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Combined metabolic activators improve cognitive functions in Alzheimer’s disease patients: a randomised, double-blinded, placebo-controlled phase-II trial
BACKGROUND: Alzheimer’s disease (AD) is associated with metabolic abnormalities linked to critical elements of neurodegeneration. We recently administered combined metabolic activators (CMA) to the AD rat model and observed that CMA improves the AD-associated histological parameters in the animals....
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9879258/ https://www.ncbi.nlm.nih.gov/pubmed/36703196 http://dx.doi.org/10.1186/s40035-023-00336-2 |
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author | Yulug, Burak Altay, Ozlem Li, Xiangyu Hanoglu, Lutfu Cankaya, Seyda Lam, Simon Velioglu, Halil Aziz Yang, Hong Coskun, Ebru Idil, Ezgi Nogaylar, Rahim Ozsimsek, Ahmet Bayram, Cemil Bolat, Ismail Oner, Sena Tozlu, Ozlem Ozdemir Arslan, Mehmet Enes Hacimuftuoglu, Ahmet Yildirim, Serkan Arif, Muhammad Shoaie, Saeed Zhang, Cheng Nielsen, Jens Turkez, Hasan Borén, Jan Uhlén, Mathias Mardinoglu, Adil |
author_facet | Yulug, Burak Altay, Ozlem Li, Xiangyu Hanoglu, Lutfu Cankaya, Seyda Lam, Simon Velioglu, Halil Aziz Yang, Hong Coskun, Ebru Idil, Ezgi Nogaylar, Rahim Ozsimsek, Ahmet Bayram, Cemil Bolat, Ismail Oner, Sena Tozlu, Ozlem Ozdemir Arslan, Mehmet Enes Hacimuftuoglu, Ahmet Yildirim, Serkan Arif, Muhammad Shoaie, Saeed Zhang, Cheng Nielsen, Jens Turkez, Hasan Borén, Jan Uhlén, Mathias Mardinoglu, Adil |
author_sort | Yulug, Burak |
collection | PubMed |
description | BACKGROUND: Alzheimer’s disease (AD) is associated with metabolic abnormalities linked to critical elements of neurodegeneration. We recently administered combined metabolic activators (CMA) to the AD rat model and observed that CMA improves the AD-associated histological parameters in the animals. CMA promotes mitochondrial fatty acid uptake from the cytosol, facilitates fatty acid oxidation in the mitochondria, and alleviates oxidative stress. METHODS: Here, we designed a randomised, double-blinded, placebo-controlled phase-II clinical trial and studied the effect of CMA administration on the global metabolism of AD patients. One-dose CMA included 12.35 g L-serine (61.75%), 1 g nicotinamide riboside (5%), 2.55 g N-acetyl-L-cysteine (12.75%), and 3.73 g L-carnitine tartrate (18.65%). AD patients received one dose of CMA or placebo daily during the first 28 days and twice daily between day 28 and day 84. The primary endpoint was the difference in the cognitive function and daily living activity scores between the placebo and the treatment arms. The secondary aim of this study was to evaluate the safety and tolerability of CMA. A comprehensive plasma metabolome and proteome analysis was also performed to evaluate the efficacy of the CMA in AD patients. RESULTS: We showed a significant decrease of AD Assessment Scale-cognitive subscale (ADAS-Cog) score on day 84 vs day 0 (P = 0.00001, 29% improvement) in the CMA group. Moreover, there was a significant decline (P = 0.0073) in ADAS-Cog scores (improvement of cognitive functions) in the CMA compared to the placebo group in patients with higher ADAS-Cog scores. Improved cognitive functions in AD patients were supported by the relevant alterations in the hippocampal volumes and cortical thickness based on imaging analysis. Moreover, the plasma levels of proteins and metabolites associated with NAD + and glutathione metabolism were significantly improved after CMA treatment. CONCLUSION: Our results indicate that treatment of AD patients with CMA can lead to enhanced cognitive functions and improved clinical parameters associated with phenomics, metabolomics, proteomics and imaging analysis. Trial registration ClinicalTrials.gov NCT04044131 Registered 17 July 2019, https://clinicaltrials.gov/ct2/show/NCT04044131 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40035-023-00336-2. |
format | Online Article Text |
