An Open-Label Study of an Herbal Topical Medication (Psirelax) for Patients with Chronic Plaque Psoriasis
An Open-Label Study of an Herbal Topical Medication (Psirelax) for Patients with Chronic Plaque Psoriasis
Joseph Shiri, Assi A. Cicurel, Arnon D. Cohen
Clalit Health Services, Siaal Research Center for Family Medicine and Primary Care, Faculty of Health Sciences, Ben-Gurion University, Beer-Sheva, Israel
Most recently recommendation issued by Maccabi Health Services.
The study was funded by an unrestricted grant from Etwal Ltd.
Background: Psirelax is an herbal topical medication indicated for the treatment of patients with psoriasis.
Objectives: To determine the efficacy of Psirelax in patients with chronic plaque psoriasis.
Methods: In an open-label study, patients with chronic plaque psoriasis were treated by application of Psirelax twice a day for a period of 4 weeks. Clinical assessment was performed using the Psoriasis Area and Severity Index (PASI).
Results: The study included 22 patients (15 men, 7 women) with a mean age of 48.9±11.8 years. Psirelax was well tolerated and there no local or systemic side effects. There was 59% reduction in PASI, from a mean of 5.9 ± 4.0 before treatment to 2.4 ± 2.4 after treatment (p<0.001). In 8 patients (36%) PASI score decreased in more than 75% (PASI75). In 16 patients (73%) PASI score decreased in more than 50% (PASI50).
Conclusions: In patients with chronic plaque psoriasis, Psirelax psoriasis treatment was well tolerated. Application of Psirelax was associated with a decrease in disease severity, as assessed by the patients and physicians.
Psoriasis is a chronic disorder which occurs in 2% of the general population. Patients with psoriasis have decreased quality of life and comparative high rates of depression. Patients with mild to moderate psoriasis are usually treated with topical medications whereas systemic therapy is usually reserved to patients with moderate to severe disease.
In recent years the complementary and alternative medicine has been used by patients with psoriasis.In a study from Israel, Ben-Arye et al have been shown that many patients with psoriasis use herbal treatments (1).
Psirelax is herbal topical medication indicated for the treatment of patients with psoriasis. Psirelax includes natural ingredients: quince seeds jelly, base cream , anti-oxidants (e.g. palm tree oil, wheat germ oil), skin softening agents (e.g. sweet almond oil), absorption aids (e.g. jojoba oil), tissue regenerating and protecting agents (e.g. grape seed oil), preservatives (e.g. paraben) and thickening agents (e.g. bee wax).
Preliminary uncontrolled observations have shown a beneficial effect of Psirelax in some patients with psoriasis. The primary objective of this study was to determine the efficacy of Psirelax topical treatment in patients with chronic plaque psoriasis.
PATIENTS AND METHODS
This was an open-label study to evaluate the tolerability of Psirelax treatment. Approval for the study was obtained from an institutional review board, and written informed consent was obtained from each patient prior to enrollment into the study. The study was conducted in accordance with the ethical principles outlined in the Declaration of Helsinki and GCP guidelines.
The study included men and women between 18 and 75 years old with a clinical diagnosis of psoriasis. All patients were in good general health and were free of any disease or physical condition which might have impaired the evaluation of plaque psoriasis. Excluded from the study were women who were pregnant, lactating, planning to become pregnant or women of child-bearing potential who have not successfully been using the same medically acceptable contraceptive methods over the previous 3 months, patients who used topical anti psoriatic therapy on the areas to be treated within one week prior to the beginning of the study, patients who received systemic biologic therapy to treat psoriasis within 12 weeks prior to the beginning of the study, patients who received systemic psoriasis therapy within 4 weeks prior to the beginning of the study, patients who received phototherapy within 4 weeks prior to the beginning of the study, patients with a recent history (within past 12 months) of alcohol or substance abuse, patients with a history of noncompliance to medical regimens and patients who had serious or unstable medical or psychological conditions that in the opinion of the Investigator could compromise the subject’s safety or successful participation in the study.
Psirelax is herbal topical medication indicated for the treatment of patients with psoriasis. Psirelax includes the following ingredients: 5%-15% quince seeds jelly, 10%-40% natural base cream (e.g. Ferntree Cottage Pure Base Cream), 55%-75% mixture of natural anti-oxidants (e.g. Vitamin E, wheat germ oil, Safflower oil), natural skin softening agents (e.g. sweet almond oil, sesame oil), natural absorption aids (e.g. jojoba oil, vegetable squalene), natural tissue regenerating and protecting agents (e.g. grape seed oil, sunflower oil), natural preservatives (e.g. paraben, tea trea essential oil, thyme essential oil, grapefruit seed extract, Vitamin E) and natural thickening agents (e.g. bee wax, aloe vera, medicinal Vaseline, coconut oil, guar gum, palm tree oil, borax).
The study was designed as an open-label study and included efficacy and safety assessments at weeks 2 and 4 after enrollment in the study.
Clinical response was measured using psoriasis area and severity index (PASI). The PASI ranges from 0 to 72 and is based on an equation that combines the percentage of affected body surface area (BSA) with an assessment of the extent and severity (erythema, desquamation and induration) of the psoriatic lesions at four anatomic sites (head, upper extremities, trunk and lower extremities).
