Endocrinology & Metabolic

Male Hypogonadism

Male hypogonadism is testosterone deficiency with associated symptoms, classified as primary (testicular) or secondary (pituitary/hypothalamic), per the Endocrine Society Clinical Practice Guideline (2018).

Symptoms

Specific symptoms (reduced libido, erectile dysfunction, loss of body hair) carry more diagnostic weight than nonspecific ones (fatigue, low mood) -- the guideline is explicit that vague symptoms alone shouldn't prompt testing.

Causes and risk

Obesity is the leading reversible cause of secondary hypogonadism in men; aging, pituitary disorders, and primary testicular conditions (including prior chemotherapy or genetic conditions like Klinefelter syndrome) also cause it.

How it is evaluated

Fasting morning testosterone (7-10 AM), confirmed on a second sample, with LH/FSH to distinguish primary from secondary. Pituitary MRI is triggered by testosterone under 150 ng/dL, elevated prolactin, or headache/visual changes.

Treatment

Weight loss is first-line for obesity-related hypogonadism and often restores testosterone without medication. Testosterone therapy is reserved for confirmed, symptomatic, non-reversible deficiency, with hematocrit and testosterone monitored at 3-6 months then annually.

When to seek care

Headache with visual changes (possible pituitary mass), or signs of a blood clot while on testosterone therapy, need prompt evaluation.

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