A Summary of a Nicotinamide Mononucleotide Clinical Study by Okabe et al. (2022)
Reviewed by Tamberlyn Blinsink, ND, MPH | Research & Development
Overview
The following summary reviews a clinical study examining oral nicotinamide mononucleotide (NMN) supplementation in the context of blood NAD⁺ levels and safety in healthy adult volunteers. The study was conducted to address a gap in human evidence regarding the safety and efficacy of oral NMN administration, as prior investigations into NMN’s effects on aging-related outcomes had been primarily limited to animal models. The authors sought to evaluate both the safety profile of NMN over a 12-week supplementation period and the resulting changes in whole blood NAD⁺ and related metabolite levels.
Summary
Oral Administration of Nicotinamide Mononucleotide Is Safe and Efficiently Increases Blood Nicotinamide Adenine Dinucleotide Levels in Healthy Subjects
Published In: Frontiers in Nutrition
Study Design: Placebo-controlled, randomized, double-blind, parallel-group trial
Participants: 30 healthy Japanese adults (ages 22–64); 15 per group (11 female, 4 male each); comparable baseline characteristics across metabolic, hepatic, and renal parameters
Dose: 250 mg NMN per day (125 mg twice daily as tablets) for 12 weeks
Outcome Measures: Physiological measurements (body weight, BMI, blood pressure, pulse rate); hematological and biochemical laboratory tests (liver enzymes, renal function, lipid panel, glucose metabolism markers, complete blood count, urinalysis); whole blood NAD metabolome (NAD⁺, NMN, NR, NAM, NA, NAMN, NAR, NAAD, MNAM) measured by LC/MS; amino acid metabolome; body composition by bioelectrical impedance analysis; adverse event monitoring via participant diary
What Was Studied: Researchers investigated the safety and tolerability of daily oral NMN supplementation over 12 weeks in healthy volunteers, as well as its ability to elevate NAD⁺ levels in whole blood. The trial also characterized the time course of NAD⁺ changes and profiled related NAD metabolites to better understand the metabolic fate of orally administered NMN in humans. Additionally, correlations between individual baseline parameters and the magnitude of NAD⁺ increase were analyzed to explore potential predictors of NMN responsiveness. Body composition and amino acid metabolome were assessed as secondary exploratory endpoints.
About the Reviewer
Name & Title: Tamberlyn Blinsink, Scientific Researcher at Solaray
Credentials: Naturopathic Doctor, Master of Public Health
Bio: Tamberlyn Blinsink, ND, MPH, a licensed naturopath who earned her Doctorate of Naturopathic Medicine from Bastyr University and her Master of Public Health from Purdue University. In addition to her experience in private practice, Dr. Blinsink, ND, MPH is a researcher in the natural products industry. She believes in giving back and has served as a lecturer at continuing education conferences and as a board member at Naturopaths Without Borders and NC Association of Naturopathic Physicians.
Reference
Okabe K, Yaku K, Uchida Y, Fukamizu Y, Sato T, Sakurai T, Tobe K, Nakagawa T. Oral Administration of Nicotinamide Mononucleotide Is Safe and Efficiently Increases Blood Nicotinamide Adenine Dinucleotide Levels in Healthy Subjects. Frontiers in Nutrition. 2022;9:868640. https://pubmed.ncbi.nlm.nih.gov/35479740/