Evidence map›Paper›PMID 32115848›Full record

ArticleHuman brain mapping2020

Modulation of amygdala reactivity following rapidly acting interventions for major depression.

Joana R A Loureiro, Amber Leaver, Megha Vasavada, Ashish K Sahib, Antoni Kubicki, Shantanu Joshi, Roger P Woods, Benjamin Wade, Eliza Congdon, Randall Espinoza and 1 more

Open access · goldAbstract read
In one paragraph

Article in Human brain mapping, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 4 pooled it
6.2field-weighted citation impact, top 3% 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, 4 syntheses or guidelines pooled it, 64 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. Trial
  10. Trial
  11. Neuroimaging correlates and predictors of response to repeated-dose intravenous ketamine in PTSD: preliminary evidence.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2021
    Trial
  12. Trial
  13. Article
  14. Review
  15. Review
  16. Ketamine for Major Depressive Disorder.Current topics in behavioral neurosciences · 2024
    Review
  17. Article
  18. Review
  19. Article
  20. Neuroimaging-Derived Biomarkers of the Antidepressant Effects of Ketamine.Biological psychiatry. Cognitive neuroscience and neuroimaging · 2023
    Review
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

11 authors at 3 institutions in 1 country.

Joana R A LoureiroDepartment of Neurology, Ahamason-Lovelace Brain Mapping Center, Los Angeles, California.ORCID 0000-0001-9550-804X
Amber LeaverNorthwestern University Clinical and Translational Sciences Institute (NUCATS), Chicago, Illinois.
Megha VasavadaDepartment of Neurology, Ahamason-Lovelace Brain Mapping Center, Los Angeles, California.
Ashish K SahibDepartment of Neurology, Ahamason-Lovelace Brain Mapping Center, Los Angeles, California.
Antoni KubickiDepartment of Neurology, Ahamason-Lovelace Brain Mapping Center, Los Angeles, California.
Shantanu JoshiDepartment of Neurology, Ahamason-Lovelace Brain Mapping Center, Los Angeles, California.
Roger P WoodsDepartment of Neurology, Ahamason-Lovelace Brain Mapping Center, Los Angeles, California.ORCID 0000-0001-9679-9571
Benjamin WadeDepartment of Neurology, Ahamason-Lovelace Brain Mapping Center, Los Angeles, California.
Eliza CongdonDepartment of Psychiatry and Biobehavioral Sciences, University of California Los Angeles, Los Angeles, California.
Randall EspinozaDepartment of Psychiatry and Biobehavioral Sciences, University of California Los Angeles, Los Angeles, California.
Katherine L NarrDepartment of Neurology, Ahamason-Lovelace Brain Mapping Center, Los Angeles, California.
Brain Mapping Foundation · USUniversity of California, Los Angeles · USNorthwestern University · 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

Electroconvulsive therapy (ECT) and ketamine treatment both induce rapidly acting antidepressant effects in patients with major depressive disorder unresponsive to standard treatments, yet their specific impact on emotion processing is unknown. Here, we examined the neural underpinnings of emotion processing within and across patients (N = 44) receiving either ECT (N = 17, mean age: 36.8, 11.0 SD) or repeated subanesthetic (0.5 mg/kg) intravenous ketamine therapy (N = 27, mean age: 37.3, 10.8 SD) using a naturalistic study design. MRI and clinical data were collected before (TP1) and after treatment (TP2); healthy controls (N = 31, mean age: 34.5, 13.5 SD) completed one MRI session (TP1). An fMRI face-matching task probed negative- and positive-valence systems. Whole-brain analysis, comparing neurofunctional changes within and across treatment groups, targeted brain regions involved in emotional facial processing, and included regions-of-interest analysis of amygdala responsivity. Main findings revealed a decrease in amygdalar reactivity after both ECT and ketamine for positive and negative emotional face processing (p < .05 family wise-error (FWE) corrected). Subthreshold changes were observed between treatments within the dorsolateral prefrontal cortex and insula (p < .005, uncorrected). BOLD change for positive faces in the inferior parietal cortex significantly correlated with overall symptom improvement, and BOLD change in frontal regions correlated with anxiety for negative faces, and anhedonia for positive faces (p < .05 FWE corrected). Both serial ketamine and ECT treatment modulate amygdala response, while more subtle treatment-specific changes occur in the larger functional network. Findings point to both common and differential mechanistic upstream systems-level effects relating to fast-acting antidepressant response, and symptoms of anxiety and anhedonia, for the processing of emotionally valenced stimuli.

Indexed as

Electroconvulsive TherapyAdultAmygdalaAntidepressive AgentsBrain MappingEmotionsFemaleHumansInjections, IntravenousKetamineMagnetic Resonance ImagingMajor Depressive DisorderMaleMiddle AgedOxygenAntidepressive AgentsKetamineOxygenamygdalaECTemotion processingketamineMDDtfMRI

Identifiers

PMID32115848
PMCPMC7268016
OpenAlexW3009996296

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.