Boost Your Testosterone Naturally | Myths Debunked & Real Advice from the Expert

29 Jun 2024 · 62 min
1:01:52

A recorded interview (June 29, 2024) where Dr. Anne Truong interviews Professor Trish (Boston University) about testosterone biology, diagnosis, clinical management and misconceptions. Key points: testosterone is a multi-system hormone (metabolic, vascular, mental and sexual), age-related decline begins ~age 40 (~1% per year) partly from ~40% loss of Leydig cells and reduced hypothalamic–pituitary signalling; free (unbound) testosterone is the biologically active fraction and is harder/expensive to measure (equilibrium dialysis or LC-MS); the commonly-cited 300 ng/dL cutoff is arbitrary (originated in an FDA advisory meeting in the 1980s); recent large randomized data (the TRAVERSE trial, ~5,000 men, up to ~4 years) reported no increase in prostate cancer or cardiovascular events with testosterone treatment; testosterone also has clinically important roles in women but is under-recognized and under‑approved. Practical advice emphasizes lifestyle (weight loss, exercise, sleep, stress reduction) and individualized titration of therapy to symptoms rather than a single lab cutoff.

Questions this video answers

Decline begins around age 40 and progresses at roughly 1% per year (as stated in the interview).

About 40% of Leydig cells are lost with age (guest's statement).

Described in the interview as about 5,000 men with follow-up up to ~4 years; the study found no increased prostate cancer or cardiovascular events with testosterone therapy (as reported).

The 300 ng/dL cutoff was described as originating informally during an FDA advisory meeting in the early 1980s (an advisor offered the number) rather than from a clinical trial.

Equilibrium dialysis and liquid chromatography–mass spectrometry (LC‑MS/MS) were named as accurate methods for measuring free testosterone; calculated free T using total T, SHBG and albumin was described as an acceptable approximation.

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