The epidemiology of acne vulgaris in late adolescence

Darren D Lynn, Tamara Umari, Cory A Dunnick, Robert P Dellavalle, Darren D Lynn, Tamara Umari, Cory A Dunnick, Robert P Dellavalle

Abstract

Importance: Acne vulgaris is the most common skin condition affecting late adolescents across the globe. Although prior studies have evaluated epidemiologic patterns of acne vulgaris in various ethnicities and regions, adequate understanding of the worldwide burden of the disease associated with patients in their late adolescence (15-19-year olds) remains lacking.

Objective: To assess the global burden of the disease associated with acne vulgaris for late adolescents (15-19-year olds) and provide an overview of the epidemiology, pathophysiology, and treatment options for acne in this population.

Design: Database summary study.

Setting: Global Burden of Disease Study 2010 database.

Participants: Global Burden of Disease regions comprised countries with prevalence of acne vulgaris between the ages of 15 and 19 years.

Main outcomes and measures: Geographic region-level disability-adjusted life year rates (per 100,000 persons) associated with acne vulgaris in years 1990 through 2010. Median percentage change in disability-adjusted life year rates was estimated for each region across the specified study period.

Conclusion and relevance: Acne vulgaris-associated disease burden exhibits global distribution and has continued to grow in prevalence over time within this population. This continued growth suggests an unmet dermatologic need worldwide for this disorder and potential opportunities for improved access and delivery of dermatologic care. Our analysis of the literature reveals numerous opportunities for enhanced patient care. To that end, we highlight some of the effective and promising treatments currently available and address important factors, such as sex, nationality, genetics, pathophysiology, and diet, as they relate to acne vulgaris in late adolescence.

Keywords: GBD; diet; epidemiology; hormones; review.

Figures

Figure 1
Figure 1
Acne vulgaris in late adolescence around the globe. Notes: (A) The proportional rate of DALYs of 15–19-year olds in a given region for acne vulgaris. (B) This figure demonstrates a similar finding when comparing developing and developed countries. Abbreviation: DALY, disability-adjusted life year.
Figure 2
Figure 2
Cellular mechanisms hypothesized to govern the pathogenesis of acne vulgaris. Abbreviations: GnRH, gonadotropin-releasing hormone; IGF, insulin growth factor; DHT, dihydrotestosterone; FoxO1, Forkhead box protein O1; mTORC, mammalian target of rapamycin.
Figure 3
Figure 3
An earlier puberty onset for females triggers a higher incidence of acne vulgaris in the younger age ranges compared to men, regardless of a country’s economic level. Note: Change in the rates of incidence across all age categories compared between 1990, 1995, 2000, and 2005 were negligible and, therefore, not included in the data set. Abbreviation: YLD, years living with the disability.

