Evidence map›Paper›PMID 24742620›Full record

ArticleBiological psychiatry2014

Development of impulse control circuitry in children of alcoholics.

Jillian E Hardee, Barbara J Weiland, Thomas E Nichols, Robert C Welsh, Mary E Soules, Davia B Steinberg, Jon-Kar Zubieta, Robert A Zucker, Mary M Heitzeg

Abstract read
In one paragraph

Article in Biological psychiatry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 2 pooled it
3.9field-weighted citation impact, top 6% 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

39 citing papers in PubMed, 2 syntheses or guidelines pooled it, 59 citations in OpenAlex.

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  10. FACTORS CONTRIBUTING TO THE ESCALATION OF ALCOHOL CONSUMPTION.Neuroscience and biobehavioral reviews · 2022
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Jillian E HardeeDepartment of Psychiatry, University of Michigan, Ann Arbor, Michigan; Addiction Research Center, University of Michigan, Ann Arbor, Michigan.
Barbara J WeilandDepartment of Psychiatry, University of Michigan, Ann Arbor, Michigan; Addiction Research Center, University of Michigan, Ann Arbor, Michigan; Department of Psychology and Neuroscience, University of Colorado, Boulder, Colorado.
Thomas E NicholsDepartment of Statistics & Warwick Manufacturing Group, University of Warwick, Coventry, United Kingdom.
Robert C WelshDepartment of Psychiatry, University of Michigan, Ann Arbor, Michigan; Department of Radiology, University of Michigan, Ann Arbor, Michigan.
Mary E SoulesDepartment of Psychiatry, University of Michigan, Ann Arbor, Michigan; Addiction Research Center, University of Michigan, Ann Arbor, Michigan.
Davia B SteinbergDepartment of Psychiatry, University of Michigan, Ann Arbor, Michigan; Addiction Research Center, University of Michigan, Ann Arbor, Michigan.
Jon-Kar ZubietaDepartment of Psychiatry, University of Michigan, Ann Arbor, Michigan; Molecular and Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, Michigan.
Robert A ZuckerDepartment of Psychiatry, University of Michigan, Ann Arbor, Michigan; Addiction Research Center, University of Michigan, Ann Arbor, Michigan.
Mary M HeitzegDepartment of Psychiatry, University of Michigan, Ann Arbor, Michigan; Addiction Research Center, University of Michigan, Ann Arbor, Michigan. Electronic address: mheitzeg@umich.edu.
University of Michigan–Ann Arbor · USUniversity of Colorado Boulder · USUniversity of Warwick · GB

Funding

Family Study of Risk for Alcoholism Over the Life CourseR37AA007065 · NIAAA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZUCKER, ROBERT ALPERT · 2003 to 2012
$10.6M
Neurocognitive Risk For Alcoholism Into AdulthoodR01AA012217 · NIAAA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HEITZEG, MARY M, ZUCKER, ROBERT ALPERT · 2000 to 2015
$7.3M
RISK AND COPING IN CHILDREN OF ALCOHOLICSR01AA007065 · NIAAA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HEITZEG, MARY M · 1987 to 2017
$6.1M
Brain Endophenotypes Modulating Drug Abuse RiskR01DA027261 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZUCKER, ROBERT ALPERT · 2009 to 2013
$3.3M
Longitudinal fMRI Study of Youth at Risk for Drug AbuseK01DA020088 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HEITZEG, MARY M · 2005 to 2009
$732k
Role of the Dopaminergic Reward System in Substance Abuse RiskK01DA031755 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WEILAND, BARBARA J · 2011 to 2014
$615k
NIAAA NIH HHS R01 AA007065NIAAA NIH HHS R01 AA012217NIAAA NIH HHS R01 AA12217NIAAA NIH HHS R37 AA007065NIAAA NIH HHS R37 AA07065NIDA NIH HHS K01 DA020088NIDA NIH HHS K01 DA031755NIDA NIH HHS R01 DA027261Wellcome Trust 100309
6 · The paper itself

Abstract

backgroundDifficulty with impulse control is heightened in children with a family history of alcohol use disorders and is a risk factor for later substance problems. Cross-sectional functional magnetic resonance imaging studies have shown altered impulse control processing in adolescents with a positive family history, yet developmental trajectories have yet to be examined.

methodsLongitudinal functional magnetic resonance imaging was conducted in children of alcoholic families (family history positive [FH+]; n = 43) and children of control families (family history negative [FH-]; n = 30) starting at ages 7-12 years. Participants performed a go/no-go task during functional magnetic resonance imaging at intervals of 1-2 years, with two to four scans performed per subject. We implemented a repeated-measures linear model fit across all subjects to conduct a whole-brain search for developmental differences between groups.

resultsPerformance improved with age in both groups, and there were no performance differences between groups. Significant between-group differences in linear age-related activation changes were found in the right caudate, middle cingulate, and middle frontal gyrus. Post hoc analyses revealed significant activation decreases with age in the caudate and middle frontal gyrus for FH- subjects and a significant increase with age in middle cingulate activation for FH+ subjects. Group differences were evident at age 7-12 years, even in alcohol- and drug-naïve participants, with FH+ subjects showing significantly blunted activation at baseline compared with FH- subjects.

conclusionsDifferences in response inhibition circuitry are visible in FH+ individuals during childhood; these differences continue into adolescence, displaying trajectories that are inconsistent with development of normal response inhibition. These patterns precede problem drinking and may be a contributing factor for subsequent substance use problems.

Indexed as

Brain MappingAge FactorsAlcoholismBrainChildChoice BehaviorCross-Sectional StudiesFemaleFunctional LateralityHumansImage Processing, Computer-AssistedImpulsive BehaviorLinear ModelsMagnetic Resonance ImagingMaleNeuropsychological TestsOxygenAdolescencealcoholismcaudatecingulatedevelopmentresponse inhibition

Identifiers

PMID24742620
PMCPMC4163541
OpenAlexW2043372518

What OpenQuestion holds

Textmetadata
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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.