Evidence map›Paper›PMID 37953411›Full record

ArticlePediatric radiology2024

Deeplasia: deep learning for bone age assessment validated on skeletal dysplasias.

Sebastian Rassmann, Alexandra Keller, Kyra Skaf, Alexander Hustinx, Ruth Gausche, Miguel A Ibarra-Arrelano, Tzung-Chien Hsieh, Yolande E D Madajieu, Markus M Nöthen, Roland Pfäffle and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Pediatric radiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
10.0field-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

26 citing papers in PubMed, 32 citations in OpenAlex.

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  20. Artificial intelligence in clinical genetics.European journal of human genetics : EJHG · 2025
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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

15 authors at 4 institutions in 1 country.

Sebastian RassmannInstitute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Venusberg-Campus 1 Building 11, 2nd Floor, 53127, Bonn, Germany.ORCID 0000-0001-7119-9473
Alexandra KellerKinderzentrum Am Johannisplatz, Leipzig, Germany.ORCID 0000-0001-9580-229X
Kyra SkafMedical Faculty, Otto-Von-Guericke-University Magdeburg, Magdeburg, Germany.
Alexander HustinxInstitute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Venusberg-Campus 1 Building 11, 2nd Floor, 53127, Bonn, Germany.ORCID 0000-0003-4592-3979
Ruth GauscheCrescNet - Wachstumsnetzwerk, Medical Faculty, University Hospital Leipzig, Leipzig, Germany.ORCID 0000-0001-5809-6330
Miguel A Ibarra-ArrelanoInstitute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Venusberg-Campus 1 Building 11, 2nd Floor, 53127, Bonn, Germany.ORCID 0000-0001-8411-4854
Tzung-Chien HsiehInstitute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Venusberg-Campus 1 Building 11, 2nd Floor, 53127, Bonn, Germany.ORCID 0000-0003-3828-4419
Yolande E D MadajieuMedical Faculty, Otto-Von-Guericke-University Magdeburg, Magdeburg, Germany.
Markus M NöthenInstitute of Human Genetics, University Hospital Bonn, Bonn, Germany.ORCID 0000-0002-8770-2464
Roland PfäffleDepartment for Pediatrics, University Hospital Leipzig, Leipzig, Germany.ORCID 0000-0001-6754-3681
Ulrike I AttenbergerDepartment of Diagnostic and Interventional Radiology, University Hospital Bonn, Bonn, Germany.
Mark BornDivision of Paediatric Radiology, Department of Radiology, University Hospital Bonn, Bonn, Germany.ORCID 0000-0002-1740-0006
Klaus MohnikeMedical Faculty, Otto-Von-Guericke-University Magdeburg, Magdeburg, Germany.ORCID 0000-0001-5113-8657
Peter M KrawitzInstitute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Venusberg-Campus 1 Building 11, 2nd Floor, 53127, Bonn, Germany.ORCID 0000-0002-3194-8625
Behnam JavanmardiInstitute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Venusberg-Campus 1 Building 11, 2nd Floor, 53127, Bonn, Germany. behnam.javanmardi@uni-bonn.de.ORCID 0000-0002-9317-6114
University Hospital Bonn · DEOtto-von-Guericke-Universität Magdeburg · DEUniversity Hospital Leipzig · DEDie Johanniter · DE

Funding

EU4Health Program of the European Union 101085231
6 · The paper itself

Abstract

backgroundSkeletal dysplasias collectively affect a large number of patients worldwide. Most of these disorders cause growth anomalies. Hence, evaluating skeletal maturity via the determination of bone age (BA) is a useful tool. Moreover, consecutive BA measurements are crucial for monitoring the growth of patients with such disorders, especially for timing hormonal treatment or orthopedic interventions. However, manual BA assessment is time-consuming and suffers from high intra- and inter-rater variability. This is further exacerbated by genetic disorders causing severe skeletal malformations. While numerous approaches to automate BA assessment have been proposed, few are validated for BA assessment on children with skeletal dysplasias.

objectiveWe present Deeplasia, an open-source prior-free deep-learning approach designed for BA assessment specifically validated on patients with skeletal dysplasias. MATERIALS AND

methodsWe trained multiple convolutional neural network models under various conditions and selected three to build a precise model ensemble. We utilized the public BA dataset from the Radiological Society of North America (RSNA) consisting of training, validation, and test subsets containing 12,611, 1,425, and 200 hand and wrist radiographs, respectively. For testing the performance of our model ensemble on dysplastic hands, we retrospectively collected 568 radiographs from 189 patients with molecularly confirmed diagnoses of seven different genetic bone disorders including achondroplasia and hypochondroplasia. A subset of the dysplastic cohort (149 images) was used to estimate the test-retest precision of our model ensemble on longitudinal data.

resultsThe mean absolute difference of Deeplasia for the RSNA test set (based on the average of six different reference ratings) and dysplastic set (based on the average of two different reference ratings) were 3.87 and 5.84 months, respectively. The test-retest precision of Deeplasia on longitudinal data (2.74 months) is estimated to be similar to a human expert.

conclusionWe demonstrated that Deeplasia is competent in assessing the age and monitoring the development of both normal and dysplastic bones.

Indexed as

AchondroplasiaDeep LearningOsteochondrodysplasiasAge Determination by SkeletonChildHumansRadiographyRetrospective StudiesArtificial intelligenceBone age measurementBone dysplasiasChildrenDeep learningGenetic diseasesRare diseases

Identifiers

PMID37953411
PMCPMC10776485
OpenAlexW4388636556

What OpenQuestion holds

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LicenceCC BY
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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.