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Efficacy of imiquimod in the treatment of alopecia areata
*Chantal Bolduc, **Harvey Lui , **David McLean,
**Jerry Shapiro *University of Montreal, Montreal, Québec,
**University of British Columbia, Vancouver, British Columbia
Alopecia areata (AA) is a relatively common,
non-scarring type of hair loss. The pathophysiology of alopecia
areata is still unclear, but an autoimmune mechanism is the
most widely accepted theory. Based on current available data,
AA appears to exhibit a TH1 cytokine profile. IL-1 has been
found to be associated with alopecia areata, and is a potent
inhibitor of hair growth in vitro. Furthermore IL-1 appears
to induce histologic changes similar to those seen in alopecia
areata. Imiquimod (Aldara) is a topical immune response modifier
that stimulates the secretion of different cytokines, most
of which are associated with a TH1 response. Although AA is
potentially associated with IL-1 and a TH1 cytokine profile,
imiquimod, which most likely enhances TH1 response, has been
used anecdotally for alopecia areata with some success. The
aim of this pilot study was to assess the potential efficacy
of imiquimod in the treatment of alopecia areata. The study
had a prospective, open-label, left-right half-head controlled
design. Only half the scalp was treated 3 times a week for
4 months, while the other side was left untreated. Hair loss
was graded semiquantitatively and photographs were taken at
baseline and serially every 4 weeks throughout the study.
The treatment was very well tolerated. Six patients with extensive
AA (40-99%) were included in the study. One patient experienced
bilateral regrowth. One patient worsened on both treated and
non treated sides. His condition was active when he entered
the study and his course was most likely unrelated to imiquimod.
The other four patients did not grow hair and kept a similar
score from baseline to the end. In conclusion, this pilot
study shows that imiquimod applied 3 times/week is unlikely
to have efficacy in severe AA.
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