Vortioxetine in major depressive disorder: from mechanisms of action to clinical studies. An updated review
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Date
2021-12-29
Authors
De Diego-Adelino, Javier
Crespo, Jose Manuel
Mora, Fernando
Neyra, Adrian
Iborra, Pedro
Gutierrez-Rojas, Luis
Salonia, Selman F.
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Taylor & francis ltd
Abstract
Introduction Vortioxetine is a multimodal-acting antidepressant that provides improvements on cognitive function aside from antidepressants and anxiolytic effects. Vortioxetine has been found to be one of the most effective and best tolerated options for major depressive disorder (MDD) in head-to-head trials. Areas covered The present review intends to gather the most relevant and pragmatic data of vortioxetine in MDD, specially focusing on new studies that emerged between 2015 and 2020. Expert opinion Vortioxetine is the first antidepressant that has shown improvements both in depression and cognitive symptoms, due to the unique multimodal mechanism of action that combine the 5-HT reuptake inhibition with modulations of other key pre- and post-synaptic 5-HT receptors (agonism of 5-HT1A receptor, partial agonism of 5-HT1B receptor, and antagonism of 5-HT3, 5-HT1D and 5-HT7 receptors). This new mechanism of action can explain the dose-dependent effect and can be responsible for its effects on cognitive functioning and improved tolerability profile. Potential analgesic and anti-inflammatory properties observed in preclinical studies as well as interesting efficacy and tolerability results of clinical studies with specific target groups render it a promising therapeutic option for patients with MDD and concomitant conditions (as menopause symptoms, pain, inflammation, apathy, sleep and/or metabolic abnormalities).
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Antidepressant, cognition, efficacy, interactions, major depressive disorder, neurotransmission, pharmacology, safety, vortioxetine, Serotonin reuptake inhibitors, Multimodal antidepressant vortioxetine, Randomized controlled-trials, Emergent sexual dysfunction, Placebo-controlled trials, Substance use disorders, Inadequate response, Double-blind, 5-ht3 receptors, Open-label