Evidence map›Paper›PMID 27036876›Full record

ArticleSocial cognitive and affective neuroscience2016

An oxytocin receptor polymorphism predicts amygdala reactivity and antisocial behavior in men.

Rebecca Waller, Nadia S Corral-Frías, Bianca Vannucci, Ryan Bogdan, Annchen R Knodt, Ahmad R Hariri, Luke W Hyde

Open access · bronzeAbstract read
In one paragraph

Article in Social cognitive and affective neuroscience, 2016. 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
12.0field-weighted citation impact, top 1% 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, 45 citations in OpenAlex.

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  6. Accumbofrontal tract integrity is related to early life adversity and feedback learning.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2021
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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 at 3 institutions in 1 country.

Rebecca WallerDepartment of Psychology, University of Michigan, Ann Arbor, USA.
Nadia S Corral-FríasDepartment of Psychological and Brain Sciences, Washington University, St. Louis, USA.
Bianca VannucciDepartment of Psychological and Brain Sciences, Washington University, St. Louis, USA.
Ryan BogdanDepartment of Psychological and Brain Sciences, Washington University, St. Louis, USA.
Annchen R KnodtDepartment of Psychology and Neuroscience, Duke University, Durham, USA.
Ahmad R HaririDepartment of Psychology and Neuroscience, Duke University, Durham, USA.
Luke W HydeDepartment of Psychology, University of Michigan, Ann Arbor, USA lukehyde@umich.edu.
Washington University in St. Louis · USDuke University · USUniversity of Michigan–Ann Arbor · US

Funding

Quantifying Individual Differences in Midlife Structural Brain Integrity Associated with Later AD/ADRD RiskR01AG049789 · NIA · DUKE UNIVERSITY · PI AHMAD R. HARIRI, TERRIE E MOFFITT · 2015 to 2026
$10.6M
Training in the Genetics and Molecular Biology of Mental DisordersT32MH014677 · NIMH · WASHINGTON UNIVERSITY · PI RICE, JOHN P. · 1985 to 2020
$3.6M
Personality and Health in Later Life: Psychosocial and Biological MechanismsR01AG045231 · NIA · WASHINGTON UNIVERSITY · PI OLTMANNS, THOMAS · 2014 to 2018
$2.9M
Neurogenetic Pathways to Drug Use in Young AdultsR01DA033369 · NIDA · DUKE UNIVERSITY · PI HARIRI, AHMAD R. · 2013 to 2016
$1.4M
NIA NIH HHS R01 AG045231NIA NIH HHS R01 AG049789NIDA NIH HHS L40 DA036468NIDA NIH HHS R01 DA033369NIMH NIH HHS L40 MH108392NIMH NIH HHS T32 MH014677
6 · The paper itself

Abstract

Variability in oxytocin (OXT) signaling is associated with individual differences in sex-specific social behavior across species. The effects of OXT signaling on social behavior are, in part, mediated through its modulation of amygdala function. Here, we use imaging genetics to examine sex-specific effects of three single-nucleotide polymorphisms in the human oxytocin receptor gene (OXTR; rs1042778, rs53576 and rs2254298) on threat-related amygdala reactivity and social behavior in 406 Caucasians. Analyses revealed that among men but not women, OXTR rs1042778 TT genotype was associated with increased right amygdala reactivity to angry facial expressions, which was uniquely related to higher levels of antisocial behavior among men. Moderated meditation analysis suggested a trending indirect effect of OXTR rs1042778 TT genotype on higher antisocial behavior via increased right amygdala reactivity to angry facial expressions in men. Our results provide evidence linking genetic variation in OXT signaling to individual differences in amygdala function. The results further suggest that these pathways may be uniquely important in shaping antisocial behavior in men.

Indexed as

Facial ExpressionSocial BehaviorAdolescentAdultAmygdalaAngerAntisocial Personality DisorderFemaleHumansMalePolymorphism, Single NucleotideReceptors, OxytocinSex FactorsYoung AdultOXTR protein, humanReceptors, OxytocinaggressionamygdalaneuroimagingneuroscienceOXTRoxytocinpsychopathologyrs1042778violence

Identifiers

PMID27036876
PMCPMC4967804
OpenAlexW2335196379

What OpenQuestion holds

Textmetadata
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.