Evidence map›Paper›PMID 35543406›Full record

ArticlePsychiatry and clinical neurosciences2022

Left DLPFC activity is associated with plasma kynurenine levels and can predict treatment response to escitalopram in major depressive disorder.

Toshiharu Kamishikiryo, Go Okada, Eri Itai, Yoshikazu Masuda, Satoshi Yokoyama, Masahiro Takamura, Manabu Fuchikami, Atsuo Yoshino, Kazuaki Mawatari, Shusuke Numata and 3 more

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In one paragraph

Article in Psychiatry and clinical neurosciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 37% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 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

13 authors at 3 institutions in 1 country.

Toshiharu KamishikiryoDepartment of Psychiatry and Neurosciences, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.ORCID https://orcid.org/0000-0002-4933-0161
Go OkadaDepartment of Psychiatry and Neurosciences, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.ORCID https://orcid.org/0000-0002-5451-8513
Eri ItaiDepartment of Psychiatry and Neurosciences, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.
Yoshikazu MasudaDepartment of Psychiatry and Neurosciences, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.
Satoshi YokoyamaDepartment of Psychiatry and Neurosciences, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.ORCID https://orcid.org/0000-0002-1309-1103
Masahiro TakamuraDepartment of Neurology, Faculty of Medicine, Shimane University, Izumo-shi, Japan.ORCID https://orcid.org/0000-0001-9742-152X
Manabu FuchikamiDepartment of Psychiatry and Neurosciences, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.
Atsuo YoshinoDepartment of Psychiatry and Neurosciences, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.ORCID https://orcid.org/0000-0002-9081-0896
Kazuaki MawatariDepartment of Preventive Environment and Nutrition, Institute of Biomedical Sciences, Tokushima University, Tokushima, Japan.ORCID https://orcid.org/0000-0003-2880-3801
Shusuke NumataDepartment of Psychiatry, Institute of Biomedical Science, Tokushima University Graduate School, Tokushima, Japan.
Akira TakahashiDepartment of Preventive Environment and Nutrition, Institute of Biomedical Sciences, Tokushima University, Tokushima, Japan.
Tetsuro OhmoriDepartment of Psychiatry, Institute of Biomedical Science, Tokushima University Graduate School, Tokushima, Japan.
Yasumasa OkamotoDepartment of Psychiatry and Neurosciences, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.ORCID https://orcid.org/0000-0001-8813-7551
Hiroshima University · JPTokushima University · JPShimane University · JP

Funding

AMED JP18dk0307076AMED JP18dm0307002AMED JP18dm0307008AMED JP20pc0101061
6 · The paper itself

Abstract

aimTo establish treatment response biomarkers that reflect the pathophysiology of depression, it is important to use an integrated set of features. This study aimed to determine the relationship between regional brain activity at rest and blood metabolites related to treatment response to escitalopram to identify the characteristics of depression that respond to treatment.

methodsBlood metabolite levels and resting-state brain activity were measured in patients with moderate to severe depression (n = 65) before and after 6-8 weeks of treatment with escitalopram, and these were compared between Responders and Nonresponders to treatment. We then examined the relationship between blood metabolites and brain activity related to treatment responsiveness in patients and healthy controls (n = 36).

resultsThirty-two patients (49.2%) showed a clinical response (>50% reduction in the Hamilton Rating Scale for Depression score) and were classified as Responders, and the remaining 33 patients were classified as Nonresponders. The pretreatment fractional amplitude of low-frequency fluctuation (fALFF) value of the left dorsolateral prefrontal cortex (DLPFC) and plasma kynurenine levels were lower in Responders, and the rate of increase of both after treatment was correlated with an improvement in symptoms. Moreover, the fALFF value of the left DLPFC was significantly correlated with plasma kynurenine levels in pretreatment patients with depression and healthy controls.

conclusionDecreased resting-state regional activity of the left DLPFC and decreased plasma kynurenine levels may predict treatment response to escitalopram, suggesting that it may be involved in the pathophysiology of major depressive disorder in response to escitalopram treatment.

Indexed as

Major Depressive DisorderEscitalopramHumansKynurenineMagnetic Resonance ImagingPrefrontal CortexTranscranial Magnetic StimulationEscitalopramKynureninedorsolateral prefrontal cortexfMRIkynureninemajor depressive disordermetabolomics

Identifiers

PMID35543406
PMCPMC9544423
OpenAlexW4280554705

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.