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New trends in pharmacological control of neuropsychiatric symptoms of dementia.

Damiana Scuteri, Maria Tiziana Corasaniti, Paolo Tonin, Pierluigi Nicotera, Giacinto Bagetta

Current opinion in pharmacology December 2021 DOI: 10.1016/j.coph.2021.09.002 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Theoretical or philosophical paper Open-label Peer reviewed
Intervention Esketamine
Key points Argues that late-life depression is a prodromal at-risk stage of Alzheimer's disease and that current pharmacological approaches for neuropsychiatric symptoms are inadequate. Proposes that microdosed psychedelics and rapid-acting esketamine could offer a first-in-class treatment for these symptoms, and calls for an open-label clinical trial to test this.

Abstract

Abnormal neuronal and synaptic plasticity occurs in Alzheimer's disease (AD) and depression. The latter, particularly late-life, has been recognized as fundamental in the identification of at-risk prodromal stages of AD. The lack of disease-modifying drugs and the off-label use of antipsychotics and antidepressants for neuropsychiatric symptoms (NPSs) have caused a season of therapeutic inappropriateness. To date, the wealth of clinical trials investigating drugs, diverse for structure and mechanism of action, has failed to provide a cure for all the spectrums of NPSs. Psychedelics in microdosing afford promotion of neurogenesis and synaptic plasticity and, recently, have been considered a revolution for the management of depression endowed with faster action and an improved side effect profile than antidepressants. In the current scenario, therefore, the rapid-acting antidepressant esketamine could represent the first-in-class for treatment of NPSs, and this deserves to be demonstrated with an open-label clinical trial.

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