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Safety and Tolerability of Nicotinamide Riboside in Heart Failure With Reduced Ejection Fraction

Wang DD, Airhart SE, Zhou B, Shireman LM, Jiang S, Melendez Rodriguez C, Kirkpatrick JN, Shen DD, Tian R, O'Brien KD
JACC. Basic to translational science 2022 7; 12; 1183-1196

Bibliography

PubMed
PMID 36644285
PubMed Central
PMC9831861
Funding
NIH/NHLBI, American Heart Association and John L. Locke Jr. Foundation support. ChromaDex supplied NR and placebo without funding the trial.
Competing interests
One author reported Cytokinetics advisory-board membership; the paper separately disclosed industry product supply.

Study snapshot

DesignRandomized placebo-controlled human trial
ModelHuman participants
Sample30 adults with stable reduced-ejection-fraction heart failure
InterventionNR titrated to 1000 mg twice daily versus placebo
Duration12-week clinical trial
EndpointsSafety; blood NAD+; PBMC respiration

What the study showed, in plain terms

NR was generally tolerated and approximately doubled whole-blood NAD+. NAD+ changes correlated with selected immune-cell respiration and inflammatory measures.

Key findings

NR was generally tolerated and approximately doubled whole-blood NAD+. NAD+ changes correlated with selected immune-cell respiration and inflammatory measures.

What this study can and cannot tell us

A small safety-focused trial; correlations in blood cells do not establish improved cardiac function, fewer admissions or survival.

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