The most credible benefit is slowing bone loss in women past menopause, backed by one solid two-year study. Sexual-function and libido claims are biologically plausible but rest mainly on laboratory and animal work. Broader longevity effects remain speculative and limited by poor absorption. Liver-injury cases and heavy product contamination make sourcing the main concern. (Full Review)
| Marker | Target | Why |
|---|---|---|
| ALT / AST (liver enzymes) | ALT and AST roughly 10–26 U/L | Detect early liver injury given the hepatotoxicity signal |
| Bilirubin | <1.0 mg/dL | Flags significant liver dysfunction |
| Blood pressure | ~110–125 / 70–80 mmHg | Capture the vessel-relaxing and adulterant-driven blood-pressure effects |
| Bone mineral density (DXA T-score) | T-score above -1.0 | Track the primary bone benefit for at-risk users |
| Bone-turnover markers (e.g., CTX, P1NP) | Mid-to-low premenopausal reference for resorption markers | Show whether bone resorption is being reduced |
| Estradiol | Age-appropriate range | Monitor the phytoestrogen activity in hormone-sensitive individuals |
Cadence: Baseline, at roughly 4–8 weeks, then every 6–12 months for longer-term use; bone density reassessed no more than annually