The Use of a Novel Nutraceutical to Treat Acne and Acne Scarring

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The-Use-of-a-Novel-Nutraceutical-to-Treat-Acne-and-Acne-Scarring Sajic Skin Science

Samina Nazarali
BMSc1 Dusan Sajic MD, PhD2

Journal of Cosmetic Dermatology, 03 Apr 2021, 21(1):405-406
DOI: 10.1111/jocd.14084 PMID: 33740839

Acne has a significant prevalence in the adolescent population, with over 95% of patients developing secondary scarring, for which there are currently suboptimal treatments.1•2 Permanent scarring is often the primary concern for patients, with continuously emerging data illustrating the significant impact it has on overall quality of life.1 An adolescent male presented to clinic with Grade 3 moderate severity acne, confined to the forehead with evidence of closed comedones, a combination of inflammatory papules and pustules, and macular erythema {Figure 1A). The patient was instructed to use adapalene 0.3%/benzoyl peroxide 2.5% and Compound A, a novel topical treatment that contains hydroxytyrosol, niacinamide, retinol, retinaldehyde, bakuchiol, green tea extract, and green cof­fee extract, for 8 weeks. Topical retinoid treatments have a well­documented efficacy for the treatment of primary acne lesions, and it has been shown that adapalene 0.3%/benzoyl peroxide 2.5% not only prevents scar formation but can reverse early scars.3 During follow-up, it was ascertained he was not able to use the adapalene/ benzoyl peroxide combination more than three times per week sec­ondary to irritation. Upon examination, it was evident that there was a significant reduction in the number of primary acne lesions; how­ever, there were numerous new erythematous post-inflammatory scars {Figure 18).

Due to the irritation, a split-face trial with adapalene 0.3%/ benzoyl peroxide 2.5% being used on the right side of the forehead and Compound A on the left was started. Four weeks later, it was noted that Compound A was non-inferior and 8 weeks later, the left side treated with Compound A, had exhibited complete resolution of acne scarring compared to the adapalene 0.3%/benzoyl perox­ide 2.5% treated side, which displayed two atrophic boxcar scars {Figure 2). This case reveals how rapidly scarring can develop, despite early treatment with a combination that was previously shown to not only reduce the risk of acne scar formation, but to reverse early scars. This highlights the importance for early intervention and elicits a need to better understand factors which make individuals more sus­ceptible to future scarring.

Bakuchiol, an ingredient of Compound A, is an alternative agent to topical retinoids and has been found to have antiprolifer­ative, anti-inflammatory, and anti-acne activity. Studies comparing retinol to bakuchiol have shown comparable efficacy4•5 ; however, bakuchiol has been shown to be better tolerated. Bakuchiol is as­sociated with fewer cutaneous side effects, specifically decreased stinging and scaling of the skin, and is not associated with photo­sensitivity.4 Hydroxytyrosol, another component of Compound A, has similarly been shown to have anti-inflammatory and anti-aging effects.6 Niacinamide, a form of vitamin B3, provides potent anti­inflammatory properties with a well-established safety profile. It is beneficial for individuals prone to post-inflammatory hyperpigmen­tation and has also been shown to improve acne lesion formation.7 Finally, green tea extract has anti-acne properties and can have a significant impact in normalizing microflora of the skin,8 an import­ant component in the development of acne and subsequent scarring.

 

 

FIGURE 1 {A)
An adolescent male on initial presentation for evaluation of acne. Evidence of moderate acne with closed comedones and inflammatory papules and pustules.


{B) 
Follow-up at 8 weeks, after using adapalene 0.3%/benzoyl peroxide 2.5% and Compound A containing hydroxytyrosol, niacinamide, retinol, bakuchiol, retinaldehyde, green tea extract, and green coffee extract. Evidence of erythematous post-inflammatory scars and mild atrophic scarring, with significant improvement of comedones

FIGURE 2
Split-face application of adapalene 0.3%/benzoyl peroxide 2.5% on the right side of the face and Compound A on the left side after 8 weeks of use. Complete resolution of atrophic scarring on the left side, with evidence of 2 boxcar scars on the right

 

These results are promising as the use of Compound A was shown to cause minimal skin irritation, potentially allowing for in­creased tolerability and thus, increased compliance. Additionally, as a topical application, it is more easily accessible compared to phys­ical, surgical, and energy-based scarring treatments. Limitations include the split-face crossover design, as there may have been in­advertent transferring of the two treatments. Furthermore, the in­ability of the patient to tolerate daily application of the adapalene 0.3%/benzoyl peroxide 2.5% cream may have affected its efficacy. Finally, this was a single subject observation; long-term studies with more patients will be essential in further evaluating the efficacy and safety of this novel compound.


 

FUNDING INFORMATION
Derma Research Group

CONFLICT OF INTEREST
The study was supported by a grant from Derma Research Group, awarded to OS. OS has also received personal fees for advisory, speaking, consulting, research, and/or other ties with Galderma Laboratories, Novartis, Bausch, Leo Pharma, Concert Pharma. SN has no conflict of interest.

ETHICAL APPROVAL
Consent was taken from the patient to have the pictures taken.
Informed consent: Written informed consent was obtained from the patient for the publication of this case report. Subject approved the images and data used. 

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