Evidence map›Paper›PMID 34911194›Full record

ArticleNeuroImage. Clinical2021

Dissociating regional gray matter density and gray matter volume in autism spectrum condition.

Lisa D Yankowitz, Benjamin E Yerys, John D Herrington, Juhi Pandey, Robert T Schultz

Abstract read
In one paragraph

Article in NeuroImage. Clinical, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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

5 authors.

Lisa D YankowitzCenter for Autism Research, Children's Hospital of Philadelphia, 2716 South St, Philadelphia, PA 19104, United States; Department of Psychology, University of Pennsylvania, 425 S. University Ave, Philadelphia, PA 19104, United States. Electronic address: lisayank@sas.upenn.edu.
Benjamin E YerysCenter for Autism Research, Children's Hospital of Philadelphia, 2716 South St, Philadelphia, PA 19104, United States; Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, 3400 Civic Center Blvd Philadelphia, PA 19105, United States.
John D HerringtonCenter for Autism Research, Children's Hospital of Philadelphia, 2716 South St, Philadelphia, PA 19104, United States; Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, 3400 Civic Center Blvd Philadelphia, PA 19105, United States.
Juhi PandeyCenter for Autism Research, Children's Hospital of Philadelphia, 2716 South St, Philadelphia, PA 19104, United States; Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, 3400 Civic Center Blvd Philadelphia, PA 19105, United States.
Robert T SchultzCenter for Autism Research, Children's Hospital of Philadelphia, 2716 South St, Philadelphia, PA 19104, United States; Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, 3400 Civic Center Blvd Philadelphia, PA 19105, United States; Department of Pediatrics Perelman School of Medicine, University of Pennsylvania, 3400 Civic Center Blvd Philadelphia, PA 19105, United States.

Funding

The Intellectual and Developmental Disabilities Research Center (IDDRC) at CHOP/PennP50HD105354 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI Michael Byrne Robinson · 2021 to 2026
$9.2M
The Intellectual and Developmental Disabilities Research Center at CHOP/PennU54HD086984 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI YUDKOFF, MARC · 2016 to 2020
$6.3M
The fusiform and amygalda in the pathobiology of autismR01MH073084 · NIMH · YALE UNIVERSITY · PI SCHULTZ, ROBERT THOMAS · 2005 to 2009
$1.6M
Developing a Community-Based ASD Research RegistryRC1MH088791 · NIMH · CHILDREN'S HOSP OF PHILADELPHIA · PI SCHULTZ, ROBERT THOMAS · 2009 to 2009
$500k
Testing the hyperspecificity hypothesis: a neural theory of autismR21MH098153 · NIMH · CHILDREN'S HOSP OF PHILADELPHIA · PI SCHULTZ, ROBERT THOMAS · 2012 to 2013
$437k
Functional Neuroimaging of Attention in AutismR21MH092615 · NIMH · CHILDREN'S HOSP OF PHILADELPHIA · PI YERYS, BENJAMIN · 2011 to 2012
$427k
NICHD NIH HHS P50 HD105354NICHD NIH HHS U54 HD086984NIMH NIH HHS R01 MH073084NIMH NIH HHS R21 MH092615NIMH NIH HHS R21 MH098153NIMH NIH HHS RC1 MH088791
6 · The paper itself

Abstract

backgroundDespite decades of research, there is continued uncertainty regarding whether autism is associated with a specific profile of gray matter (GM) structure. This inconsistency may stem from the widespread use of voxel-based morphometry (VBM) methods that combine indices of GM density and GM volume. If GM density or volume, but not both, prove different in autism, the traditional VBM approach of combining the two indices may obscure the difference. The present study measures GM density and volume separately to examine whether autism is associated with alterations in GM volume, density, or both.

methodsDifferences in MRI-based GM density and volume were examined in 6-25 year-olds with a diagnosis of autism spectrum disorder (n = 213, 80.8% male, IQ 47-154) and a typically developing (TD) sample (n = 190, 71.6% male, IQ 67-155). High-resolution T1-weighted anatomical images were collected on a single MRI scanner. Regional density and volume were estimated via whole-brain parcellation comprised of 1625 parcels. Parcel-wise analyses were conducted using generalized additive models while controlling the false discovery rate (FDR, q < 0.05). Volume differences in the 68-region Desikan-Killiany atlas derived from Freesurfer were also examined, to establish the generalizability of findings across methods.

resultsNo density differences were observed between the autistic and TD groups, either in individual parcels or whole brain mean density. Increased volume was observed in autism compared to the TD group when controlling for Age, Sex, and IQ, both at the level of the whole brain (total volume) and in 45 parcels (2.8% of total parcels). Parcels with greater volume included inferior, middle, and superior temporal gyrus, inferior and superior frontal gyrus, precuneus, and fusiform gyrus. Converging evidence from a standard Freesurfer pipeline also identified greater volume in a number of overlapping regions. LIMITATIONS: The method for determining "density" is not a direct measure of neuronal density, and this study cannot reveal underlying cellular differences. While this study represents possibly the largest single-site sample of its kind, it is underpowered to detect very small differences.

conclusionsThese results provide compelling evidence that autism is associated with regional GM volumetric differences, which are more prominent than density differences. This underscores the importance of examining volume and density separately, and suggests that direct measures of volume (e.g. region-of-interest or tensor-based morphometry approaches) may be more sensitive to autism-relevant differences in neuroanatomy than concentration/density-based approaches.

Indexed as

Autism Spectrum DisorderAutistic DisorderBrainCerebral CortexFemaleGray MatterHumansMagnetic Resonance ImagingMale

Identifiers

PMID34911194
PMCPMC8633367

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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.