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Abstract Complementary and alternative medicine approaches are popular among some patient segments
due to the perception that they are “natural” and thus are believed to be less likely to be dangerous, to be less
toxic, or to cause fewer side effects. In dermatology, these can include aromatherapy, botanicals, and essen-
tial oils (plant extracts). Preliminary evidence, biological activity studies, and small pilot clinical trials con-
ducted outside of North America, mostly in young adults, suggest that some may have value in acne
treatment. When additional research and larger clinical trials are conducted, both clinicians and patients will
be able to understand the risks and benefits compared with allopathic remedies.
© 2018 Elsevier Inc. All rights reserved.
https://doi.org/10.1016/j.clindermatol.2018.03.004
0738-081X/© 2018 Elsevier Inc. All rights reserved.
300 W.J. Winkelman
Fig. 1 Examples of essential oils and plants used to create essential oils. (Courtesy Can Stock Photo/duskbabe, with permission.)
Aromatherapy, botanicals, and essential oils in acne 301
Table 1 Organic compounds present in essential oils and their toners, treatment gels or lotions, blemish sticks, masks).21 An
proposed therapeutic actions evidence-based review of botanicals for dermatologic use re-
Organic Proposed therapeutic actions ported that TTO “may have potential to become standard treat-
compounds ment” for acne.22
Several clinical studies of TTO have been performed in acne;
Acids Anti-infectious, immunostimulants
in a single-blind study, 124 participants with mild to moderate
Aromatic Anti-infectious, immunostimulants
aldehydes acne were given either 5% TTO or 5% benzoyl peroxide.23
C10 alcohols Anti-infectious, immunostimulants There were significant reductions in inflammatory and come-
C15 and C20 Estrogen-like activity donal lesions with both treatments. TTO had a slower onset
alcohols of action but better tolerability than benzoyl peroxide.23 In a
Aldehydes Anti-infectious, calming, litholytic randomized 45-day controlled trial of 5% TTO versus vehicle
Coumarins Balancing, calming in 60 participants with mild to moderate acne, TTO, when ap-
Esters Antispasmodic, calming plied twice daily for 20 minutes and then rinsed off with water,
Lactones Balancing, calming was superior to vehicle in reducing total, inflammatory, and
Ketones Cicatrizing (wound healing), mucolytic, noninflammatory lesions (Figure 2). In addition, TTO was
litholytic, calming
well tolerated, although a small proportion of patients experi-
Oxides Expectorant, antispasmodic
enced pruritus, burning, and scaling.17 Unfortunately, a recent
Phenols Anti-infectious, immunostimulants
Phenyl methyl Anti-infectious, antispasmodic Cochrane analysis judged the evidence supporting use of TTO
esters to be of low quality due to methodological and reporting lim-
C10 terpenes Anti-infectious, cortisone-like activity itations, notably of the aforementioned study.24
C15 terpenes Antihistamines, antiallergic
From Stevensen.9 Lactobacillus-fermented Chamaecyparis obtusa leaf
extract
Placebo Group
Fig. 2 Effect of tea tree oil on acne severity index and total lesion counts (secondary outcome measure). (From Enshaieh et al,17 with
permission.)
302 W.J. Winkelman
Fig. 3 (A) Changes in inflammatory acne lesion counts and (B) noninflammatory lesion counts with Lactobacillus-fermented Chamaecyparis
obtusa (LFCO) and tea tree oil (TTO). (From Kwon et al,25 with permission.)
Aromatherapy, botanicals, and essential oils in acne 303
Fig. 4 Histologic analysis of skin. (A) Hematoxylin-eosin stain at baseline and 8 weeks with histopathologic inflammation scores at each visit
shown in the graphs (inflammation around sebaceous gland with acne lesion). Immunohistochemical stain intensity from the (B) Lactobacillus-
fermented Chamaecyparis obtusa (LFCO) side and (C) tea tree oil (TTO) side. (D) Semiquantitative reverse transcription polymerase chain reac-
tion analysis of frozen skin samples at baseline and week 8. *P b .05. GAPDH, glyceraldehyde-3-phosphate dehydrogenase. (From Kwon et al,25
with permission.)
Essential oils and aromatherapy as complemen- times per day, and employed a mask 3 times per week. A total
tary therapy in acne of 89% of participants had disease improvement versus base-
line as rated on global assessment scores. Mean decreases in
inflammatory lesions were 37%, noninflammatory lesions
Sandalwood oil
25%, and total lesions 31%. The products were generally well
tolerated, with burning, dryness, and stinging being the most
Sandalwood oil is used as a therapeutic agent in many
common treatment-related complaints.27
Asian countries to treat inflammatory and cutaneous erup-
tions.27,28 It has antibacterial actions against Staphylococcus
aureus, Staphylococcus epidermidis, and P acnes at concen-
trations of 0.06% and lower.27 Anti-inflammatory effects are Rosemary extract
thought to occur via inhibition of cyclooxygenase 1 and 2
and 12-lipoxygenase pathways, as well as in Rosemary extract contains at least three bioactive com-
lipopolysaccharide-stimulated dermal fibroblasts and keratino- pounds: rosmarinic acid, carnosol, and carnosic acid.30 These
cyte models.27 Another model that employed synthetic sandal- have different modulatory effects on cytokine production. In
wood induced wound healing in human keratinocytes.29 vivo mouse models have found inhibition of P. acnes–induced
Recently, sandalwood oil 0.5% was formulated with salicylic inflammation via inhibition/suppression of cytokine produc-
acid for evaluation in acne patients. An 8-week open-label tion. Additionally, rosemary extract may reduce nuclear factor
study involved 42 participants with mild to moderate acne kB activation and normalize Toll-like receptor protein 2
who were treated with a four-part regimen of 0.5% salicylic ac- in vitro.30 Although the addition of rosemary extract may con-
id with sandalwood in a cleanser, serum, spot treatment, and tribute anti-inflammatory actions to cosmeceutical or dermato-
mask. Participants used the cleanser twice daily, morning logic products,30 injection of rosemary extract is not
and night, applied the serum after cleansing, had the option associated with skin irritation or inflammation in the mouse
of using spot treatment on individual blemishes up to 3 to 4 model.
