Evidence map›Paper›PMID 33349451›Full record

ArticleBiological psychiatry2021

A Longitudinal Study of White Matter Development in Relation to Changes in Autism Severity Across Early Childhood.

Derek Sayre Andrews, Joshua K Lee, Danielle Jenine Harvey, Einat Waizbard-Bartov, Marjorie Solomon, Sally J Rogers, Christine Wu Nordahl, David G Amaral

Open access · greenAbstract read
In one paragraph

Article in Biological psychiatry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 3 pooled it
4.1field-weighted citation impact, top 5% 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

47 citing papers in PubMed, 3 syntheses or guidelines pooled it, 78 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

8 authors at 2 institutions in 1 country.

Derek Sayre AndrewsMedical Investigation of Neurodevelopmental Disorders Institute and Department of Psychiatry and Behavioral Sciences, School of Medicine, University of California, Davis, Sacramento, California. Electronic address: dandrews@ucdavis.edu.
Joshua K LeeMedical Investigation of Neurodevelopmental Disorders Institute and Department of Psychiatry and Behavioral Sciences, School of Medicine, University of California, Davis, Sacramento, California.
Danielle Jenine HarveyDivision of Biostatistics, Department of Public Health Sciences, University of California, Davis, Davis, California.
Einat Waizbard-BartovMedical Investigation of Neurodevelopmental Disorders Institute and Department of Psychiatry and Behavioral Sciences, School of Medicine, University of California, Davis, Sacramento, California.
Marjorie SolomonMedical Investigation of Neurodevelopmental Disorders Institute and Department of Psychiatry and Behavioral Sciences, School of Medicine, University of California, Davis, Sacramento, California.
Sally J RogersMedical Investigation of Neurodevelopmental Disorders Institute and Department of Psychiatry and Behavioral Sciences, School of Medicine, University of California, Davis, Sacramento, California.
Christine Wu NordahlMedical Investigation of Neurodevelopmental Disorders Institute and Department of Psychiatry and Behavioral Sciences, School of Medicine, University of California, Davis, Sacramento, California.
David G AmaralMedical Investigation of Neurodevelopmental Disorders Institute and Department of Psychiatry and Behavioral Sciences, School of Medicine, University of California, Davis, Sacramento, California.
University of California, Davis · USUniversity of California Davis Medical Center · US

Funding

Specifying and Treating the Anxiety Phenotype in Autism Spectrum DisorderP50HD093079 · NICHD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI AMARAL, DAVID G · 2017 to 2021
$11.4M
Rodent Behavior CoreU54HD079125 · NICHD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI ABBEDUTO, LEONARD J. · 2013 to 2019
$8.5M
Interdisciplinary Training for Autism Researchers(RMI)T32MH073124 · NIMH · UNIVERSITY OF CALIFORNIA DAVIS · PI Stephen Charles Noctor, Christine Wu Nordahl · 2004 to 2026
$6.8M
Predictors of Cognitive Development in Autism Spectrum DisorderR01MH103284 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI SOLOMON, MARJORIE · 2014 to 2024
$6.3M
Neural Phenotypes of Females with Autism Spectrum DisorderR01MH104438 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI NORDAHL, CHRISTINE WU · 2014 to 2018
$3.5M
Neurophenotypic Trajectories and Behavioral Outcomes in Autism Spectrum DisorderR01MH103371 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI AMARAL, DAVID G · 2015 to 2019
$3.4M
Neurodevelopment of cognitive control in autism: adolescence to young adulthoodR01MH106518 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI SOLOMON, MARJORIE · 2016 to 2020
$3.1M
NICHD NIH HHS P50 HD093079NICHD NIH HHS U54 HD079125NIMH NIH HHS R01 MH103284NIMH NIH HHS R01 MH103371NIMH NIH HHS R01 MH104438NIMH NIH HHS R01 MH106518NIMH NIH HHS T32 MH073124
6 · The paper itself

Abstract

backgroundCross-sectional diffusion-weighted magnetic resonance imaging studies suggest that young autistic children have alterations in white matter structure that differ from older autistic individuals. However, it is unclear whether these differences result from atypical neurodevelopment or sampling differences between young and older cohorts. Furthermore, the relationship between altered white matter development and longitudinal changes in autism symptoms is unknown.

methodsUsing longitudinal diffusion-weighted magnetic resonance imaging acquired over 2 to 3 time points between the ages of approximately 2.5 to 7.0 years in 125 autistic children and 69 typically developing control participants, we directly tested the hypothesis that autistic individuals have atypical white matter development across childhood. Additionally, we sought to determine whether changes in white matter diffusion parameters were associated with longitudinal changes in autism severity.

resultsAutistic children were found to have slower development of fractional anisotropy in the cingulum bundle, superior longitudinal fasciculus, internal capsule, and splenium of the corpus callosum. Furthermore, in the sagittal stratum, autistic individuals who increased in autism severity over time had a slower developmental trajectory of fractional anisotropy compared with individuals whose autism decreased in severity. In the uncinate fasciculus, autistic individuals who decreased in autism symptom severity also had greater increases in fractional anisotropy with age.

conclusionsThese longitudinal findings indicate that previously reported differences in diffusion-weighted magnetic resonance imaging measures between younger and older autism cohorts are attributable to an atypical developmental trajectory of white matter. Differences in white matter development between individuals whose autism severity increased, remained stable, or decreased suggest that these functional differences are associated with fiber development in the autistic brain.

Indexed as

Autistic DisorderWhite MatterAnisotropyBrainChildChild, PreschoolCross-Sectional StudiesDiffusion Magnetic Resonance ImagingHumansLongitudinal StudiesAutismDevelopmentDiffusionImagingLongitudinalWhite Matter

Identifiers

PMID33349451
PMCPMC7867569
OpenAlexW3096200516

What OpenQuestion holds

Textmetadata
LicenceTDM
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.