Document Type
Article
Publication Date
7-1-2026
Abstract
INTRODUCTION: Declining nicotinamide adenine dinucleotide (NAD+) may elevate risk of Alzheimer's disease.
METHODS: We conducted a 12-week double-blind, randomized, placebo-controlled pilot study to evaluate the safety, tolerability, and preliminary efficacy of the NAD+ precursor, nicotinamide riboside (NR), for enhancing cognitive function and cerebral blood flow (CBF) in adults with amnestic mild cognitive impairment (aMCI).
RESULTS: 42 participants completed the study (NR = 22, placebo = 20). Adherence was similar between groups with no serious adverse effects. Blood NAD+ increased twofold in the NR group. There were no improvements in cognitive function (primary outcome), total CBF, or blood pressure (secondary outcomes). Exploratory analyses revealed potential increases in regional CBF, particularly in the hippocampus.
DISCUSSION: NR effectively raises NAD+ in people with MCI but does not improve cognitive function, total CBF, or blood pressure over 12 weeks. Future studies should investigate regional effects on CBF over longer treatment durations.
Recommended Citation
Martens, Christopher; Decker, Kevin; DeConne, Theodore; Sanjana, Faria; Horvat, Fiona; Rizzi, Nicholas; Awad, Catherine; Habash, Elizabeth; Hobson, Joshua; Kramer, Mary; Armstrong, Michael; Reisdorph, Nichole; Pohlig, Ryan; Lanzi, Alyssa; Johnson, Curtis; Cohen, Matthew; and Ellison, James, "A Phase-II Randomized Controlled Pilot Study of Nicotinamide Riboside Supplementation in Older Adults With Amnestic Mild Cognitive Impairment" (2026). Department of Psychiatry and Human Behavior Faculty Papers. Paper 93.
https://jdc.jefferson.edu/phbfp/93
Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 License.
Supporting Information. Table M1.docx (31 kB)
Supporting Information. Table S1-S6.docx (33 kB)
PubMed ID
42478598
Language
English

Comments
This article is the author’s final published version in Alzheimer's and Dementia, Volume 22, Issue 7, 2026, Article number e71605.
The published version is available at https://doi.org/10.1002/alz.71605. Copyright © 2026 The Author(s).