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Antidepressant efficacy is correlated with plasma levels: mega-analysis and further evidence
The debate around optimal target dose for first-line antidepressants (ADs) is still ongoing. Along this line, therapeutic drug monitoring (TDM) represents one of the most promising tools to improve clinical outcome. Nevertheless, a few data exist regarding the concentration-effect relationship of fi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams And Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9648983/ https://www.ncbi.nlm.nih.gov/pubmed/34908537 http://dx.doi.org/10.1097/YIC.0000000000000386 |
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author | Cellini, Lorenzo De Donatis, Domenico Zernig, Gerald De Ronchi, Diana Giupponi, Giancarlo Serretti, Alessandro Xenia, Hart Conca, Andreas Florio, Vincenzo |
author_facet | Cellini, Lorenzo De Donatis, Domenico Zernig, Gerald De Ronchi, Diana Giupponi, Giancarlo Serretti, Alessandro Xenia, Hart Conca, Andreas Florio, Vincenzo |
author_sort | Cellini, Lorenzo |
collection | PubMed |
description | The debate around optimal target dose for first-line antidepressants (ADs) is still ongoing. Along this line, therapeutic drug monitoring (TDM) represents one of the most promising tools to improve clinical outcome. Nevertheless, a few data exist regarding the concentration-effect relationship of first-line ADs which limits TDM implementation in routine clinical practice. We conducted the first patient-level concentration-response mega-analysis including data acquired by us previously and explored the concentration dependency of first-line AD (206 subjects). Further, new data on mirtazapine are reported (18 subjects). Hamilton Depression Rating Scale-21 administered at baseline, at month 1 and month 3 was used as the measure of efficacy to assess antidepressant response (AR). When pooling all four first-line ADs together, normalized plasma levels and AR significantly fit a bell-shaped quadratic function with a progressive increase of AR up to around the upper normalized limit of the therapeutic reference range with a decrease of AR at higher serum levels. Our results complement the available evidence on the issue and the recent insights gained from dose-response studies. A concentration-dependent clinical efficacy, such as previously demonstrated for tricyclic compounds, also emerge for first-line ADs. Our study supports a role for TDM as a tool to optimize AD treatment to obtain maximum benefit. |
format | Online Article Text |
id | pubmed-9648983 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams And Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-96489832022-11-14 Antidepressant efficacy is correlated with plasma levels: mega-analysis and further evidence Cellini, Lorenzo De Donatis, Domenico Zernig, Gerald De Ronchi, Diana Giupponi, Giancarlo Serretti, Alessandro Xenia, Hart Conca, Andreas Florio, Vincenzo Int Clin Psychopharmacol Original Articles The debate around optimal target dose for first-line antidepressants (ADs) is still ongoing. Along this line, therapeutic drug monitoring (TDM) represents one of the most promising tools to improve clinical outcome. Nevertheless, a few data exist regarding the concentration-effect relationship of first-line ADs which limits TDM implementation in routine clinical practice. We conducted the first patient-level concentration-response mega-analysis including data acquired by us previously and explored the concentration dependency of first-line AD (206 subjects). Further, new data on mirtazapine are reported (18 subjects). Hamilton Depression Rating Scale-21 administered at baseline, at month 1 and month 3 was used as the measure of efficacy to assess antidepressant response (AR). When pooling all four first-line ADs together, normalized plasma levels and AR significantly fit a bell-shaped quadratic function with a progressive increase of AR up to around the upper normalized limit of the therapeutic reference range with a decrease of AR at higher serum levels. Our results complement the available evidence on the issue and the recent insights gained from dose-response studies. A concentration-dependent clinical efficacy, such as previously demonstrated for tricyclic compounds, also emerge for first-line ADs. Our study supports a role for TDM as a tool to optimize AD treatment to obtain maximum benefit. Lippincott Williams And Wilkins 2021-12-13 2022-03 /pmc/articles/PMC9648983/ /pubmed/34908537 http://dx.doi.org/10.1097/YIC.0000000000000386 Text en Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Cellini, Lorenzo De Donatis, Domenico Zernig, Gerald De Ronchi, Diana Giupponi, Giancarlo Serretti, Alessandro Xenia, Hart Conca, Andreas Florio, Vincenzo Antidepressant efficacy is correlated with plasma levels: mega-analysis and further evidence |
title | Antidepressant efficacy is correlated with plasma levels: mega-analysis and further evidence |
title_full | Antidepressant efficacy is correlated with plasma levels: mega-analysis and further evidence |
title_fullStr | Antidepressant efficacy is correlated with plasma levels: mega-analysis and further evidence |
title_full_unstemmed | Antidepressant efficacy is correlated with plasma levels: mega-analysis and further evidence |
title_short | Antidepressant efficacy is correlated with plasma levels: mega-analysis and further evidence |
title_sort | antidepressant efficacy is correlated with plasma levels: mega-analysis and further evidence |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9648983/ https://www.ncbi.nlm.nih.gov/pubmed/34908537 http://dx.doi.org/10.1097/YIC.0000000000000386 |
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