Evidence map›Paper›PMID 23995774›Full record

Trial reportPsychiatric genetics2013

The κ-opioid receptor gene as a predictor of response in a cocaine vaccine clinical trial.

David A Nielsen, Sara C Hamon, Thomas R Kosten

Open access · greenAbstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Psychiatric genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.7field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 25 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Pharmacogenetics of Addiction Therapy.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  7. Article
  8. Article
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  10. Review
  11. Review
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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

3 authors at 1 institution in 1 country.

David A NielsenaMenninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine bMichael E. DeBakey V.A. Medical Center (MEDVAMC), Houston, Texas cLaboratory of Statistical Genetics, The Rockefeller University, New York, New York, USA.
Sara C Hamon
Thomas R Kosten
AIDS Clinical Trials Group · US

Funding

Tiagabine and Disulfiram for Cocaine DependenceP50DA018197 · NIDA · YALE UNIVERSITY · PI NEWTON, THOMAS FREDERICK · 2004 to 2013
$12.6M
Cocaine Vaccine for Methadone Maintained PatientsR01DA015477 · NIDA · YALE UNIVERSITY · PI ROUNSAVILLE, BRUCE · 2002 to 2006
$1.7M
Innovative Multidisciplinary Education: The Statistical Genetics of AddictionR25DA026120 · NIDA · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI CHANG, SHINE, SHETE, SANJAY · 2010 to 2014
$1.5M
NIDA NIH HHS DA026120 NIH/NIDA DA026120NIDA NIH HHS P50 DA018197NIDA NIH HHS R01 DA015477NIDA NIH HHS R25 DA026120PHS HHS NIH/NIDA 5 P50 DA018197-05PHS HHS NIH/NIDA RO1 DA15477
6 · The paper itself

Abstract

objectivesWe examined the pharmacogenetic association between a variant in the κ-opioid receptor (OPRK1) gene and the response to treatment with a cocaine vaccine tested in a recent clinical trial (October 2003 to April 2005). This gene has a protective allele for opioid addiction that may act by the inhibiting dopamine activation associated with reinforcement.

methodsSixty-nine DNA samples were obtained from 114 cocaine-dependent and opioid-dependent patients who were enrolled in a 16-week phase IIb randomized double-blind placebo-controlled trial and received five vaccinations over the first 12 weeks. We genotyped 66 of these patients for the rs6473797 variant of the OPRK1 gene and compared vaccine patients with placebo patients in terms of cocaine-free urines over time.

resultsUsing repeated measures analysis of variance corrected for population structure, it was seen that vaccine pharmacotherapy reduced cocaine-positive urines significantly on the basis of the OPRK1 genotype. Among patients treated with the cocaine vaccine, those who were homozygous for the protective A allele of rs6473797 had the proportion of positive urines drop from 78 to 51% on using the vaccine (point-wise P<0.0001, experiment-wise P<0.005), whereas the positive urines of individuals carrying the nonprotective, risk G allele dropped from 82 to 77%. Strong treatment by single nucleotide polymorphism interactions reflected a lower baseline and significant reduction for placebo patients with the risk G allele (P<0.00001).

conclusionThis study indicates that a patient's OPRK1 genotype could be used to identify a subset of individuals for whom vaccine treatment may be an effective pharmacotherapy for cocaine dependence.

Indexed as

AdultCocaine-Related DisordersDemographyFemaleHumansMaleReceptors, Opioid, kappaTreatment OutcomeVaccinesOPRK1 protein, humanReceptors, Opioid, kappaVaccines

Identifiers

PMID23995774
PMCPMC3885873
OpenAlexW1981380381

What OpenQuestion holds

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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.