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Clinical Evidence for Targeting NAD Therapeutically

Overview
Publisher MDPI
Specialty Chemistry
Date 2020 Sep 18
PMID 32942582
Citations 30
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Abstract

Nicotinamide adenine dinucleotide (NAD) pharmacology is a promising class of treatments for age-related conditions that are likely to have a favorable side effect profile for human use, given the widespread use of the NAD precursor vitamin B3 supplements. However, despite several decades of active investigation and numerous possible biochemical mechanisms of action suggested, only a small number of randomized and adequately powered clinical trials of NAD upregulation as a therapeutic strategy have taken place. We conducted a systematic review of the literature, following the PRISMA guidelines, in an attempt to determine whether or not the human clinical trials performed to date support the potential benefits of NAD supplementation in a range of skin, metabolic and age-related conditions. In addition, we sought medical indications that have yielded the most promising results in the limited studies to date. We conclude that promising, yet still speculative, results have been reported for the treatment of psoriasis and enhancement of skeletal muscle activity. However, further trials are required to determine the optimal method of raising NAD levels, identifying the target conditions, and comparisons to the present standard of care for these conditions. Lastly, pharmacological methods that increase NAD levels should also be directly compared to physiological means of raising NAD levels, such as exercise programs and dietary interventions that are tailored to older individuals, and which may be more effective.

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References
1.
Lopez-Otin C, Blasco M, Partridge L, Serrano M, Kroemer G . The hallmarks of aging. Cell. 2013; 153(6):1194-217. PMC: 3836174. DOI: 10.1016/j.cell.2013.05.039. View

2.
Omran H, Almaliki M . Influence of NAD+ as an ageing-related immunomodulator on COVID 19 infection: A hypothesis. J Infect Public Health. 2020; 13(9):1196-1201. PMC: 7275989. DOI: 10.1016/j.jiph.2020.06.004. View

3.
Rodriguez Cetina Biefer H, Vasudevan A, Elkhal A . Aspects of Tryptophan and Nicotinamide Adenine Dinucleotide in Immunity: A New Twist in an Old Tale. Int J Tryptophan Res. 2017; 10:1178646917713491. PMC: 5476425. DOI: 10.1177/1178646917713491. View

4.
Lamb D, Moore J, Mesquita P, Smith M, Vann C, Osburn S . Resistance training increases muscle NAD and NADH concentrations as well as NAMPT protein levels and global sirtuin activity in middle-aged, overweight, untrained individuals. Aging (Albany NY). 2020; 12(10):9447-9460. PMC: 7288928. DOI: 10.18632/aging.103218. View

5.
de la Rubia J, Drehmer E, Platero J, Benlloch M, Caplliure-Llopis J, Villaron-Casales C . Efficacy and tolerability of EH301 for amyotrophic lateral sclerosis: a randomized, double-blind, placebo-controlled human pilot study. Amyotroph Lateral Scler Frontotemporal Degener. 2019; 20(1-2):115-122. DOI: 10.1080/21678421.2018.1536152. View