Evidence map›Paper›PMID 42377042›Full record

ReviewJournal of pregnancy2026

Urinary Congophilia in Pre-Eclampsia: A Potential Diagnostic Biomarker.

Mikyle David, Olive Khaliq, Anand Krishnan, Niren Maharaj

Abstract readReview
In one paragraph

Review in Journal of pregnancy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

4 authors.

Mikyle DavidDepartment of Obstetrics and Gynaecology, School of Clinical Medicine, Faculty of Health Sciences, University of the Free State, Bloemfontein, South Africa, ufs.ac.za.ORCID https://orcid.org/0000-0002-0688-157X
Olive KhaliqDepartment of Paediatrics and Child Health, School of Clinical Medicine, Faculty of Health Sciences, University of the Free State, Bloemfontein, South Africa, ufs.ac.za.ORCID https://orcid.org/0000-0002-9742-4525
Anand KrishnanDepartment of Haematology and Cell Biology, School of Pathology, Faculty of Health Sciences, University of the Free State, Bloemfontein, South Africa, ufs.ac.za.ORCID https://orcid.org/0000-0002-8886-8482
Niren MaharajDepartment of Obstetrics and Gynaecology, School of Clinical Medicine, Faculty of Health Sciences, University of the Free State, Bloemfontein, South Africa, ufs.ac.za.ORCID https://orcid.org/0000-0002-9210-9913

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimPre-eclampsia (PE) causes significant maternal and neonatal morbidity and mortality worldwide, particularly in low- and middle-income countries (LMICs). Current diagnostic methods, such as blood pressure monitoring and proteinuria measurement, have poor sensitivity and specificity. Although biomarkers like PlGF and sFlt-1 improve diagnostic accuracy, their clinical value is limited by cost and infrastructural constraints. The Congo red dot (CRD) test, which identifies misfolded proteins via urinary congophilia, has emerged as a low-cost, noninvasive alternative for detecting PE.

methodsThis review evaluated the diagnostic performance of the CRD test by synthesizing evidence from studies across diverse populations, including India, China, and South Africa. Methodologies encompassed prospective cohorts, case-control designs, and meta-analyses, with a focus on sensitivity, specificity, and comparative efficacy against conventional screening tools.

resultsResults indicate that the CRD test achieves high diagnostic accuracy, with reported specificity of 89.2% and sensitivity of 80.2%. The assay provides rapid results (< 3 min) without specialized equipment, demonstrating effectiveness in LMICs. However, performance variability was observed in late-onset PE, and comparative studies yielded conflicting data regarding its superiority over urinary dipstick analysis. Additionally, challenges persist in differentiating PE from other hypertensive disorders with overlapping proteinuria.

conclusionThe CRD test represents a promising diagnostic tool for PE in LMICS with limited access to advanced diagnostics. Further large-scale validation studies are required to standardize protocols, establish gestational age-specific thresholds, and clarify its role in differentiating PE from confounding conditions. Integration with existing biomarkers may enhance its clinical adoption and diagnostic precision.

Indexed as

Pre-EclampsiaBiomarkersCongo RedFemaleHumansPregnancySensitivity and SpecificityBiomarkersCongo RedCongo red dot testdiagnostic biomarkerslow-resource settingspre-eclampsiaurinary congophilia

Identifiers

PMID42377042
PMCPMC13317149

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.