Evidence map›Paper›PMID 33094897›Full record

ArticleHuman brain mapping2021

Atypical measures of diffusion at the gray-white matter boundary in autism spectrum disorder in adulthood.

Anke Bletsch, Tim Schäfer, Caroline Mann, Derek S Andrews, Eileen Daly, Maria Gudbrandsen, Amber N V Ruigrok, Robert Dallyn, Rafael Romero-Garcia, Meng-Chuan Lai and 9 more

Abstract readMulticenter Study
In one paragraph

Article in Human brain mapping, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Molecular psychiatry · 2025
    Article
  5. Article
  6. Article
  7. Imaging of the superficial white matter in health and disease.Imaging neuroscience (Cambridge, Mass.) · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
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

19 authors.

Anke BletschDepartment of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital, Goethe University, Frankfurt, Germany.ORCID 0000-0002-6857-4065
Tim SchäferDepartment of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital, Goethe University, Frankfurt, Germany.
Caroline MannDepartment of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital, Goethe University, Frankfurt, Germany.ORCID 0000-0003-2944-6244
Derek S AndrewsDepartment of Psychiatry and Behavioral Sciences at the M.I.N.D. Institute, University of California, Davis, California, USA.
Eileen DalyDepartment of Forensic and Neurodevelopmental Sciences, and the Sackler Institute for Translational Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's College, London, UK.
Maria GudbrandsenDepartment of Forensic and Neurodevelopmental Sciences, and the Sackler Institute for Translational Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's College, London, UK.
Amber N V RuigrokAutism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, UK.
Robert DallynDepartment of Forensic and Neurodevelopmental Sciences, and the Sackler Institute for Translational Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's College, London, UK.
Rafael Romero-GarciaBrain Mapping Unit, Department of Psychiatry, University of Cambridge, Cambridge, UK.
Meng-Chuan LaiAutism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, UK.
Michael V LombardoAutism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, UK.
Michael C CraigDepartment of Forensic and Neurodevelopmental Sciences, and the Sackler Institute for Translational Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's College, London, UK.
John SucklingBrain Mapping Unit, Department of Psychiatry, University of Cambridge, Cambridge, UK.
Edward T BullmoreBrain Mapping Unit, Department of Psychiatry, University of Cambridge, Cambridge, UK.
Simon Baron-CohenAutism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, UK.
MRC AIMS Consortium
Declan G M MurphyDepartment of Forensic and Neurodevelopmental Sciences, and the Sackler Institute for Translational Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's College, London, UK.
Flavio Dell'AcquaDepartment of Forensic and Neurodevelopmental Sciences, and the Sackler Institute for Translational Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's College, London, UK.
Christine EckerDepartment of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital, Goethe University, Frankfurt, Germany.

Funding

Interdisciplinary Training for Autism Researchers(RMI)T32MH073124 · NIMH · UNIVERSITY OF CALIFORNIA DAVIS · PI Stephen Charles Noctor, Christine Wu Nordahl · 2004 to 2026
$6.8M
CIHR PJT-159578Department of HealthMedical Research Council MC_G0802534Medical Research Council MR/N026063/1Medical Research Council UK G0400061NIMH NIH HHS T32 MH073124
6 · The paper itself

Abstract

Autism spectrum disorder (ASD) is a highly complex neurodevelopmental condition that is accompanied by neuroanatomical differences on the macroscopic and microscopic level. Findings from histological, genetic, and more recently in vivo neuroimaging studies converge in suggesting that neuroanatomical abnormalities, specifically around the gray-white matter (GWM) boundary, represent a crucial feature of ASD. However, no research has yet characterized the GWM boundary in ASD based on measures of diffusion. Here, we registered diffusion tensor imaging data to the structural T1-weighted images of 92 adults with ASD and 92 matched neurotypical controls in order to examine between-group differences and group-by-sex interactions in fractional anisotropy and mean diffusivity sampled at the GWM boundary, and at different sampling depths within the superficial white and into the gray matter. As hypothesized, we observed atypical diffusion at and around the GWM boundary in ASD, with between-group differences and group-by-sex interactions depending on tissue class and sampling depth. Furthermore, we identified that altered diffusion at the GWM boundary partially (i.e., ~50%) overlapped with atypical gray-white matter tissue contrast in ASD. Our study thus replicates and extends previous work highlighting the GWM boundary as a crucial target of neuropathology in ASD, and guides future work elucidating etiological mechanisms.

Indexed as

AdolescentAdultAutism Spectrum DisorderBrainDiffusion Tensor ImagingFemaleGray MatterHumansMaleMiddle AgedWhite MatterYoung Adultdiffusion tensor imagingmultimodal imagingmyelinated and unmyelinated gray mattersuperficial white matter

Identifiers

PMID33094897
PMCPMC7775996

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.