Escitalopram should be investigated in anorexia nervosa: Rationale and review of mechanisms.


Journal

Journal of psychopharmacology (Oxford, England)
ISSN: 1461-7285
Titre abrégé: J Psychopharmacol
Pays: United States
ID NLM: 8907828

Informations de publication

Date de publication:
09 2022
Historique:
pubmed: 26 8 2022
medline: 28 9 2022
entrez: 25 8 2022
Statut: ppublish

Résumé

One of the biggest ambitions in the field of anorexia nervosa (AN) research is to find a reliable and effective pharmacological treatment. The fact that currently no pharmacological treatment is safe and effective in this disease is worrying and also challenging. On the basis of the progress in our understanding of AN neurobiology, we propose that escitalopram, a widely available drug, might be a safe and effective option that needs to be investigated. Escitalopram is the only selective serotonin reuptake inhibitor, without any catecholaminergic effect. As studies have shown decreased serotonergic and increased dopaminergic transmission in AN, we hypothesized that an ideal drug for AN management should boost serotonin levels to increase serotonergic and decrease dopaminergic transmission, the two main features of escitalopram action. Here, we present a short overview of pharmacological research in AN and discuss the theoretical rationale for escitalopram use in AN. We also call for double-blind, randomized, placebo-controlled trials to test whether this theoretical framework translates into clinical efficacy.

Identifiants

pubmed: 36003008
doi: 10.1177/02698811221118340
doi:

Substances chimiques

Serotonin Uptake Inhibitors 0
Citalopram 0DHU5B8D6V
Serotonin 333DO1RDJY
Escitalopram 4O4S742ANY

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

1016-1019

Auteurs

Robertas Strumila (R)

Institute of Functional Genomics, University of Montpellier, CNRS, INSERM, Montpellier, France.
Department of Urgent and Post Urgent Psychiatry, CHU Montpellier, Montpellier, France.
Clinic of Psychiatry, Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.

Aiste Lengvenyte (A)

Institute of Functional Genomics, University of Montpellier, CNRS, INSERM, Montpellier, France.
Department of Urgent and Post Urgent Psychiatry, CHU Montpellier, Montpellier, France.
Clinic of Psychiatry, Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.

Emilie Olie (E)

Institute of Functional Genomics, University of Montpellier, CNRS, INSERM, Montpellier, France.
Department of Urgent and Post Urgent Psychiatry, CHU Montpellier, Montpellier, France.

Philippe Courtet (P)

Institute of Functional Genomics, University of Montpellier, CNRS, INSERM, Montpellier, France.
Department of Urgent and Post Urgent Psychiatry, CHU Montpellier, Montpellier, France.

Sebastien Guillaume (S)

Institute of Functional Genomics, University of Montpellier, CNRS, INSERM, Montpellier, France.
Department of Urgent and Post Urgent Psychiatry, CHU Montpellier, Montpellier, France.

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Classifications MeSH