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Real-world User-reported Benefits of a Multi-ingredient NMN-based Supplement Targeting Age-related Decline: A Brief Report

Received: 15 June 2025     Accepted: 26 June 2025     Published: 15 July 2025
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Abstract

The age-related decline in nicotinamide adenine dinucleotide (NAD⁺) contributes to mitochondrial dysfunction and oxidative stress, which may be mitigated by supplementation with NAD⁺ precursors such as nicotinamide mononucleotide (NMN). This retrospective observational study evaluated user-reported outcomes of a multi-ingredient supplement (NMN, hydroxytyrosol, ergothioneine, resveratrol, and vitamin D₃) using 196 self-reported experiences collected from the Wonderfeel Biosciences online platform (April 2022–September 2024). Among 196 analyzed users, 131 (66.8%) reported positive effects, primarily in the nervous (81%), integumentary (11%), muscular (4%), skeletal (2%), digestive (2%), and endocrine (1%) systems, while 31.6% noted neutral effects and 1.5% reported non-causal adverse events. These findings align with known mechanisms of NAD⁺ restoration and oxidative stress mitigation, suggesting complementary biological pathways. Although this real-world evidence highlights perceived improvements in energy, cognition, sleep, and skin health, the study’s limitations—including self-reported data, lack of demographic controls, and absence of biomarkers—necessitate confirmation through the prospective controlled clinical trial scheduled to commence in late 2025.

Published in International Journal of Nutrition and Food Sciences (Volume 14, Issue 4)
DOI 10.11648/j.ijnfs.20251404.12
Page(s) 193-198
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2025. Published by Science Publishing Group

Keywords

Nicotinamide Mononucleotide, Hydroxytyrosol, Ergothioneine, Resveratrol, Vitamin D, Real-world Setting, Self-reported

References
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[2] Verdin, E. NAD⁺ in aging, metabolism, and neurodegeneration. Science (2015) 350(6265): 1208-13.
[3] Imai S, Guarente L. NAD⁺ and sirtuins in aging and disease. Trends Cell Biol (2014) 24(8): 464-71.
[4] Camacho-Pereira J, Tarragó MG, Chini CC, Nin V, Escande C, Warner GM, et al. CD38 dictates age-related NAD decline and mitochondrial dysfunction through an SIRT3-dependent mechanism. Cell Metab (2016); 23(6): 1127-39.
[5] Bai P, Canto C, Oudart H, Brunyánszki A, Cen Y, Thomas C, et al. PARP-1 inhibition increases mitochondrial metabolism through SIRT1 activation. Cell Metab (2011) 13(4): 461-8.
[6] Chini CCS, Hoga KA, Warner GM, Tarragó MG, Peclat TR, Tchkonia T, et al. The NADase CD38 is induced by factors secreted from senescent cells providing a potential link between senescence and age-related cellular NAD⁺ decline. Biochem Biophys Res Commun (2019) 513(2): 486-93.
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[9] Trammell SAJ, Schmidt MS, Weidemann BJ, Redpath P, Jaksch F, Dellinger RW, et al. Nicotinamide riboside is uniquely and orally bioavailable in mice and humans. Nat Commun (2016) 7: 12948.
[10] Yi L, Maier AB, Tao R, Zhigang L, Vaidya A, Pendse S, et al. The efficacy and safety of β-nicotinamide mononucleotide (NMN) supplementation in healthy middle-aged adults: a randomized, multicenter, double-blind, placebo-controlled, parallel-group, dose-dependent clinical trial. Geroscience (2023) 45(1): 29-43.
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[12] Vilaplana-Pérez C, Auñón D, García-Flores LA, Gil-Izquierdo A. Hydroxytyrosol and potential uses in cardiovascular diseases, cancer, and AIDS. Front Nutr (2014) 1: 18.
[13] Tian X, Thorne JL, Moore BJ. Ergothioneine: an underrecognized dietary micronutrient required for healthy ageing?. Br J Nutr (2023) 129(1): 104-14.
[14] Aranow C. Vitamin D and the immune system. J Investig Med (2011) 59(6): 881-6.
[15] Sakata S, Kunimatsu R, Tanimoto K. Protective effect of ergothioneine against oxidative stress-induced chondrocyte death. Antioxidants (Basel) (2024) 13(7): 800.
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[17] Coates PM, Bailey RL, Blumberg JB, El-Sohemy A, Floyd E, Goldenberg JZ, et al. The evolution of science and regulation of dietary supplements: past, present, and future. J Nutr (2024) 154: 2335-45.
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Cite This Article
  • APA Style

