Medical Glossary

Finasteride

hair-loss

Quick Definition

Finasteride is a Type II 5-alpha-reductase inhibitor FDA-approved for male pattern hair loss (1 mg, Propecia) and benign prostatic hyperplasia (5 mg, Proscar). It works by reducing dihydrotestosterone (DHT), the androgen most directly responsible for follicular miniaturization in male pattern baldness.

In Depth

Finasteride was FDA-approved in 1992 for benign prostatic hyperplasia (BPH) and in 1997 for male pattern hair loss. It is the most-studied oral medication for androgenetic alopecia, with over 25 years of clinical follow-up data.

The 5-alpha-reductase enzyme converts testosterone to dihydrotestosterone (DHT). Finasteride selectively inhibits Type II 5-alpha-reductase, reducing serum DHT by approximately 70% and scalp DHT by a similar margin. DHT is the dominant androgen at the hair follicle in male pattern baldness; reducing DHT slows or reverses the miniaturization process.

The 5-year extension of the original Phase III trials reported that 90% of finasteride-treated men either improved or stabilized their hair count, vs 25% of placebo-treated men. Best responders are typically younger men with less advanced miniaturization.

Continued daily dosing is required to maintain results. Discontinuation generally produces reversion to the pre-treatment trajectory within 6-12 months.

The side effect profile that gets most online attention is sexual side effects (decreased libido, erectile dysfunction, ejaculation disorders) and the contested phenomenon of persistent post-finasteride syndrome (PFS). The original trials reported sexual side effects at low single-digit incidence with resolution on discontinuation in most cases. Post-marketing reports describe a smaller subset of patients with persistent symptoms after discontinuation; causation remains contested.

Topical finasteride is also available, primarily through compounding, and produces lower systemic DHT suppression while maintaining scalp DHT reduction.

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