Evidence map›Paper›PMID 41328895›Full record

ArticleJournal of magnetic resonance imaging : JMRI2026

3D Automated Segmentation of Bronchial Abnormalities on Ultrashort Echo Time MRI: A Quantitative MR Outcome in Cystic Fibrosis.

Amel Imene Hadj Bouzid, Ilyes Benlala, Baudouin Denis de Senneville, Fabien Baldacci, Julie Macey, Wadie Benhassen, Pan Su, Stephanie Bui, Maeva Zysman, Aurelien Bustin and 2 more

Abstract read
In one paragraph

Article in Journal of magnetic resonance imaging : JMRI, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Amel Imene Hadj BouzidUniv. Bordeaux, INSERM, CRCTB, UMR 1045, Bordeaux, France.ORCID https://orcid.org/0009-0009-8148-8581
Ilyes BenlalaUniv. Bordeaux, INSERM, CRCTB, UMR 1045, Bordeaux, France.
Baudouin Denis de SennevilleUniv. Bordeaux, CNRS, Bordeaux INP, IMB, UMR 5251, Talence, France.
Fabien BaldacciUniv. Bordeaux, CNRS, Bordeaux INP, LaBRI, UMR 5800, Talence, France.
Julie MaceyUniv. Bordeaux, INSERM, CRCTB, UMR 1045, Bordeaux, France.
Wadie BenhassenSiemens Healthcare SAS, Courbevoie, France.
Pan SuSiemens Medical Solutions USA, Inc., Malvern, Pennsylvania, USA.
Stephanie BuiUniv. Bordeaux, INSERM, CRCTB, UMR 1045, Bordeaux, France.
Maeva ZysmanUniv. Bordeaux, INSERM, CRCTB, UMR 1045, Bordeaux, France.
Aurelien BustinUniv. Bordeaux, INSERM, IHU LIRYC, UMR 1045, Bordeaux, France.ORCID https://orcid.org/0000-0002-2845-8617
Patrick BergerUniv. Bordeaux, INSERM, CRCTB, UMR 1045, Bordeaux, France.
Gael DournesUniv. Bordeaux, INSERM, CRCTB, UMR 1045, Bordeaux, France.ORCID https://orcid.org/0000-0002-0251-6639

Funding

Nouvelle Aquitaine Region AAPR2020-2019-8397110Vaincre La Mucoviscidose RC20250503647/1/1/80
6 · The paper itself

Abstract

backgroundCystic fibrosis (CF) monitoring relies on computed tomography (CT), but ultra-short echo time MRI (UTE-MRI) offers a radiation-free alternative. However, its clinical adoption is hindered by the laborious and subjective manual analysis, which prevents standardized quantification of bronchial abnormalities. PURPOSE: To develop a deep learning (DL) system for the segmentation of CF bronchial abnormalities on UTE-MRI and assess clinical relevance in patients undergoing cystic fibrosis transmembrane conductance regulator (CFTR) modulator treatment. STUDY TYPE: Retrospective. POPULATION: One-hundred and sixty-six CF patients were included (age = 23 ± 11, 48% male), comprising a training set (n = 97), a test set (n = 25), and an independent clinical validation cohort (n = 44). FIELD STRENGTH/SEQUENCE: 1.5T/UTE-MRI 3D gradient-echo Spiral Volume Interpolated Breath-hold Examination (VIBE) sequence. ASSESSMENT: The RiSeNet architecture was trained using paired UTE-MRI and CT scans. Its technical performance was evaluated against expert-refined segmentations and compared to state-of-the-art segmentation models using topology-aware metrics: Normalized Surface Dice (NSD) and CenterLine Dice (clDice). Clinical validation was performed by correlating automated measurements at baseline (M0) and 1-year post-CFTR modulator treatment (M12) with Bhalla scores and pulmonary function tests (FEV1%p). STATISTICAL TESTS: Student's t-test, Mann-Whitney, Wilcoxon, and Chi-square tests were used for group comparisons. The Spearman test was used to assess correlations. A p value < 0.05 was considered statistically significant.

resultsIn the test group, RiSeNet achieved significantly superior performance versus state-of-the-art with NSD scores of 0.84 for bronchiectasis, 0.90 for wall thickening, and 0.75 for mucus; and clDice scores of 0.69, 0.61, and 0.64, respectively. In the clinical validation group, significant correlations with Bhalla (ρ = -0.92/-0.85) and FEV1%p (ρ = -0.68/-0.67) were observed pre/post-CFTR modulator. Post-CFTR modulator, FEV1%p improved (69%-92%) with significant reductions in bronchiectasis (3.88-1.25), wall thickening (30.43-3.05), and mucus (53.30-11.80). DATA

conclusionRiSeNet may enable semantic segmentation of CF abnormalities on radiation-free UTE-MRI. EVIDENCE LEVEL: 3 TECHNICAL EFFICACY: 4.

Indexed as

BronchiCystic FibrosisImaging, Three-DimensionalMagnetic Resonance ImagingAdolescentAdultChildDeep LearningFemaleHumansImage Interpretation, Computer-AssistedMaleReproducibility of ResultsRetrospective StudiesTomography, X-Ray ComputedYoung Adultcystic fibrosisdeep learningElexacaftor/Tezacaftor/IvacaftorsegmentationUTE‐MRI

Identifiers

PMID41328895
PMCPMC12963807

What OpenQuestion holds

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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.