Evidence map›Paper›PMID 19462300›Full record

ReviewThe American journal of drug and alcohol abuse2009

Pharmacogenetic treatments for drug addiction: cocaine, amphetamine and methamphetamine.

Colin N Haile, Thomas R Kosten, Therese A Kosten

Open access · greenAbstract readReview
In one paragraph

Review in The American journal of drug and alcohol abuse, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 2 pooled it
3.2field-weighted citation impact, top 7% 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

37 citing papers in PubMed, 2 syntheses or guidelines pooled it, 71 citations in OpenAlex.

  1. Pooled it
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  5. Rivastigmine reduces "Likely to use methamphetamine" in methamphetamine-dependent volunteers.Progress in neuro-psychopharmacology & biological psychiatry · 2012
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  9. PGx-BasedCurrent neuropharmacology · 2026
    Article
  10. Review
  11. Dopamine Pharmacodynamics: New Insights.International journal of molecular sciences · 2024
    Review
  12. Article
  13. Pharmacogenetics of Addiction Therapy.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  14. Aberrant expression ofGeneral psychiatry · 2021
    Article
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  17. Review
  18. 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.

Colin N HaileMenninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, and Michael E DeBakey VA Medical Center, Houston, Texas 77030, USA.
Thomas R Kosten
Therese A Kosten
Michael E. DeBakey VA Medical Center · US

Funding

Target Validation Core RatsU01AA013476 · NIAAA · UNIVERSITY OF HOUSTON · PI KOSTEN, THERESE A · 2001 to 2015
$3.5M
Sex Differences in Vulnerability to Cocaine AddictionR21DA020117 · NIDA · BAYLOR COLLEGE OF MEDICINE · PI KOSTEN, THERESE A · 2008 to 2009
$679k
NIAAA NIH HHS U01 AA013476NIAAA NIH HHS U01-AA013476NIDA NIH HHS DA020117NIDA NIH HHS R21 DA020117
6 · The paper itself

Abstract

backgroundPharmacogenetics uses genetic variation to predict individual differences in response to medications and holds much promise to improve treatment of addictive disorders.

objectivesTo review how genetic variation affects responses to cocaine, amphetamine, and methamphetamine and how this information may guide pharmacotherapy.

methodsWe performed a cross-referenced literature search on pharmacogenetics, cocaine, amphetamine, and methamphetamine.

resultsWe describe functional genetic variants for enzymes dopamine-beta-hydroxylase (DbetaH), catechol-O-methyltransferase (COMT), and dopamine transporter (DAT1), dopamine D4 receptor, and brain-derived neurotrophic factor (BDNF). A single nucleotide polymorphism (SNP; C-1021T) in the DbetaH gene is relevant to paranoia associated with disulfiram pharmacotherapy for cocaine addiction. Individuals with variable number tandem repeats (VNTR) of the SLC6A3 gene 3'-untranslated region polymorphism of DAT1 have altered responses to drugs. The 10/10 repeat respond poorly to methylphenidate pharmacotherapy and the 9/9 DAT1 variant show blunted euphoria and physiological response to amphetamine. COMT, D4 receptor, and BDNF polymorphisms are linked to methamphetamine abuse and psychosis.

conclusionsDisulfiram and methylphenidate pharmacotherapies for cocaine addiction are optimized by considering polymorphisms affecting DbetaH and DAT1 respectively. Altered subjective effects for amphetamine in DAT1 VNTR variants suggest a 'protected' phenotype. SCIENTIFIC SIGNIFICANCE: Pharmacogenetic-based treatments for psychostimulant addiction are critical for successful treatment.

Indexed as

AmphetamineAmphetamine-Related DisordersCocaine-Related DisordersDisulfiramDopamine Uptake InhibitorsEnzyme InhibitorsHumansMethamphetamineMethylphenidatePharmacogeneticsPolymorphism, Single NucleotideAmphetamineDisulfiramDopamine Uptake InhibitorsEnzyme InhibitorsMethamphetamineMethylphenidate

Identifiers

PMID19462300
PMCPMC2754046
OpenAlexW2163816715

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.