Evidence map›Paper›PMID 35138551›Full record

ReviewHepatology international2022

Conventional and artificial intelligence-based imaging for biomarker discovery in chronic liver disease.

Jérémy Dana, Aïna Venkatasamy, Antonio Saviano, Joachim Lupberger, Yujin Hoshida, Valérie Vilgrain, Pierre Nahon, Caroline Reinhold, Benoit Gallix, Thomas F Baumert

Open access · greenAbstract readReview
In one paragraph

Review in Hepatology international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
7.0field-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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Genetic analysis of imaging-derived phenotypes.Nature reviews. Genetics · 2026
    Review
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  17. Radiology of fibrosis part II: abdominal organs.Journal of translational medicine · 2024
    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

10 authors at 4 institutions in 4 countries.

Jérémy DanaInstitut de Recherche sur les Maladies Virales et Hépatiques, Institut National de la Santé et de la Recherche Médicale (Inserm), U1110, 3 Rue Koeberlé, 67000, Strasbourg, France. jeremy.dana@etu.unistra.fr.ORCID http://orcid.org/0000-0003-0352-4128
Aïna VenkatasamyInstitut Hospitalo-Universitaire (IHU), Strasbourg, France.
Antonio SavianoInstitut de Recherche sur les Maladies Virales et Hépatiques, Institut National de la Santé et de la Recherche Médicale (Inserm), U1110, 3 Rue Koeberlé, 67000, Strasbourg, France.
Joachim LupbergerInstitut de Recherche sur les Maladies Virales et Hépatiques, Institut National de la Santé et de la Recherche Médicale (Inserm), U1110, 3 Rue Koeberlé, 67000, Strasbourg, France.
Yujin HoshidaLiver Tumor Translational Research Program, Division of Digestive and Liver Diseases, Department of Internal Medicine, Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, USA.
Valérie VilgrainRadiology Department, Hôpital Beaujon, Université de Paris, CRI, INSERM 1149, APHP. Nord, Paris, France.
Pierre NahonLiver Unit, Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpitaux Universitaires Paris Seine Saint-Denis, Bobigny, France.
Caroline ReinholdDepartment of Diagnostic Radiology, McGill University, Montreal, Canada.
Benoit GallixInstitut Hospitalo-Universitaire (IHU), Strasbourg, France.
Thomas F BaumertInstitut de Recherche sur les Maladies Virales et Hépatiques, Institut National de la Santé et de la Recherche Médicale (Inserm), U1110, 3 Rue Koeberlé, 67000, Strasbourg, France. thomas.baumert@unistra.fr.
Inserm · FRMcGill University · CAMcGill University Health Centre · CAThe University of Texas Southwestern Medical Center · US

Funding

Reverse-engineering precision liver cancer chemopreventionR01CA233794 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI HOSHIDA, YUJIN · 2019 to 2023
$3.5M
Molecular Prognostic Indicators in Liver Cirrhosis and CancerR01DK099558 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HOSHIDA, YUJIN · 2013 to 2016
$2.6M
Integrative genomic framework for dissecting regulatory mechanisms underlying hepatocellular carcinomaR21CA209940 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI POCHET, NATHALIE · 2017 to 2018
$402k
Spatial and temporal profiling to unravel the host cell responses to hepatitis B virus infectionR03AI131066 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI POCHET, NATHALIE · 2018 to 2019
$181k
Agence Nationale de la Recherche ANR-10-IAHU-02European Research Council 671231European Research Council ERC-AdG-2014-671231-HEPCIRNCI NIH HHS R01 CA233794NCI NIH HHS R21 CA209940NIAID NIH HHS R03 AI131066NIDDK NIH HHS R01 DK099558
6 · The paper itself

Abstract

Chronic liver diseases, resulting from chronic injuries of various causes, lead to cirrhosis with life-threatening complications including liver failure, portal hypertension, hepatocellular carcinoma. A key unmet medical need is robust non-invasive biomarkers to predict patient outcome, stratify patients for risk of disease progression and monitor response to emerging therapies. Quantitative imaging biomarkers have already been developed, for instance, liver elastography for staging fibrosis or proton density fat fraction on magnetic resonance imaging for liver steatosis. Yet, major improvements, in the field of image acquisition and analysis, are still required to be able to accurately characterize the liver parenchyma, monitor its changes and predict any pejorative evolution across disease progression. Artificial intelligence has the potential to augment the exploitation of massive multi-parametric data to extract valuable information and achieve precision medicine. Machine learning algorithms have been developed to assess non-invasively certain histological characteristics of chronic liver diseases, including fibrosis and steatosis. Although still at an early stage of development, artificial intelligence-based imaging biomarkers provide novel opportunities to predict the risk of progression from early-stage chronic liver diseases toward cirrhosis-related complications, with the ultimate perspective of precision medicine. This review provides an overview of emerging quantitative imaging techniques and the application of artificial intelligence for biomarker discovery in chronic liver disease.

Indexed as

Elasticity Imaging TechniquesFatty LiverHypertension, PortalLiver NeoplasmsArtificial IntelligenceBiomarkersDisease ProgressionHumansLiverLiver CirrhosisMagnetic Resonance ImagingBiomarkersChronic liver diseaseDeep learningElastographyHisto-pathological featuresMachine learningPejorative evolutionQuantitative biomarkersRadiomics

Identifiers

PMID35138551
PMCPMC9177703
OpenAlexW4210844307

What OpenQuestion holds

Textmetadata
LicenceTDM
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.