Evidence map›Paper›PMID 24576686›Full record

Trial reportBiological psychiatry2014

Testosterone rapidly increases neural reactivity to threat in healthy men: a novel two-step pharmacological challenge paradigm.

Stefan M M Goetz, Lingfei Tang, Moriah E Thomason, Michael P Diamond, Ahmad R Hariri, Justin M Carré

Registry-linked trialOpen access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Biological psychiatry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02734238 (Physiological and Psychological Effects of Testosterone During Severe Energy Deficit and Recovery), which is not on this map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
26.1field-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.

NCT02734238 phase4completednot on this mapstarted 2016, after this paper: background citation

Physiological and Psychological Effects of Testosterone During Severe Energy Deficit and Recovery: a Randomized, Placebo Controlled Trial

TypeinterventionalSponsorPennington Biomedical Research CenterRan2016 to 2017Enrolled53ConditionsCaloric Restriction, ExerciseArmsSesame Oil, testosterone enanthate
3 · Its place in the literature

Who cites it

50 citing papers in PubMed, 187 citations in OpenAlex.

  1. Investigating the effects of single-dose intranasal testosterone on economic preferences in a large randomized trial of men.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  2. Effect of exogenous testosterone on cooperation depends on personality and time pressure.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2019
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  8. Prenatal Interferon-Alpha Exposure Induces Autism-Like Neurobehavioral and Neurochemical Alterations in Male Offspring.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Stefan M M GoetzDepartment of Psychology, Wayne State University, Detroit, Michigan.
Lingfei TangDepartment of Psychology, Wayne State University, Detroit, Michigan.
Moriah E ThomasonMerrill Palmer Skillman Institute, Wayne State University, Detroit, Michigan; Department of Pediatrics, Wayne State University, Detroit, Michigan.
Michael P DiamondDepartment of Obstetrics and Gynecology, Georgia Regents University, Augusta, Georgia.
Ahmad R HaririDepartment of Pediatrics, Wayne State University, Detroit, Michigan; Department of Psychology and Neuroscience, Duke University, Durham, North Carolina; Institute for Genome Sciences and Policy, Duke University, Durham, North Carolina.
Justin M CarréDepartment of Psychology, Wayne State University, Detroit, Michigan; Department of Psychology, Nipissing University, North Bay, Ontario, Canada. Electronic address: justinca@nipissingu.ca.
Wayne State University · USAugusta University · USNipissing University · CA

Funding

In Utero Assessment of the Human Neural Connectome and Later Child BehaviorR01MH110793 · NIMH · WAYNE STATE UNIVERSITY · PI THOMASON, MORIAH E · 2016 to 2021
$2.7M
Self-Regulation Failure: Identifying and Modifying a Risk PhenotypeR01DA031579 · NIDA · DUKE UNIVERSITY · PI HARIRI, AHMAD R., STRAUMAN, TIMOTHY J · 2010 to 2012
$1.9M
Neurogenetic Pathways to Drug Use in Young AdultsR01DA033369 · NIDA · DUKE UNIVERSITY · PI HARIRI, AHMAD R. · 2013 to 2016
$1.4M
Consequences of prenatal toxicant exposure on fetal brain functionR21ES026022 · NIEHS · MICHIGAN STATE UNIVERSITY · PI BURT, S. ALEXANDRA, THOMASON, MORIAH E · 2015 to 2016
$451k
NIDA NIH HHS R01 DA031579NIDA NIH HHS R01 DA033369NIEHS NIH HHS R21 ES026022NIMH NIH HHS R01 MH110793
6 · The paper itself

Abstract

backgroundPrevious research suggests that testosterone (T) plays a key role in shaping competitive and aggressive behavior in humans, possibly by modulating threat-related neural circuitry. However, this research has been limited by the use of T augmentation that fails to account for baseline differences and has been conducted exclusively in women. Thus, the extent to which normal physiologic concentrations of T affect threat-related brain function in men remains unknown.

methodsIn the current study, we use a novel two-step pharmacologic challenge protocol to overcome these limitations and to evaluate causal modulation of threat- and aggression-related neural circuits by T in healthy young men (n = 16). First, we controlled for baseline differences in T through administration of a gonadotropin releasing hormone antagonist. Once a common baseline was established across participants, we then administered T to within the normal physiologic range. During this second step of the protocol we acquired functional neuroimaging data to examine the impact of T augmentation on neural circuitry supporting threat and aggression.

resultsGonadotropin releasing hormone antagonism successfully reduced circulating concentrations of T and brought subjects to a common baseline. Administration of T rapidly increased circulating T concentrations and was associated with heightened reactivity of the amygdala, hypothalamus, and periaqueductal grey to angry facial expressions.

conclusionsThese findings provide novel causal evidence that T rapidly potentiates the response of neural circuits mediating threat processing and aggressive behavior in men.

Indexed as

Facial ExpressionAdolescentAdultAggressionBlood Chemical AnalysisBrainCross-Over StudiesDouble-Blind MethodGonadotropin-Releasing HormoneHormone AntagonistsHumansMagnetic Resonance ImagingMaleNeuropsychological TestsOxygenPhotic StimulationGonadotropin-Releasing HormoneHormone AntagonistsOxygenTestosteroneAggressionamygdalaandrogensangeremotionfMRItestosterone

Identifiers

PMID24576686
PMCPMC9552187
OpenAlexW2074347579

What OpenQuestion holds

Textmetadata
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Registered trials

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.