Kynurenic acid is a potential overlapped biomarker between diagnosis and treatment response for depression from metabolome analysis

Abstract Since optimal treatment at an early stage leads to remission of symptoms and recovery of function, putative biomarkers leading to early diagnosis and prediction of therapeutic responses are desired. The current study aimed to use a metabolomic approach to extract metabolites involved in bot...

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Autores principales: Hisayuki Erabi, Go Okada, Chiyo Shibasaki, Daiki Setoyama, Dongchon Kang, Masahiro Takamura, Atsuo Yoshino, Manabu Fuchikami, Akiko Kurata, Takahiro A. Kato, Shigeto Yamawaki, Yasumasa Okamoto
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Publicado: Nature Portfolio 2020
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Acceso en línea:https://doaj.org/article/0d8b0e005edb4e1fa3026c8f98f91b71
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spelling oai:doaj.org-article:0d8b0e005edb4e1fa3026c8f98f91b712021-12-02T18:37:07ZKynurenic acid is a potential overlapped biomarker between diagnosis and treatment response for depression from metabolome analysis10.1038/s41598-020-73918-z2045-2322https://doaj.org/article/0d8b0e005edb4e1fa3026c8f98f91b712020-10-01T00:00:00Zhttps://doi.org/10.1038/s41598-020-73918-zhttps://doaj.org/toc/2045-2322Abstract Since optimal treatment at an early stage leads to remission of symptoms and recovery of function, putative biomarkers leading to early diagnosis and prediction of therapeutic responses are desired. The current study aimed to use a metabolomic approach to extract metabolites involved in both the diagnosis of major depressive disorder (MDD) and the prediction of therapeutic response for escitalopram. We compared plasma metabolites of MDD patients (n = 88) with those in healthy participants (n = 88) and found significant differences in the concentrations of 20 metabolites. We measured the Hamilton Rating Scale for Depression (HRSD) on 62 patients who completed approximately six-week treatment with escitalopram before and after treatment and found that kynurenic acid and kynurenine were significantly and negatively associated with HRSD reduction. Only one metabolite, kynurenic acid, was detected among 73 metabolites for overlapped biomarkers. Kynurenic acid was lower in MDD, and lower levels showed a better therapeutic response to escitalopram. Kynurenic acid is a metabolite in the kynurenine pathway that has been widely accepted as being a major mechanism in MDD. Overlapping biomarkers that facilitate diagnosis and prediction of the treatment response may help to improve disease classification and reduce the exposure of patients to less effective treatments in MDD.Hisayuki ErabiGo OkadaChiyo ShibasakiDaiki SetoyamaDongchon KangMasahiro TakamuraAtsuo YoshinoManabu FuchikamiAkiko KurataTakahiro A. KatoShigeto YamawakiYasumasa OkamotoNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 10, Iss 1, Pp 1-8 (2020)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Hisayuki Erabi
Go Okada
Chiyo Shibasaki
Daiki Setoyama
Dongchon Kang
Masahiro Takamura
Atsuo Yoshino
Manabu Fuchikami
Akiko Kurata
Takahiro A. Kato
Shigeto Yamawaki
Yasumasa Okamoto
Kynurenic acid is a potential overlapped biomarker between diagnosis and treatment response for depression from metabolome analysis
description Abstract Since optimal treatment at an early stage leads to remission of symptoms and recovery of function, putative biomarkers leading to early diagnosis and prediction of therapeutic responses are desired. The current study aimed to use a metabolomic approach to extract metabolites involved in both the diagnosis of major depressive disorder (MDD) and the prediction of therapeutic response for escitalopram. We compared plasma metabolites of MDD patients (n = 88) with those in healthy participants (n = 88) and found significant differences in the concentrations of 20 metabolites. We measured the Hamilton Rating Scale for Depression (HRSD) on 62 patients who completed approximately six-week treatment with escitalopram before and after treatment and found that kynurenic acid and kynurenine were significantly and negatively associated with HRSD reduction. Only one metabolite, kynurenic acid, was detected among 73 metabolites for overlapped biomarkers. Kynurenic acid was lower in MDD, and lower levels showed a better therapeutic response to escitalopram. Kynurenic acid is a metabolite in the kynurenine pathway that has been widely accepted as being a major mechanism in MDD. Overlapping biomarkers that facilitate diagnosis and prediction of the treatment response may help to improve disease classification and reduce the exposure of patients to less effective treatments in MDD.
format article
author Hisayuki Erabi
Go Okada
Chiyo Shibasaki
Daiki Setoyama
Dongchon Kang
Masahiro Takamura
Atsuo Yoshino
Manabu Fuchikami
Akiko Kurata
Takahiro A. Kato
Shigeto Yamawaki
Yasumasa Okamoto
author_facet Hisayuki Erabi
Go Okada
Chiyo Shibasaki
Daiki Setoyama
Dongchon Kang
Masahiro Takamura
Atsuo Yoshino
Manabu Fuchikami
Akiko Kurata
Takahiro A. Kato
Shigeto Yamawaki
Yasumasa Okamoto
author_sort Hisayuki Erabi
title Kynurenic acid is a potential overlapped biomarker between diagnosis and treatment response for depression from metabolome analysis
title_short Kynurenic acid is a potential overlapped biomarker between diagnosis and treatment response for depression from metabolome analysis
title_full Kynurenic acid is a potential overlapped biomarker between diagnosis and treatment response for depression from metabolome analysis
title_fullStr Kynurenic acid is a potential overlapped biomarker between diagnosis and treatment response for depression from metabolome analysis
title_full_unstemmed Kynurenic acid is a potential overlapped biomarker between diagnosis and treatment response for depression from metabolome analysis
title_sort kynurenic acid is a potential overlapped biomarker between diagnosis and treatment response for depression from metabolome analysis
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/0d8b0e005edb4e1fa3026c8f98f91b71
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