Evidence map›Paper›PMID 36369209›Full record

ArticleRespiratory research2022

A fully automated deep learning pipeline for micro-CT-imaging-based densitometry of lung fibrosis murine models.

Elena Vincenzi, Alice Fantazzini, Curzio Basso, Annalisa Barla, Francesca Odone, Ludovica Leo, Laura Mecozzi, Martina Mambrini, Erica Ferrini, Nicola Sverzellati and 1 more

Abstract read
In one paragraph

Article in Respiratory research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Review
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  6. Article
  7. Imaging technologies in experimental pulmonary fibrosis research: essential tool for enhanced translational relevance.European respiratory review : an official journal of the European Respiratory Society · 2025
    Review
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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

11 authors.

Elena VincenziDepartment of Computer Science, Bioengineering, Robotics and Systems Engineering, University of Genoa, Genoa, Italy.
Alice FantazziniCamelot Biomedical System S.R.L, Via Al Ponte Reale 2/20, 16124, Genoa, Italy.
Curzio BassoCamelot Biomedical System S.R.L, Via Al Ponte Reale 2/20, 16124, Genoa, Italy.
Annalisa BarlaDepartment of Computer Science, Bioengineering, Robotics and Systems Engineering, University of Genoa, Genoa, Italy.
Francesca OdoneDepartment of Computer Science, Bioengineering, Robotics and Systems Engineering, University of Genoa, Genoa, Italy.
Ludovica LeoDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Laura MecozziDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Martina MambriniDepartment of Veterinary Science, University of Parma, Parma, Italy.
Erica FerriniDepartment of Veterinary Science, University of Parma, Parma, Italy.
Nicola SverzellatiDepartment of Medicine and Surgery, University of Parma, Parma, Italy.
Franco Fabio StellariChiesi Farmaceutici S.P.A, Corporate Pre-Clinical Research and Development, Largo Belloli, 11/A, 43122, Parma, Italy. fb.stellari@chiesi.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic pulmonary fibrosis, the archetype of pulmonary fibrosis (PF), is a chronic lung disease of a poor prognosis, characterized by progressively worsening of lung function. Although histology is still the gold standard for PF assessment in preclinical practice, histological data typically involve less than 1% of total lung volume and are not amenable to longitudinal studies. A miniaturized version of computed tomography (µCT) has been introduced to radiologically examine lung in preclinical murine models of PF. The linear relationship between X-ray attenuation and tissue density allows lung densitometry on total lung volume. However, the huge density changes caused by PF usually require manual segmentation by trained operators, limiting µCT deployment in preclinical routine. Deep learning approaches have achieved state-of-the-art performance in medical image segmentation. In this work, we propose a fully automated deep learning approach to segment right and left lung on µCT imaging and subsequently derive lung densitometry. Our pipeline first employs a convolutional network (CNN) for pre-processing at low-resolution and then a 2.5D CNN for higher-resolution segmentation, combining computational advantage of 2D and ability to address 3D spatial coherence without compromising accuracy. Finally, lungs are divided into compartments based on air content assessed by density. We validated this pipeline on 72 mice with different grades of PF, achieving a Dice score of 0.967 on test set. Our tests demonstrate that this automated tool allows for rapid and comprehensive analysis of µCT scans of PF murine models, thus laying the ground for its wider exploitation in preclinical settings.

Indexed as

Deep LearningPulmonary FibrosisAnimalsDensitometryDisease Models, AnimalMiceX-Ray MicrotomographyDeep learningDrug discoveryMicro-computed tomographyPreclinicalSegmentation

Identifiers

PMID36369209
PMCPMC9651107

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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.