Evidence map›Paper›PMID 27271503›Full record

ArticlePloS one2016

A Whole-Brain Investigation of White Matter Microstructure in Adolescents with Conduct Disorder.

Sagari Sarkar, Flavio Dell'Acqua, Seán Froudist Walsh, Nigel Blackwood, Stephen Scott, Michael C Craig, Quinton Deeley, Declan G M Murphy

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

8 citing papers in PubMed, 19 citations in OpenAlex.

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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

8 authors at 4 institutions in 2 countries.

Sagari SarkarKing's College London, Sackler Institute for Translational Neurodevelopment and the Department of Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, London, United Kingdom.
Flavio Dell'AcquaKing's College London, Sackler Institute for Translational Neurodevelopment and the Department of Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, London, United Kingdom.
Seán Froudist WalshFriedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York, United States of America.
Nigel BlackwoodKing's College London, Sackler Institute for Translational Neurodevelopment and the Department of Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, London, United Kingdom.
Stephen ScottKing's College London, Department of Child and Adolescent Psychiatry, Institute of Psychiatry, Psychology and Neuroscience, London, United Kingdom.
Michael C CraigKing's College London, Sackler Institute for Translational Neurodevelopment and the Department of Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, London, United Kingdom.
Quinton DeeleyKing's College London, Sackler Institute for Translational Neurodevelopment and the Department of Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, London, United Kingdom.
Declan G M MurphyKing's College London, Sackler Institute for Translational Neurodevelopment and the Department of Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, London, United Kingdom.
King's College London · GBCentre for Mental Health · GBAllen Institute for Brain Science · USSouth London and Maudsley NHS Foundation Trust · GB

Funding

Department of Health RP-PG-0606-1045Medical Research Council G0400061Medical Research Council MR/N026063/1
6 · The paper itself

Abstract

backgroundThe biological basis of severe antisocial behaviour in adolescents is poorly understood. We recently reported that adolescents with conduct disorder (CD) have significantly increased fractional anisotropy (FA) of the uncinate fasciculus (a white matter (WM) tract that connects the amygdala to the frontal lobe) compared to their non-CD peers. However, the extent of WM abnormality in other brain regions is currently unclear.

methodsWe used tract-based spatial statistics to investigate whole brain WM microstructural organisation in 27 adolescent males with CD, and 21 non-CD controls. We also examined relationships between FA and behavioural measures. Groups did not differ significantly in age, ethnicity, or substance use history.

resultsThe CD group, compared to controls, had clusters of significantly greater FA in 7 brain regions corresponding to: 1) the bilateral inferior and superior cerebellar peduncles, corticopontocerebellar tract, posterior limb of internal capsule, and corticospinal tract; 2) right superior longitudinal fasciculus; and 3) left cerebellar WM. Severity of antisocial behavior and callous-unemotional symptoms were significantly correlated with FA in several of these regions across the total sample, but not in the CD or control groups alone.

conclusionsAdolescents with CD have significantly greater FA than controls in WM regions corresponding predominantly to the fronto-cerebellar circuit. There is preliminary evidence that variation in WM microstructure may be dimensionally related to behaviour problems in youngsters. These findings are consistent with the hypothesis that antisocial behaviour in some young people is associated with abnormalities in WM 'connectivity'.

Indexed as

AdolescentAdolescent BehaviorAnisotropyAntisocial Personality DisorderBrain MappingCase-Control StudiesChildConduct DisorderDiffusion Tensor ImagingDrug UsersHumansMaleWhite MatterYoung Adult

Identifiers

PMID27271503
PMCPMC4894575
OpenAlexW2419308306

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.