References

    1. Seattle WI. GBD Compare. Seattle: University of Washington; 2013.
    1. Rea JN, Newhouse ML, Halil T. Skin disease in Lambeth. A community study of prevalence and use of medical care. Br J Prev Soc Med. 1976;30(2):107–114.
    1. Wolkenstein P, Grob JJ, Bastuji-Garin S, Ruszczynski S, Roujeau JC, Revuz J. French people and skin diseases: results of a survey using a representative sample. Arch Dermatol. 2003;139(12):1614–1619. discussion 1619.
    1. Johnson MT, Roberts J. Skin conditions and related need for medical care among persons 1–74 years. United States 1971–1974. Vital Health Stat. 1978;11(212):i–v. 1–72.
    1. Bhate K, Williams HC. Epidemiology of acne vulgaris. Br J Dermatol. 2013;168(3):474–485.
    1. Quarles FN, Johnson BA, Badreshia S, et al. Acne vulgaris in richly pigmented patients. Dermatol Ther. 2007;20(3):122–127.
    1. Davis EC, Callender VD. A review of acne in ethnic skin: pathogenesis, clinical manifestations, and management strategies. J Clin Aesthet Dermatol. 2010;3(4):24–38.
    1. Pochi PE, Strauss JS. Sebaceous gland activity in black skin. Dermatol Clin. 1988;6(3):349–351.
    1. Grimes P, Edison BL, Green BA, Wildnauer RH. Evaluation of inherent differences between African American and white skin surface properties using subjective and objective measures. Cutis. 2004;73(6):392–396.
    1. Bagatin E, Timpano DL, Guadanhim LR, et al. Acne vulgaris: prevalence and clinical forms in adolescents from Sao Paulo, Brazil. An Bras Dermatol. 2014;89(3):428–435.
    1. Perkins AC, Cheng CE, Hillebrand GG, Miyamoto K, Kimball AB. Comparison of the epidemiology of acne vulgaris among Caucasian, Asian, Continental Indian and African American women. J Eur Acad Dermatol Venereol. 2011;25(9):1054–1060.
    1. Halder RM, Nootheti PK. Ethnic skin disorders overview. J Am Acad Dermatol. 2003;48(6 Suppl):S143–S148.
    1. Callender VD. Acne in ethnic skin: special considerations for therapy. Dermatol Ther. 2004;17(2):184–195.
    1. Friedman HL. The health of adolescents: beliefs and behaviour. Soc Sci Med. 1989;29(3):309–315.
    1. Tan JK, Vasey K, Fung KY. Beliefs and perceptions of patients with acne. J Am Acad Dermatol. 2001;44(3):439–445.
    1. Magin P, Pond D, Smith W, Watson A. A systematic review of the evidence for ‘myths and misconceptions’ in acne management: diet, face-washing and sunlight. Fam Pract. 2005;22(1):62–70.
    1. Plewig G, Fulton JE, Kligman AM. Pomade acne. Arch Dermatol. 1970;101(5):580–584.
    1. Jugeau S, Tenaud I, Knol AC, et al. Induction of toll-like receptors by Propionibacterium acnes. Br J Dermatol. 2005;153(6):1105–1113.
    1. Kim J. Review of the innate immune response in acne vulgaris: activation of Toll-like receptor 2 in acne triggers inflammatory cytokine responses. Dermatology. 2005;211(3):193–198.
    1. Danby FW. Acne Causes and Practical Management. Hoboken, NJ: Wiley Blackwell; 2015.
    1. Parker LN. Adrenarche. Endocrinol Metab Clin North Am. 1991;20(1):71–83.
    1. Martinez G, Copen CE, Abma JC. Teenagers in the United States: sexual activity, contraceptive use, and childbearing, 2006–2010 national survey of family growth. Vital Health Stat. 2011;23(31):1–35.
    1. Calman KC, Muir AV, Milne JA, Young H. Survey of the distribution of steroid dehydrogenases in sebaceous glands of human skin. Br J Dermatol. 1970;82(6):567–571.
    1. Melnik BC. The role of transcription factor FoxO1 in the pathogenesis of acne vulgaris and the mode of isotretinoin action. G Ital Dermatol Venereol. 2010;145(5):559–571.
    1. Melnik BC, Zouboulis CC. Potential role of FoxO1 and mTORC1 in the pathogenesis of Western diet-induced acne. Exp Dermatol. 2013;22(5):311–315.
    1. Caprio S, Plewe G, Diamond MP, et al. Increased insulin secretion in puberty: a compensatory response to reductions in insulin sensitivity. J Pediatr. 1989;114(6):963–967.
    1. Melnik BC. Is nuclear deficiency of FoxO1 due to increased growth factor/PI3K/Akt-signalling in acne vulgaris reversed by isotretinoin treatment? Br J Dermatol. 2010;162:1398–1400.