Additional objective of this study was an assessment of the tolerability of Psirelax which was achieved by assessing local and systemic side effects at each visit.
Sample Size Calculation
A calculation assuming a 40% response rate in patients treated with Psirelax demonstrated that a target sample size of 20 patients is sufficient to demonstrate preliminary effectiveness of treatment.
Safety analyses were carried out on all patients who received Psirelax for one
Analyses of efficacy measures were based on the intent-to-treat cohort. Descriptive statistics were used to summarize efficacy end-points.Results of continuous variables are shown as means ± SD. To analyze statistically significant differences in continuous parameters before and after treatment, Wilcoxon test were used. Dichotomous variables were analyzed using Fisher exact tests. Logistic and linear regressions were used for multivariate analyses. P values ≤ .05 were considered statistically significant.
The study included 22 patients (15 men, 7 women) with a mean age of 48.9±11.8 years. Psirelax was well tolerated and there no local or systemic side effects. All patients included in the study completed the 4 week follow-up period. The screening process identified 3 other patients that were excluded from analysis for technical reasons.
Application of Psirelax was associated with a decrease in disease severity, as assessed by PASI. There was a 59% reduction in PASI, from a mean of 5.9 ± 4.0 before treatment to 2.4 ± 2.4 after treatment (p=0.0001). In 8 patients (36%) PASI score decreased in more than 75% (PASI75). In 16 patients (73%) PASI score decreased in more than 50% (PASI50). The reduction in PASI was pronounced in women as compared to men (57% of women achieved PASI75 as compared to 26% in men), and showed a tendency for better results in patients younger then 40 years (PASI75 was 40% in patients younger than 40 years, 36% in patients between 40-60 years and 33% in patients above 60 years) (Table I).
In the current study we tested the safety and efficacy of a novel herbal topical medication (Psirelax) for patients with chronic plaque psoriasis. Psirelax includes natural ingredients such as quince seeds, sweet almond oil, jojoba oil, grape seed oil and bee wax.
The results of the study show that Psirelax was well tolerated. No adverse events were observed. Application of Psirelax was associated with a decrease in disease severity, as assessed by the patients and physicians.
Complementary medicine includes therapeutic modalities that derive from traditional and philosophical systems of medicine, which view health and disease in the context of human totality of body and mind. Thus, the effect of Psirelax observed in our patients demonstrates the beneficial effect this new complementary medication in patients with psoriasis.
Psirelax contains a unique blend of natural herbal oils and seeds that have effects of oiling and emulsifying the skin with possible anti-inflammatory and immune modulating activities.
Psirelax ingredients include sunflower seed oil which contains high levels of essential fatty acids (e.g. linoleic acid) that have skin barrier-enhancing properties. A sunflower oleodistillate has been shown to increase the epidermal key lipid synthesis and to reduce inflammation in vitro and in animal models. Sunflower oleodistillate has been shown to activate peroxisome proliferative-activated receptor-alpha in vitro, which stimulates keratinocyte differentiation, improve barrier function, and enhance lipid metabolism in the skin. Some studies have been shown the efficacy of sunflower seed oil in atopic dermatitis (4).
Psirelax also contains wheat germ oil was which was never studied in the treatment of psoriasis. A study showing improvement in rheumatoid arthritis patients taking wheat germ, proposed that a modulation of apoptosis is responsible for the effect (6). Other natural oils used in Psirelax include sweet almond oil and jojoba oil. The oil form makes these natural oils effective as emollient and moisturizer for human skin (7). Sweet almond oil has a weak anti bacterial effect and may be used as demulcent, while jojoba oil has healing effects on acne, sunburn, and chapped skin. Small scale studies have proven that sweet almond oil and jojoba oil has a beneficial effect in patients with psoriasis by the skin’s inflammatory process. Patients treated with the oils showed clinical improvement after treatment (7-9).
Quince is used topically as a compression for injuries, inflammation of the joints, injuries of the nipples, and skin lacerations. A topical lotion is used to soothe the eyes. Sweet almond is used topically as an emollient for chapped skin, to soothe mucous membranes and as a weak antibacterial (7). Aloe Vera (Barbadensis) was studied for the treatment of psoriasis. Applying aloe extract 0.5% cream topically 3 times daily for 4 weeks significantly improved and increased the resolution of psoriatic plaques compared to placebo (10). Aloe extract cream seems to reduce desquamation, erythema, and infiltration, and generate significant improvement of lesions in a double blind placebo controlled studies (11-12).
Beeswax is used by honey bees to build their honeycomb cells. Beeswax provides protective effects to human skin against contact irritants and allergens (13-14). The benefits of beeswax for psoriasis treatment are supported by a research which studied the healing effect of the combination beeswax, honey, and olive oil on patients with psoriasis and atopic dermatitis (15).
It is possible that the outcome of Psirelax treatment observed in the current study were attributed to placebo affect or to the lubrication affect of Psirelax formula. However, these preliminary results are encouraging and suggest that a double blind placebo controlled study should be conducted to further assess the efficacy of Psirelax in patients with psoriasis.
May 23, 2017