Global photographic assessment of men aged 18 to 60 years with male pattern hair loss receiving finasteride 1 mg or placebo - 11/08/12
Male Pattern Hair Loss Study Group
Abstract |
Background |
Finasteride (1 mg) has been shown to increase vertex hair growth in men aged 18 to 60 years with male pattern hair loss and to increase frontal scalp hair growth in subjects aged 18 to 41 years.
Objective |
A secondary efficacy analysis was conducted to determine effects of finasteride (1 mg) on scalp hair growth in the 4 distinct scalp regions affected by male pattern hair loss.
Methods |
Multicenter, double-blind studies randomized patients with vertex hair loss (men aged 18-41 and 41-60 years) to finasteride (1 mg/d) or placebo. Efficacy was evaluated by review of standardized clinical photographs (global photographic assessment) of the vertex, anterior/mid scalp regions, and frontal and temporal hairlines over 24 months relative to baseline.
Results |
At 24 months, treatment with finasteride resulted in statistically significant (P ≤ .05) hair growth versus placebo in all scalp regions. There was also a significant decrease in hair loss in the younger men treated with finasteride in all areas, but only in the vertex and anterior/mid scalp regions in the older men. A slightly higher incidence of drug-related sexual adverse experiences was reported in the finasteride group than in the placebo group, irrespective of age.
Limitations |
These studies enrolled men with vertex pattern hair loss; therefore, the findings may not be extrapolated to men with predominantly anterior/mid scalp, frontal, or temporal hair loss.
Conclusion |
Based on global photographic assessment, finasteride (1 mg) is able to increase hair growth in all areas of the scalp affected by male pattern hair loss.
Le texte complet de cet article est disponible en PDF.Key words : androgenetic alopecia, dihydrotestosterone, finasteride, male pattern hair loss, 5⍺-reductase inhibitor
Plan
Funding for this study was provided by Merck. |
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Disclosure: All 3 dermatologist authors (E. A. O., D. A. W., and R. S.) were investigators and consultants in the past when these studies were first conducted. Dr Olsen is on the Merck CTCL Advisory Board. Dr Savin is an investigator for Merck. Mr Rodgers and Drs Johnson-Levonas, Round, Rotonda, and Kaufman are employees of Merck. Dr Whiting has no conflicts of interest to declare. |
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Reprints not available from the authors. |
Vol 67 - N° 3
P. 379-386 - septembre 2012 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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