Evidence map›Paper›PMID 29020372›Full record

Trial reportThe international journal of neuropsychopharmacology2017

Tolcapone-Enhanced Neurocognition in Healthy Adults: Neural Basis and Predictors.

Savita G Bhakta, Gregory A Light, Jo A Talledo, Bryan Balvaneda, Erica Hughes, Alexis Alvarez, Brinda K Rana, Jared W Young, Neal R Swerdlow

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The international journal of neuropsychopharmacology, 2017. 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
1.3field-weighted citation impact, top 21% 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, 25 citations in OpenAlex.

  1. Cortical dopamine reduces the impact of motivational biases governing automated behaviour.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
    Trial
  2. EEG reveals that dextroamphetamine improves cognitive control through multiple processes in healthy participants.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
    Trial
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. Article
  8. Lessons learned by giving amphetamine to antipsychotic-medicated schizophrenia patients.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2019
    Article
  9. Cross-Species Neurophysiological Biomarkers of Attentional Dysfunction in Schizophrenia: Bridging the Translational Gap.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
    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

9 authors at 2 institutions in 1 country.

Savita G BhaktaDepartment of Psychiatry, University of California, San Diego, La Jolla, California; Research Service MIRECC, VISN 22, Veterans Affairs San Diego Healthcare System, San Diego, California.
Gregory A LightDepartment of Psychiatry, University of California, San Diego, La Jolla, California; Research Service MIRECC, VISN 22, Veterans Affairs San Diego Healthcare System, San Diego, California.
Jo A TalledoDepartment of Psychiatry, University of California, San Diego, La Jolla, California; Research Service MIRECC, VISN 22, Veterans Affairs San Diego Healthcare System, San Diego, California.
Bryan BalvanedaDepartment of Psychiatry, University of California, San Diego, La Jolla, California; Research Service MIRECC, VISN 22, Veterans Affairs San Diego Healthcare System, San Diego, California.
Erica HughesDepartment of Psychiatry, University of California, San Diego, La Jolla, California; Research Service MIRECC, VISN 22, Veterans Affairs San Diego Healthcare System, San Diego, California.
Alexis AlvarezDepartment of Psychiatry, University of California, San Diego, La Jolla, California; Research Service MIRECC, VISN 22, Veterans Affairs San Diego Healthcare System, San Diego, California.
Brinda K RanaDepartment of Psychiatry, University of California, San Diego, La Jolla, California; Research Service MIRECC, VISN 22, Veterans Affairs San Diego Healthcare System, San Diego, California.
Jared W YoungDepartment of Psychiatry, University of California, San Diego, La Jolla, California; Research Service MIRECC, VISN 22, Veterans Affairs San Diego Healthcare System, San Diego, California.
Neal R SwerdlowDepartment of Psychiatry, University of California, San Diego, La Jolla, California; Research Service MIRECC, VISN 22, Veterans Affairs San Diego Healthcare System, San Diego, California.
University of California, San Diego · USVA San Diego Healthcare System · US

Funding

UC San Diego Clinical and Translational Research InstituteKL2TR001444 · NCATS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DEPP, COLIN A. · 2015 to 2024
$15.4M
Pharmacologic augmentation of neurocognition and cognitive training in psychosisR01MH059803 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SWERDLOW, NEAL R · 1999 to 2018
$4.5M
Memantine effects on sensorimotor gating and neurocognition in schizophreniaR01MH094320 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SWERDLOW, NEAL R · 2012 to 2020
$2.6M
A model organism of brain circuitry and behavioral switching for bipolar disorderR01MH104344 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI YOUNG, JARED WILLIAM · 2014 to 2017
$1.7M
Institute for Clinical and Translational ScienceKL2TR000147 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI COOPER, DAN M · 2012 to 2015
$940k
NCATS NIH HHS KL2 TR000147NCATS NIH HHS KL2 TR001444NIMH NIH HHS R01 MH059803NIMH NIH HHS R01 MH094320NIMH NIH HHS R01 MH104344
6 · The paper itself

Abstract

Background: Failure of procognitive drug trials in schizophrenia may reflect the clinical heterogeneity of schizophrenia, underscoring the need to identify biomarkers of treatment sensitivity. We used an experimental medicine design to test the procognitive effects of a putative procognitive agent, tolcapone, using an electroencephalogram-based cognitive control task in healthy subjects. Methods: Healthy men and women (n=27; ages 18-35 years), homozygous for either the Met/Met or Val/Val rs4680 genotype, received placebo and tolcapone 200 mg orally across 2 test days separated by 1 week in a double-blind, randomized, counterbalanced, within-subject design. On each test day, neurocognitive performance was assessed using the MATRICS Consensus Cognitive Battery and an electroencephalogram-based 5 Choice-Continuous Performance Test. Results: Tolcapone enhanced visual learning in low-baseline MATRICS Consensus Cognitive Battery performers (d=0.35) and had an opposite effect in high performers (d=0.5), and enhanced verbal fluency across all subjects (P=.03) but had no effect on overall MATRICS Consensus Cognitive Battery performance. Tolcapone reduced false alarm rate (d=0.8) and enhanced frontal P200 amplitude during correctly identified nontarget trials (d=0.6) in low-baseline 5 Choice-Continuous Performance Test performers and had opposite effects in high performers (d=0.5 and d=0.25, respectively). Tolcapone's effect on frontal P200 amplitude and false alarm rate was correlated (rs=-0.4, P=.05). All neurocognitive effects of tolcapone were independent of rs4680 genotype. Conclusion: Tolcapone enhanced neurocognition and engaged electroencephalogram measures relevant to cognitive processes in specific subgroups of healthy individuals. These findings support an experimental medicine model for identifying procognitive treatments and provide a strong basis for future biomarker-informed procognitive studies in schizophrenia patients.

Indexed as

Brain MappingAdolescentAdultBenzophenonesBrainCatechol O-MethyltransferaseCatechol O-Methyltransferase InhibitorsChoice BehaviorCognitionCross-Over StudiesDouble-Blind MethodEvoked PotentialsFemaleGenotypeHealthy VolunteersHumansBenzophenonesCatechol O-MethyltransferaseCatechol O-Methyltransferase InhibitorsCOMT protein, humanNitrophenolsTolcaponebiomarkercognitioncognitive controlCOMT inhibitorevent related potentialtolcapone

Identifiers

PMID29020372
PMCPMC5716101
OpenAlexW2745562678

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.