    1. 8/1 M. Parents and Teachers: Teen Growth and Development, Years 15 to 17; 2015. [Accessed May 29, 2015]. Available from: .
    1. Smith CP, Dunger DB, Williams AJ, et al. Relationship between insulin, insulin-like growth factor I, and dehydroepiandrosterone sulfate concentrations during childhood, puberty, and adult life. J Clin Endocrinol Metab. 1989;68(5):932–937.
    1. Plant TM. Neuroendocrine control of the onset of puberty. Front Neuroendocrinol. 2015;38:73–88.
    1. Stathakis V, Kilkenny M, Marks R. Descriptive epidemiology of acne vulgaris in the community. Australas J Dermatol. 1997;38(3):115–123.
    1. French SA, Story M, Neumark-Sztainer D, Fulkerson JA, Hannan P. Fast food restaurant use among adolescents: associations with nutrient intake, food choices and behavioral and psychosocial variables. Int J Obes Relat Metab Disord. 2001;25(12):1823–1833.
    1. Drewnowski A, Popkin BM. The nutrition transition: new trends in the global diet. Nutr Rev. 1997;55(2):31–43.
    1. Kwon HH, Yoon JY, Hong JS, Jung JY, Park MS, Suh DH. Clinical and histological effect of a low glycaemic load diet in treatment of acne vulgaris in Korean patients: a randomized, controlled trial. Acta Derm Venereol. 2012;92(3):241–246.
    1. Ismail NH, Manaf ZA, Azizan NZ. High glycemic load diet, milk and ice cream consumption are related to acne vulgaris in Malaysian young adults: a case control study. BMC Dermatol. 2012;12:13.
    1. Zouboulis CC, Jourdan E, Picardo M. Acne is an inflammatory disease and alterations of sebum composition initiate acne lesions. J Eur Acad Dermatol Venereol. 2014;28(5):527–532.
    1. Melnik B. Dietary intervention in acne: Attenuation of increased mTORC1 signaling promoted by Western diet. Dermatoendocrinol. 2012;4(1):20–32.
    1. Smith RN, Mann NJ, Braue A, Makelainen H, Varigos GA. The effect of a high-protein, low glycemic-load diet versus a conventional, high glycemic-load diet on biochemical parameters associated with acne vulgaris: a randomized, investigator-masked, controlled trial. J Am Acad Dermatol. 2007;57(2):247–256.
    1. Burris J, Rietkerk W, Woolf K. Acne: the role of medical nutrition therapy. J Acad Nutr Diet. 2013;113(3):416–430.
    1. Robinson HM. The acne problem. South Med J. 1949;42(12):1050–1060. illust.
    1. Adebamowo CA, Spiegelman D, Danby FW, Frazier AL, Willett WC, Holmes MD. High school dietary dairy intake and teenage acne. J Am Acad Dermatol. 2005;52(2):207–214.
    1. Adebamowo CA, Spiegelman D, Berkey CS, et al. Milk consumption and acne in adolescent girls. Dermatol Online J. 2006;12(4):1.
    1. Adebamowo CA, Spiegelman D, Berkey CS, et al. Milk consumption and acne in teenaged boys. J Am Acad Dermatol. 2008;58(5):787–793.
    1. Koldovsky O. Hormones in milk. Life Sci. 1980;26(22):1833–1836.
    1. Yeung A, Sheehan J. Hormone Concentrations in Milk and Milk Products [Letter from FDA Center for Food Safety and Applied Nutrition] Washington, DC: US Food and Drug Administration; 2012.
    1. Millward DJ, Layman DK, Tome D, Schaafsma G. Protein quality assessment: impact of expanding understanding of protein and amino acid needs for optimal health. Am J Clin Nutr. 2008;87(5):1576s–1581s.
    1. Delnevo CD, Bover Manderski MT, Giovino GA. Youth tobacco use and electronic cigarettes. JAMA Pediatr. 2014;168:775–776.
    1. Administration SAaMHS . Results from the 2010 National Survey on Drug Use and Health: Mental Health Findings. Rockville, MD: Substance Abuse and Mental Health Services Administration; 2012.
    1. Dutra LM, Glantz SA. Electronic cigarettes and conventional cigarette use among US adolescents: a cross-sectional study. JAMA Pediatr. 2014;168(7):610–617.
    1. Carroll Chapman SL, Wu LT. E-cigarette prevalence and correlates of use among adolescents versus adults: a review and comparison. J Psychiatr Res. 2014;54:43–54.
    1. Klaz I, Kochba I, Shohat T, Zarka S, Brenner S. Severe acne vulgaris and tobacco smoking in young men. J Invest Dermatol. 2006;126(8):1749–1752.
