Evidence map›Paper›PMID 20141248›Full record

ArticleJournal of abnormal psychology2010

Polymorphisms of the mu-opioid receptor and dopamine D4 receptor genes and subjective responses to alcohol in the natural environment.

Lara A Ray, Robert Miranda, Jennifer W Tidey, John E McGeary, James MacKillop, Chad J Gwaltney, Damaris J Rohsenow, Robert M Swift, Peter M Monti

Abstract read
In one paragraph

Article in Journal of abnormal psychology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 6 pooled it
5.6field-weighted citation impact, top 3% 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

80 citing papers in PubMed, 6 syntheses or guidelines pooled it, 122 citations in OpenAlex.

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  5. Subjective response to alcohol challenge: a quantitative review.Alcoholism, clinical and experimental research · 2011
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  19. Event-level associations between objective and subjective alcohol intoxication and driving after drinking across the college years.Psychology of addictive behaviors : journal of the Society of Psychologists in Addictive Behaviors · 2012
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  20. Pharmacogenetics of naltrexone in asian americans: a randomized placebo-controlled laboratory study.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2012
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20 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

9 authors at 2 institutions in 1 country.

Lara A RayCenter for Alcohol and Addiction Studies, Brown University and Department of Psychology, University of California, Los Angeles, Los Angeles, CA 90095-1563, USA. lararay@psych.ucla.edu
Robert Miranda
Jennifer W Tidey
John E McGeary
James MacKillop
Chad J Gwaltney
Damaris J Rohsenow
Robert M Swift
Peter M Monti
Brown University · USProvidence College · US

Funding

ALCOHOL INTERVENTION/TREATMENT OUTCOME RESEARCH TRAININGT32AA007459 · NIAAA · BROWN UNIVERSITY · PI ROBERT MIRANDA, PETER M. MONTI · 1986 to 2026
$13.3M
NALTREXONE, CRAVING AND DRINKING: ECOLOGICAL ASSESSMENTR01AA007850 · NIAAA · BROWN UNIVERSITY · PI MIRANDA, ROBERT · 1988 to 2015
$8.4M
Elucidating Mechanisms of Pharmacotherapy for AlcoholismK23AA014966 · NIAAA · BROWN UNIVERSITY · PI MIRANDA, ROBERT · 2004 to 2008
$714k
NIAAA NIH HHS 1K23 AA014966NIAAA NIH HHS 2R01 AA07850NIAAA NIH HHS K23 AA014966NIAAA NIH HHS R01 AA007850NIAAA NIH HHS T32 AA007459NIAAA NIH HHS T32 AA07459
6 · The paper itself

Abstract

Polymorphisms of the mu-opioid receptor (OPRM1) and dopamine D4 receptor (DRD4) genes are associated with subjective responses to alcohol and urge to drink under laboratory conditions. This study examined these associations in the natural environment using ecological momentary assessment. Participants were non-treatment-seeking heavy drinkers (n = 112, 52% female, 61% alcohol dependent) who enrolled in a study of naltrexone effects on craving and drinking in the natural environment. Data were culled from 5 consecutive days of drinking reports prior to medication randomization. Analyses revealed that, after drinking, carriers of the Asp40 allele of the OPRM1 gene reported higher overall levels of vigor and lower levels negative mood, as compared to homozygotes for the Asn40 variant. Carriers of the long allele (i.e., >or=7 tandem repeats) of the DRD4 endorsed greater urge to drink than homozygotes for the short allele. Effects of OPRM1 and DRD4 variable-number-of-tandem-repeats genotypes appear to be alcohol dose-dependent. Specifically, carriers of the DRD4-L allele reported slight decreases in urge to drink at higher levels of estimated blood alcohol concentration (eBAC), and Asp40 carriers reported decreases in vigor and increases in negative mood as eBAC rose, as compared to carriers of the major allele for each gene. Self-reported vigor and urge to drink were positively associated with alcohol consumption within the same drinking episode. This study extends findings on subjective intoxication, urge to drink, and their genetic bases from controlled laboratory to naturalistic settings.

Indexed as

EnvironmentAdultAlcoholismFemaleHumansMaleNaltrexoneNarcotic AntagonistsPolymorphism, GeneticReceptors, Dopamine D4Receptors, Opioid, muTandem Repeat SequencesDRD4 protein, humanNaltrexoneNarcotic AntagonistsOPRM1 protein, humanReceptors, Dopamine D4Receptors, Opioid, mu

Identifiers

PMID20141248
PMCPMC3703617
OpenAlexW2044560641

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.