Evidence map›Paper›PMID 34256607›Full record

Trial reportThe American journal of psychiatry2021

Effects of Gabapentin on Dorsal Anterior Cingulate Cortex GABA and Glutamate Levels and Their Associations With Abstinence in Alcohol Use Disorder: A Randomized Clinical Trial.

James J Prisciandaro, Michaela Hoffman, Truman R Brown, Konstantin Voronin, Sarah Book, Emily Bristol, Raymond F Anton

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The American journal of psychiatry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
2.3field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 27 citations in OpenAlex.

  1. Pooled it
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  8. Review
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  13. Alcohol Use Disorder and Chronic Pain: An Overlooked Epidemic.The American journal of psychiatry · 2024
    Review
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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 1 institution in 1 country.

James J PrisciandaroDepartment of Psychiatry and Behavioral Sciences, Addiction Sciences Division (Prisciandaro, Hoffman, Voronin, Book, Bristol, Anton), and Department of Radiology (Brown), Medical University of South Carolina, Charleston.
Michaela HoffmanDepartment of Psychiatry and Behavioral Sciences, Addiction Sciences Division (Prisciandaro, Hoffman, Voronin, Book, Bristol, Anton), and Department of Radiology (Brown), Medical University of South Carolina, Charleston.
Truman R BrownDepartment of Psychiatry and Behavioral Sciences, Addiction Sciences Division (Prisciandaro, Hoffman, Voronin, Book, Bristol, Anton), and Department of Radiology (Brown), Medical University of South Carolina, Charleston.
Konstantin VoroninDepartment of Psychiatry and Behavioral Sciences, Addiction Sciences Division (Prisciandaro, Hoffman, Voronin, Book, Bristol, Anton), and Department of Radiology (Brown), Medical University of South Carolina, Charleston.
Sarah BookDepartment of Psychiatry and Behavioral Sciences, Addiction Sciences Division (Prisciandaro, Hoffman, Voronin, Book, Bristol, Anton), and Department of Radiology (Brown), Medical University of South Carolina, Charleston.
Emily BristolDepartment of Psychiatry and Behavioral Sciences, Addiction Sciences Division (Prisciandaro, Hoffman, Voronin, Book, Bristol, Anton), and Department of Radiology (Brown), Medical University of South Carolina, Charleston.
Raymond F AntonDepartment of Psychiatry and Behavioral Sciences, Addiction Sciences Division (Prisciandaro, Hoffman, Voronin, Book, Bristol, Anton), and Department of Radiology (Brown), Medical University of South Carolina, Charleston.
Medical University of South Carolina · US

Funding

TREATING ETHANOL WITHDRAWAL WITH LORAZEPAM/NALTREXONEP50AA010761 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI Patrick J. Mulholland · 1996 to 2026
$46.8M
Gabapentin for Restoring GABA/glutamate Homeostasis in Co-occurring Bipolar and Cannabis Use Disorders: A Randomized, Double-blind, Placebo-controlled, Parallel-group, Clinical MRI StudyR01DA054275 · NIDA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI PRISCIANDARO, JAMES JOSEPH · 2021 to 2025
$3.1M
Imaging Framework for Testing GABAergic/glutamatergic Drugs in Bipolar AlcoholicsR01AA025365 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI PRISCIANDARO, JAMES JOSEPH · 2017 to 2022
$2.7M
Gabapentin for Relapse Prevention: Alc. Withdrawal-Brain GABA/Glutamate EffectsR01AA022364 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI ANTON, RAYMOND F · 2014 to 2017
$2.0M
NIAAA NIH HHS P50 AA010761NIAAA NIH HHS R01 AA022364NIAAA NIH HHS R01 AA025365NIDA NIH HHS R01 DA054275
6 · The paper itself

Abstract

objectiveAlthough gabapentin has demonstrated efficacy in mitigating alcohol withdrawal symptoms and preventing relapse drinking in individuals with alcohol use disorder (AUD), the neurobiological mechanisms of action underlying these therapeutic effects remain unknown. The present study evaluated changes in GABA and glutamate levels in the dorsal anterior cingulate cortex (dACC) as candidate mechanisms of action.

methodsIn a 16-week randomized clinical trial, 68 adults with AUD, including a history of alcohol withdrawal syndrome, received 1,200 mg/day of gabapentin (N=37) or placebo (N=31) and nine medical management visits after ≥72 hours of abstinence. Proton MR spectroscopy (

resultsThe effects of gabapentin on GABA and glutamate levels were significantly associated with participants' percent days abstinent during early treatment. Specifically, gabapentin was associated with greater increases in glutamate and greater decreases in GABA levels in participants who remained mostly or entirely abstinent, and yet the opposite in participants who drank on more than half of the days preceding the second scan. Furthermore, gabapentin-treated participants with greater increases in glutamate levels during early treatment had significantly more percent days abstinent across the remainder of the study, relative to placebo-treated participants.

conclusionsIn addition to providing insight into the mechanisms through which gabapentin may promote abstinence in individuals with AUD, this study also provides evidence for a biomarker of efficacious treatment that may be used to evaluate other glutamatergic or GABAergic medications for AUD and related conditions.

Indexed as

AdultAlcoholismDouble-Blind MethodFemaleGabapentingamma-Aminobutyric AcidGlutamic AcidGyrus CinguliHumansMaleMiddle AgedProton Magnetic Resonance SpectroscopySubstance Withdrawal SyndromeGabapentingamma-Aminobutyric AcidGlutamic AcidAlcoholAnticonvulsantsNeuroimagingSubstance-Related and Addictive Disorders

Identifiers

PMID34256607
PMCPMC9161238
OpenAlexW3179005331

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.