Nicotinamide Riboside

ID: nicotinamide_riboside

Aliases: NR, Niagen, nicotinamide riboside chloride

Type: compound

Route/form: oral supplement in most human trials; IV NR has limited emerging clinic data

Status: supplement

Evidence level: human RCT

Best data tier: human controlled/review

Support scope: human, review/regulatory

Source types: human_rct, human_trial, review

Linked sources: 4

Broad outcomes: Cardiovascular / lipids / blood pressure, Fat loss / metabolic health, Gut / immune / inflammation, Longevity / mitochondrial / redox, Muscle growth / performance / recovery

Reading note: These are curation notes anchored to linked sources, not a clinical recommendation or protocol.

Targets / mechanism

Optimization domains

Research basis

Limits, risks, and missing evidence

Risk flags

Linked papers, labels, and reviews

  1. Chronic nicotinamide riboside supplementation is well-tolerated and elevates NAD+ in healthy middle-aged and older adults
    human_rct / pubmed_nr_healthy_older_2018
    Randomized crossover human NR study; supports oral NAD+ metabolome elevation and tolerability, with exploratory cardiovascular/metabolic endpoints.
  2. A randomized placebo-controlled clinical trial of nicotinamide riboside in obese men: safety, insulin-sensitivity, and lipid-mobilizing effects
    human_rct / pubmed_nr_obese_men_2018
    Direct human NR trial in obese insulin-resistant men; useful negative/limited-effect context for insulin sensitivity and fat-loss claims.
  3. Nicotinamide Riboside Augments the Aged Human Skeletal Muscle NAD+ Metabolome and Induces Transcriptomic and Anti-inflammatory Signatures
    human_trial / pubmed_nr_aged_muscle_2019
    Aged human skeletal-muscle NR study; supports tissue NAD metabolome and transcriptomic signals, not a demonstrated hypertrophy or performance protocol.
  4. Therapeutic Potential of NAD-Boosting Molecules: The In Vivo Evidence
    review / pubmed_nad_boosting_molecules_review_2018
    Broad NAD-boosting review covering NR, NMN, CD38, PARP, sirtuins, aging, metabolic disease, and translational caveats.