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


Journal

Psychiatry and clinical neurosciences
ISSN: 1440-1819
Titre abrégé: Psychiatry Clin Neurosci
Pays: Australia
ID NLM: 9513551

Informations de publication

Date de publication:
Aug 2022
Historique:
revised: 16 03 2022
received: 26 11 2021
accepted: 24 04 2022
pubmed: 12 5 2022
medline: 12 8 2022
entrez: 11 5 2022
Statut: ppublish

Résumé

To 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. Blood 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). Thirty-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. Decreased 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.

Identifiants

pubmed: 35543406
doi: 10.1111/pcn.13373
pmc: PMC9544423
doi:

Substances chimiques

Kynurenine 343-65-7
Escitalopram 4O4S742ANY

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

367-376

Subventions

Organisme : AMED
ID : JP20pc0101061
Organisme : AMED
ID : JP18dk0307076
Organisme : AMED
ID : JP18dm0307008
Organisme : AMED
ID : JP18dm0307002

Informations de copyright

© 2022 The Authors. Psychiatry and Clinical Neurosciences published by John Wiley & Sons Australia, Ltd on behalf of Japanese Society of Psychiatry and Neurology.

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Auteurs

Toshiharu Kamishikiryo (T)

Department of Psychiatry and Neurosciences, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.

Go Okada (G)

Department of Psychiatry and Neurosciences, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.

Eri Itai (E)

Department of Psychiatry and Neurosciences, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.

Yoshikazu Masuda (Y)

Department of Psychiatry and Neurosciences, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.

Satoshi Yokoyama (S)

Department of Psychiatry and Neurosciences, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.

Masahiro Takamura (M)

Department of Neurology, Faculty of Medicine, Shimane University, Izumo-shi, Japan.

Manabu Fuchikami (M)

Department of Psychiatry and Neurosciences, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.

Atsuo Yoshino (A)

Department of Psychiatry and Neurosciences, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.

Kazuaki Mawatari (K)

Department of Preventive Environment and Nutrition, Institute of Biomedical Sciences, Tokushima University, Tokushima, Japan.

Shusuke Numata (S)

Department of Psychiatry, Institute of Biomedical Science, Tokushima University Graduate School, Tokushima, Japan.

Akira Takahashi (A)

Department of Preventive Environment and Nutrition, Institute of Biomedical Sciences, Tokushima University, Tokushima, Japan.

Tetsuro Ohmori (T)

Department of Psychiatry, Institute of Biomedical Science, Tokushima University Graduate School, Tokushima, Japan.

Yasumasa Okamoto (Y)

Department of Psychiatry and Neurosciences, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.

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