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The Possible Application of Ketamine in the Treatment of Depression in Alzheimer’s Disease
Depression is a leading cause of disability globally, with a prevalence of 3.8% among the whole population, 5% of the adult population, and 5.7% of the elderly population over 60 years of age. There is evidence that depression is linked to certain neurodegenerative diseases, one being Alzheimer’s di...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036213/ https://www.ncbi.nlm.nih.gov/pubmed/35466206 http://dx.doi.org/10.3390/neurolint14020025 |
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author | Mohammad Shehata, Islam Masood, Waniyah Nemr, Nouran Anderson, Alexandra Bhusal, Kamal Edinoff, Amber N. Cornett, Elyse M. Kaye, Adam M. Kaye, Alan D. |
author_facet | Mohammad Shehata, Islam Masood, Waniyah Nemr, Nouran Anderson, Alexandra Bhusal, Kamal Edinoff, Amber N. Cornett, Elyse M. Kaye, Adam M. Kaye, Alan D. |
author_sort | Mohammad Shehata, Islam |
collection | PubMed |
description | Depression is a leading cause of disability globally, with a prevalence of 3.8% among the whole population, 5% of the adult population, and 5.7% of the elderly population over 60 years of age. There is evidence that depression is linked to certain neurodegenerative diseases, one being Alzheimer’s disease (AD). The efficacy of conventional antidepressants to treat depression in AD is conflicting, especially regarding selective serotonin reuptake inhibitors (SSRIs). A recent systemic review and meta-analysis of 25 randomized controlled trials including fourteen antidepressant medications showed no high efficacy in treating AD patients’ symptoms. However, ketamine, a nonselective N-methyl-D-aspartate (NMDA) receptor antagonist, can mediate a wide range of pharmacological effects, including neuroprotection, anti-inflammatory and anticancer properties, multimodal analgesia, and treatment of depression, suicidal attempts, and status epilepticus. Esketamine, which is ketamine formulated as a nasal spray, was approved by the Federal Drug Administration (FDA) in March 2019 as an adjuvant drug to treat treatment-resistant depression. NMDA receptor antagonists treat AD through offsetting AD-related pathological stimulation of subtypes of glutamate receptors in the central nervous system. Recent clinical findings suggest that ketamine may provide neuroprotection and reduce neuropsychiatric symptoms associated with AD. In the present investigation, we evaluate the potential role of ketamine and its postulated mechanism in AD management. |
format | Online Article Text |
id | pubmed-9036213 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-90362132022-04-26 The Possible Application of Ketamine in the Treatment of Depression in Alzheimer’s Disease Mohammad Shehata, Islam Masood, Waniyah Nemr, Nouran Anderson, Alexandra Bhusal, Kamal Edinoff, Amber N. Cornett, Elyse M. Kaye, Adam M. Kaye, Alan D. Neurol Int Review Depression is a leading cause of disability globally, with a prevalence of 3.8% among the whole population, 5% of the adult population, and 5.7% of the elderly population over 60 years of age. There is evidence that depression is linked to certain neurodegenerative diseases, one being Alzheimer’s disease (AD). The efficacy of conventional antidepressants to treat depression in AD is conflicting, especially regarding selective serotonin reuptake inhibitors (SSRIs). A recent systemic review and meta-analysis of 25 randomized controlled trials including fourteen antidepressant medications showed no high efficacy in treating AD patients’ symptoms. However, ketamine, a nonselective N-methyl-D-aspartate (NMDA) receptor antagonist, can mediate a wide range of pharmacological effects, including neuroprotection, anti-inflammatory and anticancer properties, multimodal analgesia, and treatment of depression, suicidal attempts, and status epilepticus. Esketamine, which is ketamine formulated as a nasal spray, was approved by the Federal Drug Administration (FDA) in March 2019 as an adjuvant drug to treat treatment-resistant depression. NMDA receptor antagonists treat AD through offsetting AD-related pathological stimulation of subtypes of glutamate receptors in the central nervous system. Recent clinical findings suggest that ketamine may provide neuroprotection and reduce neuropsychiatric symptoms associated with AD. In the present investigation, we evaluate the potential role of ketamine and its postulated mechanism in AD management. MDPI 2022-03-22 /pmc/articles/PMC9036213/ /pubmed/35466206 http://dx.doi.org/10.3390/neurolint14020025 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Mohammad Shehata, Islam Masood, Waniyah Nemr, Nouran Anderson, Alexandra Bhusal, Kamal Edinoff, Amber N. Cornett, Elyse M. Kaye, Adam M. Kaye, Alan D. The Possible Application of Ketamine in the Treatment of Depression in Alzheimer’s Disease |
title | The Possible Application of Ketamine in the Treatment of Depression in Alzheimer’s Disease |
title_full | The Possible Application of Ketamine in the Treatment of Depression in Alzheimer’s Disease |
title_fullStr | The Possible Application of Ketamine in the Treatment of Depression in Alzheimer’s Disease |
title_full_unstemmed | The Possible Application of Ketamine in the Treatment of Depression in Alzheimer’s Disease |
title_short | The Possible Application of Ketamine in the Treatment of Depression in Alzheimer’s Disease |
title_sort | possible application of ketamine in the treatment of depression in alzheimer’s disease |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036213/ https://www.ncbi.nlm.nih.gov/pubmed/35466206 http://dx.doi.org/10.3390/neurolint14020025 |
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