| Treatment of Alopecia Areata and Alopecia Totalis
With Viviscal® (Special Marine Extract Compound)
A. Lassus*, J. Santalahti*, M.
Sellmann**
*Helsinki Research Centre-Stora Roberts-Gatan 8 A
1, SF-00120 Helsinki, Finland
**Dermatological Clinic - Freidrich-Ebert -Platz
17, 51373 Leverkusen, Germany
SUMMARY
Twenty patients with
alopecia areata (mean duration 9 years) and 20 patients with alopecia
totalis (mean duration of 7 years) were treated with 2 pills of Viviscal®
Liniment once daily and Viviscal® shampoo 2-3 times/week for eight
months. Viviscal® is a preparation containing mainly compound of marine
extract and colloidal silicic acid. Both group included 10 females and
10 males. All patients had earlier received topical steroids and 15 had
had been treated with systemical corricosteroids. Most of them had also
been treated with topical minoxidil and photochemotherapy. Seventeen of
the patients with alopecia areata (85%) were completely cured and two
showed significant improvement. One of the patients in this group
deteriorated during the treatment period. Five (25%) of the patients
with alopecia totalis were completely cured and four (20%) showed
significant improvement, while 11 patients developed only minimal vellus
hair. This promising study showed that Viviscal® is a further complement
to the rather short list of remedies which alter the clinical course of
alopecia areata and alopecia totalis.
INTRODUCTION
The treatment of alopecia
areata and alopecia totalis is usually disappointing and treatment
results are difficult to interpret because of spontaneous remissions and
recurrences. Topical, intra-lesional or systemical corticosteroid
therapy is usually tried, but the benefit is questionable. Systematical
corticosteroid treatment may be effective in some cases, but the
maintenance doses needed are often too high. In 1977 promising results
with the use of topical dinitrochlorbence were reported(1).
Later reports that topically used squaric acid may induce regrowth of
hair in even severe cases of alopecia areata have been published(2).
These treatments have, however, probed to be too topically irritant for
practical use. Ultraviolet light has been recommended, but its benefit
has not been confirmed. However, it has been reported to stimulate
regrowth in some cases(3). In 1974, Rollier and Warcewski(4)
first reported that methoxsalen (8-MOP) in combination with natural
sunlight may induce hair growth. In 1978, Weissmann et al. (5)
reported that the use of topical 8-MOP and UVA-light induced good
regrowth in patients with alopecia areata. Similar results were reported
by Lassus et al in 1980 and 1984(6,7).
In 1992 Lassus et al.(8)
reported excellent regrowth of hair in young males with hereditary
androgenic alopecia by using Viviscal® an oral food supplement of mainly
marine origin. The present study which was initiated in October 1992 is
a therapeutical evaluation of the effect of oral and topical Viviscal® ;
for treatment of alopecia areata and alopecia totalis.
PATIENTS AND METHODS
Twenty patients with alopecia
areata and 20 patients with alpecia totalis were treated. All had had
alopecia for at least two years. In both groups, 10 males and 10 females
were treated (Table 1). The mean age of the patients as well as mean
weight, length, mean duration of alopecia, site of baldness, earlier
treatments and concomitant diseases are illustrated in Table 1.
Before treatment and at each
re-examination the cumulative surface-area of the bald areas was
measured and the size was expressed in square centimetres. The scalp
area showing regrowth of permanent hair was measured and regrowth was
expressed as a percentage of the total bald area. All patients took two
pills of Viviscal® daily for an eight-month period and applied every
evening topically a 1.0% liniment containing the same active ingredients
as that of the pills. All patients except those with no hair at any time
used a 1.0% shampoo with the same active ingredients as in the Viviscal®
pills, 2-3 times weekly.
Pre-examinations were carried out
bi-monthly, which involved measuring the regrowth of permanent hair, the
degree of hair loss and a photography of the involved areas. In
addition, the thickness of epidermis and dermis was measured by the use
of a Dermascan-C(9) equipment, an elasticity index was
measured with the use of a Dermaflex-A(10) equipment, Cortex
Ltd., Denmark and an erythemal index with an erythemal meter(11),
Diastron Ltd., UK. All measurements were carried out from the same bald
site of the scalp.
Statistical methods were applied to
continuous as well as categorical data collected during the study.
Categorical data variables were analysed with a standard X-test for
homogenity and Fischer's exact test was also used. Results were
generated statistically significant if the corresponding P-value was
<0.05, but lower than or equal to 0.10.
RESULTS
All patients were treated for
eight months and showed excellent compliance. In the alopecia areata
group the mean bald areas were 118 cm2 at baseline. At the
end of the trial 17 patients showed complete regrowth, two had a
regrowth > 50% as compared with baseline and one patient showed
deterioration (the bald areas had increased size from 63 cm2
to 113 cm2). That was a 43-year-old female who responded well
in the beginning of the study, but started to loose hair again after
four months of treatment. In the whole group the mean area of baldness
was 9.5 cm2 after treatment. The difference as compared with
the area of baldness at baseline reached high statistical significant (P
<0.001).
In the alopecia totalis group, five
patients showed complete regrowth, one patient a regrowth > 50% and
three patients a moderate regrowth of permanent hair (30-50%). The
remaining 11 patients only minor increase of vellus hair.
All patients in the alpecia areata
group had increased hair loss at baseline which had completely stopped
after two months of treatment. Nineteen of the 20 patients showed no
abnormal hair loss at the end of the treatment.
As shown in Table 3, epidermis had
significantly become thicker in both groups during the treatment while
the thickness of dermis had remained approximately unchanged. The
elasticity index and the erythemal index had significantly increased in
both groups.
The only adverse reaction observed
during the treatment period was a mild drying of the skin surface of the
scalp with concomitant mild scaling. However, this did not require
treatment or cause withdrawal from the study.
DISCUSSION
The idea of carrying out the
present study came from earlier observations that Viviscal® stimulates
hair growth in males with hereditary androgenic alopecia(8). In order to
evaluate the effect of Viviscal® in the treatment of alopecia areata,
only severe cases without signs of spontaneous regrowth were included in
the study. Considering the severe nature of the treated cases, the
results were definitely impressive and support earlier results(8)
that Viviscal® seems to be highly effective for inducing hair growth. In
particular the results in the alopecia totalis group were promising and
a longer period of treatment could have further improved results. In
contrast to the effect of corticosteroids, Viviscal® and
photochemotherapy, seem to be effective in atopic subjects with alopecia
areata or alopecia totalis.
The mechanism by which Viviscal®
induces regrowth of permanent hair is still not clear. An
immunosuppressive effect in combination with increased nutrition may be
of importance. However, the mode of action of photochemotherapy is
neither clear.
The present findings definitely
suggest that Viviscal® may be a new alternative for treatment of
alopecia areata and alopecia totalis.
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