MitoQ is a redesigned antioxidant that collects inside the cell's energy-producing compartments. Human trials repeatedly show better artery widening, but mainly where vessel function is already impaired, fading to nothing in regular exercisers. Endurance, physical function and neurological outcomes showed no gain. Lifespan claims rest on animals. Side effects are mild; years of continuous use are untested. (Full Review)
| Marker | Target | Why |
|---|---|---|
| Flow-mediated dilation | Above 7% | The primary documented endpoint |
| Carotid-femoral pulse wave velocity | Below 7.6 m/s | Large-artery stiffness |
| Blood pressure (home, seated) | Below 120/80 mmHg | Cheap proxy for vascular effect |
| Oxidised low-density lipoprotein | No established target; track the change from the individual's own baseline, aiming for a fall | The marker that moved in the vascular trial |
| High-sensitivity C-reactive protein | Below 1.0 mg/L | Systemic inflammation context |
| Alanine aminotransferase | 10–26 U/L in men, 7–20 U/L in women | Liver injury, the one enzyme MitoQ moved |
| Estimated glomerular filtration rate with urine albumin-to-creatinine ratio | Above 90 mL/min/1.73 m² and below 10 mg/g | Safety floor for the unresolved kidney signal |
Cadence: Home blood pressure weekly for the first month, then monthly. Blood panel and kidney measures at three months, then every six to twelve months while use continues. Vascular imaging, where done at baseline, repeated at three months.