Evidence map›Paper›PMID 33620746›Full record

Trial reportAddiction (Abingdon, England)2021

Reward drinking and naltrexone treatment response among young adult heavy drinkers.

Corey R Roos, Krysten W Bold, Katie Witkiewitz, Robert F Leeman, Kelly S DeMartini, Lisa M Fucito, William R Corbin, Karl Mann, Henry R Kranzler, Stephanie S O'Malley

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Addiction (Abingdon, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.6field-weighted citation impact, top 10% 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, 29 citations in OpenAlex.

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  12. Comparing the psychometric properties of reward and relief drinking measures.Experimental and clinical psychopharmacology · 2024
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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

10 authors at 6 institutions in 2 countries.

Corey R RoosDepartment of Psychiatry, Yale School of Medicine, New Haven, CT, USA.ORCID 0000-0002-0086-770X
Krysten W BoldDepartment of Psychiatry, Yale School of Medicine, New Haven, CT, USA.
Katie WitkiewitzDepartment of Psychology, University of New Mexico, Albuquerque, NM, USA.ORCID 0000-0002-1086-3067
Robert F LeemanDepartment of Psychiatry, Yale School of Medicine, New Haven, CT, USA.
Kelly S DeMartiniDepartment of Psychiatry, Yale School of Medicine, New Haven, CT, USA.
Lisa M FucitoDepartment of Psychiatry, Yale School of Medicine, New Haven, CT, USA.ORCID 0000-0001-9410-2830
William R CorbinDepartment of Psychology, Arizona State University, Tempe, AZ, USA.
Karl MannCentral Institute of Mental Health, Medical Faculty Mannheim, University of Heidelberg, Mannheim, Germany.
Henry R KranzlerPerelman School of Medicine, University of Pennsylvania and Crescenz VAMC, Philadelphia, PA, USA.ORCID 0000-0002-1018-0450
Stephanie S O'MalleyDepartment of Psychiatry, Yale School of Medicine, New Haven, CT, USA.
Yale University · USArizona State University · USHeidelberg University · DEPhiladelphia VA Medical Center · USUniversity of Florida Health · USUniversity of New Mexico · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
SUBSTANCE ABUSEK12DA000167 · NIDA · YALE UNIVERSITY · PI STEPHANIE S O'MALLEY, Marc N Potenza · 1991 to 2026
$17.7M
Research Training Fellowship in Substance use and Addiction (RTFSA)T32DA007238 · NIDA · YALE UNIVERSITY · PI BRIAN D. KILUK, ISMENE L. PETRAKIS · 1988 to 2026
$5.7M
Southern HIV and Alcohol Research Consortium Administrative and Research Support CoreU24AA022002 · NIAAA · UNIVERSITY OF FLORIDA · PI COOK, ROBERT L · 2012 to 2022
$5.5M
Mobile Combined Alcohol and HIV Prevention Including PrEP Uptake/Adherence for High-Risk Young MenUH3AA026214 · NIAAA · UNIVERSITY OF FLORIDA · PI LEEMAN, ROBERT F · 2019 to 2021
$1.1M
Web-Based Mindfulness Treatment to Prevent Relapse to Substance UseK23AT011342 · NCCIH · YALE UNIVERSITY · PI ROOS, COREY · 2020 to 2024
$823k
DEVELOPMENT OF A MULTIMODAL MOBILE SLEEP INTERVENTION USING WEARABLE TECHNOLOGY TO REDUCE HEAVY DRINKING IN YOUNG ADULTSR34AA026021 · NIAAA · YALE UNIVERSITY · PI FUCITO, LISA M · 2018 to 2020
$753k
A Smartphone App to Capture Impaired Inhibitory Control as a Novel Moderate Drinking Tool for Young AdultsR21AA026918 · NIAAA · UNIVERSITY OF FLORIDA · PI HONE, LIANA SENNETH ELLIOTT · 2019 to 2020
$447k
NCATS NIH HHS UL1 TR001863NCCIH NIH HHS K23 AT011342NIAAA NIH HHS R21 AA026918NIAAA NIH HHS R34 AA026021NIAAA NIH HHS U24 AA022002NIAAA NIH HHS UH3AA026214NIDA NIH HHS K12 DA000167NIDA NIH HHS T32 DA007238
6 · The paper itself

Abstract

aimsTheory-driven, exploratory study to: (i) identify a reward drinking phenotype in young adults; (ii) evaluate this phenotype as a predictor of naltrexone response; and (iii) examine mechanisms of naltrexone in reward drinkers.

designSecondary analysis of a randomized controlled trial.

settingUSA.

participantsA total of 128 young adult (ages 18-25) heavy drinkers.

interventionsNaltrexone versus placebo. MEASUREMENTS: Daily surveys assessed affect, urge, drinking, and context. The Drinking Motives Questionnaire was used to identify phenotypes based on reward (enhancement motives) and relief (coping motives) drinking.

findingsWe identified three profiles: "Low reward/Low relief" (14.1%; low enhancement/low coping motives); "Reward drinkers" (62.2%; high enhancement/low coping motives); and "High reward/High relief" (22.7%; high enhancement/high coping motives). Among reward drinkers (versus low profile), naltrexone significantly reduced percent days drinking to intoxication (blood alcohol concentration [BAC] ≥0.08) (PDI) (d = 0.56; 95% CI [0.17, 0.96]) and percent high intensity drinking days (PHID) (8/10 drinks for women/men) (d = 0.32; 95% CI [0.01, 0.68]). Among the high reward/high relief profile drinkers (versus low profile), naltrexone reduced PHID (d = 0.69; 95% CI [0.02, 1.50]). Using profile-informed cutoffs and observed scores (for clinical applicability): (i) among cutoff-derived reward drinkers, we found a medium-to-large (d = 0.66; 95% CI [0.24, 1.16]) and small effect (d = 0.28; 95% CI [0.04, 0.72]) of naltrexone in reducing PDI and PHID, respectively; and (ii) among the cutoff-derived high reward/high relief subgroup, we found a medium-to-large effect (d = 0.63; 95% CI [0.05, 1.1]) of naltrexone in reducing PHID. Among reward drinkers (not other profiles), naltrexone reduced drinking on days a drinking event occurred by weakening the within-day association between positive affect and urges (P < 0.05).

conclusionsNaltrexone has pronounced effects in reducing risky drinking among young adult reward drinkers (high reward/low relief) by reducing urges on days when individuals have higher positive affect and are exposed to a drinking event. Naltrexone also appears to reduce risky drinking among young adult high reward/high relief drinkers, but not via the same mechanism.

Indexed as

AlcoholismNaltrexoneAdolescentAdultAlcohol DrinkingBlood Alcohol ContentFemaleHumansMaleRewardYoung AdultBlood Alcohol ContentNaltrexoneHeavy drinkingmechanismsnaltrexoneprecision medicinereward drinkeryoung adults

Identifiers

PMID33620746
PMCPMC8328878
OpenAlexW3133115917

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.