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Platelet-Derived Growth Factor as an Antidepressant Treatment Selection Biomarker: Higher Levels Selectively Predict Better Outcomes with Bupropion-SSRI Combination
BACKGROUND: Platelet derived growth factor is integral to maintenance of blood brain barrier, increases in response to blood brain barrier disruption, and may reflect neuroinflammation. Based on previous reports of better outcomes with dopaminergic antidepressants in depressed patients with elevated...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5737519/ https://www.ncbi.nlm.nih.gov/pubmed/29016822 http://dx.doi.org/10.1093/ijnp/pyx060 |
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author | Jha, Manish K Minhajuddin, Abu Gadad, Bharathi S Trivedi, Madhukar H |
author_facet | Jha, Manish K Minhajuddin, Abu Gadad, Bharathi S Trivedi, Madhukar H |
author_sort | Jha, Manish K |
collection | PubMed |
description | BACKGROUND: Platelet derived growth factor is integral to maintenance of blood brain barrier, increases in response to blood brain barrier disruption, and may reflect neuroinflammation. Based on previous reports of better outcomes with dopaminergic antidepressants in depressed patients with elevated inflammatory biomarkers, we hypothesize that elevated peripheral platelet derived growth factor levels can serve as a powerful biomarker for selecting dopaminergic antidepressants. METHODS: Platelet derived growth factor, basic fibroblast growth factor, and granulocyte colony stimulating factor were measured as part of Bioplex Pro human cytokine 27-plex kit in participants of the Combining Medications to Enhance Depression Outcomes trial who provided baseline plasma (n=166) and were treated with either bupropion-plus-escitalopram, escitalopram-plus-placebo, or venlafaxine-plus-mirtazapine. Differential changes in overall symptom severity and anhedonia as well as side effects were tested with a treatment-arm-by-biomarker interaction in mixed model analyses. Effect of biomarkers with significant interaction was calculated in subsequent analyses stratified by treatment arm. RESULTS: There was a significant treatment-arm-by-platelet derived growth factor interaction for depression severity (P=.03) and anhedonia (P=.008) but not for side effects (P=.44). Higher baseline platelet derived growth factor level was associated with greater reduction in depression severity (effect size=0.71, P=.015) and anhedonia (effect size=0.66, P=.02) in the bupropion- selective serotonin reuptake inhibitor but not the other two treatment arms. There was no significant treatment-arm-by-biomarker interaction for both depression severity and side effects with the other two biomarkers. CONCLUSION: As compared with selective serotonin reuptake inhibitor monotherapy or venlafaxine-plus-mirtazapine, bupropion-plus-escitalopram selectively improves anhedonia, which in turn results in improved overall depression severity in depressed patients with elevated platelet derived growth factor levels. |
format | Online Article Text |
id | pubmed-5737519 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57375192018-01-09 Platelet-Derived Growth Factor as an Antidepressant Treatment Selection Biomarker: Higher Levels Selectively Predict Better Outcomes with Bupropion-SSRI Combination Jha, Manish K Minhajuddin, Abu Gadad, Bharathi S Trivedi, Madhukar H Int J Neuropsychopharmacol Regular Research Articles BACKGROUND: Platelet derived growth factor is integral to maintenance of blood brain barrier, increases in response to blood brain barrier disruption, and may reflect neuroinflammation. Based on previous reports of better outcomes with dopaminergic antidepressants in depressed patients with elevated inflammatory biomarkers, we hypothesize that elevated peripheral platelet derived growth factor levels can serve as a powerful biomarker for selecting dopaminergic antidepressants. METHODS: Platelet derived growth factor, basic fibroblast growth factor, and granulocyte colony stimulating factor were measured as part of Bioplex Pro human cytokine 27-plex kit in participants of the Combining Medications to Enhance Depression Outcomes trial who provided baseline plasma (n=166) and were treated with either bupropion-plus-escitalopram, escitalopram-plus-placebo, or venlafaxine-plus-mirtazapine. Differential changes in overall symptom severity and anhedonia as well as side effects were tested with a treatment-arm-by-biomarker interaction in mixed model analyses. Effect of biomarkers with significant interaction was calculated in subsequent analyses stratified by treatment arm. RESULTS: There was a significant treatment-arm-by-platelet derived growth factor interaction for depression severity (P=.03) and anhedonia (P=.008) but not for side effects (P=.44). Higher baseline platelet derived growth factor level was associated with greater reduction in depression severity (effect size=0.71, P=.015) and anhedonia (effect size=0.66, P=.02) in the bupropion- selective serotonin reuptake inhibitor but not the other two treatment arms. There was no significant treatment-arm-by-biomarker interaction for both depression severity and side effects with the other two biomarkers. CONCLUSION: As compared with selective serotonin reuptake inhibitor monotherapy or venlafaxine-plus-mirtazapine, bupropion-plus-escitalopram selectively improves anhedonia, which in turn results in improved overall depression severity in depressed patients with elevated platelet derived growth factor levels. Oxford University Press 2017-07-23 /pmc/articles/PMC5737519/ /pubmed/29016822 http://dx.doi.org/10.1093/ijnp/pyx060 Text en © The Author 2017. Published by Oxford University Press on behalf of CINP. http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Regular Research Articles Jha, Manish K Minhajuddin, Abu Gadad, Bharathi S Trivedi, Madhukar H Platelet-Derived Growth Factor as an Antidepressant Treatment Selection Biomarker: Higher Levels Selectively Predict Better Outcomes with Bupropion-SSRI Combination |
title | Platelet-Derived Growth Factor as an Antidepressant Treatment Selection
Biomarker: Higher Levels Selectively Predict Better Outcomes with Bupropion-SSRI
Combination |
title_full | Platelet-Derived Growth Factor as an Antidepressant Treatment Selection
Biomarker: Higher Levels Selectively Predict Better Outcomes with Bupropion-SSRI
Combination |
title_fullStr | Platelet-Derived Growth Factor as an Antidepressant Treatment Selection
Biomarker: Higher Levels Selectively Predict Better Outcomes with Bupropion-SSRI
Combination |
title_full_unstemmed | Platelet-Derived Growth Factor as an Antidepressant Treatment Selection
Biomarker: Higher Levels Selectively Predict Better Outcomes with Bupropion-SSRI
Combination |
title_short | Platelet-Derived Growth Factor as an Antidepressant Treatment Selection
Biomarker: Higher Levels Selectively Predict Better Outcomes with Bupropion-SSRI
Combination |
title_sort | platelet-derived growth factor as an antidepressant treatment selection
biomarker: higher levels selectively predict better outcomes with bupropion-ssri
combination |
topic | Regular Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5737519/ https://www.ncbi.nlm.nih.gov/pubmed/29016822 http://dx.doi.org/10.1093/ijnp/pyx060 |
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