Evidence map›Paper›PMID 36351970›Full record

ArticleScientific reports2022

Maternal plasma proteome profiling of biomarkers and pathogenic mechanisms of early-onset and late-onset preeclampsia.

Hao Chen, Ingrid Aneman, Valentina Nikolic, Natasa Karadzov Orlic, Zeljko Mikovic, Milan Stefanovic, Zoran Cakic, Hristina Jovanovic, Stephanie E L Town, Matthew P Padula and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

20 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  9. Pathophysiological mechanisms in severe preeclampsia: role of upregulated proteins in blood pressure, extracellular matrix and immunity.Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia · 2025
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  12. Review
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  14. Predicting Preterm Birth Using Proteomics.Clinics in perinatology · 2024
    Review
  15. Article
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  17. Placenta: an old organ with new functions.Frontiers in immunology · 2024
    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

11 authors at 3 institutions in 2 countries.

Hao ChenSchool of Life Sciences, Faculty of Science, University of Technology Sydney, Ultimo, NSW, Australia.
Ingrid AnemanSchool of Life Sciences, Faculty of Science, University of Technology Sydney, Ultimo, NSW, Australia.
Valentina NikolicDepartment of Pharmacology and Toxicology, Faculty of Medicine, University of Nis, Nis, Serbia.
Natasa Karadzov OrlicDepartment of Gynaecology and Obstetrics, Narodni Front, Belgrade, Serbia.
Zeljko MikovicDepartment of Gynaecology and Obstetrics, Narodni Front, Belgrade, Serbia.
Milan StefanovicDepartment of Gynaecology and Obstetrics, Faculty of Medicine, University of Nis, Nis, Serbia.
Zoran CakicDepartment of Gynaecology and Obstetrics, General Hospital of Leskovac, Leskovac, Serbia.
Hristina JovanovicDepartment of Pharmacology and Toxicology, Faculty of Medicine, University of Nis, Nis, Serbia.
Stephanie E L TownSchool of Life Sciences, Faculty of Science, University of Technology Sydney, Ultimo, NSW, Australia.
Matthew P PadulaSchool of Life Sciences, Faculty of Science, University of Technology Sydney, Ultimo, NSW, Australia. matthew.padula@uts.edu.au.
Lana McClementsSchool of Life Sciences, Faculty of Science, University of Technology Sydney, Ultimo, NSW, Australia. lana.mcclements@uts.edu.au.
University of Technology Sydney · AUUniversity of Nis · RSUniversity of Belgrade · RS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Preeclampsia is still the leading cause of morbidity and mortality in pregnancy without a cure. There are two phenotypes of preeclampsia, early-onset (EOPE) and late-onset (LOPE) with poorly defined pathogenic differences. This study aimed to facilitate better understanding of the mechanisms of pathophysiology of EOPE and LOPE, and identify specific biomarkers or therapeutic targets. In this study, we conducted an untargeted, label-free quantitative proteomic analyses of plasma samples from pregnant women with EOPE (n = 17) and LOPE (n = 11), and age, BMI-matched normotensive controls (n = 18). Targeted proteomics approach was also employed to validate a subset of proteins (n = 17). In total, there were 26 and 20 differentially abundant proteins between EOPE or LOPE, and normotensive controls, respectively. A series of angiogenic and inflammatory proteins, including insulin-like growth factor-binding protein 4 (IGFBP4; EOPE: FDR = 0.0030 and LOPE: FDR = 0.00396) and inter-alpha-trypsin inhibitor heavy chain H2-4 (ITIH2-4), were significantly altered in abundance in both phenotypes. Through validation we confirmed that ITIH2 was perturbed only in LOPE (p = 0.005) whereas ITIH3 and ITIH4 were perturbed in both phenotypes (p < 0.05). Overall, lipid metabolism/transport proteins associated with atherosclerosis were highly abundant in LOPE, however, ECM proteins had a more pronounced role in EOPE. The complement cascade and binding and uptake of ligands by scavenger receptors, pathways, were associated with both EOPE and LOPE.

Indexed as

Pre-EclampsiaBiomarkersEosine Yellowish-(YS)FemaleHumansPhosphatidylethanolaminesPregnancyProteomeProteomicsBiomarkersEosine Yellowish-(YS)eosinylphosphatidylethanolaminePhosphatidylethanolaminesProteome

Identifiers

PMID36351970
PMCPMC9646706
OpenAlexW4308735430

What OpenQuestion 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 OpenQuestion graph.