Evidence map›Paper›PMID 26790664›Full record

ArticleMolecular diagnosis & therapy2016

Circulating Maternal Total Cell-Free DNA, Cell-Free Fetal DNA and Soluble Endoglin Levels in Preeclampsia: Predictors of Adverse Fetal Outcome? A Cohort Study.

Radwa Marawan AbdelHalim, Dalia Ibrahim Ramadan, Reham Zeyada, Ahmed Soliman Nasr, Iman Atef Mandour

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In one paragraph

Article in Molecular diagnosis & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
3.4field-weighted citation impact, top 9% 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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Liquid Biopsy in Adverse Neurodevelopment of Children: Problems and Prospects.Methods in molecular biology (Clifton, N.J.) · 2023
    Review
  6. Cell-free DNA as a potential biomarker for preeclampsia.Expert review of molecular diagnostics · 2021
    Article
  7. Article
  8. Article
  9. Review
  10. 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

5 authors at 1 institution in 1 country.

Radwa Marawan AbdelHalimDepartment of Clinical and Chemical Pathology, Kasr Al-ainy School of Medicine, Cairo University, Kasr Al-Ainy Street, Cairo, 11562, Egypt.
Dalia Ibrahim RamadanDepartment of Clinical and Chemical Pathology, Kasr Al-ainy School of Medicine, Cairo University, Kasr Al-Ainy Street, Cairo, 11562, Egypt. dramadan7371@yahoo.com.
Reham ZeyadaDepartment of Clinical and Chemical Pathology, Kasr Al-ainy School of Medicine, Cairo University, Kasr Al-Ainy Street, Cairo, 11562, Egypt.
Ahmed Soliman NasrDepartment of Obstetrics and Gynecology, Kasr Al-ainy School of Medicine, Cairo University, Cairo, Egypt.
Iman Atef MandourDepartment of Clinical and Chemical Pathology, Kasr Al-ainy School of Medicine, Cairo University, Kasr Al-Ainy Street, Cairo, 11562, Egypt.
Cairo University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe diagnosis of preeclampsia (PE) is based on the measurement of maternal blood pressure and proteinuria; however, these parameters are not used in the prediction of adverse fetal outcomes that may occur due to fetal stress. The plasma concentrations of total cell-free DNA (cf-DNA), cell-free fetal DNA (cff-DNA) and soluble endoglin (sEng) are higher in women with established PE than in normotensive controls, and the increase is particularly marked in those with severe PE. We aimed to evaluate the levels of cf-DNA, cff-DNA and sEng in pregnant Egyptian women with PE in order to assess the severity of the disease and to detect their potential utility in the future prediction of time of delivery and adverse fetal outcome. SUBJECTS AND

methodsThe study included 107 pregnant females with established PE during their third trimester (51 with mild PE and 56 with severe PE), together with 93 normotensive pregnant women. Absolute quantitation of the hemoglobin subunit beta (HBB) and testis-specific protein, Y-linked 1 (TSPY1) genes for the measurement of cf-DNA and cff-DNA in maternal blood, respectively, was carried out using real-time polymerase chain reaction (PCR) together with the measurement of serum sEng using ELISA.

resultsAn almost twofold increase in cf-DNA and cff-DNA was detected in the severe PE group over the mild group, and both were significantly different from the control group. Significantly higher levels of cf-DNA, cff-DNA and sEng, with variable magnitudes, were detected in the preterm labor and unfavorable fetal outcome groups compared with the term and favorable outcome groups, respectively. The three markers were almost equivalent with regard to the area under the curve for predicting adverse fetal outcome in the severe PE group. The same was also true for cf-DNA and cff-DNA within the mild PE group.

conclusionsIncorporation of cf-DNA, cff-DNA and sEng into the prenatal care service should be considered as a serious addition for the screening and detection of adverse pregnancy outcomes in view of their significant elevations in cases of preeclamptic women whose babies ultimately suffered a poor outcome.

Indexed as

AdolescentAdultbeta-GlobinsCell Cycle ProteinsCohort StudiesDNAEarly DiagnosisEndoglinFemaleHumansPre-EclampsiaPregnancyPregnancy OutcomePregnancy Trimester, FirstPrenatal DiagnosisYoung Adultbeta-GlobinsCell Cycle ProteinsDNAEndoglinENG protein, humanTSPY1 protein, human

Identifiers

PMID26790664
OpenAlexW2285039707

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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.