© Springer Nature Singapore Pte Ltd. 2018
Ichiro Katayama, Hiroyuki Murota and Takahiro Satoh (eds.)Evolution of Atopic Dermatitis in the 21st Centuryhttps://doi.org/10.1007/978-981-10-5541-6_2929. Clinical Questions: Lifestyle of Japan and Atopic Dermatitis
(1)
Division of Skin Surface Sensing, Department of Dermatology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan
Abstract
Although the etiology and pathogenesis of atopic dermatitis (AD) are not fully understood, genetic and environmental factors are apparently involved in the onset and exacerbation of AD in a mutually interactive manner.
AD had become a very common skin disease from the 1950s through the 1970s in Japan. The incidence of AD in the Japanese population demonstrated an increase up to the 1990s but appeared to level off thereafter. These changes coincide with an era of rapid economic growth and have been attributed to the adoption of elements of a “Western” lifestyle such as diet or housing. Meanwhile, the Japanese also have specific traditions such as bathing. In addition, unpredictable climate change is occurring not only in Japan but also around the world.
What exactly are the lifestyle and other environmental ingredients that are responsible for the changing incidence of AD in Japan? This chapter reviewed selected environmental and lifestyle factors characterized in terms of the most significant influence on the prevalence and course of AD, especially in Japan.
Keywords
Atopic dermatitisClimateAir pollutionBathDiet29.1 Introduction: Atopic Dermatitis and Environmental Factors
Atopic dermatitis (AD) is a common, chronic or chronically relapsing, severely pruritic, eczematous skin disease. The incidence of AD is generally considered to be increasing worldwide. Standardized questionnaire data from almost a million children aged 6–7 years and 13–14 years in the International Study of Asthma and Allergies in Childhood (ISAAC) suggest that AD is not a problem confined only to developed countries, with a high prevalence being found in many developing cities undergoing rapid demographic change [1]. Although the etiology and pathogenesis of AD are not fully understood, recent studies demonstrate that it involves a complex interaction of skin barrier dysfunction, exposure to external allergens or microbes, Th2-prone immune response, and itch-scratch behavior. Allergic reactions in AD are considered multifactorial, heterogeneous disorders caused by an interaction of environmental and genetic factors.
Genetic and environmental factors appear to be involved in the onset and exacerbation of AD in a mutually interactive manner. In 1993, Schultz Larsen et al. reported that the pairwise concordance rate of AD in monozygotic twins was 72%, while it was only 23% in their dizygotic counterparts [2]. Interestingly, the results of a similar study from the same country published in 2007 indicated that the concordance rate seemed to be affected by environmental factors even in genetically identical twins. In the 11,515 pairs of twins, the pairwise concordance rate of AD was 57% and 21% in the monozygotic and dizygotic twins, respectively [3]. AD-inducing environmental factors, as yet unknown, had shown increased effects in industrialized and developing countries and seemed to trigger the onset of AD in almost all individuals who were genetically predisposed to the disease.
Recent data regarding the burden of AD suggest that the picture in the developing world may soon resemble that of wealthier nations, in which AD affects over 20% of children. In the case of Japan, AD had become a very common skin disease from the 1950s through the 1970s. The incidence of AD in the Japanese population demonstrated an increase up to the 1990s, but appeared to level off thereafter [4, 5]. These changes coincide with an era of rapid economic growth and have been attributed to the adoption of a “Western” lifestyle. However, what exactly are the lifestyle and other environmental ingredients that are responsible for the changing incidence of AD? The objective of this chapter was to review selected environmental and lifestyle factors characterized in terms of the most significant influence on the prevalence and course of AD in Japan.
