Evidence map›Paper›PMID 37108840›Full record

ReviewInternational journal of molecular sciences2023

Biochemical Screening for Fetal Trisomy 21: Pathophysiology of Maternal Serum Markers and Involvement of the Placenta.

Jean Guibourdenche, Marie-Clémence Leguy, Guillaume Pidoux, Marylise Hebert-Schuster, Christelle Laguillier, Olivia Anselem, Gilles Grangé, Fidéline Bonnet, Vassilis Tsatsaris

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
9.3field-weighted citation impact, top 2% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Combined triple screening and BMI models for gestational diabetes prediction.Turkish journal of obstetrics and gynecology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. PAPPA's role in female reproduction.Reproduction (Cambridge, England) · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Placental Related Disorders of Pregnancy 2.0.International journal of molecular sciences · 2023
    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

9 authors at 4 institutions in 1 country.

Jean GuibourdencheHormonologie CHU Cochin AP-HP, 75014 Paris, France.ORCID 0000-0003-3968-6890
Marie-Clémence LeguyHormonologie CHU Cochin AP-HP, 75014 Paris, France.
Guillaume PidouxINSERM UMR-S1180, 75014 Paris, France.ORCID 0000-0002-5074-429X
Marylise Hebert-SchusterFaculté de Santé, Université Paris Cité, 75014 Paris, France.ORCID 0000-0002-8221-4023
Christelle LaguillierHormonologie CHU Cochin AP-HP, 75014 Paris, France.ORCID 0000-0002-2704-9774
Olivia AnselemFHU Préma, 75014 Paris, France.
Gilles GrangéFHU Préma, 75014 Paris, France.
Fidéline BonnetHormonologie CHU Cochin AP-HP, 75014 Paris, France.
Vassilis TsatsarisFaculté de Santé, Université Paris Cité, 75014 Paris, France.
Université Paris Cité · FRAssistance Publique – Hôpitaux de Paris · FRHôpital Cochin · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is now well established that maternal serum markers are often abnormal in fetal trisomy 21. Their determination is recommended for prenatal screening and pregnancy follow-up. However, mechanisms leading to abnormal maternal serum levels of such markers are still debated. Our objective was to help clinicians and scientists unravel the pathophysiology of these markers via a review of the main studies published in this field, both in vivo and in vitro, focusing on the six most widely used markers (hCG, its free subunit hCGβ, PAPP-A, AFP, uE3, and inhibin A) as well as cell-free feto-placental DNA. Analysis of the literature shows that mechanisms underlying each marker's regulation are multiple and not necessarily directly linked with the supernumerary chromosome 21. The crucial involvement of the placenta is also highlighted, which could be defective in one or several of its functions (turnover and apoptosis, endocrine production, and feto-maternal exchanges and transfer). These defects were neither constant nor specific for trisomy 21, and might be more or less pronounced, reflecting a high variability in placental immaturity and alteration. This explains why maternal serum markers can lack both specificity and sensitivity, and are thus restricted to screening.

Indexed as

Down SyndromeBiomarkersChorionic Gonadotropin, beta Subunit, HumanFemaleHumansPlacentaPregnancyPregnancy-Associated Plasma Protein-APrenatal DiagnosisTrisomyBiomarkersChorionic Gonadotropin, beta Subunit, HumanPregnancy-Associated Plasma Protein-Acell free fetal DNAfetal aneuploidyhCGhCG free β subunitinhibin Amaternal bloodPAPP-Aplacentaprenatal screeningunconjugated estriol

Identifiers

PMID37108840
PMCPMC10146970
OpenAlexW4366833039

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.