Vasopressin Surrogate Marker Copeptin as a Potential Novel Endocrine Biomarker for Antidepressant Treatment Response in Major Depression: A Pilot Study
BackgroundMajor depressive disorder (MDD) constitutes the leading cause of disability worldwide. Although efficacious antidepressant pharmacotherapies exist for MDD, only about 40–60% of the patients respond to initial treatment. However, there is still a lack of robustly established and applicable...
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2020-05-01
|
Series: | Frontiers in Psychiatry |
Subjects: | |
Online Access: | https://www.frontiersin.org/article/10.3389/fpsyt.2020.00453/full |
_version_ | 1818962476151078912 |
---|---|
author | Agorastos Agorastos Agorastos Agorastos Agorastos Agorastos Anne Sommer Alexandra Heinig Klaus Wiedemann Cüneyt Demiralay |
author_facet | Agorastos Agorastos Agorastos Agorastos Agorastos Agorastos Anne Sommer Alexandra Heinig Klaus Wiedemann Cüneyt Demiralay |
author_sort | Agorastos Agorastos |
collection | DOAJ |
description | BackgroundMajor depressive disorder (MDD) constitutes the leading cause of disability worldwide. Although efficacious antidepressant pharmacotherapies exist for MDD, only about 40–60% of the patients respond to initial treatment. However, there is still a lack of robustly established and applicable biomarkers for antidepressant response in everyday clinical practice.ObjectiveThis study targets the assessment of the vasopressin (AVP) surrogate marker Copeptin (CoP), as a potential peripheral hypothalamic-level biomarker of antidepressant treatment response in MDD.MethodsWe measured baseline and dynamic levels of plasma CoP along with plasma ACTH and cortisol (CORT) in drug-naive outpatients with MDD before and after overnight manipulation of the hypothalamic-pituitary-adrenal (HPA) axis [i.e., stimulation (metyrapone) and suppression (dexamethasone)] on three consecutive days and their association with treatment response to 4 weeks of escitalopram treatment.ResultsOur findings suggest significantly higher baseline and post-metyrapone plasma CoP levels in future non-responders, a statistically significant invert association between baseline CoP levels and probability of treatment response and a potential baseline plasma CoP cut-off level of above 2.9 pmol/L for future non-response screening. Baseline and dynamic plasma ACTH and CORT levels showed no association with treatment response.ConclusionsThis pilot study provide first evidence in humans that CoP may represent a novel, clinically easily applicable, endocrine biomarker of antidepressant response, based on a single-measurement, cut-off level. These findings, underline the role of the vasopressinergic system in the pathophysiology of MDD and may represent a significant new tool in the clinical and biological phenotyping of MDD enhancing individual-tailored therapies. |
first_indexed | 2024-12-20T12:29:55Z |
format | Article |
id | doaj.art-09945bb9fa1e4dfa979ae35b087094ed |
institution | Directory Open Access Journal |
issn | 1664-0640 |
language | English |
last_indexed | 2024-12-20T12:29:55Z |
publishDate | 2020-05-01 |
publisher | Frontiers Media S.A. |
record_format | Article |
series | Frontiers in Psychiatry |
spelling | doaj.art-09945bb9fa1e4dfa979ae35b087094ed2022-12-21T19:40:44ZengFrontiers Media S.A.Frontiers in Psychiatry1664-06402020-05-011110.3389/fpsyt.2020.00453542392Vasopressin Surrogate Marker Copeptin as a Potential Novel Endocrine Biomarker for Antidepressant Treatment Response in Major Depression: A Pilot StudyAgorastos Agorastos0Agorastos Agorastos1Agorastos Agorastos2Anne Sommer3Alexandra Heinig4Klaus Wiedemann5Cüneyt Demiralay6Department of Psychiatry and Psychotherapy, University Medical Center Hamburg-Eppendorf, Hamburg, GermanyDepartment of Psychiatry, Division of Neurosciences, Faculty of Health Sciences, School of Medicine, Aristotle University of Thessaloniki, Thessaloniki, GreeceVA Center of Excellence for Stress and Mental Health (CESAMH), VA San Diego Healthcare System, San Diego, CA, United StatesDepartment of Psychiatry and Psychotherapy, University Medical Center Hamburg-Eppendorf, Hamburg, GermanyDepartment of Psychiatry and Psychotherapy, University Medical Center Hamburg-Eppendorf, Hamburg, GermanyDepartment of Psychiatry and Psychotherapy, University Medical Center Hamburg-Eppendorf, Hamburg, GermanyDepartment of Psychiatry and Psychotherapy, University Medical Center Hamburg-Eppendorf, Hamburg, GermanyBackgroundMajor depressive disorder (MDD) constitutes the leading cause of disability worldwide. Although