Chronic nicotinamide mononucleotide supplementation elevates blood nicotinamide adenine dinucleotide levels and alters muscle function in healthy older men
Masaki Igarashi et al. · npj Aging · 2022
Evidence type: Human randomized trialInterpretive weight: LimitedResearch area: NAD-related and physical-function measures
PopulationHealthy Japanese men aged 65 years or older
Sample42 randomized; a test-food allocation error after week 6 materially reduced the interpretable 12-week efficacy sample
InterventionNMN 250 mg/day versus placebo for up to 12 weeks
EndpointsWhole-blood NAD+ and NAD-related metabolites; Gait speed; Grip strength; Body composition; Safety and tolerability
What the publication reported
This placebo-controlled trial examined 250 mg/day NMN in healthy older men. NMN increased whole-blood NAD+ and related metabolites and was reported as well tolerated.
The publication reported nominal improvements in gait speed and left-hand grip performance, while body-composition outcomes did not significantly improve. The authors themselves noted that the muscle-function findings require validation in larger studies.
Interpretation is complicated by a test-food allocation error after six weeks that caused participants to receive the opposite intervention during part of the study, reducing the cleanly interpretable 12-week efficacy sample.
Key findings
Whole-blood NAD+ and multiple NAD-related metabolites increased with NMN supplementation.
No significant deleterious safety effect was reported.
Gait speed and left-grip performance showed nominally significant improvements that the authors described as needing validation.
Body composition did not significantly change.
A test-food allocation error materially limits interpretation of longer-duration efficacy comparisons.
What it cannot establish
The study enrolled only older men, limiting generalizability by sex and age.
A test-food allocation error after week 6 compromised the intended 12-week treatment assignment.
The muscle-function findings were nominal and require replication in larger trials.
Body-composition outcomes were null.
The study was funded by the NMN supplier, and three authors were company employees.
HealthspanX claim boundary: This record supports NAD pharmacodynamic evidence in older men and exploratory physical-function findings. It does not establish general anti-aging, sarcopenia-treatment, longevity, or product-equivalence claims.