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alopecia areata epidemiology and clinical disease patterns

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Alopecia areata epidemiology and clinical disease patterns

Epidemiology, the study of the distribution and determinants of health conditions in human populations, was originally concerned with the investigation and control of infectious diseases, but now has evolved into a powerful tool for analyzing many kinds of health events, including occurrence and prevalence of alopecia areata. Epidemiological information with respect to alopecia areata obtained from study samples of a target population is as crucial to the disease description as clinical and pathological findings are.

Epidemiologic analysis and observations of alopecia areata are available from USA, Japan and European countries, and this valuable information is used to plan and evaluate strategies to prevent hair loss, and as guide to management of patients in whom the condition has already developed.

Alopecia areata is common throughout the world and can occur at any age, but approximately 50 percent of cases are seen in children and young adults before the age of 20. Statistical data on the prevalence of alopecia areata in the United States, as determined from the First National Health and Nutrition Examination Survey conducted from 1971 through 1974, indicated that every 158 out of 100,000 persons, or roughly 0.1 to 0.2 percent of the population, was affected by alopecia areata. Some research literature has estimated that about 1.7% of the population presents at least one episode of Alopecia Areata during their life. Both sexes are equally affected, though some conflicting reports indicate a higher incidence of alopecia areata in females or males.

Ikeda analyzed the case histories of 1,989 patients with alopecia areata at Kyoto University in Japan and assigned them to one of four arbitrary types of alopecia areata. Under the Ikeda classification system:

  • 83 percent of the cases were of Type I alopecia areata, characterized by the "round" or patchy type of commonly found alopecia areata. Individuals with type I alopecia areata had no family history of alopecia areata and carried a good prognosis, with no history of hypertension, atopy, or endocrine disorders.
  • 10 percent of cases in this study were categorized as Type II (atopic type) alopecia areata, and was described as clinically having hair loss in a round, ophiasis-patterned, reticular, or indeterminate shape. These patients with type II alopecia areata had a history of asthma, allergic rhinitis, or dermatitis. The hair loss in these patients lasted longer than those with type I alopecia areata and was associated with seasonal recurrences. Over 75 percent of these patients went on to develop alopecia totalis or total loss of scalp hair.
  • Patients with type III (prehypertensive type) alopecia areata had chronic disease activity and a reticular pattern of hair loss. This means that the patients experienced loss of hair in one site concurrent with spontaneous hair re-growth in another area of hair loss. The frequency of this type of alopecia areata was 4 percent, and alopecia totalis developed in 39 percent of these cases. A point to be noted is that the incidence of parental hypertension in this group was 95 percent, compared with 10 percent in the common type, 11 percent in the atopic group, and 21 percent in a control population.
  • Patients with type IV (combined or endocrine-autoimmune) alopecia areata were usually over 40 years of age and had either round, reticular, or ophiasis pattern (band like pattern of hair loss affecting the temporal and occipital regions of the scalp) alopecia areata for a prolonged period. The frequency of this type of alopecia areata was 3 percent, and alopecia totalis developed in 10 percent of this group.

Studies by other investigators in due course have confirmed many of Ikeda’s conclusions.

An evaluation study by Muller and Winkelmann of 736 patients with alopecia areata at the Mayo Clinic between 1945 and 1954 reported that 30 percent of patients developed alopecia totalis (54 percent of the children and 24 percent of the adults). They also observed that the proportion of patients presenting with alopecia totalis declined with each decade of life.

In an attempt to co-relate puberty and prognosis of alopecia areata patients, Walker and Rothman reviewed 230 patients with alopecia areata at the University of Chicago Clinics during the period from 1928 to 1948. This included 40 patients who went on to develop alopecia totalis or alopecia universalis. They reported:

  • Of those patients who developed alopecia areata before puberty, 50 percent eventually developed alopecia totalis and none fully recovered from the episode.
  • In comparison, only 23 percent of those who developed patchy alopecia areata after puberty became totally bald and only 5 percent of these patients fully recovered.
  • The duration of the initial alopecia areata episode until complete hair re-growth was within 6 months in 31 percent of the patients and within 1 year in 50 percent. They also pointed out that 34 percent of the patients never recovered from the initial episode.
  • The overall incidence of relapse or of experiencing another episode of alopecia areata was 86 percent, although it reached 100 percent if patients were followed for 20 years. Those patients with alopecia totalis tended to remain persistently bald.

Detailed data on the natural history of alopecia areata and on the epidemiology of disease is useful information that helps researchers to understand who gets this disease, how it progresses, and its co-relation with the other diseases with which it is associated. Human epidemiology shows that there is a higher incidence of alopecia areata in genetically related individuals, suggesting that genes affect alopecia areata.

Epidemiological studies to investigate associations between alopecia areata and MHC class II antigens have helped to spur research towards uncovering the possible autoimmune pathogenesis of alopecia areata. The documentation of this data also helps new investigators, who do not have access to their own group of carefully defined alopecia areata patients, to conduct immunologic and other studies, in the hope of discovering the dark secrets of this enigmatic disease.


Alopecia areata epidemiology and clinical disease patterns references

  • Safavi K. Prevalence of alopecia areata in the First National Health and Nutrition Examination Survey. Arch Dermatol. 1992 May;128(5):702. PMID: 1575541
  • Safavi KH, Muller SA, Suman VJ, Moshell AN, Melton LJ 3rd. Incidence of alopecia areata in Olmsted County, Minnesota, 1975 through 1989. Mayo Clin Proc. 1995 Jul;70(7):628-33. PMID: 7791384
  • Ikeda T. A new classification of alopecia areata. Dermatologica. 1965;131(6):421-45. PMID: 5864736
  • Muller SA, Winkelmann RK. Alopecia areata an evaluation of 736 patients. Arch Dermatol. 1963 Sep;88:290-7. PMID: 14043621

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