Piceatannol for Health & Longevity - Quick Reference Sheet

Piceatannol for Health & Longevity

Created on 06/26/2026 – Quick Reference based on Evidence Review created using AI4L / Opus 4.8 Audit

Piceatannol is a resveratrol-related plant compound from passion-fruit seeds, sold as a niche supplement. Human evidence is thin: short studies hint at better insulin response in overweight men and modest skin benefits, while broader claims rest on cell and animal work. It clears the body fast, seems well tolerated short-term, but stays early-stage. (Full Review)

Protocol

Standard Dose
20 mg/day
Only human-tested oral dose, as passion-fruit-seed extract, taken for 8 weeks
Dosing Pattern
Once daily
Once-daily is the only evidence-based pattern despite rapid clearance
Best Time of Day
With a meal
Reasonable to align with post-meal metabolic handling; no timing study exists
Time to effect
Metabolic Markers
8 weeks
Insulin and blood-pressure changes were measured at this point in the trial
SIRT1 Expression
2 weeks
Raised SIRT1 gene activity in blood after two weeks of dosing
Skin Outcomes
Over weeks
Skin hydration and wrinkle outcomes accrued gradually over weeks

Benefits

Contraindications
  • Pregnancy or breastfeeding
  • Bleeding disorders or surgery within ~2 weeks
  • Anticoagulant use without supervision
  • Hormone-sensitive cancers
Key Interactions
  • Anticoagulant and antiplatelet drugs (warfarin, apixaban, rivaroxaban, aspirin, clopidogrel)
  • Over-the-counter NSAIDs (ibuprofen, naproxen, high-dose aspirin)
  • Blood-thinning supplements (fish oil, high-dose vitamin E, ginkgo, garlic, curcumin)
  • Additive antioxidant/sirtuin supplements (resveratrol, pterostilbene, quercetin)
  • COMT-dependent drugs and substrates (entacapone, catecholamine-based medications)

Risk & Side Effects

  • High:
  • Medium:
  • Low: Generally mild tolerability with limited safety data
  • Speculative: Bleeding / antiplatelet risk; estrogenic / hormonal activity; drug-metabolism interactions; pregnancy and lactation uncertainty

Monitoring

Marker Target Why
Fasting insulin 2–5 µIU/mL Most direct marker of the trial's primary benefit
Fasting glucose 75–90 mg/dL Tracks glucose control alongside insulin
HbA1c < 5.4% Longer-term (3-month) glucose average
Blood pressure < 120/80 mmHg Trial showed reductions in overweight men
Resting heart rate 50–70 bpm Reduced in the trial subgroup
hs-CRP < 1.0 mg/L Gauges any anti-inflammatory effect
Lipid panel (LDL, HDL, triglycerides) LDL < 100 mg/dL; triglycerides < 100 mg/dL Cardiovascular mechanism is proposed

Cadence: Baseline, then around 8–12 weeks, and thereafter every 6–12 months if use continues

Qualitative Assessment

  • Energy levels and exercise tolerance
  • Skin hydration and appearance
  • Body composition and waist measurement
  • General well-being and any signs of easy bruising or bleeding