    1. Schafer T, Nienhaus A, Vieluf D, Berger J, Ring J. Epidemiology of acne in the general population: the risk of smoking. Br J Dermatol. 2001;145(1):100–104.
    1. Capitanio B, Sinagra JL, Ottaviani M, Bordignon V, Amantea A, Picardo M. Acne and smoking. Dermatoendocrinol. 2009;1(3):129–135.
    1. Pelle E, Miranda EP, Fthenakis C, Mammone T, Marenus K, Maes D. Cigarette smoke-induced lipid peroxidation in human skin and its inhibition by topically applied antioxidants. Skin Pharmacol Appl Skin Physiol. 2002;15(1):63–68.
    1. Halvorsen JA, Stern RS, Dalgard F, Thoresen M, Bjertness E, Lien L. Suicidal ideation, mental health problems, and social impairment are increased in adolescents with acne: a population-based study. J Invest Dermatol. 2011;131(2):363–370.
    1. Silverberg JI, Silverberg NB. Epidemiology and extracutaneous comorbidities of severe acne in adolescence: a US population-based study. Br J Dermatol. 2014;170(5):1136–1142.
    1. Smithard A, Glazebrook C, Williams HC. Acne prevalence, knowledge about acne and psychological morbidity in mid-adolescence: a community-based study. Br J Dermatol. 2001;145(2):274–279.
    1. Spencer EH, Ferdowsian HR, Barnard ND. Diet and acne: a review of the evidence. Int J Dermatol. 2009;48(4):339–347.
    1. Wen L, Jiang G, Zhang X, Lai R, Wen X. Relationship between acne and psychological burden evaluated by ASLEC and HADS surveys in high school and college students from central China. Cell Biochem Biophys. 2015;71(2):1083–1088.
    1. Bettoli V, Zauli S. The epidemiology and comorbidities of severe acne in children aged 0–17 years. Br J Dermatol. 2014;170(5):1013–1014.
    1. Bowe WP, Hoffstad O, Margolis DJ. Upper respiratory tract infection in household contacts of acne patients. Dermatology. 2007;215(3):213–218.
    1. Levy RM, Huang EY, Roling D, Leyden JJ, Margolis DJ. Effect of antibiotics on the oropharyngeal flora in patients with acne. Arch Dermatol. 2003;139(4):467–471.
    1. Margolis DJ, Bowe WP, Hoffstad O, Berlin JA. Antibiotic treatment of acne may be associated with upper respiratory tract infections. Arch Dermatol. 2005;141(9):1132–1136.
    1. Bataille V, Snieder H, MacGregor AJ, Sasieni P, Spector TD. The influence of genetics and environmental factors in the pathogenesis of acne: a twin study of acne in women. J Invest Dermatol. 2002;119(6):1317–1322.
    1. Friedman GD. Twin studies of disease heritability based on medical records: application to acne vulgaris. Acta Genet Med Gemellol (Roma) 1984;33(3):487–495.
    1. Schackert K, Scholz S, Steinbauer-Rosenthal I, Albert ED, Wank R, Plewig G. Letter: HL-A antigens in acne conglobata: a negative study. Arch Dermatol. 1974;110(3):468.
    1. Wong SS, Pritchard MH, Holt PJ. Familial acne fulminans. Clin Exp Dermatol. 1992;17(5):351–353.
    1. Ando I, Kukita A, Soma G, Hino H. A large number of tandem repeats in the polymorphic epithelial mucin gene is associated with severe acne. J Dermatol. 1998;25(3):150–152.
    1. Klinger B, Anin S, Silbergeld A, Eshet R, Laron Z. Development of hyperandrogenism during treatment with insulin-like growth factor-I (IGF-I) in female patients with Laron syndrome. Clin Endocrinol (Oxf) 1998;48(1):81–87.
    1. Melnik BC, John SM, Plewig G. Acne: risk indicator for increased body mass index and insulin resistance. Acta Derm Venereol. 2013;93(6):644–649.
    1. Zouboulis CC. Acne as a chronic systemic disease. Clin Dermatol. 2014;32(3):389–396.
    1. Simonart T. Newer approaches to the treatment of acne vulgaris. Am J Clin Dermatol. 2012;13(6):357–364.
    1. Dreno B. Topical antibacterial therapy for acne vulgaris. Drugs. 2004;64(21):2389–2397.
    1. Gollnick HP. From new findings in acne pathogenesis to new approaches in treatment. J Eur Acad Dermatol Venereol. 2015;29(Suppl 5):1–7.
    1. Webster G. Combination azelaic acid therapy for acne vulgaris. J Am Acad Dermatol. 2000;43(2 pt 3):S47–S50.
