Evidence map›Paper›PMID 29210332›Full record

ArticlePharmacogenomics2018

Dopamine gene variants in opioid addiction: comparison of dependent patients, nondependent users and healthy controls.

Matthew Randesi, Wim van den Brink, Orna Levran, Vadim Yuferov, Peter Blanken, Jan M van Ree, Jurg Ott, Mary Jeanne Kreek

Abstract read
In one paragraph

Article in Pharmacogenomics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

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  9. VMAT2 gene (Pharmacogenomics · 2019
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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 at 4 institutions in 3 countries.

Matthew RandesiLaboratory of the Biology of Addictive Diseases, The Rockefeller University, 1230 York Ave, New York, NY 10065, USA.
Wim van den BrinkCentral Committee on the Treatment of Heroin Addicts (CCBH), Universiteitsweg 100, 3584 CG Utrecht, The Netherlands.
Orna LevranLaboratory of the Biology of Addictive Diseases, The Rockefeller University, 1230 York Ave, New York, NY 10065, USA.
Vadim YuferovLaboratory of the Biology of Addictive Diseases, The Rockefeller University, 1230 York Ave, New York, NY 10065, USA.
Peter BlankenCentral Committee on the Treatment of Heroin Addicts (CCBH), Universiteitsweg 100, 3584 CG Utrecht, The Netherlands.
Jan M van ReeCentral Committee on the Treatment of Heroin Addicts (CCBH), Universiteitsweg 100, 3584 CG Utrecht, The Netherlands.
Jurg OttLaboratory of Statistical Genetics, The Rockefeller University, 1230 York Ave, New York, NY 10065, USA.
Mary Jeanne KreekLaboratory of the Biology of Addictive Diseases, The Rockefeller University, 1230 York Ave, New York, NY 10065, USA.
Rockefeller University · USAcademic Medical Center · NLParnassia Groep · NLUniversity Medical Center Utrecht · NL

Funding

UNIQUE RNA STRUCTURE OF CAUSATIVE AGENT FOR DELTA HEPATITISP50DA005130 · NIDA · ROCKEFELLER UNIVERSITY · PI UNTERWALD, ELLEN M · 1987 to 2001
$5.0M
ADDICTIONS: GENOTYPES, POLYMOPHISMS, AND FUNCTIONR01DA012848 · NIDA · ROCKEFELLER UNIVERSITY · PI KREEK, MARY J · 1999 to 2003
$4.5M
NIDA NIH HHS P50 DA005130NIDA NIH HHS R01 DA012848
6 · The paper itself

Abstract

aimTo determine whether specific dopaminergic system gene variants are associated with opioid dependence. PATIENTS &

methodsSubjects included 153 healthy controls, 163 opioid exposed, but not dependent and 281 opioid dependent. Genotypes of 90 variants in 13 genes were examined.

resultsThe most significant results were obtained for DA β-hydroxylase variants, rs2073837 and rs1611131, which were associated with protection from addiction (q = 0.0172, 0.0415, respectively) and the functional TH variant, rs2070762, was associated with more risk (q = 0.0387). The three variants also showed a combined effect that remained significant after correction for multiple testing (p

conclusionThese data offer support that dopaminergic gene variants have a role in opioid dependence and warrant further study.

Indexed as

AdultAnalgesics, OpioidBehavior, AddictiveCase-Control StudiesDopamineDopamine beta-HydroxylaseFemaleGenotypeHumansMaleOpioid-Related DisordersPolymorphism, Single NucleotideRiskAnalgesics, OpioidDopamineDopamine beta-HydroxylaseDBHdrug addictionTH

Identifiers

PMID29210332
PMCPMC6826863
OpenAlexW2773721473

What OpenQuestion holds

Textmetadata
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.