304 W.J. Winkelman
Jeju essential oil 7. Sawni A, Singh A. Complementary, holistic, and integrative medicine: ac-
ne. Pediatr Rev. 2013;34:91-93.
8. Agnew T, Leach M, Segal L. The clinical impact and cost-effectiveness of
Jeju essential oil is derived from Thymus plants.31 Jeju es- essential oils and aromatherapy for the treatment of acne vulgaris: a proto-
sential oil may have antibacterial activities with effects col for a randomized controlled trial. J Altern Complement Med. 2014;20:
against P acnes,31 according to a 2009 study, in which the 399-405.
researchers suggest the agent may be useful for treating 9. Stevensen CJ. Aromatherapy in dermatology. Clin Dermatol. 1998;16:
689-694.
acne patients. 10. Mahmood T, Akhtar N, Khan BA, et al. Outcomes of 3% green tea emul-
sion on skin sebum production in male volunteers. Bosn J Basic Med Sci.
2010;10:260-264.
11. Fowler Jr JF, Woolery-Lloyd H, Waldorf H, et al. Innovations in natural
Korean citrus ingredients and their use in skin care. J Drugs Dermatol. 2010;9:
S72-81. quiz s82-73.
Citrus oils from Citrus obovoides and Citrus natsudaidai 12. Chularojanamontri L, Tuchinda P, Kulthanan K, et al. Moisturizers for ac-
ne: what are their constituents? J Clin Aesthet Dermatol. 2014;7:36-44.
have been tested for antibacterial activity against P. acnes
13. U.S. Food & Drug Administration. Is it a cosmetic, a drug, or both?
and S. epidermidis.32 Results indicated lower P. acnes secre- (Or is it soap?). Available at: https://www.fda.gov/Cosmetics/
tion of interleukin 8 and tumor necrosis factor α, suggesting GuidanceRegulation/LawsRegulations/ucm074201.htm. Accessed Octo-
potential utility in acne.32 ber 19, 2017.
14. Federal Food, Drug, and Cosmetic Act, 21 USC §301 et seq. 1938.
15. Kiecolt-Glaser JK, Graham JE, Malarkey WB, et al. Olfactory influences
on mood and autonomic, endocrine, and immune function. Psychoneur-
Conclusions oendocrinology. 2008;33:328-339.
16. Hammer KA. Treatment of acne with tea tree oil (melaleuca) products: a
review of efficacy, tolerability and potential modes of action. Int J Antimi-
Currently there is weak clinical evidence that TTO 5% may crob Agents. 2015;45:106-110.
be used as an alternative acne therapy. Several agents may be 17. Enshaieh S, Jooya A, Siadat AH, et al. The efficacy of 5% topical tea tree
helpful as complementary therapy due to biologic plausibility, oil gel in mild to moderate acne vulgaris: a randomized, double-blind
placebo-controlled study. Indian J Dermatol Venereol Leprol. 2007;73:
but there is little clinical evidence. There is as yet no proof of
22-25.
psychosocial outcome effectiveness, cost effectiveness, or any 18. Carson CF, Riley TV. Antimicrobial activity of the major components of
other economic advantages, and no insights into impact on post- the essential oil of Melaleuca alternifolia. J Appl Bacteriol. 1995;78:
inflammatory hyperpigmentation in patients with darker skin 264-269.
tones. Despite the lack of evidence, dermatologists would be 19. Brand C, Ferrante A, Prager RH, et al. The water-soluble components of
the essential oil of Melaleuca alternifolia (tea tree oil) suppress the produc-
served well to at least understand complementary and
tion of superoxide by human monocytes, but not neutrophils, activated
alternative remedies when their patients ask about such agents in vitro. Inflamm Res. 2001;50:213-219.
and their potential clinical value in the management of their 20. Koh KJ, Pearce AL, Marshman G, et al. Tea tree oil reduces
acne. histamine-induced skin inflammation. Br J Dermatol. 2002;147:
1212-1217.
21. Rosamilia LL. Over-the-counter treatments for acne and rosacea. Semin
Cutan Med Surg. 2016;35:87-95.
Acknowledgments 22. Reuter J, Merfort I, Schempp CM. Botanicals in dermatology: an
evidence-based review. Am J Clin Dermatol. 2010;11:247-267.
23. Bassett IB, Pannowitz DL, Barnetson RS. A comparative study of tea-tree
Valerie Sanders assisted in the preparation of the oil versus benzoylperoxide in the treatment of acne. Med J Aust.
manuscript. 1990;153:455-458.
24. Cao H, Yang G, Wang Y, et al. Complementary therapies for acne vul-
garis. Cochrane Database Syst Rev. 2015;1:CD009436.
25. Kwon HH, Yoon JY, Park SY, et al. Comparison of clinical and
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