Cargando…
Creatine as a Therapeutic Target in Alzheimer's Disease
Alzheimer's disease (AD) is the most prevalent neurodegenerative disease, affecting approximately 6.5 million older adults in the United States. Development of AD treatment has primarily centered on developing pharmaceuticals that target amyloid-β (Aβ) plaques in the brain, a hallmark pathologi...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Nutrition
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10594571/ https://www.ncbi.nlm.nih.gov/pubmed/37881206 http://dx.doi.org/10.1016/j.cdnut.2023.102011 |
_version_ | 1785124680935407616 |
---|---|
author | Smith, Aaron N. Morris, Jill K. Carbuhn, Aaron F. Herda, Trent J. Keller, Jessica E. Sullivan, Debra K. Taylor, Matthew K. |
author_facet | Smith, Aaron N. Morris, Jill K. Carbuhn, Aaron F. Herda, Trent J. Keller, Jessica E. Sullivan, Debra K. Taylor, Matthew K. |
author_sort | Smith, Aaron N. |
collection | PubMed |
description | Alzheimer's disease (AD) is the most prevalent neurodegenerative disease, affecting approximately 6.5 million older adults in the United States. Development of AD treatment has primarily centered on developing pharmaceuticals that target amyloid-β (Aβ) plaques in the brain, a hallmark pathological biomarker that precedes symptomatic AD. Though recent clinical trials of novel drugs that target Aβ have demonstrated promising preliminary data, these pharmaceuticals have a poor history of developing into AD treatments, leading to hypotheses that other therapeutic targets may be more suitable for AD prevention and treatment. Impaired brain energy metabolism is another pathological hallmark that precedes the onset of AD that may provide a target for intervention. The brain creatine (Cr) system plays a crucial role in maintaining bioenergetic flux and is disrupted in AD. Recent studies using AD mouse models have shown that supplementing with Cr improves brain bioenergetics, as well as AD biomarkers and cognition. Despite these promising findings, no human trials have investigated the potential benefits of Cr supplementation in AD. This narrative review discusses the link between Cr and AD and the potential for Cr supplementation as a treatment for AD. |
format | Online Article Text |
id | pubmed-10594571 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Nutrition |
record_format | MEDLINE/PubMed |
spelling | pubmed-105945712023-10-25 Creatine as a Therapeutic Target in Alzheimer's Disease Smith, Aaron N. Morris, Jill K. Carbuhn, Aaron F. Herda, Trent J. Keller, Jessica E. Sullivan, Debra K. Taylor, Matthew K. Curr Dev Nutr Review Alzheimer's disease (AD) is the most prevalent neurodegenerative disease, affecting approximately 6.5 million older adults in the United States. Development of AD treatment has primarily centered on developing pharmaceuticals that target amyloid-β (Aβ) plaques in the brain, a hallmark pathological biomarker that precedes symptomatic AD. Though recent clinical trials of novel drugs that target Aβ have demonstrated promising preliminary data, these pharmaceuticals have a poor history of developing into AD treatments, leading to hypotheses that other therapeutic targets may be more suitable for AD prevention and treatment. Impaired brain energy metabolism is another pathological hallmark that precedes the onset of AD that may provide a target for intervention. The brain creatine (Cr) system plays a crucial role in maintaining bioenergetic flux and is disrupted in AD. Recent studies using AD mouse models have shown that supplementing with Cr improves brain bioenergetics, as well as AD biomarkers and cognition. Despite these promising findings, no human trials have investigated the potential benefits of Cr supplementation in AD. This narrative review discusses the link between Cr and AD and the potential for Cr supplementation as a treatment for AD. American Society for Nutrition 2023-09-29 /pmc/articles/PMC10594571/ /pubmed/37881206 http://dx.doi.org/10.1016/j.cdnut.2023.102011 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Review Smith, Aaron N. Morris, Jill K. Carbuhn, Aaron F. Herda, Trent J. Keller, Jessica E. Sullivan, Debra K. Taylor, Matthew K. Creatine as a Therapeutic Target in Alzheimer's Disease |
title | Creatine as a Therapeutic Target in Alzheimer's Disease |
title_full | Creatine as a Therapeutic Target in Alzheimer's Disease |
title_fullStr | Creatine as a Therapeutic Target in Alzheimer's Disease |
title_full_unstemmed | Creatine as a Therapeutic Target in Alzheimer's Disease |
title_short | Creatine as a Therapeutic Target in Alzheimer's Disease |
title_sort | creatine as a therapeutic target in alzheimer's disease |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10594571/ https://www.ncbi.nlm.nih.gov/pubmed/37881206 http://dx.doi.org/10.1016/j.cdnut.2023.102011 |
work_keys_str_mv | AT smithaaronn creatineasatherapeutictargetinalzheimersdisease AT morrisjillk creatineasatherapeutictargetinalzheimersdisease AT carbuhnaaronf creatineasatherapeutictargetinalzheimersdisease AT herdatrentj creatineasatherapeutictargetinalzheimersdisease AT kellerjessicae creatineasatherapeutictargetinalzheimersdisease AT sullivandebrak creatineasatherapeutictargetinalzheimersdisease AT taylormatthewk creatineasatherapeutictargetinalzheimersdisease |