Evidence map›Paper›PMID 40804017›Full record

ArticlePrenatal diagnosis2025

The Value of Enhancing Sonographic Phenotyping to Improve the Diagnostic Yield of Noninvasive Prenatal Diagnosis (NIPD) for Achondroplasia.

Camille Verebi, Victor Gravrand, Claire Guerini, Olivia Anselem, Nicolas Vaucouleur, Lucie Orhant Boimard, Rachida Ben Ouazzou, Ceren Demirtas, France Leturcq, Thierry Bienvenu and 3 more

Abstract read
In one paragraph

Article in Prenatal diagnosis, 2025. 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. 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

13 authors.

Camille VerebiService de Médecine Génomique des maladies de système et d'organe, Fédération de Génétique et de Médecine Génomique, AP-HP.Centre-Université de Paris, Hôpital Cochin, Paris, France.ORCID 0000-0002-0524-4827
Victor GravrandService de Médecine Génomique des maladies de système et d'organe, Fédération de Génétique et de Médecine Génomique, AP-HP.Centre-Université de Paris, Hôpital Cochin, Paris, France.
Claire GueriniMaternité Port Royal, CPDPN de Cochin Port Royal, Service d'obstétrique, AP-HP.Centre-Université de Paris, Hôpital Cochin, Paris, France.
Olivia AnselemMaternité Port Royal, CPDPN de Cochin Port Royal, Service d'obstétrique, AP-HP.Centre-Université de Paris, Hôpital Cochin, Paris, France.ORCID 0000-0002-1516-3203
Nicolas VaucouleurService de Médecine Génomique des maladies de système et d'organe, Fédération de Génétique et de Médecine Génomique, AP-HP.Centre-Université de Paris, Hôpital Cochin, Paris, France.
Lucie Orhant BoimardService de Médecine Génomique des maladies de système et d'organe, Fédération de Génétique et de Médecine Génomique, AP-HP.Centre-Université de Paris, Hôpital Cochin, Paris, France.
Rachida Ben OuazzouService de Médecine Génomique des maladies de système et d'organe, Fédération de Génétique et de Médecine Génomique, AP-HP.Centre-Université de Paris, Hôpital Cochin, Paris, France.
Ceren DemirtasService de Médecine Génomique des maladies de système et d'organe, Fédération de Génétique et de Médecine Génomique, AP-HP.Centre-Université de Paris, Hôpital Cochin, Paris, France.
France LeturcqService de Médecine Génomique des maladies de système et d'organe, Fédération de Génétique et de Médecine Génomique, AP-HP.Centre-Université de Paris, Hôpital Cochin, Paris, France.
Thierry BienvenuService de Médecine Génomique des maladies de système et d'organe, Fédération de Génétique et de Médecine Génomique, AP-HP.Centre-Université de Paris, Hôpital Cochin, Paris, France.
Vassilis TsatsarisMaternité Port Royal, CPDPN de Cochin Port Royal, Service d'obstétrique, AP-HP.Centre-Université de Paris, Hôpital Cochin, Paris, France.
Emmanuelle PannierMaternité Port Royal, CPDPN de Cochin Port Royal, Service d'obstétrique, AP-HP.Centre-Université de Paris, Hôpital Cochin, Paris, France.
Juliette NectouxService de Médecine Génomique des maladies de système et d'organe, Fédération de Génétique et de Médecine Génomique, AP-HP.Centre-Université de Paris, Hôpital Cochin, Paris, France.ORCID 0000-0001-5584-1112

Funding

Agence de la Biomédecine 22AMP009Agence de la Biomédecine R13188KKAssociation Vaincre la Mucoviscidose RC20160501509Association Vaincre la Mucoviscidose RC20200502668
6 · The paper itself

Abstract

objectivesAchondroplasia is the most common form of skeletal dysplasia and is usually suspected in the third trimester of pregnancy based on abnormal sonographic findings. Non-invasive prenatal diagnosis (NIPD), based on the detection of pathogenic FGFR3 variants in maternal plasma, provides an accurate genetic confirmation. The aim of this study was to identify the sonographic markers most strongly associated with achondroplasia, with the intention of enhancing the specificity of NIPD referrals and improving diagnostic efficiency, thereby supporting clinicians in their diagnostic approach.

methodsA retrospective cohort study was conducted on 275 NIPD tests performed in the laboratory between 2017 and 2023. Of these, 176 were requested due to sonographic abnormalities suggestive of achondroplasia. Sonographic reports were systematically reviewed to identify key ultrasound features correlated with a positive NIPD result.

resultsAmong the NIPD tests ordered due to sonographic anomalies, 34.1% were confirmed positive for achondroplasia. Abnormal proximal end of the femur, frontal bossing, and a pronounced nasal saddle were the most specific markers, achieving a diagnostic yield of 87.5% when all three features were present. In contrast, short femur length alone had a poor diagnostic yield (8.9%).

conclusionTargeted sonographic phenotyping significantly improves the diagnostic yield of NIPD for achondroplasia. These findings support the need for more refined prenatal screening guidelines to enhance test specificity and optimise patient care as new achondroplasia treatments emerge.

Indexed as

AchondroplasiaNoninvasive Prenatal TestingUltrasonography, PrenatalAdultCohort StudiesFemaleHumansPhenotypePregnancyReceptor, Fibroblast Growth Factor, Type 3Retrospective StudiesFGFR3 protein, humanReceptor, Fibroblast Growth Factor, Type 3achondroplasiaFGFR3noninvasive prenatal diagnosisprenatal screeningultrasound phenotyping

Identifiers

PMID40804017
PMCPMC12530346

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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.