Evidence map›Paper›PMID 33615749›Full record

ArticleNeuropsychopharmacology reports2021

Functional connectivity between the amygdala and subgenual cingulate gyrus predicts the antidepressant effects of ketamine in patients with treatment-resistant depression.

Tomoyuki Nakamura, Masaru Tomita, Naoki Horikawa, Masatoshi Ishibashi, Ken Uematsu, Teruyuki Hiraki, Toshi Abe, Naohisa Uchimura

Open access · goldAbstract read
In one paragraph

Article in Neuropsychopharmacology reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 2 pooled it
2.6field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 2 syntheses or guidelines pooled it, 28 citations in OpenAlex.

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  12. Neuroimaging-Derived Biomarkers of the Antidepressant Effects of Ketamine.Biological psychiatry. Cognitive neuroscience and neuroimaging · 2023
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  18. Prefrontal cortex and depression.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
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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

8 authors at 1 institution in 1 country.

Tomoyuki NakamuraDepartment of Neuropsychiatry, Kurume University School of Medicine, Kurume City, Japan.ORCID 0000-0001-7421-7921
Masaru TomitaDepartment of Neuropsychiatry, Kurume University School of Medicine, Kurume City, Japan.
Naoki HorikawaDepartment of Neuropsychiatry, Kurume University School of Medicine, Kurume City, Japan.
Masatoshi IshibashiDepartment of Neuropsychiatry, Kurume University School of Medicine, Kurume City, Japan.
Ken UematsuUematsu Mental Clinic, Chikugo City, Japan.
Teruyuki HirakiDepartment of Anaesthesiology, Kurume University School of Medicine, Kurume City, Japan.
Toshi AbeDepartment of Radiology, Kurume University School of Medicine, Kurume City, Japan.
Naohisa UchimuraDepartment of Neuropsychiatry, Kurume University School of Medicine, Kurume City, Japan.
Kurume University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimApproximately one-third of patients with major depressive disorder develop treatment-resistant depression. One-third of patients with treatment-resistant depression demonstrate resistance to ketamine, which is a novel antidepressant effective for this disorder. The objective of this study was to examine the utility of resting-state functional magnetic resonance imaging for the prediction of treatment response to ketamine in treatment-resistant depression.

methodsAn exploratory seed-based resting-state functional magnetic resonance imaging analysis was performed to examine baseline resting-state functional connectivity differences between ketamine responders and nonresponders before treatment with multiple intravenous ketamine infusions.

resultsFifteen patients with treatment-resistant depression received multiple intravenous subanesthetic (0.5 mg/kg/40 minutes) ketamine infusions, and nine were identified as responders. The exploratory resting-state functional magnetic resonance imaging analysis identified a cluster of significant baseline resting-state functional connectivity differences associating ketamine response between the amygdala and subgenual anterior cingulate gyrus in the right hemisphere. Using anatomical region of interest analysis of the resting-state functional connectivity, ketamine response was predicted with 88.9% sensitivity and 100% specificity. The resting-state functional connectivity of significant group differences between responders and nonresponders retained throughout the treatment were considered a trait-like feature of heterogeneity in treatment-resistant depression.

conclusionThis study suggests the possible clinical utility of resting-state functional magnetic resonance imaging for predicting the antidepressant effects of ketamine in treatment-resistant depression patients and implicated resting-state functional connectivity alterations to determine the trait-like pathophysiology underlying treatment response heterogeneity in treatment-resistant depression.

Indexed as

KetamineMajor Depressive DisorderAmygdalaAntidepressive AgentsDepressionGyrus CinguliHumansAntidepressive AgentsKetaminefunctional connectivityketamineresting-state functional MRItreatment-resistant depressiontreatment response prediction

Identifiers

PMID33615749
PMCPMC8340826
OpenAlexW3129697370

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.