Leopoldo Duailibe Nogueira Santos MD
Department of Dermatology and Skin Science University of British Columbia, Vancouver, Canada
University of British Columbia, Vancouver, CanadaJerry Shapiro MD FRCPC
Department of Dermatology and Skin Science University of British Columbia,Vancouver, Canada The Ronald O. Perelman Department of Dermatology New York University Langone Medical Center, New York, NY
University of British Columbia,Vancouver, CanadaMinoxidil
The literature shows that minoxidil acts by shortening telogen
phase and increasing hair diameter especially in miniaturized
hairs. The mechanism of action is not established yet
but the hypothesis involves increasing level/activity of vascular
endothelial growth factor (VEGF). New insights into its
mechanism are the stimulation of production of PGE2 and
minoxidil influences on androgen receptor.1
Topical minoxidil 5% solution has been proved to work better
than minoxidil 2% in men.2 Minoxidil 5% foam once daily is as
effective as minoxidil 2% solution twice daily in women.3 Approximately
40% of male patients experience hair regrowth with
5% minoxidil and therapeutic response should be seen within
3-6 months. A new method to detect patient responsiveness to
the treatment has been suggested using sulfotransferase activity
in plucked hair.4
Minoxidil is a topical treatment that should be applied on
dry scalp twice daily. It is a lifelong treatment and hair shedding
can occur in the first 1-3 months. The most common
side effects are irritant dermatitis, contact dermatitis, and hypertrichosis
on the face. The latter side effect is not of much
consequence is adult males. Topical minoxidil is available in
solution as the 2% and 5% and as a 5% foam.
5-alpha-reductase Inhibitors (5ARI)
This group of medications inhibit the 5-alpha-reductase enzyme
type I, II, and/or III resulting in decreased conversion of
testosterone to dihydrotestosterone (DHT).
Finasteride mainly inhibits type II/III enzyme. The approved
dose to MPHL is 1mg daily. Two thirds of the patients are
expected to improve their condition and one third to stabilized
hair loss. Patients are asked to be on finasteride for one
year until deciding to discontinue if there is no improvement.
Improvement is not only due to hair regrowth but also to
changes in hair growth rate (length) and thickness.5
Dutasteride inhibits types I/II of 5-alfa-reductase enzyme.
It is three times more potent than finasteride. Dustasteride
0.5mg is prescribed off-label for MPHL. Olsen et al found that
2.5mg of dutasteride was superior to 0.5mg in promoting
hair growth. Also 2.5mg was more efficient in suppressing
scalp DHT compared to 0.5mg dutasteride and 5mg finasteride
(79% x 51% x 41%). As a result, 2.5mg dutasteride was
associated with higher prevalence of sexual complaints (decreased
libido).6 Jeung et al treated non-responders to 1mg
finasteride with 0.5mg dutasteride. Following 6 months of
dutasteride, 75% of the patients showed improvement on
global photographic assessment and phototrichogram. How-