Evidence map›Paper›PMID 36013052›Full record

ArticleJournal of clinical medicine2022

Expression of ABCA1 Transporter and LXRA/LXRB Receptors in Placenta of Women with Late Onset Preeclampsia.

Hubert Wolski, Marcin Ożarowski, Grażyna Kurzawińska, Anna Bogacz, Marlena Wolek, Małgorzata Łuszczyńska, Krzysztof Drews, Aleksandra E Mrozikiewicz, Przemysław Ł Mikołajczak, Radosław Kujawski and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Subtype specific immune-metabolic reprogramming in preeclampsia revealed by multiomics and serum biomarkers.Hypertension research : official journal of the Japanese Society of Hypertension · 2026
    Article
  2. Review
  3. Review
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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

13 authors at 2 institutions in 1 country.

Hubert WolskiDivision of Perinatology and Women's Disease, Poznań University of Medical Sciences, 61-701 Poznan, Poland.
Marcin OżarowskiDepartment of Biotechnology, Institute of Natural Fibres and Medicinal Plants, 60-630 Poznan, Poland.ORCID 0000-0003-2305-3116
Grażyna KurzawińskaDivision of Perinatology and Women's Disease, Poznań University of Medical Sciences, 61-701 Poznan, Poland.
Anna BogaczDepartment of Stem Cells and Regenerative Medicine, Institute of Natural Fibres and Medicinal Plants, 60-630 Poznan, Poland.ORCID 0000-0001-5455-8315
Marlena WolekDepartment of Stem Cells and Regenerative Medicine, Institute of Natural Fibres and Medicinal Plants, 60-630 Poznan, Poland.
Małgorzata ŁuszczyńskaDepartment of Stem Cells and Regenerative Medicine, Institute of Natural Fibres and Medicinal Plants, 60-630 Poznan, Poland.
Krzysztof DrewsDivision of Perinatology and Women's Disease, Poznań University of Medical Sciences, 61-701 Poznan, Poland.
Aleksandra E MrozikiewiczDepartment of Infertility and Reproductive Endocrinology, Poznań University of Medical Sciences, 61-701 Poznan, Poland.
Przemysław Ł MikołajczakDepartment of Pharmacology, Poznań University of Medical Sciences, 61-701 Poznan, Poland.ORCID 0000-0002-1252-6523
Radosław KujawskiDepartment of Pharmacology, Poznań University of Medical Sciences, 61-701 Poznan, Poland.ORCID 0000-0002-2389-0689
Bogusław CzernyDepartment of Stem Cells and Regenerative Medicine, Institute of Natural Fibres and Medicinal Plants, 60-630 Poznan, Poland.
Tomasz M KarpińskiDepartment of Medical Microbiology, Poznań University of Medical Sciences, 61-701 Poznan, Poland.ORCID 0000-0001-6599-9204
Agnieszka Seremak-MrozikiewiczDivision of Perinatology and Women's Disease, Poznań University of Medical Sciences, 61-701 Poznan, Poland.
Poznan University of Medical Sciences · PLInstitute of Natural Fibres and Medicinal Plants · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAppropriate levels of cholesterol are necessary for the mother and developing fetus, but theirexcess may cause preeclampsia. The ABCA1 transporter mediates the secretion of cholesterol and is highly regulated at the transcriptional level via the nuclear liver X receptors (LXRs).

methodsSixteen preeclamptic and 39 normotensives healthy women with uncomplicated pregnancies were involved in the case-control study. The placental levels of ABCA1, LXRA and LXRB mRNA were quantified by real-time quantitative PCR. The concentrations of ABCA1, LXRA and LXRB proteins from the placenta were determined using an enzyme-linked immunosorbent assay Results: We found in the logistic regression model significantly lower placental expression of LXRB mRNA (crude OR = 0.26, 95% CI: 0.07-0.94,

conclusionsOur results suggest that high placenta LXRA mRNA and LXRA protein expression levels decrease the risk of late-onset preeclampsia. These nuclear receptors could play a role in the development of preeclampsia through disturbances of lipid metabolism.

Indexed as

adenosine triphosphate-binding cassette transporter A1 (ABCA1)gene expressionliver X receptors (LXRs)preeclampsia (PE)protein level

Identifiers

PMID36013052
PMCPMC9410380
OpenAlexW4292163451

What OpenQuestion holds

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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.