TLDR Dutasteride is more efficient than finasteride, but individual results vary.
This study analyzed the pharmacogenetics of finasteride and dutasteride, two drugs used to treat prostatic diseases. The study found that both drugs are slow, time-dependent inhibitors of steroid 5α-reductase type II, with dutasteride being a more efficient inhibitor than finasteride for most enzyme variants. However, there is significant pharmacogenetic variation for both drugs, which should be taken into account when designing treatment protocols. The study suggests that pharmacogenetic analysis could be used to determine which drug would be most effective for individual patients.
408 citations,
May 2004 in “The Journal of clinical endocrinology and metabolism/Journal of clinical endocrinology & metabolism” Dutasteride more effectively lowers DHT levels in men with enlarged prostates than finasteride.
42 citations,
February 1998 in “The Journal of Steroid Biochemistry and Molecular Biology” PNU 157706 is a more effective treatment than finasteride for conditions caused by DHT, like enlarged prostate and hair loss.
24 citations,
January 1996 in “The Prostate” Finasteride is a safe and effective long-term treatment for prostate enlargement, reducing prostate volume and related symptoms.
70 citations,
June 1993 in “Biochemistry” Finasteride slowly binds to 5-alpha-reductase, affecting enzyme stability and inhibitor potency.
3 citations,
October 1995 in “International Journal of Dermatology” Finasteride helps treat skin issues like acne and baldness by blocking testosterone conversion.
30 citations,
August 1992 in “The Journal of Clinical Endocrinology and Metabolism” Finasteride doesn't affect hormone levels in normal men.
211 citations,
November 1990 in “The Journal of Steroid Biochemistry and Molecular Biology” Finasteride effectively treats BPH, but needs more trials to understand potential.