Evidence map›Paper›PMID 39367038›Full record

ArticleScientific reports2024

Development of non-invasive biomarkers for pre-eclampsia through data-driven cardiovascular network models.

Claudia Popp, Jason M Carson, Alex B Drysdale, Hari Arora, Edward D Johnstone, Jenny E Myers, Raoul van Loon

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. High frame ratebioRxiv : the preprint server for biology · 2026
    Article
  2. Article
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.

Claudia PoppBiomedical Engineering Simulation and Testing Lab, Department of Biomedical Engineering, Faculty of Science and Engineering, Swansea University, Swansea, SA1 8EN, UK.
Jason M CarsonBiomedical Engineering Simulation and Testing Lab, Department of Biomedical Engineering, Faculty of Science and Engineering, Swansea University, Swansea, SA1 8EN, UK.
Alex B DrysdaleBiomedical Engineering Simulation and Testing Lab, Department of Biomedical Engineering, Faculty of Science and Engineering, Swansea University, Swansea, SA1 8EN, UK.
Hari AroraBiomedical Engineering Simulation and Testing Lab, Department of Biomedical Engineering, Faculty of Science and Engineering, Swansea University, Swansea, SA1 8EN, UK.
Edward D JohnstoneDivision of Developmental Biology, Maternal and Fetal Health Research Centre, Faculty of Medicine Biology and Health, University of Manchester, Manchester, UK.
Jenny E MyersDivision of Developmental Biology, Maternal and Fetal Health Research Centre, Faculty of Medicine Biology and Health, University of Manchester, Manchester, UK.
Raoul van LoonBiomedical Engineering Simulation and Testing Lab, Department of Biomedical Engineering, Faculty of Science and Engineering, Swansea University, Swansea, SA1 8EN, UK. r.vanloon@swansea.ac.uk.

Funding

Wellcome Trust
6 · The paper itself

Abstract

Computational models can be at the basis of new powerful technologies for studying and classifying disorders like pre-eclampsia, where it is difficult to distinguish pre-eclamptic patients from non-pre-eclamptic based on pressure when patients have a track record of hypertension. Computational models now enable a detailed analysis of how pregnancy affects the cardiovascular system. Therefore, new non-invasive biomarkers were developed that can aid the classification of pre-eclampsia through the integration of six different measured non-invasive cardiovascular signals. Datasets of 21 pregnant women (no early onset pre-eclampsia, n = 12; early onset pre-eclampsia, n = 9) were used to create personalised cardiovascular models through computational modelling resulting in predictions of blood pressure and flow waveforms in all major and minor vessels of the utero-ovarian system. The analysis performed revealed that the new predictors PPI (pressure pulsatility index) and RI (resistance index) calculated in arcuate and radial/spiral arteries are able to differentiate between the 2 groups of women (t-test scores of p < .001) better than PI (pulsatility index) and RI (Doppler calculated in the uterine artery) for both supervised and unsupervised classification. In conclusion, two novel high-performing biomarkers for the classification of pre-eclampsia have been identified based on blood velocity and pressure predictions in the smaller placental vasculatures where non-invasive measurements are not feasible.

Indexed as

BiomarkersPre-EclampsiaAdultBlood Flow VelocityBlood PressureFemaleHumansModels, CardiovascularPregnancyBiomarkersClinical diagnosisDigital twinHypertensionMachine learningPregnancyPulse wave velocityUterine doppler waveforms

Identifiers

PMID39367038
PMCPMC11452701

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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.