Evidence map›Paper›PMID 38241324›Full record

ArticlePloS one2024

Diagnostics of preeclampsia based on Congo red binding to urinary components: Rationales and limitations.

Sergei A Fedotov, Maria S Khrabrova, Elena S Vashukova, Andrey S Glotov, Anastasia O Anpilova, Vladimir A Dobronravov, Maria E Velizhanina, Aleksandr A Rubel

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2024. 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
0.6field-weighted citation impact, top 35% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  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

8 authors at 2 institutions in 2 countries.

Sergei A FedotovLaboratory of Amyloid Biology, Saint Petersburg University, St. Petersburg, Russia.ORCID 0000-0002-7428-120X
Maria S KhrabrovaLaboratory of Amyloid Biology, Saint Petersburg University, St. Petersburg, Russia.
Elena S VashukovaDepartment of Genomic Medicine, D.O. Ott Research Institute of Obstetrics, Gynecology and Reproductology, St. Petersburg, Russia.
Andrey S GlotovDepartment of Genomic Medicine, D.O. Ott Research Institute of Obstetrics, Gynecology and Reproductology, St. Petersburg, Russia.ORCID 0000-0002-7465-4504
Anastasia O AnpilovaLaboratory of Amyloid Biology, Saint Petersburg University, St. Petersburg, Russia.ORCID 0000-0001-8419-6909
Vladimir A DobronravovResearch Institute of Nephrology, Pavlov University, St. Petersburg, Russia.
Maria E VelizhaninaLaboratory of Amyloid Biology, Saint Petersburg University, St. Petersburg, Russia.ORCID 0000-0002-9005-527X
Aleksandr A RubelLaboratory of Amyloid Biology, Saint Petersburg University, St. Petersburg, Russia.ORCID 0000-0001-6203-2006
St Petersburg University · RUResearch Institute of Obstetrics and Gynecology named after D.O. Ott · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Preeclampsia is a disorder that can occur during pregnancy and is one of the leading causes of death among pregnant women. This disorder occurs after the 20th week of pregnancy and is characterized by arterial hypertension, proteinuria, fetoplacental, and multiple organ dysfunctions. Despite the long history of studying preeclampsia, its etiology and pathogenesis remain poorly understood, and therapy is symptomatic. One of the factors of the disorder is believed to be misfolded proteins that are prone to form amyloid aggregates. The CRD tests, utilizing the binding of the amyloid-specific dye Congo red to urine components, demonstrate high efficiency in diagnosing preeclampsia. However, these tests have also been found to be positive in other disorders with proteinuria, presumably associated with concomitant amyloidosis. To assess the limitations of the CRD tests, we examined urine congophilia and protein components mediating Congo red positivity in patients with proteinuria, including preeclampsia, amyloid and non-amyloid nephropathies. We stained the urine samples and calculated congophilia levels. We also assessed the contribution of large protein aggregates to congophilia values using ultracentrifugation and determined the molecular weights of congophilic urinary proteins using centrifugal concentrators. All proteinuric groups demonstrate positive results in the CRD tests and congophilia levels were more than two times higher compared with the control non-proteinuric groups (p <0.01). There was a strong correlation between urine protein excretion and congophilia in amyloid nephropathy (rs = 0.76), non-amyloid nephropathies (rs = 0.90), and preeclampsia (rs = 0.90). Removal of large aggregates from urine did not affect the congophilia levels. Separation of urine protein fractions revealed congophilic components in the range of 30-100 kDa, including monomeric serum albumin. Our results indicate limitations of CRD tests in preeclampsia diagnostics in women with renal disorders and underscore the need for further research on the mechanisms of Congo red binding with urine components.

Indexed as

AmyloidosisHypertensionPre-EclampsiaAmyloidAmyloidogenic ProteinsCongo RedFemaleHumansPregnancyProteinuriaAmyloidAmyloidogenic ProteinsCongo Red

Identifiers

PMID38241324
PMCPMC10798433
OpenAlexW4391019831

What OpenQuestion holds

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LicenceCC BY
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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.