Evidence map›Paper›PMID 40162283›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Deep Learning Study of Alkaptonuria Spinal Disease Assesses Global and Regional Severity and Detects Occult Treatment Status.

Kendall A Flaharty, Vibha Chandrasekar, Irene J Castillo, Dat Duong, Carlos R Ferreira, Suzanna Ledgister Hanchard, Ping Hu, Rebekah L Waikel, Francis Rossignol, Wendy J Introne and 1 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. 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

5 · Who and what money

Authors and funding

11 authors.

Kendall A FlahartyMedical Genomics Unit, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.ORCID 0009-0000-9473-1354
Vibha ChandrasekarMedical Genomics Unit, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
Irene J CastilloHuman Biochemical Genetics Section, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
Dat DuongMedical Genomics Unit, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
Carlos R FerreiraUnit on Skeletal Genomics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA.ORCID 0000-0002-2697-1046
Suzanna Ledgister HanchardMedical Genomics Unit, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
Ping HuMedical Genomics Unit, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
Rebekah L WaikelMedical Genomics Unit, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
Francis RossignolHuman Biochemical Genetics Section, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
Wendy J IntroneHuman Biochemical Genetics Section, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
Benjamin D SolomonMedical Genomics Unit, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.

Funding

Skeletal and Metabolic Translational MedicineZIAHD009024 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI FERREIRA, CARLOS · 2025 to 2025
$2.5M
Intramural NIH HHS ZIA HD009024Intramural NIH HHS ZIA HG200406
6 · The paper itself

Abstract

Deep learning (DL) is increasingly used to analyze medical imaging, but is less refined for rare conditions, which require novel pre-processing and analytical approaches. To assess DL in the context of rare diseases, we focused on alkaptonuria (AKU), a rare disorder that affects the spine and involves other sequelae; treatments include the medication nitisinone. Since assessing X-rays to determine disease severity can be a slow, manual process requiring considerable expertise, we aimed to determine whether our DL methods could accurately identify overall spine severity, severity at specific regions of the spine, and whether DL could detect whether patients were receiving nitisinone. We evaluated DL performance versus clinical experts using cervical and lumbar spine radiographs. DL models predicted global severity scores (30-point scale) within 1.72 ± 1.96 points of expert clinician scores for cervical and 2.51 ± 1.96 points for lumbar radiographs. For region-specific metrics, we assessed the degree of narrowing, calcium, and vacuum phenomena at each intervertebral space (IVS). Our model's narrowing scores were within 0.191-0.557 points from clinician scores (6-point scale), calcium was predicted with 78-90% accuracy (present, absent, or disc fusion), while vacuum disc phenomenon predictions were less consistent (41-90%). Intriguingly, DL models predicted nitisinone treatment status with 68-77% accuracy, while expert clinicians appeared unable to discern nitisinone status (51% accuracy) (p = 2.0 × 10

Identifiers

PMID40162283
PMCPMC11952612

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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.