JOURNAL OF COSMETIC SCIENCE 28 The individual lesion’s erythema and infl ammation was also reduced by the multi-prong treatment. The degree of infl ammation on the acne sites is reported in Figure 2. As ob- served in Figure 2 there was a marked reduction in acne lesion infl ammation after two and three days for lesions treated with the regimen. The regimen appeared to be more effective in reducing acne-induced erythema having an area under the curve of 14.37, which is 11% less than the untreated control after 24 hours. This increased effi cacy is clearly shown by the distinct reduction in acne lesion size and erythema on the site treated with the four-prong approach over time. The regimen reduced lesion size by 70% and erythema by 65% within six days of treatment. DISCUSSION The clinical assessment of acne treatments has historically been based on global evalua- tion of the patient or the lesion counts. These methods require long-term treatment and multiple time points to evaluate the treatment’s effectiveness. However, recently devel- oped treatment modalities, e.g., lasers, work in a shorter time frame, and these methods therefore require evaluation methods that are accurate on a shorter time scale. There is also a growing consumer interest in products that work in hours or days as opposed to weeks. This requires an understanding of the life cycle of individual comedones. Previously it has been reported that a comedone cycle has a lifespan of 12–14 days (17). We also observed that individual comedones appear to have a lifespan of about 12–14 days on average. The acne lesion will naturally resolve over this time and can be notice- ably improved in days. The lesions appear to be largest and most infl amed at day 7 or at the midpoint of the cycle. This resolution can be improved or accelerated by conventional treatments. Improvement can therefore be measured by the speed of resolution of the individual lesions and not only by a global score or total lesion count. Based on the confi nes and conditions of this study, there was a distinct reduction in acne lesion size and erythema on the site treated with the new regimen within days of treat- ment. This regimen appeared to be the most effective in reducing acne lesion size, with over 80% of the lesion size and erythema alleviated within six days of treatment. Figure 2. Average erythema of individual acne lesions measured daily for eight days (excluding Sunday). Erythema was assessed as described in Methods on a scale of 1–3 by an expert for a control lesion (black bars) and a treated lesion (grey bars). The area under the curve was 12.41 cm for the treated lesion and 16.09 cm for the untreated lesion (p = 0.0271).
RAPID ASSESSMENT OF ANTI-ACNE PRODUCT 29 CONCLUSION We have developed a method to evaluate acne treatments that can reduce individual lesions in days as opposed to weeks. This method will help to assess new treatments and thereby improve the treatment design. REFERENCES (1) H. Gollnick, Current concepts of the pathogenesis of acne: Implications for drug treatment, Drugs, 63(15), 1579–1596 (2003). (2) S. A. Buchner, Acne and its drug treatment, Ther. Umsch., 47(8), 670–674 (1990). (3) J. J. Leyden, Antibiotic resistance in the topical treatment of acne vulgaris, Cutis., 73(Suppl 6), 6–10 (2004). (4) R. A. Bojar and K. T. Holland, Acne and Propionibacterium acnes, Clin. Dermatol., 22(5), 375–379 (2004). (5) J. J. Leyden, Effect of topical benzoyl peroxide/clindamycin versus topical clindamycin and vehicle in the reduction of Propionibacterium acnes, Cutis, 69(6), 475–480 (2002). (6) A. M. Kligman, The growing importance of topical retinoids in clinical dermatology: A retrospective and prospective analysis, J. Am. Acad. Dermatol, 39(2 Pt 3), S2–S7 (1998). (7) C. C. Zouboulis, Acne and sebaceous gland function, Clinics Dermatol., 22, 360–366 (2004). (8) A. Jeremy, D. Holland, S. Roberts, K. Thomson, and W. Cunliffe, Infl ammatory events are involved in acne lesion initiation, J. Invest. Dermatol., 121, 20–27 (2003). (9) B. S. Allen and J. G. Smith, Jr., Various parameters for grading acne vulgaris, Arch. Dermatol., 118(1), 23–25 (1982). (10) S. Lidén, K. Göransson, and L. Odsell, Clinical evaluation in acne, Acta Derm Venereol. (Stockh.), 89(Suppl.), 47–52 (1980). (11) B. M. Burke and W. J. Cunliffe, The assessment of acne vulgaris—The Leeds technique, Br. J. Dermatol., 111(1), 83–92 (1984). (12) T. J. Wilt, A. Ishani, G. Stark, R. MacDonald, J. Lau, and C. Mulrow, J.A.M.A., 280(18), 1604–1609 (1998). (13) H. Nukaya, H. Yamashiro, H. Fukazawa, H. Ishida, and K. Tsuji, Isolation of inhibitors of TPA- induced mouse ear edema from hoelen, Poria cocos, Chem. Pharm. Bull., 44(4), 847–849 (1996). (14) M. Jang, L. Cai, G. O. Udeani, K. V. Slowing, C. F. Thomas, C. W. Beecher, H. H. Fong, N. R. Farnsworth, A. D. Kinghorn, R. G. Mehta, R. C. Moon, and J. M. Pezzuto, Cancer chemopreventive activity of resveratrol, a natural product derived from grapes, Science, 275(5297), 218–220 (1997). (15) A. M. Kligman, J. J. Leyden, and R. Stewart, New uses for benzoyl peroxide: A broad spectrum antimi- crobial agent, Int. J. Dermatol., 16(5), 413–417 (1977). (16) J. S. Samuelson, An accurate photographic method for grading acne: Initial use in a double-blind clini- cal comparison of minocycline and tetracycline, J. Am. Acad. Dermatol., 12(3), 461–467 (1985). (17) J. A. Witkowski and L. C. Parish, The assessment of acne: An evaluation of grading and lesion counting in the measurement of acne, Clin. Dermatol., 22(5), 394–397 (2004). (18) C. H. Cook, R. L. Centner, and S. E. Michaels, An acne grading method using photographic standards, Arch. Dermatol., 115(5), 571–575 (1979). (19) W. Cunliffe, D. Holland, and A. Jeremy, Comedone formation: Etiology, clinical presentation, and treatment, Clinics Dermatol., 22, 367–374 (2004).
Previous Page Next Page