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An Exploratory Pilot Study with Plasma Protein Signatures Associated with Response of Patients with Depression to Antidepressant Treatment for 10 Weeks

Major depressive disorder (MDD) is a leading cause of global disability with a chronic and recurrent course. Recognition of biological markers that could predict and monitor response to drug treatment could personalize clinical decision-making, minimize unnecessary drug exposure, and achieve better...

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Autores principales: Kim, Eun Young, Ahn, Hee-Sung, Lee, Min Young, Yu, Jiyoung, Yeom, Jeonghun, Jeong, Hwangkyo, Min, Hophil, Lee, Hyun Jeong, Kim, Kyunggon, Ahn, Yong Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7692261/
https://www.ncbi.nlm.nih.gov/pubmed/33126421
http://dx.doi.org/10.3390/biomedicines8110455
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author Kim, Eun Young
Ahn, Hee-Sung
Lee, Min Young
Yu, Jiyoung
Yeom, Jeonghun
Jeong, Hwangkyo
Min, Hophil
Lee, Hyun Jeong
Kim, Kyunggon
Ahn, Yong Min
author_facet Kim, Eun Young
Ahn, Hee-Sung
Lee, Min Young
Yu, Jiyoung
Yeom, Jeonghun
Jeong, Hwangkyo
Min, Hophil
Lee, Hyun Jeong
Kim, Kyunggon
Ahn, Yong Min
author_sort Kim, Eun Young
collection PubMed
description Major depressive disorder (MDD) is a leading cause of global disability with a chronic and recurrent course. Recognition of biological markers that could predict and monitor response to drug treatment could personalize clinical decision-making, minimize unnecessary drug exposure, and achieve better outcomes. Four longitudinal plasma samples were collected from each of ten patients with MDD treated with antidepressants for 10 weeks. Plasma proteins were analyzed qualitatively and quantitatively with a nanoflow LC−MS/MS technique. Of 1153 proteins identified in the 40 longitudinal plasma samples, 37 proteins were significantly associated with response/time and clustered into six according to time and response by the linear mixed model. Among them, three early-drug response markers (PHOX2B, SH3BGRL3, and YWHAE) detectable within one week were verified by liquid chromatography-multiple reaction monitoring/mass spectrometry (LC-MRM/MS) in the well-controlled 24 patients. In addition, 11 proteins correlated significantly with two or more psychiatric measurement indices. This pilot study might be useful in finding protein marker candidates that can monitor response to antidepressant treatment during follow-up visits within 10 weeks after the baseline visit.
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spelling pubmed-76922612020-11-28 An Exploratory Pilot Study with Plasma Protein Signatures Associated with Response of Patients with Depression to Antidepressant Treatment for 10 Weeks Kim, Eun Young Ahn, Hee-Sung Lee, Min Young Yu, Jiyoung Yeom, Jeonghun Jeong, Hwangkyo Min, Hophil Lee, Hyun Jeong Kim, Kyunggon Ahn, Yong Min Biomedicines Article Major depressive disorder (MDD) is a leading cause of global disability with a chronic and recurrent course. Recognition of biological markers that could predict and monitor response to drug treatment could personalize clinical decision-making, minimize unnecessary drug exposure, and achieve better outcomes. Four longitudinal plasma samples were collected from each of ten patients with MDD treated with antidepressants for 10 weeks. Plasma proteins were analyzed qualitatively and quantitatively with a nanoflow LC−MS/MS technique. Of 1153 proteins identified in the 40 longitudinal plasma samples, 37 proteins were significantly associated with response/time and clustered into six according to time and response by the linear mixed model. Among them, three early-drug response markers (PHOX2B, SH3BGRL3, and YWHAE) detectable within one week were verified by liquid chromatography-multiple reaction monitoring/mass spectrometry (LC-MRM/MS) in the well-controlled 24 patients. In addition, 11 proteins correlated significantly with two or more psychiatric measurement indices. This pilot study might be useful in finding protein marker candidates that can monitor response to antidepressant treatment during follow-up visits within 10 weeks after the baseline visit. MDPI 2020-10-28 /pmc/articles/PMC7692261/ /pubmed/33126421 http://dx.doi.org/10.3390/biomedicines8110455 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, Eun Young
Ahn, Hee-Sung
Lee, Min Young
Yu, Jiyoung
Yeom, Jeonghun
Jeong, Hwangkyo
Min, Hophil
Lee, Hyun Jeong
Kim, Kyunggon
Ahn, Yong Min
An Exploratory Pilot Study with Plasma Protein Signatures Associated with Response of Patients with Depression to Antidepressant Treatment for 10 Weeks
title An Exploratory Pilot Study with Plasma Protein Signatures Associated with Response of Patients with Depression to Antidepressant Treatment for 10 Weeks
title_full An Exploratory Pilot Study with Plasma Protein Signatures Associated with Response of Patients with Depression to Antidepressant Treatment for 10 Weeks
title_fullStr An Exploratory Pilot Study with Plasma Protein Signatures Associated with Response of Patients with Depression to Antidepressant Treatment for 10 Weeks
title_full_unstemmed An Exploratory Pilot Study with Plasma Protein Signatures Associated with Response of Patients with Depression to Antidepressant Treatment for 10 Weeks
title_short An Exploratory Pilot Study with Plasma Protein Signatures Associated with Response of Patients with Depression to Antidepressant Treatment for 10 Weeks
title_sort exploratory pilot study with plasma protein signatures associated with response of patients with depression to antidepressant treatment for 10 weeks
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7692261/
https://www.ncbi.nlm.nih.gov/pubmed/33126421
http://dx.doi.org/10.3390/biomedicines8110455
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