Norheim · Nature aging 2024 · randomized, double-blind, placebo-controlled trial · n=40

Effect of nicotinamide riboside on airway inflammation in COPD: a randomized, placebo-controlled trial.

Cited 38 times in the scientific literature.

Level 2 - randomized trial

Individual randomized controlled trial

PubMed 39548320 · doi:10.1038/s43587-024-00758-1 · record verified 2026-08-29

What was done

A randomized, double-blind, placebo-controlled clinical trial evaluated oral supplementation with the NAD+ precursor nicotinamide riboside (NR) for 6 weeks, followed by a 12-week post-treatment follow-up, in 40 patients with stable chronic obstructive pulmonary disease (COPD). The primary outcome was the change in sputum interleukin-8 (IL-8) from baseline to week 6. Secondary outcomes included whole-blood NAD+ levels and plasma IL-6, along with exploratory analyses of airway genomic integrity pathways and epigenetic aging.

What was found

The estimated treatment difference between NR and placebo in sputum IL-8 after 6 weeks was -52.6% (95% CI: -75.7% to -7.6%; P = 0.030). This reduction persisted 12 weeks after the end of treatment (-63.7%; 95% CI: -85.7% to -7.8%; P = 0.034). NR treatment increased whole-blood NAD+ levels by more than twofold, while plasma IL-6 levels were unchanged. Exploratory analyses indicated upregulation of gene pathways related to genomic integrity in the airways and reduced epigenetic aging.

Why it matters

This trial provides preliminary evidence that replenishing NAD+ via nicotinamide riboside can reduce airway inflammation in stable COPD. It highlights a potential metabolic approach to targeting age-related mechanisms in chronic lung disease.

Limits

The sample size is small (n = 40), leading to wide confidence intervals around the primary estimate. The abstract does not report functional or clinical outcomes such as spirometry (FEV1), exacerbations, quality of life, or safety and tolerability data. The specific dosage of nicotinamide riboside is not stated in the abstract.

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