    Cifuentes, L. F., Salzman, A. (2025). Real-world User-reported Benefits of a Multi-ingredient NMN-based Supplement Targeting Age-related Decline: A Brief Report. International Journal of Nutrition and Food Sciences, 14(4), 193-198. https://doi.org/10.11648/j.ijnfs.20251404.12

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    ACS Style

    Cifuentes, L. F.; Salzman, A. Real-world User-reported Benefits of a Multi-ingredient NMN-based Supplement Targeting Age-related Decline: A Brief Report. Int. J. Nutr. Food Sci. 2025, 14(4), 193-198. doi: 10.11648/j.ijnfs.20251404.12

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    AMA Style

    Cifuentes LF, Salzman A. Real-world User-reported Benefits of a Multi-ingredient NMN-based Supplement Targeting Age-related Decline: A Brief Report. Int J Nutr Food Sci. 2025;14(4):193-198. doi: 10.11648/j.ijnfs.20251404.12

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  • @article{10.11648/j.ijnfs.20251404.12,
      author = {Luis Fernando Cifuentes and Andrew Salzman},
      title = {Real-world User-reported Benefits of a Multi-ingredient NMN-based Supplement Targeting Age-related Decline: A Brief Report
    },
      journal = {International Journal of Nutrition and Food Sciences},
      volume = {14},
      number = {4},
      pages = {193-198},
      doi = {10.11648/j.ijnfs.20251404.12},
      url = {https://doi.org/10.11648/j.ijnfs.20251404.12},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijnfs.20251404.12},
      abstract = {The age-related decline in nicotinamide adenine dinucleotide (NAD⁺) contributes to mitochondrial dysfunction and oxidative stress, which may be mitigated by supplementation with NAD⁺ precursors such as nicotinamide mononucleotide (NMN). This retrospective observational study evaluated user-reported outcomes of a multi-ingredient supplement (NMN, hydroxytyrosol, ergothioneine, resveratrol, and vitamin D₃) using 196 self-reported experiences collected from the Wonderfeel Biosciences online platform (April 2022–September 2024). Among 196 analyzed users, 131 (66.8%) reported positive effects, primarily in the nervous (81%), integumentary (11%), muscular (4%), skeletal (2%), digestive (2%), and endocrine (1%) systems, while 31.6% noted neutral effects and 1.5% reported non-causal adverse events. These findings align with known mechanisms of NAD⁺ restoration and oxidative stress mitigation, suggesting complementary biological pathways. Although this real-world evidence highlights perceived improvements in energy, cognition, sleep, and skin health, the study’s limitations—including self-reported data, lack of demographic controls, and absence of biomarkers—necessitate confirmation through the prospective controlled clinical trial scheduled to commence in late 2025.},
     year = {2025}
    }
    

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    AB  - The age-related decline in nicotinamide adenine dinucleotide (NAD⁺) contributes to mitochondrial dysfunction and oxidative stress, which may be mitigated by supplementation with NAD⁺ precursors such as nicotinamide mononucleotide (NMN). This retrospective observational study evaluated user-reported outcomes of a multi-ingredient supplement (NMN, hydroxytyrosol, ergothioneine, resveratrol, and vitamin D₃) using 196 self-reported experiences collected from the Wonderfeel Biosciences online platform (April 2022–September 2024). Among 196 analyzed users, 131 (66.8%) reported positive effects, primarily in the nervous (81%), integumentary (11%), muscular (4%), skeletal (2%), digestive (2%), and endocrine (1%) systems, while 31.6% noted neutral effects and 1.5% reported non-causal adverse events. These findings align with known mechanisms of NAD⁺ restoration and oxidative stress mitigation, suggesting complementary biological pathways. Although this real-world evidence highlights perceived improvements in energy, cognition, sleep, and skin health, the study’s limitations—including self-reported data, lack of demographic controls, and absence of biomarkers—necessitate confirmation through the prospective controlled clinical trial scheduled to commence in late 2025.
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