Evidence map›Paper›PMID 25521358›Full record

ArticlePharmacogenomics2014

Dopaminergic pathway polymorphisms and heroin addiction: further support for association of CSNK1E variants.

Orna Levran, Einat Peles, Matthew Randesi, Joel Correa da Rosa, Jurg Ott, John Rotrosen, Miriam Adelson, Mary Jeanne Kreek

Abstract read
In one paragraph

Article in Pharmacogenomics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
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

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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

21 citing papers in PubMed.

  1. Review
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  4. Frontiers in pharmacology · 2025
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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

8 authors.

Orna LevranThe Laboratory of the Biology of Addictive Diseases, The Rockefeller University, New York, NY 10065, USA.
Einat Peles
Matthew Randesi
Joel Correa da Rosa
Jurg Ott
John Rotrosen
Miriam Adelson
Mary Jeanne Kreek

Funding

TRANSFORMING TRANSLATIONAL SCIENCE AND EDUCATION TO BENEFIT HUMAN HEALTHUL1RR024143 · NCRR · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY · 2006 to 2011
$49.1M
Transforming Translational Science and Education to Benefit Human HealthUL1TR000043 · NCATS · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY · 2012 to 2015
$26.8M
NCATS NIH HHS UL1 TR000043NCRR NIH HHS UL1 RR024143NCRR NIH HHS UL1RR024143
6 · The paper itself

Abstract

BACKGROUND &

aimThe dopaminergic pathways have been implicated in the etiology of drug addictions. The aim of this study was to determine if variants in dopaminergic genes are associated with heroin addiction. MATERIALS &

methodsThe study includes 828 former heroin addicts and 232 healthy controls, of predominantly European ancestry. Ninety seven SNPs (13 genes) were analyzed.

resultsNine nominally significant associations were observed at CSNK1E, ANKK1, DRD2 and DRD3.

conclusionThe results support our previous report of association of CSNK1E SNP rs1534891 with protection from heroin addiction. CSNK1E interacts with circadian rhythms and DARPP-32 and has been implicated in negative regulation of sensitivity to opioids in rodents. It may be a target for drug addiction treatment. Original submitted 8 August 2014; Revision submitted 8 October 2014.

Indexed as

Genetic Predisposition to DiseaseAdultAnalgesics, OpioidCasein Kinase 1 epsilonCircadian RhythmDopamineDopamine and cAMP-Regulated Phosphoprotein 32FemaleGenetic Association StudiesGenotypeHaplotypesHeroin DependenceHumansLinkage DisequilibriumMaleMiddle AgedAnalgesics, OpioidCasein Kinase 1 epsilonDopamineDopamine and cAMP-Regulated Phosphoprotein 32PPP1R1B protein, humancasein kinase 1εcircadian rhythmsdopaminergic reward pathwaysheroin addictionSNP rs1534891

Identifiers

PMID25521358
PMCPMC4288976

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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.