A real condition with a commercial problem. The gap between the diagnosis and the advertising is where the harm sits.
Male hypogonadism is a genuine clinical condition: the testes fail to produce adequate testosterone, sperm, or both. It has identifiable causes, agreed diagnostic criteria, and treatment that helps the men who have it.
It has also become the commercial engine of an entire clinic sector, and the gap between the diagnosis and the marketing is where the harm sits.
Professional guidelines — the Endocrine Society's among them — are consistent, and the requirements are stricter than most advertising implies. All of the following:
A single afternoon blood test followed by a prescription meets none of this.
Primary hypogonadism is a testicular problem — low testosterone with high LH and FSH, because the pituitary is shouting and nothing is answering.
Secondary is a pituitary or hypothalamic problem — low testosterone with low or inappropriately normal LH and FSH.
That second pattern matters because it can indicate something that needs finding: a pituitary tumour, haemochromatosis, significant illness. Treating the testosterone without asking why it is low can mean treating a symptom of something else entirely. Measuring LH and FSH costs little and is how that is avoided.
This is the heart of it. In men seen by metabolic clinics, low testosterone is frequently a consequence rather than a cause:
Each of these is treatable, and treating it may raise testosterone without any hormone being prescribed. A work‑up that does not look for them will find low testosterone and stop there — which is convenient for a clinic that sells testosterone.
Four recurring moves, all identifiable from the outside:
Treatment raises haematocrit, which is why a baseline full blood count is required and why it is monitored. It affects the prostate, which is why PSA is checked in older men.
On cardiovascular risk, the picture improved with the TRAVERSE trial, which did not find an excess of major cardiac events in men with hypogonadism and cardiovascular risk. It did report more cases of atrial fibrillation and pulmonary embolism. "Reassuring but not without signals" is the fair summary, and a clinic claiming it is proven safe is overstating a real result.
Men who genuinely have this condition benefit from treatment, and under‑diagnosis is a real problem too. The argument here is only for the work‑up: two morning samples, the full panel around them, reversible causes excluded, and a conversation about fertility — before anything is prescribed.
Every patient starts the same way: thirty minutes with a physician, then a full biomarker panel drawn at a laboratory near you. Whether any medicine follows is your doctor’s decision, made after reading your results with you.
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