Evidence map›Paper›PMID 32552879›Full record

ArticleMolecular autism2020

Evidence against the "normalization" prediction of the early brain overgrowth hypothesis of autism.

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

Open access · goldAbstract read
In one paragraph

Article in Molecular autism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% of its field
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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
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  13. Unified framework for early stage status prediction of autism based on infant structural magnetic resonance imaging.Autism research : official journal of the International Society for Autism Research · 2021
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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

6 authors at 1 institution in 1 country.

Lisa D YankowitzCenter for Autism Research, Children's Hospital of Philadelphia, 2716 South St, Philadelphia, PA, 19104, USA. lisayank@sas.upenn.edu.ORCID 0000-0003-2604-5840
John D HerringtonCenter for Autism Research, Children's Hospital of Philadelphia, 2716 South St, Philadelphia, PA, 19104, USA.
Benjamin E YerysCenter for Autism Research, Children's Hospital of Philadelphia, 2716 South St, Philadelphia, PA, 19104, USA.
Joseph A PereiraCenter for Autism Research, Children's Hospital of Philadelphia, 2716 South St, Philadelphia, PA, 19104, USA.
Juhi PandeyCenter for Autism Research, Children's Hospital of Philadelphia, 2716 South St, Philadelphia, PA, 19104, USA.
Robert T SchultzCenter for Autism Research, Children's Hospital of Philadelphia, 2716 South St, Philadelphia, PA, 19104, USA.
Children's Hospital of Philadelphia · US

Funding

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 U54 HD086984NIMH NIH HHS R01 MH073084NIMH NIH HHS R21 MH092615NIMH NIH HHS R21 MH098153NIMH NIH HHS RC1 MH088791
6 · The paper itself

Abstract

backgroundThe frequently cited Early Overgrowth Hypothesis of autism spectrum disorder (ASD) postulates that there is overgrowth of the brain in the first 2 years of life, which is followed by a period of arrested growth leading to normalized brain volume in late childhood and beyond. While there is consistent evidence for early brain overgrowth, there is mixed evidence for normalization of brain volume by middle childhood. The outcome of this debate is important to understanding the etiology and neurodevelopmental trajectories of ASD.

methodsBrain volume was examined in two very large single-site samples of children, adolescents, and adults. The primary sample comprised 456 6-25-year-olds (ASD n = 240, typically developing controls (TDC) n = 216), including a large number of females (n = 102) and spanning a wide IQ range (47-158). The replication sample included 175 males. High-resolution T1-weighted anatomical MRI images were examined for group differences in total brain, cerebellar, ventricular, gray, and white matter volumes.

resultsThe ASD group had significantly larger total brain, cerebellar, gray matter, white matter, and lateral ventricular volumes in both samples, indicating that brain volume remains enlarged through young adulthood, rather than normalizing. There were no significant age or sex interactions with diagnosis in these measures. However, a significant diagnosis-by-IQ interaction was detected in the larger sample, such that increased brain volume was related to higher IQ in the TDCs, but not in the ASD group. Regions-of-significance analysis indicated that total brain volume was larger in ASD than TDC for individuals with IQ less than 115, providing a potential explanation for prior inconsistent brain size results. No relationships were found between brain volume and measures of autism symptom severity within the ASD group. LIMITATIONS: Our cross-sectional sample may not reflect individual changes over time in brain volume and cannot quantify potential changes in volume prior to age 6.

conclusionsThese findings challenge the "normalization" prediction of the brain overgrowth hypothesis by demonstrating that brain enlargement persists across childhood into early adulthood. The findings raise questions about the clinical implications of brain enlargement, since we find that it neither confers cognitive benefits nor predicts increased symptom severity in ASD.

Indexed as

Models, BiologicalAdolescentAdultAutistic DisorderBrainChildEducational StatusFemaleGray MatterHumansIntelligenceMagnetic Resonance ImagingMaleOrgan SizeParentsRacial GroupsAdolescentAutismBrain volumeIQMRIStructural imaging

Identifiers

PMID32552879
PMCPMC7301552
OpenAlexW3035817353

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.