Nicotinamide riboside reliably raises the blood pool of a cellular energy coenzyme. Walking in peripheral artery disease and Parkinson movement symptoms are the main clinical hints, still limited. Blood pressure, metabolism, muscle mass, and thinking scores lack consistent human gains. Safety over weeks to a few months is generally favorable, with mild stomach symptoms. Extending healthy human life remains unproven. (Full Review)
| Marker | Target | Why |
|---|---|---|
| Whole-blood NAD+ | No established functional target; track change from personal baseline | Confirms target engagement |
| Homocysteine | <8 µmol/L | Methylation drain from nicotinamide clearance |
| hs-CRP | <1.0 mg/L | Systemic inflammation |
| AST / ALT | <30 U/L | Hepatic tolerance |
| Systolic / diastolic blood pressure | <120/80 mmHg | Vascular response |
| eGFR | >90 mL/min/1.73 m² when attainable; otherwise track slope | Renal handling of NAD catabolites |
| LDL cholesterol | Functional often <70–100 mg/dL depending on risk | Combination-product lipid signal |
Cadence: Baseline metabolic panel, blood counts, lipids, seated blood pressure, and whole-blood NAD+ (homocysteine and B-vitamin status at high dose); NAD+ at 4 weeks, then every 3–6 months with homocysteine, liver enzymes, and blood pressure