Combined Metabolic Activators Improves Cognitive Functions in Alzheimer’s Disease Patients

Author:

YULUG BURAK1,ALTAY OZLEM2,LI XIANGYU2,HANOGLU LUTFU3,CANKAYA SEYDA1,LAM SIMON4,VELIOGLU HALIL AZIZ3,YANG HONG2,COSKUN EBRU3,IDIL EZGI5,NOGAYLAR RAHIM1,OZSIMSEK AHMET1,BAYRAM CEMIL6,BOLAT ISMAIL6,ONER SENA7,TOZLU OZLEM OZDEMIR7,ARSLAN MEHMET ENES7,HACIMUFTUOGLU AHMET6,YILDIRIM SERKAN6,ARIF MUHAMMAD2,SHOAIE SAEED2,ZHANG CHENG2,NIELSEN JENS8,TURKEZ HASAN6,BOREN JAN9,UHLEN MATHIAS2,Mardinoglu Adil10ORCID

Affiliation:

1. Alanya Alaaddin Keykubat Üniversitesi: Alanya Alaaddin Keykubat Universitesi

2. KTH Royal Institute of Technology: Kungliga Tekniska Hogskolan

3. Istanbul Medipol University: Istanbul Medipol Universitesi

4. King's College London - Strand Campus: King's College London

5. Alanya Alaaddin Keykubat University: Alanya Alaaddin Keykubat Universitesi

6. Ataturk University: Ataturk Universitesi

7. Erzurum Technical University: Erzurum Teknik Universitesi

8. Chalmers University of Technology: Chalmers tekniska hogskola

9. University of Gothenburg: Goteborgs Universitet

10. Royal Institute of Technology

Abstract

Abstract Background: Alzheimer’s disease (AD) is associated with metabolic abnormalities linked to critical elements of neurodegeneration. We recently administrated Combined Metabolic Activators (CMA) to the AD rat model and observed that administration of CMA activated the mitochondrial functions and eventually improved the AD-associated histological parameters in the animals. CMA consists of NAD+ and glutathione precursors and includes L-serine, nicotinamide riboside, N-acetyl-L-cysteine, and L-carnitine tartrate. Methods: Here, we designed a randomised, double-blinded, placebo-controlled phase-II trial and studied the effect of CMA administration on the global metabolism of AD patients. The primary endpoint was on the difference in cognitive 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. We also performed a comprehensive human plasma metabolome and proteome analysis. Results: Based on our analysis, we showed a significant decrease of ADAS-Cog scores on Day 84 vs Day 0 (p=0.00001, 29% improvement) in the CMA group. Moreover, there was a significant enhancement (p=0.0073) in ADAS-Cog scores between CMA and placebo groups in patients with higher ADAS-Cog scores. Improved cognitive functions were endorsed with relevant hippocampal volumes and cortical thickness alterations. Moreover, the plasma levels of proteins and metabolites associated with NAD+ and glutathione metabolism are significantly improved after treatment. Conclusion: In conclusion, our results show that treating AD patients with CMA leads to enhanced cognitive functions associated with the improved metabolome, proteome and structural neuroimaging parameters, suggesting a role for such a therapeutic regimen in treating patients, especially with severe AD.Trial registration: ClinicalTrials.gov NCT04044131 Registered 17 July 2019, https://clinicaltrials.gov/ct2/show/NCT04044131

Publisher

Research Square Platform LLC

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