Title: Androgenic Alopecia Malepattern baldness Common baldness
1Androgenic Alopecia (Male-pattern baldness
Common baldness)
- Commonest type of hair loss. May be a
physiological process. - Prevalence rate is almost 100 in certain races.
- Mode of inheritance unknown.
2Pathophysiology
- Normally
- On the top Androgen-sensitive follicles
- On the sides and back of the scalp
androgen-independent follicles - In genetically predisposed individuals(Under
Influence of Androgens) - Terminal hair follicles are transformed into
vellus. - Shortened anagen and an increased telogen.
- Decreased growth of hair on the scalp as well as
axilla
3Role of DHT
- T converted to DHT with the help of 5
?-reductase. - Persons with an inherited deficiency of type II5
?-reductase castrated prepubertal boys or
eunuchs do not develop androgenic alopecia - Under the influence of DHT, the terminal follicle
is converted to a vellus follicle - High concentrations of DHT seen in the scalp of
patients with androgenic alopecia.
4Finasteride - Effects on semen production
- No effect since
- Testosterone is responsible for spermatogenesis
- Men with an inherited deficiency of 5 ?-reductase
still have normal sperm development.
5Pharmacokinetic properties of oral finasteride
after repeated administration of 1 mg/day or
after single dose of 5 mg.
Day 1 Day 17 Cmax (?g/L) 6.5 9.2 38.1 tmax
(h) 1.6 1.3 1.8 t½ (h) 4.5 4.8 4.7 AUC0-24 (?g/L/h
) 38.2 53.2 180.6
6Finasteride - 1mg
- Clinical Efficacy
- Evaluated in three phase III placebo-controlled
studies, each of 1 years duration - Additionally, the two studies in men with mild to
moderate vertex hair loss continued in a blinded
manner for a second year. - A total of 1879 male patients aged between18 and
41 years were enrolled in the trials. - A wide spectrum of patients (vertex and frontal
hair loss) were enrolled in the study.
7Finasteride 1 MgIn Frontal Male Pattern Hair
Loss
- Double-blind placebo-controlled trial (n 326).
- End points included hair counts in the frontal
scalp, patient self-assessment, investigator
assessment and evaluation of global photographs. - Finasteride 1 mg significantly increased scalp
hair counts in the frontal area (P - Cosmetic improvement was noted by patients,
investigators and global reviewers. - Aust J Dermatol 1997 38 (Suppl.2 ) 101-2
8Finasteride-1 Mg Tolerability
- Not significantly different from that of placebo
except for sexual functional disorders - Sexual adverse events were reported in (3.8)
finasteride compared with (2.1) placebo
recipients and comprised decreased libido(1.8
vs. 1.3), ejaculation disorders (1.2 vs. 0.7)
and erectile dysfunction (1.3 vs. 0.7) - Resolved in many patients who reported them but
remained on therapy. It also resolved in those
who stopped therapy. - Small reductions (from 0.7 to 0.5 ng/ml) in serum
prostate-specific antigen (PSA) may be seen.
Hence double the reported PSA before interpreting.
9Finasteride 1mg - Indications
- Treatment of men with male pattern hair loss and
to prevent further hair loss in these patients.
10Finasteride-1mg - Dosage Administration
- 1mg/day taken with or without food. Continue for
at least 3 months before assessing. Effects are
reversed within 12 months of stopping therapy - Dosage adjustment unnecessary in elderly or in
renal insufficiency. - Contraindicated in women.
11Patient 1
Baseline
Month 12
Month 24
J Am Acad Dermatol 1998 39578-89
12Hair count mean change from baseline ( SE) from
the combined US and international studies for men
who entered the extension studies.
J Am Acad Dermatol 1998 39578-89
13Investigator assessment mean rating score ( 1
SE) from the combined US and international
studies for men who entered the extension studies.
J Am Acad Dermatol 1998 39578-89
14Treatment-related sexual adverse events reported
with finasteride. Men with male pattern hair loss
were randomised to receive oral finasteride 1
mg/day (n945) or placebo (n934) for 1 year.
p 0.041 vs. placebo
Drugs 1999 57(1) 111-126
15Finasteride in frontal hair lossHair count mean
change from baseline ( 1 SE).
All patients 1 mg
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J Am Acad Dermatol 1999 40 930-7.