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Examining Endothelial Function and Platelet Reactivity in Patients with Depression before and after SSRI Therapy

Although it is recognized that patients with major depressive disorder (MDD) are at increased risk of developing cardiovascular disease (CVD) the mechanisms responsible remain unknown. Endothelial dysfunction is one of the first signs of CVD. Using two techniques, flow-mediated dilatation in respons...

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Autores principales: Dawood, Tye, Barton, David A., Lambert, Elisabeth A., Eikelis, Nina, Lambert, Gavin W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4757642/
https://www.ncbi.nlm.nih.gov/pubmed/26924994
http://dx.doi.org/10.3389/fpsyt.2016.00018
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author Dawood, Tye
Barton, David A.
Lambert, Elisabeth A.
Eikelis, Nina
Lambert, Gavin W.
author_facet Dawood, Tye
Barton, David A.
Lambert, Elisabeth A.
Eikelis, Nina
Lambert, Gavin W.
author_sort Dawood, Tye
collection PubMed
description Although it is recognized that patients with major depressive disorder (MDD) are at increased risk of developing cardiovascular disease (CVD) the mechanisms responsible remain unknown. Endothelial dysfunction is one of the first signs of CVD. Using two techniques, flow-mediated dilatation in response to reactive hyperemia and laser Doppler velocimetry with iontophoresis, we examined endothelial function in the forearm before and after serotonin-specific reuptake inhibitor (SSRI) treatment in 31 patients with MDD. Measurement of intercellular adhesion molecule-1, vascular cell adhesion molecule-1, soluble P-selectin, and noradrenaline in plasma was also performed. Prior to treatment, markers of endothelial and vascular function and platelet reactivity were within the normal range. Following SSRI therapy (95 ± 5 days) symptoms of depression were reduced (paired difference between pre- and post-treatment Hamilton rating −18 ± 1, P < 0.001) with 19 patients recovered and 4 remitted. There occurred no significant change in markers of endothelial or vascular function following SSRI therapy. The improvement in Hamilton depression rating in response to therapy could be independently predicted by the baseline arterial plasma noradrenaline concentration (r(2) = 0.36, P = 0.003). In this cohort of patients with MDD, SSRI therapy did not influence endothelial function or markers of vascular or platelet reactivity. Patient response to SSRI therapy could be predicted by the initial circulating level of noradrenaline, with noradrenaline levels being lower in responders.
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spelling pubmed-47576422016-02-26 Examining Endothelial Function and Platelet Reactivity in Patients with Depression before and after SSRI Therapy Dawood, Tye Barton, David A. Lambert, Elisabeth A. Eikelis, Nina Lambert, Gavin W. Front Psychiatry Psychiatry Although it is recognized that patients with major depressive disorder (MDD) are at increased risk of developing cardiovascular disease (CVD) the mechanisms responsible remain unknown. Endothelial dysfunction is one of the first signs of CVD. Using two techniques, flow-mediated dilatation in response to reactive hyperemia and laser Doppler velocimetry with iontophoresis, we examined endothelial function in the forearm before and after serotonin-specific reuptake inhibitor (SSRI) treatment in 31 patients with MDD. Measurement of intercellular adhesion molecule-1, vascular cell adhesion molecule-1, soluble P-selectin, and noradrenaline in plasma was also performed. Prior to treatment, markers of endothelial and vascular function and platelet reactivity were within the normal range. Following SSRI therapy (95 ± 5 days) symptoms of depression were reduced (paired difference between pre- and post-treatment Hamilton rating −18 ± 1, P < 0.001) with 19 patients recovered and 4 remitted. There occurred no significant change in markers of endothelial or vascular function following SSRI therapy. The improvement in Hamilton depression rating in response to therapy could be independently predicted by the baseline arterial plasma noradrenaline concentration (r(2) = 0.36, P = 0.003). In this cohort of patients with MDD, SSRI therapy did not influence endothelial function or markers of vascular or platelet reactivity. Patient response to SSRI therapy could be predicted by the initial circulating level of noradrenaline, with noradrenaline levels being lower in responders. Frontiers Media S.A. 2016-02-18 /pmc/articles/PMC4757642/ /pubmed/26924994 http://dx.doi.org/10.3389/fpsyt.2016.00018 Text en Copyright © 2016 Dawood, Barton, Lambert, Eikelis and Lambert. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Dawood, Tye
Barton, David A.
Lambert, Elisabeth A.
Eikelis, Nina
Lambert, Gavin W.
Examining Endothelial Function and Platelet Reactivity in Patients with Depression before and after SSRI Therapy
title Examining Endothelial Function and Platelet Reactivity in Patients with Depression before and after SSRI Therapy
title_full Examining Endothelial Function and Platelet Reactivity in Patients with Depression before and after SSRI Therapy
title_fullStr Examining Endothelial Function and Platelet Reactivity in Patients with Depression before and after SSRI Therapy
title_full_unstemmed Examining Endothelial Function and Platelet Reactivity in Patients with Depression before and after SSRI Therapy
title_short Examining Endothelial Function and Platelet Reactivity in Patients with Depression before and after SSRI Therapy
title_sort examining endothelial function and platelet reactivity in patients with depression before and after ssri therapy
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4757642/
https://www.ncbi.nlm.nih.gov/pubmed/26924994
http://dx.doi.org/10.3389/fpsyt.2016.00018
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