efficacious antidepressant pharmacotherapies exist for MDD, only about 40–60% of the patients respond to initial treatment. However, there is still a lack of robustly established and applicable biomarkers for antidepressant response in everyday clinical practice.ObjectiveThis study targets the assessment of the vasopressin (AVP) surrogate marker Copeptin (CoP), as a potential peripheral hypothalamic-level biomarker of antidepressant treatment response in MDD.MethodsWe measured baseline and dynamic levels of plasma CoP along with plasma ACTH and cortisol (CORT) in drug-naive outpatients with MDD before and after overnight manipulation of the hypothalamic-pituitary-adrenal (HPA) axis [i.e., stimulation (metyrapone) and suppression (dexamethasone)] on three consecutive days and their association with treatment response to 4 weeks of escitalopram treatment.ResultsOur findings suggest significantly higher baseline and post-metyrapone plasma CoP levels in future non-responders, a statistically significant invert association between baseline CoP levels and probability of treatment response and a potential baseline plasma CoP cut-off level of above 2.9 pmol/L for future non-response screening. Baseline and dynamic plasma ACTH and CORT levels showed no association with treatment response.ConclusionsThis pilot study provide first evidence in humans that CoP may represent a novel, clinically easily applicable, endocrine biomarker of antidepressant response, based on a single-measurement, cut-off level. These findings, underline the role of the vasopressinergic system in the pathophysiology of MDD and may represent a significant new tool in the clinical and biological phenotyping of MDD enhancing individual-tailored therapies.https://www.frontiersin.org/article/10.3389/fpsyt.2020.00453/fullcopeptinvasopressin (AVP)depressionhypothalamus-pituitary-adrenal axis (HPA axis)cortisolbiomarker |
spellingShingle | Agorastos Agorastos Agorastos Agorastos Agorastos Agorastos Anne Sommer Alexandra Heinig Klaus Wiedemann Cüneyt Demiralay Vasopressin Surrogate Marker Copeptin as a Potential Novel Endocrine Biomarker for Antidepressant Treatment Response in Major Depression: A Pilot Study Frontiers in Psychiatry copeptin vasopressin (AVP) depression hypothalamus-pituitary-adrenal axis (HPA axis) cortisol biomarker |
title | Vasopressin Surrogate Marker Copeptin as a Potential Novel Endocrine Biomarker for Antidepressant Treatment Response in Major Depression: A Pilot Study |
title_full | Vasopressin Surrogate Marker Copeptin as a Potential Novel Endocrine Biomarker for Antidepressant Treatment Response in Major Depression: A Pilot Study |
title_fullStr | Vasopressin Surrogate Marker Copeptin as a Potential Novel Endocrine Biomarker for Antidepressant Treatment Response in Major Depression: A Pilot Study |
title_full_unstemmed | Vasopressin Surrogate Marker Copeptin as a Potential Novel Endocrine Biomarker for Antidepressant Treatment Response in Major Depression: A Pilot Study |
title_short | Vasopressin Surrogate Marker Copeptin as a Potential Novel Endocrine Biomarker for Antidepressant Treatment Response in Major Depression: A Pilot Study |
title_sort | vasopressin surrogate marker copeptin as a potential novel endocrine biomarker for antidepressant treatment response in major depression a pilot study |
topic | copeptin vasopressin (AVP) depression hypothalamus-pituitary-adrenal axis (HPA axis) cortisol biomarker |
url | https://www.frontiersin.org/article/10.3389/fpsyt.2020.00453/full |
work_keys_str_mv | AT agorastosagorastos vasopressinsurrogatemarkercopeptinasapotentialnovelendocrinebiomarkerforantidepressanttreatmentresponseinmajordepressionapilotstudy AT agorastosagorastos vasopressinsurrogatemarkercopeptinasapotentialnovelendocrinebiomarkerforantidepressanttreatmentresponseinmajordepressionapilotstudy AT agorastosagorastos vasopressinsurrogatemarkercopeptinasapotentialnovelendocrinebiomarkerforantidepressanttreatmentresponseinmajordepressionapilotstudy AT annesommer vasopressinsurrogatemarkercopeptinasapotentialnovelendocrinebiomarkerforantidepressanttreatmentresponseinmajordepressionapilotstudy AT alexandraheinig vasopressinsurrogatemarkercopeptinasapotentialnovelendocrinebiomarkerforantidepressanttreatmentresponseinmajordepressionapilotstudy AT klauswiedemann vasopressinsurrogatemarkercopeptinasapotentialnovelendocrinebiomarkerforantidepressanttreatmentresponseinmajordepressionapilotstudy AT cuneytdemiralay vasopressinsurrogatemarkercopeptinasapotentialnovelendocrinebiomarkerforantidepressanttreatmentresponseinmajordepressionapilotstudy |