Evidence map›Paper›PMID 32643995›Full record

ArticleJournal of psychopharmacology (Oxford, England)2021

Brain entropy and neurotrophic molecular markers accompanying clinical improvement after ketamine: Preliminary evidence in adolescents with treatment-resistant depression.

Abhrajeet V Roy, Michelle Thai, Bonnie Klimes-Dougan, Mindy Westlund Schreiner, Bryon A Mueller, Christina Sophia Albott, Kelvin O Lim, Mark Fiecas, Susannah J Tye, Kathryn R Cullen

Open access · greenAbstract read
In one paragraph

Article in Journal of psychopharmacology (Oxford, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 3 pooled it
2.0field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 3 syntheses or guidelines pooled it, 29 citations in OpenAlex.

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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

10 authors at 4 institutions in 2 countries.

Abhrajeet V RoyDepartment of Psychiatry and Behavioral Sciences, Medical School, University of Minnesota, Minneapolis, USA.
Michelle ThaiDepartment of Psychology, College of Liberal Arts, University of Minnesota, Minneapolis, USA.
Bonnie Klimes-DouganDepartment of Psychology, College of Liberal Arts, University of Minnesota, Minneapolis, USA.
Mindy Westlund SchreinerDepartment of Psychiatry, University of Utah, Salt Lake City, USA.
Bryon A MuellerDepartment of Psychiatry and Behavioral Sciences, Medical School, University of Minnesota, Minneapolis, USA.
Christina Sophia AlbottDepartment of Psychiatry and Behavioral Sciences, Medical School, University of Minnesota, Minneapolis, USA.
Kelvin O LimDepartment of Psychiatry and Behavioral Sciences, Medical School, University of Minnesota, Minneapolis, USA.
Mark FiecasDivision of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, USA.
Susannah J TyeQueensland Brain Institute, The University of Queensland, Brisbane, Australia.
Kathryn R CullenDepartment of Psychiatry and Behavioral Sciences, Medical School, University of Minnesota, Minneapolis, USA.ORCID 0000-0001-9631-3770
University of Minnesota Medical Center · USUniversity of Minnesota · USThe University of Queensland · AUUniversity of Utah · US

Funding

University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR000114 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R · 2012 to 2015
$35.0M
University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR002494 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R, WEISDORF, DANIEL J · 2018 to 2022
$34.9M
TRD4 - Ultrahigh Field Engineering and SafetyP41EB027061 · NIBIB · UNIVERSITY OF MINNESOTA · PI Gregory John Metzger · 2019 to 2026
$11.7M
UNIVERSITY OF MINNESOTA CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTE (UMN CTSI)UL1RR033183 · NCRR · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R · 2011 to 2011
$8.9M
NMR Imaging and SpectroscopyP41EB015894 · NIBIB · UNIVERSITY OF MINNESOTA · PI UGURBIL, KAMIL · 2012 to 2017
$8.4M
Institutional Center Cores for Advanced NeuroimagingP30NS076408 · NINDS · UNIVERSITY OF MINNESOTA · PI UGURBIL, KAMIL · 2012 to 2020
$4.2M
Comorbidity: Substance Use Disorders and Other Psychiatric ConditionsT32DA037183 · NIDA · UNIVERSITY OF MINNESOTA · PI Anna Zilverstand · 2014 to 2026
$3.2M
High Performance Connectome Upgrade for Human 3T MR ScannerS10OD017974 · OD · UNIVERSITY OF MINNESOTA · PI LIM, KELVIN O. · 2014 to 2014
$600k
NCATS NIH HHS UL1 TR000114NCATS NIH HHS UL1 TR002494NCRR NIH HHS UL1 RR033183NIBIB NIH HHS P41 EB015894NIBIB NIH HHS P41 EB027061NIDA NIH HHS T32 DA037183NIH HHS S10 OD017974NINDS NIH HHS P30 NS076408
6 · The paper itself

Abstract

backgroundCurrent theory suggests that treatment-resistant depression (TRD) involves impaired neuroplasticity resulting in cognitive and neural rigidity, and that clinical improvement may require increasing brain flexibility and adaptability.

aimsIn this hypothesis-generating study, we sought to identify preliminary evidence of brain flexibility correlates of clinical change within the context of an open-label ketamine trial in adolescents with TRD, focusing on two promising candidate markers of neural flexibility: (a) entropy of resting-state functional magnetic resonance imaging (fMRI) signals; and (b) insulin-stimulated phosphorylation of mammalian target of rapamycin (mTOR) and glycogen synthase-3-beta (GSK3β) in peripheral blood mononuclear cells.

methodsWe collected resting-state functional magnetic resonance imaging data and blood samples from 13 adolescents with TRD before and after a series of six ketamine infusions over 2 weeks. Usable pre/post ketamine data were available from 11 adolescents for imaging and from 10 adolescents for molecular signaling. We examined correlations between treatment response and changes in the central and peripheral flexibility markers.

resultsDepression reduction correlated with increased nucleus accumbens entropy. Follow-up analyses suggested that physiological changes were associated with treatment response. In contrast to treatment non-responders (

conclusionsThese data provide preliminary evidence that changes in neural flexibility may underlie symptom relief in adolescents with TRD following ketamine. Future research with adequately powered samples is needed to confirm resting-state entropy and insulin-stimulated mTOR and GSK3β as brain flexibility markers and candidate targets for future clinical trials. CLINICAL TRIAL NAME: Ketamine in adolescents with treatment-resistant depression

Indexed as

AdolescentAntidepressive AgentsBiomarkersBrainDepressive Disorder, Treatment-ResistantEntropyExcitatory Amino Acid AntagonistsFemaleHumansKetamineLeukocytes, MononuclearMagnetic Resonance ImagingMaleNerve Growth FactorsNucleus AccumbensAntidepressive AgentsBiomarkersExcitatory Amino Acid AntagonistsKetamineNerve Growth FactorsadolescentsdepressionentropyKetaminemTOR/GSK3βneuroplasticity

Identifiers

PMID32643995
PMCPMC8569740
OpenAlexW3040929984

What Socratic 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 Socratic graph.