5-Alpha reductase inhibitors in androgenetic alopecia: Shifting paradigms, current concepts, comparative efficacy, and safety

Dermatol Ther. 2020 May;33(3):e13379. doi: 10.1111/dth.13379. Epub 2020 Apr 24.

Abstract

Androgenetic alopecia (AGA) is a multifactorial disease that carries a significant psychological burden with it. Dihydrotestosterone, the main pathogenic androgen in AGA, is produced by conversion of testosterone, which is catalyzed by the 5-alpha reductase (5-AR) isoenzyme family. Finasteride and dutasteride are inhibitors of these enzymes. Finasteride, which is a single receptor 5-alpha reductase inhibitor (5-ARI), acts by blocking dihydrotestosterone (DHT). Dutasteride, a dual receptor DHT blocker, has a higher potency than its predecessor, finasteride. This review corroborates the evidence of superiority of dutasteride over finasteride, and its comparable safety profile concerning fertility, teratogenicity, neurotoxicity, and hepatotoxicity.

Keywords: 5-alpha reductase inhibitors; androgenetic alopecia; dutasteride; finasteride.

Publication types

  • Review

MeSH terms

  • 5-alpha Reductase Inhibitors* / adverse effects
  • Alopecia / drug therapy
  • Androgen Antagonists
  • Dutasteride / adverse effects
  • Finasteride* / adverse effects
  • Humans

Substances

  • 5-alpha Reductase Inhibitors
  • Androgen Antagonists
  • Finasteride
  • Dutasteride