Evidence map›Paper›PMID 21730016›Full record

Trial reportJournal of psychopharmacology (Oxford, England)2012

Chronic tiagabine administration and aggressive responding in individuals with a history of substance abuse and antisocial behavior.

Joshua L Gowin, Charles E Green, Joseph L Alcorn, Alan C Swann, F Gerard Moeller, Scott D Lane

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of psychopharmacology (Oxford, England), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 45% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pharmacological interventions for antisocial personality disorder.The Cochrane database of systematic reviews · 2020
    Pooled it
  2. Review
  3. Review
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

6 authors at 2 institutions in 1 country.

Joshua L GowinProgram in Neuroscience, Graduate School of Biomedical Sciences, University of Texas Health Science Center, Houston, TX, USA.
Charles E Green
Joseph L Alcorn
Alan C Swann
F Gerard Moeller
Scott D Lane
The University of Texas Health Science Center at Houston · USCenter for Clinical Research (United States) · US

Funding

Translational MR Imaging in Cocaine Pharmacotherapy DevelopmentP50DA009262 · NIDA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI GREEN, CHARLES EDWARD · 1994 to 2014
$26.9M
DRUGS OF ABUSE AND HUMAN AGGRESSIVE BEHAVIORR01DA003166 · NIDA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI LANE, SCOTT D · 1985 to 2010
$2.7M
Serotonin, Impulsivity, and Substance AbuseK02DA000403 · NIDA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MOELLER, FREDERICK GERARD · 2000 to 2011
$1.2M
NIDA NIH HHS K02 DA000403NIDA NIH HHS K02 DA 00403NIDA NIH HHS P50 DA009262NIDA NIH HHS R01 DA003166NIDA NIH HHS R01 DA 03166
6 · The paper itself

Abstract

Anticonvulsants, notably those which modulate GABA activity, have shown efficacy in reducing aggressive behavior. Previously, we found dose-related decreases in human aggressive responding following acute tiagabine administration. Here, we examined the effects of chronic tiagabine over a 5-week period. Twelve individuals at increased risk for aggressive and violent behavior (currently on parole/probation with personality and/or substance use disorders) were randomly assigned to placebo (n = 6) or an escalating dose sequence of placebo, 4 mg, 8 mg, 12 mg, placebo (n = 6). Data were analyzed using both frequentist and Bayesian mixed models, evaluating aggressive behavior as a function of time, dose condition, and their interaction. For aggressive responding, there was a significant interaction of drug condition and time. Aggression in the tiagabine condition decreased for each additional week in the study, while participants in the placebo condition failed to demonstrate similar change over time. For monetary-reinforced responding, no drug or drug by time interactions were observed, suggesting specificity of drug effects on aggression. The small number of subjects limits the generality of the findings, and previous studies with tiagabine are limited to acute dosing and case report investigations. However, the present data provide an indication that tiagabine merits further examination as an agent for management of impulsive aggression.

Indexed as

AdultAggressionAnticonvulsantsAntisocial Personality DisorderBayes TheoremDiagnostic and Statistical Manual of Mental DisordersDose-Response Relationship, DrugFemaleGABA Uptake InhibitorsHumansImpulsive BehaviorMaleNipecotic AcidsPatient DropoutsPsychiatric Status Rating ScalesSubstance-Related DisordersAnticonvulsantsGABA Uptake InhibitorsNipecotic AcidsTiagabine

Identifiers

PMID21730016
PMCPMC4777893
OpenAlexW2139784860

What OpenQuestion holds

Textmetadata
LicenceTDM
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.