Evidence map›Paper›PMID 32061453›Full record

ArticleEuropean neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology2020

Single and repeated ketamine treatment induces perfusion changes in sensory and limbic networks in major depressive disorder.

Ashish K Sahib, Joana R A Loureiro, Megha M Vasavada, Antoni Kubicki, Shantanu H Joshi, Kai Wang, Roger P Woods, Eliza Congdon, Danny J J Wang, Michael L Boucher and 2 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02165449 (Translational Biomarkers of Fast Acting Therapies in Major Depression), which is not on this map. Cited by 23 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 3 pooled it
3.1field-weighted citation impact, top 8% 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.

NCT02165449 phase1completednot on this map

Translational Biomarkers of Fast Acting Therapies in Major Depression

TypeinterventionalSponsorUniversity of California, Los AngelesRan2014 to 2019Enrolled60ConditionsMajor Depressive DisorderArmsKetamine
3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 3 syntheses or guidelines pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Region- and time- specific effects of ketamine on cerebral blood flow: a randomized controlled trial.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Trial
  7. Trial
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Neuroimaging-Derived Biomarkers of the Antidepressant Effects of Ketamine.Biological psychiatry. Cognitive neuroscience and neuroimaging · 2023
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Effects of Serial Ketamine Infusions on Corticolimbic Functional Connectivity in Major Depression.Biological psychiatry. Cognitive neuroscience and neuroimaging · 2021
    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

12 authors at 2 institutions in 1 country.

Ashish K SahibDepartment of Neurology, Ahamason-Lovelace Brain Mapping Center, United States.
Joana R A LoureiroDepartment of Neurology, Ahamason-Lovelace Brain Mapping Center, United States.
Megha M VasavadaDepartment of Neurology, Ahamason-Lovelace Brain Mapping Center, United States.
Antoni KubickiDepartment of Neurology, Ahamason-Lovelace Brain Mapping Center, United States.
Shantanu H JoshiDepartment of Neurology, Ahamason-Lovelace Brain Mapping Center, United States.
Kai WangLaboratory of FMRI Technology (LOFT), Stevens Neuroimaging and Informatics Institute, University of Southern California, Los Angeles, CA, United States.
Roger P WoodsDepartment of Neurology, Ahamason-Lovelace Brain Mapping Center, United States.
Eliza CongdonDepartment of Psychiatry and Biobehavioral Sciences, University of California Los Angeles, 635 Charles E Young Drive South Suite, Los Angeles, CA 90095-7334, United States.
Danny J J WangLaboratory of FMRI Technology (LOFT), Stevens Neuroimaging and Informatics Institute, University of Southern California, Los Angeles, CA, United States.
Michael L BoucherDepartment of Psychiatry and Biobehavioral Sciences, University of California Los Angeles, 635 Charles E Young Drive South Suite, Los Angeles, CA 90095-7334, United States.
Randall EspinozaDepartment of Psychiatry and Biobehavioral Sciences, University of California Los Angeles, 635 Charles E Young Drive South Suite, Los Angeles, CA 90095-7334, United States.
Katherine L NarrDepartment of Neurology, Ahamason-Lovelace Brain Mapping Center, United States; Department of Psychiatry and Biobehavioral Sciences, University of California Los Angeles, 635 Charles E Young Drive South Suite, Los Angeles, CA 90095-7334, United States. Electronic address: narr@ucla.edu.
Neurobehavioral Systems · USUniversity of Southern California · US

Funding

Perturbation of the treatment resistant depression connectome by fast-acting therapiesU01MH110008 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ESPINOZA, RANDALL, NARR, KATHERINE L · 2016 to 2019
$5.5M
Biomarkers of fast acting therapies in major depressionK24MH102743 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI NARR, KATHERINE L · 2014 to 2018
$889k
NIMH NIH HHS K24 MH102743NIMH NIH HHS U01 MH110008
6 · The paper itself

Abstract

Ketamine infusion therapy can produce fast-acting antidepressant effects in patients with major depressive disorder (MDD). Yet, how single and repeated ketamine treatment induces brain systems-level neuroplasticity underlying symptom improvement is unknown. Advanced multiband imaging (MB) pseudo-continuous arterial spin labeling (pCASL) perfusion MRI data was acquired from patients with treatment resistant depression (TRD) (N = 22, mean age=35.2 ± 9.95 SD, 27% female) at baseline, and 24 h after receiving single, and four subanesthetic (0.5 mg/kg) intravenous ketamine infusions. Changes in global and regional CBF were compared across time points, and relationships with overall mood, anhedonia and apathy were examined. Comparisons between patients at baseline and controls (N = 18, mean age=36.11 ± 14.5 SD, 57% female) established normalization of treatment effects. Results showed increased regional CBF in the cingulate and primary and higher-order visual association regions after first ketamine treatment. Baseline CBF in the fusiform, and acute changes in CBF in visual areas were related to symptom improvement after single and repeated ketamine treatment, respectively. In contrast, after serial infusion therapy, decreases in regional CBF were observed in the bilateral hippocampus and right insula with ketamine treatment. Findings demonstrate that neurophysiological changes occurring with single and repeated ketamine treatment follow both a regional and temporal pattern including sensory and limbic regions. Initial changes are observed in the posterior cingulate and precuneus and primary and higher-order visual areas, which relate to clinical responses. However, repeated exposure to ketamine, though not relating to clinical outcome, appears to engage deeper limbic structures and insula. ClinicalTrials.gov: Biomarkers of Fast Acting Therapies in Major Depression, https://clinicaltrials.gov/ct2/show/NCT02165449, NCT02165449.

Indexed as

AdultAffectAnhedoniaApathyBrain MappingCerebrovascular CirculationDepressive Disorder, Treatment-ResistantExcitatory Amino Acid AntagonistsFemaleHumansKetamineLimbic SystemMagnetic Resonance ImagingMajor Depressive DisorderMaleMiddle AgedExcitatory Amino Acid AntagonistsKetamineCBFFusiformInsulaKetamineMB pCASLMDD

Identifiers

PMID32061453
PMCPMC8869841
OpenAlexW3006626252

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.