Evidence map›Paper›PMID 39931027›Full record

ArticleGigaScience2025

Opaque ontology: neuroimaging classification of ICD-10 diagnostic groups in the UK Biobank.

Ty Easley, Xiaoke Luo, Kayla Hannon, Petra Lenzini, Janine Bijsterbosch

Abstract read
In one paragraph

Article in GigaScience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Ty EasleyDepartment of Radiology, Washington University School of Medicine, Saint Louis, Missouri 63110, USA.ORCID 0000-0002-8215-2598
Xiaoke LuoDepartment of Radiology, Washington University School of Medicine, Saint Louis, Missouri 63110, USA.ORCID 0009-0006-8028-3822
Kayla HannonDepartment of Radiology, Washington University School of Medicine, Saint Louis, Missouri 63110, USA.ORCID 0000-0002-6340-6791
Petra LenziniDepartment of Radiology, Washington University School of Medicine, Saint Louis, Missouri 63110, USA.ORCID 0009-0003-1446-8034
Janine BijsterboschDepartment of Radiology, Washington University School of Medicine, Saint Louis, Missouri 63110, USA.ORCID 0000-0002-1385-9178

Funding

The role of late life depression in cognitive decline and Alzheimer's Disease riskR01MH128286 · NIMH · WASHINGTON UNIVERSITY · PI Janine Diane Bijsterbosch · 2022 to 2026
$2.7M
A High Performance Research Image Repository (RIR) for the Washington University Center of High Performance Computing (CHPC)S10OD030477 · OD · WASHINGTON UNIVERSITY · PI MARCUS, DANIEL SCOTT · 2021 to 2021
$1.9M
HCP-2.0: Ascertaining Network Mechanisms and Analytics of Emotional Dysfunction (HARMONY)R01MH132962 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI BIJSTERBOSCH, JANINE DIANE, NARR, KATHERINE L · 2023 to 2024
$1.6M
Acquisition of a next-generation computing clusterS10OD025200 · OD · WASHINGTON UNIVERSITY · PI TOBIAS, MALCOLM · 2019 to 2019
$597k
National Science Foundation DGE-2139839NIH HHS NIMH R01 MH128286NIH HHS S10 OD025200NIH HHS S10 OD030477NIH S10 1S10OD025200-01A1NIMH NIH HHS R01 MH128286NIMH NIH HHS R01 MH132962Washington University Research Computing and Informatics Facility
6 · The paper itself

Abstract

backgroundThe use of machine learning to classify diagnostic cases versus controls defined based on diagnostic ontologies such as the International Classification of Diseases, Tenth Revision (ICD-10) from neuroimaging features is now commonplace across a wide range of diagnostic fields. However, transdiagnostic comparisons of such classifications are lacking. Such transdiagnostic comparisons are important to establish the specificity of classification models, set benchmarks, and assess the value of diagnostic ontologies.

resultsWe investigated case-control classification accuracy in 17 different ICD-10 diagnostic groups from Chapter V (mental and behavioral disorders) and Chapter VI (diseases of the nervous system) using data from the UK Biobank. Classification models were trained using either neuroimaging (structural or functional brain magnetic resonance imaging feature sets) or sociodemographic features. Random forest classification models were adopted using rigorous shuffle-splits to estimate stability as well as accuracy of case-control classifications. Diagnostic classification accuracies were benchmarked against age classification (oldest vs. youngest) from the same feature sets and against additional classifier types (k-nearest neighbors and linear support vector machine). In contrast to age classification accuracy, which was high for all feature sets, few ICD-10 diagnostic groups were classified significantly above chance (namely, demyelinating diseases based on structural neuroimaging features and depression based on sociodemographic and functional neuroimaging features).

conclusionThese findings highlight challenges with the current disease classification system, leading us to recommend caution with the use of ICD-10 diagnostic groups as target labels in brain-based disease prediction studies.

Indexed as

Biological Specimen BanksInternational Classification of DiseasesNeuroimagingAdultAgedCase-Control StudiesFemaleHumansMachine LearningMagnetic Resonance ImagingMaleMiddle AgedUK BiobankUnited Kingdommachine learningmental health disordersnervous system diseasesneuroimagingUK Biobank

Identifiers

PMID39931027
PMCPMC11811528

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.