Evidence map›Paper›PMID 30848494›Full record

ArticleAlcoholism, clinical and experimental research2019

Naltrexone Acutely Enhances Connectivity Between the Ventromedial Prefrontal Cortex and a Left Frontoparietal Network.

Amanda Elton, Samantha Dove, Cory N Spencer, Donita L Robinson, Charlotte A Boettiger

Open access · greenAbstract read
In one paragraph

Article in Alcoholism, clinical and experimental research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 23 citations in OpenAlex.

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  9. Acute depletion of dopamine precursors in the human brain: effects on functional connectivity and alcohol attentional bias.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

5 authors at 1 institution in 1 country.

Amanda EltonDepartment of Psychology and Neuroscience, University of North Carolina, Chapel Hill, North Carolina.ORCID 0000-0001-9027-1442
Samantha DoveDepartment of Psychology and Neuroscience, University of North Carolina, Chapel Hill, North Carolina.
Cory N SpencerDepartment of Psychology and Neuroscience, University of North Carolina, Chapel Hill, North Carolina.
Donita L RobinsonBowles Center for Alcohol Studies, University of North Carolina, Chapel Hill, North Carolina.ORCID 0000-0001-7540-3363
Charlotte A BoettigerDepartment of Psychology and Neuroscience, University of North Carolina, Chapel Hill, North Carolina.ORCID 0000-0003-1853-1574
University of North Carolina at Chapel Hill · US

Funding

UNC ARC Information/Dissemination CoreP60AA011605 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Clyde W Hodge · 2003 to 2026
$46.3M
Supplement to Molecular and Cellular Studies on Alcohol's ActionsT32AA007573 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FULTON T CREWS, Thomas L. Kash · 1997 to 2026
$9.3M
Genetic and Epigenetic Regulation of COMT, a Key Moderator of Cognitive DeclineR01NR017221 · NINR · VIRGINIA COMMONWEALTH UNIVERSITY · PI SWIFT-SCANLAN, THERESA · 2018 to 2022
$2.1M
The neural mechanisms of risk for alcohol use disorder among college studentsK01AA026334 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ELTON, AMANDA L · 2018 to 2022
$770k
NIAAA NIH HHS K01 AA026334NIAAA NIH HHS P60 AA011605NIAAA NIH HHS T32 AA007573NINR NIH HHS R01 NR017221
6 · The paper itself

Abstract

backgroundNaltrexone, an opioid receptor antagonist that is Food and Drug Administration approved for treating alcohol use disorder (AUD), reduces alcohol craving and intake. Despite known pharmacological properties, little is known regarding the effects of naltrexone on neural circuit function. Thus, a data-driven examination of the neural effects of naltrexone in human subjects may offer novel insight into its treatment mechanisms.

methodsTwenty-one alcohol using males (22 to 39) participated in a double-blind, placebo-controlled crossover study of the effects of naltrexone on brain voxel-wise functional connectivity (FC) using intersubject FC correlation mapping. We first cross-correlated the time series from each gray matter voxel to produce a 6,356 × 6,356 FC matrix for each subject and session. We then subtracted the placebo FC matrix from the naltrexone FC matrix. To identify brain regions demonstrating significant reconfiguration of whole-brain FC patterns following naltrexone treatment, we statistically quantified the consistency of patterns of voxel FC changes across subjects. Permutation testing identified significant clusters of voxels undergoing significant reconfiguration. Using the identified clusters in a seed-based FC analysis, we then compared the FC patterns of affected brain areas on placebo versus naltrexone in a paired t-test. Ridge regression analyses identified self-report measures, including substance use, that significantly predicted individual differences in FC among naltrexone-modulated regions.

resultsTwo clusters in the rostral anterior cingulate cortex (rACC)/ventromedial prefrontal cortex (vmPFC) demonstrated significant modulation of FC by naltrexone. Using these 2 proximal clusters as a single seed, specific FC changes were identified in regions associated with a left frontoparietal network (increasing), as well as visual and motor regions (decreasing). Stronger FC between the rACC/vmPFC and this set of regions on placebo was associated with more external locus of control, whereas weaker connectivity was associated with greater substance use problems. Naltrexone strengthened these connections most among individuals who reported greater drinking to cope.

conclusionsEnhancing connectivity between the rACC/vmPFC, implicated in alcohol craving, and components of a left frontoparietal network involved in executive control may represent an effective strategy for the treatment of AUD.

Indexed as

AdultAlcohol DeterrentsCross-Over StudiesDouble-Blind MethodExecutive FunctionFemaleHumansMagnetic Resonance ImagingMaleNaltrexoneNerve NetParietal LobePrefrontal CortexYoung AdultAlcohol DeterrentsNaltrexonefMRIMedial Prefrontal CortexNaltrexoneResting State

Identifiers

PMID30848494
PMCPMC6528472
OpenAlexW2922290742

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.