Kepler University Linz, Linz, Austria.
Birgit SchützMedical Genetics, Center for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria.
Mario MikulaMedical Genetics, Center for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria.
Xiaowei ZhuDepartments of Psychiatry Stanford University School of Medicine, Stanford, CA.
Alexander E UrbanDepartments of Psychiatry Stanford University School of Medicine, Stanford, CA.
Roberta L HannibalGenetics, Stanford University School of Medicine, Stanford, CA.
Julie BakerGenetics, Stanford University School of Medicine, Stanford, CA.
Martin KnöflerDepartment of Obstetrics and Gynecology, Reproductive Biology Unit, Center for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria.
Herbert StanglDepartments of Medical Chemistry Center for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria.
Jürgen PollheimerDepartment of Obstetrics and Gynecology, Reproductive Biology Unit, Center for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria clemens.roehrl@fh-wels.at juergen.pollheimer@meduniwien.ac.at.
Clemens RöhrlDepartments of Medical Chemistry Center for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria clemens.roehrl@fh-wels.at juergen.pollheimer@meduniwien.ac.at.ORCID 0000-0002-1192-0748
Medical University of Vienna · ATStanford University · USJohannes Kepler University of Linz · ATUniversity of Applied Sciences Upper Austria · AT

Funding

Austrian Science Fund FWF P 31470
6 · The paper itself

Abstract

During pregnancy, extravillous trophoblasts (EVTs) invade the maternal decidua and remodel the local vasculature to establish blood supply for the growing fetus. Compromised EVT function has been linked to aberrant pregnancy associated with maternal and fetal morbidity and mortality. However, metabolic features of this invasive trophoblast subtype are largely unknown. Using primary human trophoblasts isolated from first trimester placental tissues, we show that cellular cholesterol homeostasis is differentially regulated in EVTs compared with villous cytotrophoblasts. Utilizing RNA-sequencing, gene set-enrichment analysis, and functional validation, we provide evidence that EVTs display increased levels of free and esterified cholesterol. Accordingly, EVTs are characterized by increased expression of the HDL-receptor, scavenger receptor class B type I, and reduced expression of the LXR and its target genes. We further reveal that EVTs express elevated levels of hydroxy-delta-5-steroid dehydrogenase 3 beta- and steroid delta-isomerase 1 (HSD3B1) (a rate-limiting enzyme in progesterone synthesis) and are capable of secreting progesterone. Increasing cholesterol export by LXR activation reduced progesterone secretion in an ABCA1-dependent manner. Importantly, HSD3B1 expression was decreased in EVTs of idiopathic recurrent spontaneous abortions, pointing toward compromised progesterone metabolism in EVTs of early miscarriages. Here, we provide insights into the regulation of cholesterol and progesterone metabolism in trophoblastic subtypes and its putative relevance in human miscarriage.

Indexed as

Abortion, HabitualCholesterolComputational BiologyFemaleHomeostasisHumansPregnancyProgesteroneSequence Analysis, RNATrophoblastsCholesterolProgesteroneadenosine 5′-triphosphate binding cassette transporter A1early miscarriageHSD3B1nuclear receptor/liver X receptorplacentarecurrent spontaneous abortionscavenger receptor class B type Itrophoblast

Identifiers

PMID31530576
PMCPMC6824492
OpenAlexW2974754276

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.