Evidence map›Paper›PMID 27241058›Full record

ReviewThe pharmacogenomics journal2016

COMT val158met moderation of dopaminergic drug effects on cognitive function: a critical review.

J P Schacht

Abstract readReview
In one paragraph

Review in The pharmacogenomics journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 2 pooled it
7.0field-weighted citation impact, top 2% 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

58 citing papers in PubMed, 2 syntheses or guidelines pooled it, 107 citations in OpenAlex.

  1. Pooled it
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  10. Dopaminergic Genetic Variation Influences Aripiprazole Effects on Alcohol Self-Administration and the Neural Response to Alcohol Cues in a Randomized Trial.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
    Trial
  11. Catechol-Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  12. Article
  13. Article
  14. Hydroethanolic Extract ofTheScientificWorldJournal · 2025
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  20. Heliyon · 2023
    Article
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

1 author at 1 institution in 1 country.

J P SchachtDepartment of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, SC, USA.
Medical University of South Carolina · US

Funding

TREATING ETHANOL WITHDRAWAL WITH LORAZEPAM/NALTREXONEP50AA010761 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI HOWARD C. BECKER · 1996 to 2026
$46.8M
Neural Connectivity and the Transition to Alcohol DependenceR00AA021419 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI SCHACHT, JOSEPH P. · 2015 to 2017
$747k
Neural Connectivity and the Transition to Alcohol DependenceK99AA021419 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI SCHACHT, JOSEPH P. · 2013 to 2014
$208k
NIAAA NIH HHS K99 AA021419NIAAA NIH HHS P50 AA010761NIAAA NIH HHS R00 AA021419
6 · The paper itself

Abstract

The relationship between dopamine (DA) tone in the prefrontal cortex (PFC) and PFC-dependent cognitive functions (for example, working memory, selective attention, executive function) may be described by an inverted-U-shaped function, in which both excessively high and low DA is associated with impairment. In the PFC, the COMT val158met single nucleotide polymorphism (rs4680) confers differences in catechol-O-methyltransferase (COMT) efficacy and DA tone, and individuals homozygous for the val allele display significantly reduced cortical DA. Many studies have investigated whether val158met genotype moderates the effects of dopaminergic drugs on PFC-dependent cognitive functions. A review of 25 such studies suggests evidence for this pharmacogenetic effect is mixed for stimulants and COMT inhibitors, which have greater effects on D1 receptors, and strong for antipsychotics, which have greater effects on D2 receptors. Overall, COMT val158met genotype represents an enticing target for identifying individuals who are more likely to respond positively to dopaminergic drugs.

Indexed as

Pharmacogenomic VariantsPolymorphism, Single NucleotideAnimalsAntipsychotic AgentsCatechol O-MethyltransferaseCatechol O-Methyltransferase InhibitorsCognitionDopamineDopamine AgentsDopamine AgonistsGene FrequencyHeterozygoteHomozygoteHumansPatient SelectionPharmacogeneticsAntipsychotic AgentsCatechol O-MethyltransferaseCatechol O-Methyltransferase InhibitorsCOMT protein, humanDopamineDopamine AgentsDopamine AgonistsDRD1 protein, humanDRD2 protein, humanReceptors, Dopamine D1Receptors, Dopamine D2

Identifiers

PMID27241058
PMCPMC5028240
OpenAlexW2426421998

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.