Evidence map›Paper›PMID 32612502›Full record

ReviewFrontiers in neuroscience2020

One Is Not Enough: Understanding and Modeling Polysubstance Use.

Elizabeth A Crummy, Timothy J O'Neal, Britahny M Baskin, Susan M Ferguson

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in neuroscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 181 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
181citing papers in PubMed, 2 pooled it
16.1field-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.

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

181 citing papers in PubMed, 2 syntheses or guidelines pooled it, 314 citations in OpenAlex.

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121 more citing papers are in PubMed but not listed here.

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

4 authors at 1 institution in 1 country.

Elizabeth A CrummyGraduate Program in Neuroscience, University of Washington, Seattle, WA, United States.
Timothy J O'NealGraduate Program in Neuroscience, University of Washington, Seattle, WA, United States.
Britahny M BaskinGraduate Program in Neuroscience, University of Washington, Seattle, WA, United States.
Susan M FergusonCenter for Neurobiology of Addiction, Pain, and Emotion, University of Washington, Seattle, WA, United States.
University of Washington · US

Funding

TRAINING IN THE MOLECULAR PHARMACOLOGY OF ABUSED DRUGST32DA007278 · NIDA · UNIVERSITY OF WASHINGTON · PI Susan Marie Ferguson, Paul E. M. Phillips · 1993 to 2026
$9.8M
Role of specific cortico-basal ganglia pathways in animal models of addictionR01DA036582 · NIDA · SEATTLE CHILDREN'S HOSPITAL · PI FERGUSON, SUSAN MARIE · 2014 to 2018
$2.3M
Elucidating the role of direct and indirect pathway medium spiny neurons in opioid addictionF31DA047012 · NIDA · SEATTLE CHILDREN'S HOSPITAL · PI O'NEAL, TIMOTHY JOSEPH · 2018 to 2021
$95k
NIDA NIH HHS F31 DA047012NIDA NIH HHS R01 DA036582NIDA NIH HHS T32 DA007278
6 · The paper itself

Abstract

Substance use disorder (SUD) is a chronic, relapsing disease with a highly multifaceted pathology that includes (but is not limited to) sensitivity to drug-associated cues, negative affect, and motivation to maintain drug consumption. SUDs are highly prevalent, with 35 million people meeting criteria for SUD. While drug use and addiction are highly studied, most investigations of SUDs examine drug use in isolation, rather than in the more prevalent context of comorbid substance histories. Indeed, 11.3% of individuals diagnosed with a SUD have concurrent alcohol and illicit drug use disorders. Furthermore, having a SUD with one substance increases susceptibility to developing dependence on additional substances. For example, the increased risk of developing heroin dependence is twofold for alcohol misusers, threefold for cannabis users, 15-fold for cocaine users, and 40-fold for prescription misusers. Given the prevalence and risk associated with polysubstance use and current public health crises, examining these disorders through the lens of co-use is essential for translatability and improved treatment efficacy. The escalating economic and social costs and continued rise in drug use has spurred interest in developing preclinical models that effectively model this phenomenon. Here, we review the current state of the field in understanding the behavioral and neural circuitry in the context of co-use with common pairings of alcohol, nicotine, cannabis, and other addictive substances. Moreover, we outline key considerations when developing polysubstance models, including challenges to developing preclinical models to provide insights and improve treatment outcomes.

Indexed as

addictionneurobiology of addictionneuronal signaling and behaviorpolydrugpreclinical modelsreviewreward circuitrysubstance use

Identifiers

PMID32612502
PMCPMC7309369
OpenAlexW3035858980

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.