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Short Communication
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Efficacy of Vitamin E to Prevent Dermal Complications of Isotretinoin |
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Farideh Goforoushan,
Hamideh Azimi
and
Mohamad Goldust
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ABSTRACT
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Acne treatment depends on whether patents have a mild, moderate, or severe type of acne. The aim of this study was to compare the using of Isotretinoin (Rokutan) with and without oral vitamin E in treating acne. This study was performed on 60 patients on 0.5 mg/kg/day isotretinoin treatment for 6 months. The first group received 800 IU day-1 Vit E during treatment and the second group recieved 800 Iu day-1 cod liver oil capsules. All patients were observed for the complications at 1th, 4th and 6th weeks during treatment. Cheilitis was the most common side effect among these patients (69%). Epistaxis was the second side effect in both groups (22%). Other side effects were xerosis, pruritus, epigastric pain and nail fragility. The frequency and the severity of complications were less common at 4th and 6th weeks of treatment. Isotretinoin is a useful and effective drug in treating severe and treatment-resistance acne lesions.
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Received: December 08, 2012;
Accepted: February 16, 2013;
Published: March 27, 2013
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INTRODUCTION
Acne is a common skin disease of pilosebaceous unit affecting both genders
during maturity and its activity often decreases through termination of this
period. However, its severity and duration vary in different individuals (Vender
and Vender, 2012). Lesions are more prevalent and severe in skin areas with
more sebaceous glands (Gan et al., 2012). Drugs
effective in treating acne include vitamin A, benzoyl peroxide and antibiotics
(Landis et al., 2012). Isotretinoin is an oral
vitamin A-based retinoid resulting in long-term recovery period. The drug affects
all factors playing a role in acne creating but it has more side effects including
teratogenic quality of the drug (Mehra et al., 2012).
The drug has indication in severe nodulocystic and phlogistic acne, moderate
acne which does not respond to common treatments, patients suffering from acne
scar, more sebum skin, negative gram folliculate, fulminate acne, pyoderma faciale
and finally patients fearing deformity (Bergler-Czop and
Brzezinska-Wcislo, 2012). The side effects are drug-dependent and they can
be controlled by decreasing the drug dosage (Alonso-de-Celada
et al., 2012). The present study aims at comparative evaluation of
Isotretinoin with and without oral vitamin E in treating acne.
MATERIALS AND METHODS Sixty patients suffering from acne were selected during May 2011 to May 2012 according to the following criteria: patients with more than moderate severity of face acne, patients with slight acne suffering from scar and pigmentation after inflammatory, patients with acne resisting against common treatments. The understudy patients were divided into two groups using simple and alternate random method. Group I was treated with 0.5 mg/kg/day of Rokutan and 800 unit of oral vitamin E. The group II (control group) was treated with 0.5 mg/kg/day of Rokutan and cod liver oil capsules which is free from vitamin E. After starting the treatment and during 1st, 4th and 6th weeks of the plan, the patients were visited by dermatologist considering dermal-mucous complications. At the end of the study, response-to-treatment evaluation was as very good (in case of decreasing more than 50% of size and number of lesions) and moderate (in case of decreasing less than 50% of size and number of lesions). The obtained data was analyzed using SPSS-16 software, statistical tests of T-test, Man Whitney and Chi square. Fischer test was used, if required. The results were stated as frequency percentage and mean and p<0.05 values are regarded as meaningful. RESULTS
There were totally 60 patients divided into two case and control groups. The
case group was consisted of 30 cases (11 males and 19 females) and there were
30 cases (13 males and 17 females) in the control group. The mean age was 21.88±8.65
(test group = 22.57±9.12 and control group = 21.20±8.82). There
was no meaningful difference between these two groups considering mean age (p
= 0.497).
Table 1: |
Frequency distribution of acne severity and gender of patients
in two separate test and control groups |
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Value in parameter are expressed as percentage |
Considering acne severity, most patients suffered from mild or severe acne
(Table 1). The lesions were observed on face of 24 subjects
(9 males and 5 females), face and shoulders of 8 cases (3 males and 5 females)
and face, shoulder, back and chest of 28 patients. Chelate was the most common
dermal-mucous complication during 1st, 4th and 6th weeks after treatment in
both groups. At the end of the study, response to treatment with Rokutan was
very good and acceptable in 39 subjects (22 of the case and 17 of control groups)
and was moderate in 21 subjects (including 8 of the case and 13 of the control
group). Mean time of the symptoms outbreak was 4.05 and 3.33 years in patients
of the test and control groups, respectively. There is no significant difference
between two case and control groups considering gender (p = 0.93). During 1st
and 4th weeks of treatment, meaningful difference was not observed in the case
group in comparison with the control group considering prevalence of dermal-mucous
complications of Rokutan. At the 6th week of treatment, chelate prevalence in
the test group was meaningfully less than that of the control group (p = 0.037).
Dermal-mucous complications were more prevalent in both groups during the 1st
week of treatment in comparison with the 4th and 6th weeks.
DISCUSSION
Rokutan is a useful drug in treating severe and treatment-resistance acne (Erturan
et al., 2012). In about 65% of cases, treatment results with rokutan
were very good and acceptable. In their study conducted on effects of rokutan
in treating acne in Australia, Cooper et al. (2013)
introduced the drug as a healthy and useful product in treating moderate to
severe acne as well as treatment-resistance acne and suggested a significant
difference between results of treating with rokutan and other therapeutic methods.
Stein and Lebwohl (2001), from New York suggested that
consumption of 800 units of vitamin E (alpha tocopherol) per day may decrease
Isotretinoin complications in treating acne or acitretin in treating psoriasis.
According to the present study, in patients received vitamin E along with rokutan,
chelate prevalence in the test group during 6th week after treatment was less
that the control one. In other cases, there was no difference in results of
both groups. Vitamin E effects in decreasing severity of rokutan side effects.
There was no significant difference between two groups considering severity
of created side effects (Strauss et al., 2000).
In our study, there was no meaningful difference regarding prevalence of side
effects during 1st and 4th weeks after treatment. Dosage of the consumed rokutan
is one of reasons of unchanged prevalence of the created side effects. It was
the same in both groups. Rokutan is a useful and effective drug in treating
severe and treatment-resistance acne lesions. It is also effective in treating
moderate to severe as well as slight acne associated with scar. Cheilitis is
the most prevalent side effect of rokutan. During 6th week of treatment, its
prevalence significantly decreases via concurrent consumption of vitamin E.
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