id | pubmed-9879258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-98792582023-01-27 Combined metabolic activators improve cognitive functions in Alzheimer’s disease patients: a randomised, double-blinded, placebo-controlled phase-II trial Yulug, Burak Altay, Ozlem Li, Xiangyu Hanoglu, Lutfu Cankaya, Seyda Lam, Simon Velioglu, Halil Aziz Yang, Hong Coskun, Ebru Idil, Ezgi Nogaylar, Rahim Ozsimsek, Ahmet Bayram, Cemil Bolat, Ismail Oner, Sena Tozlu, Ozlem Ozdemir Arslan, Mehmet Enes Hacimuftuoglu, Ahmet Yildirim, Serkan Arif, Muhammad Shoaie, Saeed Zhang, Cheng Nielsen, Jens Turkez, Hasan Borén, Jan Uhlén, Mathias Mardinoglu, Adil Transl Neurodegener Research BACKGROUND: Alzheimer’s disease (AD) is associated with metabolic abnormalities linked to critical elements of neurodegeneration. We recently administered combined metabolic activators (CMA) to the AD rat model and observed that CMA improves the AD-associated histological parameters in the animals. CMA promotes mitochondrial fatty acid uptake from the cytosol, facilitates fatty acid oxidation in the mitochondria, and alleviates oxidative stress. METHODS: Here, we designed a randomised, double-blinded, placebo-controlled phase-II clinical trial and studied the effect of CMA administration on the global metabolism of AD patients. One-dose CMA included 12.35 g L-serine (61.75%), 1 g nicotinamide riboside (5%), 2.55 g N-acetyl-L-cysteine (12.75%), and 3.73 g L-carnitine tartrate (18.65%). AD patients received one dose of CMA or placebo daily during the first 28 days and twice daily between day 28 and day 84. The primary endpoint was the difference in the cognitive function and daily living activity scores between the placebo and the treatment arms. The secondary aim of this study was to evaluate the safety and tolerability of CMA. A comprehensive plasma metabolome and proteome analysis was also performed to evaluate the efficacy of the CMA in AD patients. RESULTS: We showed a significant decrease of AD Assessment Scale-cognitive subscale (ADAS-Cog) score on day 84 vs day 0 (P = 0.00001, 29% improvement) in the CMA group. Moreover, there was a significant decline (P = 0.0073) in ADAS-Cog scores (improvement of cognitive functions) in the CMA compared to the placebo group in patients with higher ADAS-Cog scores. Improved cognitive functions in AD patients were supported by the relevant alterations in the hippocampal volumes and cortical thickness based on imaging analysis. Moreover, the plasma levels of proteins and metabolites associated with NAD + and glutathione metabolism were significantly improved after CMA treatment. CONCLUSION: Our results indicate that treatment of AD patients with CMA can lead to enhanced cognitive functions and improved clinical parameters associated with phenomics, metabolomics, proteomics and imaging analysis. Trial registration ClinicalTrials.gov NCT04044131 Registered 17 July 2019, https://clinicaltrials.gov/ct2/show/NCT04044131 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40035-023-00336-2. BioMed Central 2023-01-26 /pmc/articles/PMC9879258/ /pubmed/36703196 http://dx.doi.org/10.1186/s40035-023-00336-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Yulug, Burak Altay, Ozlem Li, Xiangyu Hanoglu, Lutfu Cankaya, Seyda Lam, Simon Velioglu, Halil Aziz Yang, Hong Coskun, Ebru Idil, Ezgi Nogaylar, Rahim Ozsimsek, Ahmet Bayram, Cemil Bolat, Ismail Oner, Sena Tozlu, Ozlem Ozdemir Arslan, Mehmet Enes Hacimuftuoglu, Ahmet Yildirim, Serkan Arif, Muhammad Shoaie, Saeed Zhang, Cheng Nielsen, Jens Turkez, Hasan Borén, Jan Uhlén, Mathias Mardinoglu, Adil Combined metabolic activators improve cognitive functions in Alzheimer’s disease patients: a randomised, double-blinded, placebo-controlled phase-II trial |
title | Combined metabolic activators improve cognitive functions in Alzheimer’s disease patients: a randomised, double-blinded, placebo-controlled phase-II trial |
title_full | Combined metabolic activators improve cognitive functions in Alzheimer’s disease patients: a randomised, double-blinded, placebo-controlled phase-II trial |
title_fullStr | Combined metabolic activators improve cognitive functions in Alzheimer’s disease patients: a randomised, double-blinded, placebo-controlled phase-II trial |
title_full_unstemmed | Combined metabolic activators improve cognitive functions in Alzheimer’s disease patients: a randomised, double-blinded, placebo-controlled phase-II trial |
title_short | Combined metabolic activators improve cognitive functions in Alzheimer’s disease patients: a randomised, double-blinded, placebo-controlled phase-II trial |
title_sort | combined metabolic activators improve cognitive functions in alzheimer’s disease patients: a randomised, double-blinded, placebo-controlled phase-ii trial |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9879258/ https://www.ncbi.nlm.nih.gov/pubmed/36703196 http://dx.doi.org/10.1186/s40035-023-00336-2 |
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