Evidence map›Paper›PMID 25637908›Full record

ArticleBehavioural brain research2015

Monoamine oxidase A (MAOA) genotype predicts greater aggression through impulsive reactivity to negative affect.

David S Chester, C Nathan DeWall, Karen J Derefinko, Steven Estus, Jessica R Peters, Donald R Lynam, Yang Jiang

Abstract read
In one paragraph

Article in Behavioural brain research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–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

25 citing papers in PubMed.

  1. Trial
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  10. Single-Dose of Testosterone and theFrontiers in behavioral neuroscience · 2020
    Article
  11. Article
  12. Identification of Single Nucleotide Polymorphisms in PorcineAnimals : an open access journal from MDPI · 2019
    Article
  13. Review
  14. Article
  15. Review
  16. Article
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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

7 authors.

David S ChesterDepartment of Psychology, University of Kentucky, 0003 Kastle Hall, Lexington, KY 40506, USA. Electronic address: davidchester@uky.edu.
C Nathan DeWallDepartment of Psychology, University of Kentucky, 0003 Kastle Hall, Lexington, KY 40506, USA.
Karen J DerefinkoDepartment of Psychology, University of Kentucky, 0003 Kastle Hall, Lexington, KY 40506, USA.
Steven EstusDepartment of Physiology, University of Kentucky, Lexington, KY, USA; Sanders-Brown Center on Aging, University of Kentucky, Lexington, KY, USA.
Jessica R PetersDepartment of Psychology, University of Kentucky, 0003 Kastle Hall, Lexington, KY 40506, USA.
Donald R LynamDepartment of Psychological Sciences, Purdue University, West Lafayette, IN, USA.
Yang JiangSanders-Brown Center on Aging, University of Kentucky, Lexington, KY, USA; Department of Behavioral Science, University of Kentucky, Lexington, KY, USA.

Funding

Training and Pilot CoreP50DA005312 · NIDA · UNIVERSITY OF KENTUCKY · PI BARDO, MICHAEL T · 1987 to 2016
$19.5M
Kentucky Center for Clinical and Translational ScienceUL1TR000117 · NCATS · UNIVERSITY OF KENTUCKY · PI KERN, PHILIP A · 2012 to 2015
$13.3M
HIV NEUROTOXICITY--MECHANISM &MODULATION BY CANABINOIDSR01DA007304 · NIDA · UNIVERSITY OF MINNESOTA TWIN CITIES · PI THAYER, STANLEY A · 1992 to 2024
$5.0M
Research Training in Drug Abuse BehaviorT32DA035200 · NIDA · UNIVERSITY OF KENTUCKY · PI CRAIG R RUSH, William Walton Stoops · 2013 to 2026
$4.4M
HIV Neurotoxicity-Mechanism &Modulation by CannabinoidsR37DA007304 · NIDA · UNIVERSITY OF MINNESOTA TWIN CITIES · PI THAYER, STANLEY A · 2004 to 2013
$3.1M
RESEARCH TRAINING IN DRUG ABUSE BEHAVIORT32DA007304 · NIDA · UNIVERSITY OF KENTUCKY · PI RUSH, CRAIG R · 1998 to 2012
$3.1M
NCATS NIH HHS UL1 TR000117NCATS NIH HHS UL1TR000117NIDA NIH HHS DA007304NIDA NIH HHS P50 DA005312NIDA NIH HHS P50-DA05312NIDA NIH HHS R01 DA007304NIDA NIH HHS R37 DA007304NIDA NIH HHS T32 DA007304NIDA NIH HHS T32 DA035200NIDA NIH HHS T32DA035200
6 · The paper itself

Abstract

Low functioning MAOA genotypes have been reliably linked to increased reactive aggression, yet the psychological mechanisms of this effect remain largely unknown. The low functioning MAOA genotype's established link to diminished inhibition and greater reactivity to conditions of negative affect suggest that negative urgency, the tendency to act impulsively in the context of negative affect, may fill this mediating role. Such MAOA carriers may have higher negative urgency, which may in turn predict greater aggressive responses to provocation. To test these hypotheses, 277 female and male participants were genotyped for an MAOA SNP yet to be linked to aggression (rs1465108), and then reported their negative urgency and past aggressive behavior. We replicated the effect of the low functioning MAOA genotype on heightened aggression, which was mediated by greater negative urgency. These results suggest that disrupted serotonergic systems predispose individuals towards aggressive behavior by increasing impulsive reactivity to negative affect.

Indexed as

AggressionImpulsive BehaviorPolymorphism, Single NucleotideAdolescentFemaleGenotypeGenotyping TechniquesHumansMaleModels, NeurologicalModels, PsychologicalMonoamine OxidasePsychological TestsYoung AdultMonoamine OxidaseAggressionGeneticsImpulsivityMAOANegative urgencyUPPS model

Identifiers

PMID25637908
PMCPMC4351151

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.