Evidence map›Paper›PMID 29251836›Full record

ArticleAutism research : official journal of the International Society for Autism Research2018

Longitudinal development of thalamic and internal capsule microstructure in autism spectrum disorder.

Kristine McLaughlin, Brittany G Travers, Olga I Dadalko, Douglas C Dean, Do Tromp, Nagesh Adluru, Daniel Destiche, Abigail Freeman, Molly D Prigge, Alyson Froehlich and 7 more

Abstract read
In one paragraph

Article in Autism research : official journal of the International Society for Autism Research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

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

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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

17 authors.

Kristine McLaughlinWaisman Center, University of Wisconsin-Madison, Madison, Wisconsin.
Brittany G TraversWaisman Center, University of Wisconsin-Madison, Madison, Wisconsin.ORCID 0000-0002-8161-3858
Olga I DadalkoWaisman Center, University of Wisconsin-Madison, Madison, Wisconsin.
Douglas C DeanWaisman Center, University of Wisconsin-Madison, Madison, Wisconsin.
Do TrompWaisman Center, University of Wisconsin-Madison, Madison, Wisconsin.
Nagesh AdluruWaisman Center, University of Wisconsin-Madison, Madison, Wisconsin.
Daniel DesticheWaisman Center, University of Wisconsin-Madison, Madison, Wisconsin.
Abigail FreemanWaisman Center, University of Wisconsin-Madison, Madison, Wisconsin.
Molly D PriggeWaisman Center, University of Wisconsin-Madison, Madison, Wisconsin.
Alyson FroehlichPediatrics, University of Utah, Salt Lake City, Utah.
Tyler C DuffieldPsychology/Neuroscience Center, Brigham Young University, Provo, Utah.
Brandon A ZielinskiPediatrics, University of Utah, Salt Lake City, Utah.
Erin D BiglerPsychology/Neuroscience Center, Brigham Young University, Provo, Utah.
Nicholas LangeHarvard Psychiatry & McLean Hospital, Belmont, Massachusetts.
Jeff S AndersonRadiology, University of Utah, Salt Lake City, Utah.
Andrew L AlexanderWaisman Center, University of Wisconsin-Madison, Madison, Wisconsin.
Janet E LainhartWaisman Center, University of Wisconsin-Madison, Madison, Wisconsin.

Funding

WISCONSIN CENTER ON MENTAL RETARDATION: CORE SUPPORTP30HD003352 · NICHD · UNIVERSITY OF WISCONSIN-MADISON · PI SVAREN, JOHN P · 1985 to 2015
$25.2M
Atypical Late Neurodevelopment in Autism: A Longitudinal MRI and DTI StudyR01MH080826 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI LAINHART, JANET ELIZABETH · 2007 to 2020
$6.5M
POSTDOCTORAL TRAINING IN MENTAL RETARDATION RESEARCHT32HD007489 · NICHD · UNIVERSITY OF WISCONSIN-MADISON · PI Sigan L Hartley · 1995 to 2026
$6.0M
Waisman Intellectual and Developmental Disabilities Research Center Down Syndrome RegistryU54HD090256 · NICHD · UNIVERSITY OF WISCONSIN-MADISON · PI POLLAK, SETH D · 2016 to 2020
$6.0M
Biological Determinants of Brain Variation in AutismR01MH097464 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI LAINHART, JANET ELIZABETH, LANGE, NICHOLAS T · 2013 to 2017
$2.9M
The Microstructural Basis of Abnormal Connectivity in AutismR01MH084795 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI LAINHART, JANET ELIZABETH · 2009 to 2013
$1.9M
Longitudinal Characterization of Functional Connectivity in AutismK08MH092697 · NIMH · UNIVERSITY OF UTAH · PI ANDERSON, JEFFREY · 2011 to 2015
$912k
Brain Network Development in Normal and Autistic ChildrenK08MH100609 · NIMH · UNIVERSITY OF UTAH · PI ZIELINSKI, BRANDON A. · 2014 to 2017
$759k
BRAIN CONNECTIVITY AND THE ROLE OF MYELIN IN AUTISM SPECTRUM DISORDERSK99MH110596 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI DEAN III, DOUGLAS CARL · 2017 to 2018
$270k
NICHD NIH HHS P30 HD003352NICHD NIH HHS T32 HD007489NICHD NIH HHS U54 HD090256NIMH NIH HHS K08 MH092697NIMH NIH HHS K08 MH100609NIMH NIH HHS K99 MH110596NIMH NIH HHS R01 MH080826NIMH NIH HHS R01 MH084795NIMH NIH HHS R01 MH097464
6 · The paper itself

Abstract

The thalamus is a key sensorimotor relay area that is implicated in autism spectrum disorder (ASD). However, it is unknown how the thalamus and white-matter structures that contain thalamo-cortical fiber connections (e.g., the internal capsule) develop from childhood into adulthood and whether this microstructure relates to basic motor challenges in ASD. We used diffusion weighted imaging in a cohort-sequential design to assess longitudinal development of the thalamus, and posterior- and anterior-limbs of the internal capsule (PLIC and ALIC, respectively) in 89 males with ASD and 56 males with typical development (3-41 years; all verbal). Our results showed that the group with ASD exhibited different developmental trajectories of microstructure in all regions, demonstrating childhood group differences that appeared to approach and, in some cases, surpass the typically developing group in adolescence and adulthood. The PLIC (but not ALIC nor thalamus) mediated the relation between age and finger-tapping speed in both groups. Yet, the gap in finger-tapping speed appeared to widen at the same time that the between-group gap in the PLIC appeared to narrow. Overall, these results suggest that childhood group differences in microstructure of the thalamus and PLIC become less robust in adolescence and adulthood. Further, finger-tapping speed appears to be mediated by the PLIC in both groups, but group differences in motor speed that widen during adolescence and adulthood suggest that factors beyond the microstructure of the thalamus and internal capsule may contribute to atypical motor profiles in ASD. Autism Res 2018, 11: 450-462. © 2017 International Society for Autism Research, Wiley Periodicals, Inc. LAY SUMMARY: Microstructure of the thalamus, a key sensory and motor brain area, appears to develop differently in individuals with autism spectrum disorder (ASD). Microstructure is important because it informs us of the density and organization of different brain tissues. During childhood, thalamic microstructure was distinct in the ASD group compared to the typically developing group. However, these group differences appeared to narrow with age, suggesting that the thalamus continues to dynamically change in ASD into adulthood.

Indexed as

AdolescentAdultAutism Spectrum DisorderChildChild, PreschoolCohort StudiesDiffusion Magnetic Resonance ImagingHumansInternal CapsuleLongitudinal StudiesMaleThalamusYoung Adultautism spectrum disorderdiffusion magnetic resonance imaginginternal capsulethalamuswhite matter

Identifiers

PMID29251836
PMCPMC5867209

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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.