Evidence map›Paper›PMID 30322710›Full record

ArticleBiological psychiatry. Cognitive neuroscience and neuroimaging2019

Resilience to Risk for Psychopathology: The Role of White Matter Microstructural Development in Adolescence.

Scott A Jones, Angelica M Morales, Bonnie J Nagel

Open access · greenAbstract read
In one paragraph

Article in Biological psychiatry. Cognitive neuroscience and neuroimaging, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

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  15. Altered frontostriatal white matter microstructure is associated with familial alcoholism and future binge drinking in adolescence.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2019
    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

3 authors at 1 institution in 1 country.

Scott A JonesDepartment of Behavioral Neuroscience, Oregon Health & Science University, Portland, Oregon.
Angelica M MoralesDepartment of Behavioral Neuroscience, Oregon Health & Science University, Portland, Oregon.
Bonnie J NagelDepartment of Behavioral Neuroscience, Oregon Health & Science University, Portland, Oregon; Department of Psychiatry, Oregon Health & Science University, Portland, Oregon. Electronic address: nagelb@ohsu.edu.
Oregon Health & Science University · US

Funding

Timing Effects of Heavy Alcohol Initiation on Adolescent NeurodevelopmentR01AA017664 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI NAGEL, BONNIE J · 2009 to 2020
$3.7M
NIAAA NIH HHS R01 AA017664
6 · The paper itself

Abstract

backgroundOne major risk factor for the development of psychopathology is a family history of psychopathology (FHP). Cross-sectional studies have shown that FHP is associated with alterations in white matter microstructure in adolescents without current psychopathology; however, whether these associations persist throughout adolescence, particularly in those who remain resilient to developing psychopathology, is unclear.

methodsSixty-six adolescents underwent diffusion-weighted imaging at baseline (12-16 years of age) and at one or two follow-up visits (142 total scans). Adolescents' parents completed a modified Family History Assessment Module to calculate FHP density (FHPD) based on familial alcohol use, substance use, and major depressive, generalized anxiety, substance-induced mood, and antisocial personality disorders. The relationship between FHPD and white matter microstructural development was examined using multilevel modeling.

resultsFHPD was associated with significant alterations in white matter microstructure at baseline; in the bilateral superior corona radiata and left superior longitudinal fasciculus, these effects were transient (FHPD was associated with altered white matter microstructure only in early adolescence), while effects in the posterior limb of the internal capsule were persistent. Associations between FHPD and white matter microstructure in the body of the corpus callosum emerged later in adolescence.

conclusionsThis prospective, longitudinal study provides novel information indicating that the association between FHP and white matter microstructure previously observed in adolescents is transient in most regions but may persist into late adolescence in other regions, despite current resilience to developing psychopathology. Future studies are necessary to determine if these persistent alterations are associated with onset of psychopathology later in life.

Indexed as

Resilience, PsychologicalAdolescentBrainChildDiffusion Magnetic Resonance ImagingFemaleGenetic Predisposition to DiseaseHumansLongitudinal StudiesMaleMedical History TakingMental DisordersProspective StudiesWhite MatterAdolescenceFamily historyFractional anisotropyLongitudinalMRIPsychopathology

Identifiers

PMID30322710
PMCPMC6368895
OpenAlexW2888789883

What OpenQuestion holds

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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.