●Tissue Selectivity: 10:1 anabolic-to-androgenic ratio, surpassing testosterone's 1:1 profile.
●Oral Efficacy: No injections required, with stable plasma concentrations over 24 hours.
●Muscle Memory Preservation: Upregulates MyoD expression, enhancing rebound growth post-cycle.
Risks and Controversies
●HPTA Suppression: Doses ≥5 mg/day suppress LH/FSH by 50–70%, necessitating post-cycle therapy (PCT).
●Lipid Dysregulation: Reduces HDL by 20% and elevates LDL by 15% in 12-week cycles.
●AR Desensitization: Chronic use (>6 months) downregulates muscle AR expression by 30%, diminishing returns.
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