Evidence map›Paper›PMID 40890480›Full record

ArticlePediatric research2026

Pulmonary T2* quantification of fetuses with congenital diaphragmatic hernia: a retrospective, case-controlled, MRI pilot study.

Carla L Avena-Zampieri, Alena Uus, Alexia Egloff, Joseph Davidson, Jana Hutter, Caroline L Knight, Megan Hall, Maria Deprez, Kelly Payette, Mary Rutherford and 2 more

Abstract read
In one paragraph

Article in Pediatric research, 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

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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

12 authors.

Carla L Avena-ZampieriDepartment of Women and Children's Health, King's College London, London, United Kingdom. carla.avena_zampieri@kcl.ac.uk.ORCID http://orcid.org/0000-0002-5455-2789
Alena UusBiomedical Engineering Department, School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom.
Alexia EgloffBiomedical Engineering Department, School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom.
Joseph DavidsonUniversity College London/Great Ormond Street Institute of Child Health, London, United Kingdom.
Jana HutterBiomedical Engineering Department, School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom.
Caroline L KnightDepartment of Women and Children's Health, King's College London, London, United Kingdom.
Megan HallDepartment of Women and Children's Health, King's College London, London, United Kingdom.
Maria DeprezBiomedical Engineering Department, School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom.
Kelly PayetteBiomedical Engineering Department, School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom.
Mary RutherfordBiomedical Engineering Department, School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom.
Anne GreenoughDepartment of Women and Children's Health, King's College London, London, United Kingdom.
Lisa StoryDepartment of Women and Children's Health, King's College London, London, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAdvanced MRI techniques, motion-correction and T2*-relaxometry, may provide information regarding functional properties of pulmonary tissue. We assessed whether lung volumes and pulmonary T2* values in fetuses with congenital diaphragmatic hernia (CDH) were lower than controls and differed between survivors and non-survivors.

methodsWomen with uncomplicated pregnancies (controls) and those with a CDH had a fetal MRI on a 1.5 T imaging system encompassing T2 single shot fast spin echo sequences and gradient echo single shot echo planar sequences providing T2* data. Motion-correction was performed using slice-to-volume reconstruction, T2* maps were generated using in-house pipelines. Lungs were segmented separately using a pre-trained 3D-deep-learning pipeline.

resultsDatasets from 33 controls and 12 CDH fetuses were analysed. The mean ± SD gestation at scan was 28.3 ± 4.3 for controls and 27.6 ± 4.9 weeks for CDH cases. CDH lung volumes were lower than controls in both non-survivors and survivors for both lungs combined (5.76 ± 3.59 [cc], mean difference = 15.97, 95% CI: -24.51--12.9, p < 0.001 and 5.73 ± 2.96 [cc], mean difference = 16, 95% CI: 1.91-11.53, p = 0.008) and for the ipsilateral lung (1.93 ± 2.09 [cc], mean difference = 19.8, 95% CI: -28.48--16.45, p < 0.001 1.58 ± 1.18 [cc], mean difference=20.15, 95% CI: 5.96-15.97, p < 0.001). Mean pulmonary T2* values were lower in non-survivors in both lungs, the ipsilateral and contralateral lungs compared with the control group (81.83 ± 26.21 ms, mean difference = 31.13, 95% CI: -58.14--10.32, p = 0.006; 81.05 ± 26.84 ms, mean difference = 31.91, 95% CI: -59.02--10.82, p = 0.006; 82.62 ± 36.31 ms, mean difference = 30.34, 95% CI: -58.84--8.25, p = 0.011) but no difference was observed between controls and CDH cases that survived.

conclusionsMean pulmonary T2* values were lower in CDH fetuses compared to controls and CDH cases who died compared to survivors. Mean pulmonary T2* values may have a prognostic function in CDH fetuses. IMPACT: This study provides original motion-corrected assessment of the morphologic and functional properties of the ipsilateral and contralateral fetal lungs in the context of CDH. Mean pulmonary T2* values were lower in CDH fetuses compared to controls and in cases who died compared to survivors. Mean pulmonary T2* values may have a role in prognostication. Reduction in pulmonary T2* values in CDH fetuses suggests altered pulmonary development, contributing new insights into antenatal assessment.

Indexed as

FetusHernias, Diaphragmatic, CongenitalLungMagnetic Resonance ImagingPrenatal DiagnosisCase-Control StudiesFemaleGestational AgeHumansPilot ProjectsPregnancyRetrospective Studies

Identifiers

PMID40890480
PMCPMC13433260

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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.