Evidence map›Paper›PMID 40468437›Full record

ArticleMolecular autism2025

Subgrouping autism and ADHD based on structural MRI population modelling centiles.

Clara Pecci-Terroba, Meng-Chuan Lai, Michael V Lombardo, Bhismadev Chakrabarti, Amber N V Ruigrok, John Suckling, Evdokia Anagnostou, Jason P Lerch, Margot J Taylor, Rob Nicolson and 12 more

Abstract read
In one paragraph

Article in Molecular autism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
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

22 authors.

Clara Pecci-TerrobaDepartment of Psychology, University of Cambridge, Cambridge, UK.ORCID 0000-0002-6379-582X
Meng-Chuan LaiAutism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, UK.ORCID 0000-0002-9593-5508
Michael V LombardoLaboratory for Autism and Neurodevelopmental Disorders, Center for Neuroscience and Cognitive Systems, Istituto Italiano Di Tecnologia, Rovereto, Italy.ORCID 0000-0001-6780-8619
Bhismadev ChakrabartiCentre for Autism, School of Psychology and Clinical Language Sciences, University of Reading, Reading, UK.ORCID 0000-0002-6649-7895
Amber N V RuigrokAutism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, UK.ORCID 0000-0001-7711-8056
John SucklingBrain Mapping Unit, Department of Psychiatry, University of Cambridge, Cambridge, UK.ORCID 0000-0002-5098-1527
Evdokia AnagnostouHolland Bloorview Kids Rehabilitation Hospital, Bloorview Research Institute Toronto, University of Toronto, Toronto, ON, Canada.ORCID 0000-0002-3455-9887
Jason P LerchProgram in Neurosciences and Mental Health, Research Institute, The Hospital for Sick Children, Toronto, ON, Canada.ORCID 0000-0001-6164-2881
Margot J TaylorProgram in Neurosciences and Mental Health, Research Institute, The Hospital for Sick Children, Toronto, ON, Canada.ORCID 0000-0002-3534-9750
Rob NicolsonDepartment of Psychiatry, University of Western Ontario, London, ON, Canada.ORCID 0000-0001-7086-7038
Stelios GeorgiadesMcMaster University, Hamilton, ON, Canada.
Jennifer CrosbieDepartment of Psychiatry, The Hospital for Sick Children, Toronto, ON, Canada.ORCID 0000-0002-8710-3322
Russell SchacharDepartment of Psychiatry, The Hospital for Sick Children, Toronto, ON, Canada.ORCID 0000-0002-2015-4395
Elizabeth KelleyDepartment of Psychology, Queen's University, Kingston, ON, Canada.ORCID 0000-0001-7742-6542
Jessica JonesCentre for Neuroscience Studies, Queen's University, Kingston, ON, Canada.ORCID 0000-0002-1116-4321
Paul D ArnoldMathison Centre for Mental Health Research & Education, Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.ORCID 0000-0003-2496-4624
Jakob SeidlitzDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA.ORCID 0000-0002-8164-7476
Aaron F Alexander-BlochDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA.ORCID 0000-0001-6554-1893
Edward T BullmoreBrain Mapping Unit, Department of Psychiatry, University of Cambridge, Cambridge, UK.ORCID 0000-0002-8955-8283
Simon Baron-CohenAutism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, UK.ORCID 0000-0001-9217-2544
Saashi A BedfordDepartment of Psychology, University of Cambridge, Cambridge, UK. ajb349@cam.ac.uk.ORCID 0000-0002-0491-5342
Richard A I BethlehemDepartment of Psychology, University of Cambridge, Cambridge, UK. rb643@cam.ac.uk.ORCID 0000-0002-0714-0685

Funding

Detection of ASD at the 1st birthday as standard of care: The Get SET Early ModelR01MH104446 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI PIERCE, KAREN L · 2014 to 2018
$6.0M
Precision brain charts for imaging-genomics of schizophrenia and the psychosis spectrumR01MH133843 · NIMH · CHILDREN'S HOSP OF PHILADELPHIA · PI Aaron Felix Alexander-Bloch · 2023 to 2026
$3.2M
Discovering Neural Biomarkers of Language and Social Development in ASD ToddlersR01DC016385 · NIDCD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI COURCHESNE, ERIC, PIERCE, KAREN L · 2017 to 2021
$3.0M
NIDCD NIH HHS R01 DC016385NIMH NIH HHS R01 MH104446NIMH NIH HHS R01 MH133843Wellcome Trust 214322\Z\18\Z
6 · The paper itself

Abstract

backgroundAutism and attention deficit hyperactivity disorder (ADHD) are two highly heterogeneous neurodevelopmental conditions with variable underlying neurobiology. Imaging studies have yielded varied results, and it is now clear that there is unlikely to be one characteristic neuroanatomical profile of either condition. Parsing this heterogeneity could allow us to identify more homogeneous subgroups, either within or across conditions, which may be more clinically informative. This has been a pivotal goal for neurodevelopmental research using both clinical and neuroanatomical features, though results thus far have again been inconsistent with regards to the number and characteristics of subgroups.

methodsHere, we use population modelling to cluster a multi-site dataset based on global and regional centile scores of cortical thickness, surface area and grey matter volume. We use HYDRA, a novel semi-supervised machine learning algorithm which clusters based on differences to controls and compare its performance to a traditional clustering approach.

resultsWe identified distinct subgroups within autism and ADHD, as well as across diagnosis, often with opposite neuroanatomical alterations relatively to controls. These subgroups were characterised by different combinations of increased or decreased patterns of morphometrics. We did not find significant clinical differences across subgroups. LIMITATIONS: Crucially, however, the number of subgroups and their membership differed vastly depending on chosen features and the algorithm used, highlighting the impact and importance of careful method selection.

conclusionsWe highlight the importance of examining heterogeneity in autism and ADHD and demonstrate that population modelling is a useful tool to study subgrouping in autism and ADHD. We identified subgroups with distinct patterns of alterations relative to controls but note that these results rely heavily on the algorithm used and encourage detailed reporting of methods and features used in future studies.

Indexed as

Attention Deficit Disorder with HyperactivityAutistic DisorderMagnetic Resonance ImagingAdolescentAlgorithmsChildCluster AnalysisFemaleHumansMachine LearningMaleADHDAutismNeuroimagingPopulation modellingStructural MRISubgrouping

Identifiers

PMID40468437
PMCPMC12135403

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.