    1. Strauss JS, Krowchuk DP, Leyden JJ, et al. American Academy of Dermatology/American Academy of Dermatology Association Guidelines of care for acne vulgaris management. J Am Acad Dermatol. 2007;56(4):651–663.
    1. Dawson AL, Dellavalle RP. Acne vulgaris. BMJ. 2013;346:f2634.
    1. Gollnick H, Cunliffe W, Berson D, et al. Management of acne: a report from a global alliance to improve outcomes in acne. J Am Acad Dermatol. 2003;49(1 Suppl):S1–S37.
    1. Simonart T, Dramaix M, De Maertelaer V. Efficacy of tetracyclines in the treatment of acne vulgaris: a review. Br J Dermatol. 2008;158(2):208–216.
    1. Thiboutot D, Gollnick H, Bettoli V, et al. Global Alliance to Improve Outcomes in Acne New insights into the management of acne: an update from the Global Alliance to Improve Outcomes in Acne group. J Am Acad Dermatol. 2009;60(5 Suppl):S1–S50.
    1. Harper JC. An update on the pathogenesis and management of acne vulgaris. J Am Acad Dermatol. 2004;51(1 Suppl):S36–S38.
    1. Nast A, Dreno B, Bettoli V, et al. European evidence-based (S3) guidelines for the treatment of acne. J Eur Acad Dermatol Venereol. 2012;26(Suppl 1):1–29.
    1. Chivot M. Retinoid therapy for acne. A comparative review. Am J Clin Dermatol. 2005;6(1):13–19.
    1. DiGiovanna JJ. Systemic retinoid therapy. Dermatol Clin. 2001;19(1):161–167.
    1. Chivot M. Retinoid therapy for acne. A comparative review. Am J Clin Dermatol. 2005;6(1):13–19.
    1. DiGiovanna JJ. Systemic retinoid therapy. Dermatol Clin. 2001;19(1):161–167.
    1. Panzer C, Wise S, Fantini G, et al. Impact of oral contraceptives on sex hormone-binding globulin and androgen levels: a retrospective study in women with sexual dysfunction. J Sex Med. 2006;3(1):104–113.
    1. Prevost N, English JC. Isotretinoin: update on controversial issues. J Pediatr Adolesc Gynecol. 2013;26(5):290–293.
    1. Haider A, Shaw JC. Treatment of acne vulgaris. JAMA. 2004;292(6):726–735.
    1. Newman MD, Bowe WP, Heughebaert C, Shalita AR. Therapeutic considerations for severe nodular acne. Am J Clin Dermatol. 2011;12(1):7–14.
    1. Kohler C, Tschumi K, Bodmer C, Schneiter M, Birkhaeuser M. Effect of finasteride 5 mg (Proscar) on acne and alopecia in female patients with normal serum levels of free testosterone. Gynecol Endocrinol. 2007;23(3):142–145.
    1. Panzer C, Wise S, Fantini G, et al. Impact of oral contraceptives on sex hormone-binding globulin and androgen levels: a retrospective study in women with sexual dysfunction. J Sex Med. 2006;3(1):104–113.
    1. Thorneycroft H, Gollnick H, Schellschmidt I. Superiority of a combined contraceptive containing drospirenone to a triphasic preparation containing norgestimate in acne treatment. Cutis. 2004;74(2):123–130.
    1. Farmer RD, Lawrenson RA, Thompson CR, Kennedy JG, Hambleton IR. Population-based study of risk of venous thromboembolism associated with various oral contraceptives. Lancet. 1997;349(9045):83–88.
    1. Phillips A, Hahn DW, McGuire JL. Preclinical evaluation of norgestimate, a progestin with minimal androgenic activity. Am J Obstet Gynecol. 1992;167(4 pt 2):1191–1196.
    1. Corson SL. Efficacy and clinical profile of a new oral contraceptive containing norgestimate. US clinical trials. Acta Obstet Gynecol Scand Suppl. 1990;152:25–31.
    1. Collier R. Scrutiny of Diane-35 due to potential dangers of off-label prescribing. CMAJ. 2013;185:E217–E218.
    1. Brahm J, Brahm M, Segovia R, et al. Acute and fulminant hepatitis induced by flutamide: case series report and review of the literature. Ann Hepatol. 2011;10(1):93–98.
    1. Cilotti A, Danza G, Serio M. Clinical application of 5alpha-reductase inhibitors. J Endocrinol Invest. 2001;24(3):199–203.
    1. Biggar RJ, Andersen EW, Wohlfahrt J, Melbye M. Spironolactone use and the risk of breast and gynecologic cancers. Cancer Epidemiol. 2013;37(6):870–875.
    1. Joseph MA, Jayaseelan E, Ganapathi B, Stephen J. Hidradenitis suppurativa treated with finasteride. J Dermatolog Treat. 2005;16(2):75–78.

Source: PubMed

3
订阅