29.2 What Are the Factors in Climate that Have Effects on AD?
29.2.1 Temperature and Humidity
Climate can have a major impact on symptoms of AD. Many published data show that cold and dry weather increase the prevalence and risk of flares in patients with AD [6–10]. An ecological analysis was conducted using information on long-term climatic conditions in the different study areas from the World Weather Guide [6]. Among latitude, altitude, average outdoor temperature, and relative outdoor humidity, AD symptoms correlate positively with latitude and negatively with annual outdoor temperature, but correlations were not observed with any of the other factors. In a cross-sectional population-based survey of schoolchildren from ten Spanish centers in three different climatic regions, AD was positively associated with precipitation and humidity and was negatively associated with temperature and the number of sunny hours [7]. In a study of Taiwanese schoolchildren, no associations were found for the highest monthly means of temperature, whereas the annual means and the lowest monthly means of temperature were negatively related to flexural eczema but only in girls [8]. These results show that AD is significantly dependent on meteorological conditions. Studies that have researched flare factors in established AD support this notion, as lower outdoor temperatures, especially in combination with skin irritants, can contribute to the worsening of disease, whereas indoor climate seems less important [9]. However, the relationship between outdoor climate and disease flares is complex, with some children reporting worsening in the summer and others in winter, and the effects of outdoor temperature, ultraviolet (UV) light, and humidity are likely to interact. Engebretsen KA et al. reviewed the literature regarding the effect of environmental humidity and temperature on skin barrier function and dermatitis and conclude that low humidity and low temperatures lead to a general decrease in skin barrier function and increased susceptibility toward mechanical stress [10].
In Japan, yearly average temperature and humidity differ from region to region. The national yearly average temperature and humidity are 15.8 °C and 69%, respectively. The yearly average temperature and humidity of Hokkaido, Tokyo, and Okinawa are 9.8 °C/69%, 16.9 °C/61%, and 23.1 °C/74%, respectively. A cross-sectional study of the prevalence of AD conducted by the Japanese Ministry of Health, Labour and Welfare actually confirmed that the lowest prevalence of AD was found in Okinawa, where the highest temperature occurred. Hayashi et al. reported that the prevalence of AD in Gifu, with a temperate climate (15.8 °C/64%), was significantly higher than that in Itoman (in Okinawa), with a subtropical climate [11]. Significantly lower rates of current AD in the Ogasawara Islands (23.3 °C/78%), which are located away from mainland Japan and belong to a subtropical area, were also observed compared to previous reports from Japan [12]. In our population-based survey of children aged 5 years and younger on Ishigaki Island, Okinawa, Japan (Kyushu University Ishigaki Atopic Dermatitis Study: KIDS), the AD prevalence on Ishigaki Island was apparently lower than that reported by a research team of the Japanese Ministry of Health, Labour and Welfare [13]. They reported that the national mean prevalence of AD was 12.8% in individuals aged 4 months, 9.8% in those aged 18 months, 13.2% in those aged 3 years, 11.8% in those aged 6–7 years, 10.6% in those aged 12–13 years, and 8.2% in those aged 18 years. The AD prevalence on Ishigaki Island (6.3%) was approximately half that of children of corresponding ages in mainland Japan. In addition, although five types of loss-of-function mutations in the filaggrin (FLG) gene isolated in previous Japanese FLG mutation studies were identified, the frequency of FLG loss-of-function mutation in children of the KIDS cohort was not significantly different between the AD and non-AD groups (7.9% and 6.1%, respectively, p = 0.174), suggesting that FLG loss-of-function mutations are not always a predisposing factor for AD prevalence [14]. There are many possible explanations for this, such as different pathogens, dietary habits, or flora. However, we believe that the high temperature (24.4 °C) and humidity (73.1%) of Ishigaki Island might reduce the incidence of AD, presumably reducing the onset of AD in those who have FLG mutations or a defect in enzymes that digest filaggrin. This study definitively showed that the involvement of the interaction of environmental and genetic factors in AD onset differs from region to region. Extremes of climate might suppress the effects of genetic factors.
29.2.2 Season
Although it has been generally accepted that seasonal aggravation of skin symptoms is a basic feature of AD, recent studies have suggested a decrease in the seasonal dependence of the dermatosis in European countries [15]. In Japan, the difference in climate in each of the four seasons is fairly clear-cut. Uenishi et al. examined the incidence of seasonal deterioration of AD in Japanese subjects. Of 682 patients aged 3–30 years with AD, 452 (66%) showed a seasonal aggravation of skin symptoms, and 230 (34%) experienced perennial deterioration. The overall incidences of exacerbation in spring, summer, autumn, and winter were 25%, 19%, 11%, and 36%, respectively [16]. In 1967, Masuda reported that the incidences of deterioration in spring, summer, autumn, and winter were 22%, 38%, 13%, and 34%, respectively [17]. Considering these results makes it evident that a real decrease in the incidence of seasonal aggravation of AD has occurred in Japan and that the incidence of summer deterioration has greatly decreased. The authors speculated that an important cause of the decrease in summer deterioration of AD may be a change in attitudes regarding the use of soap for bathing. In the 1960s, dermatologists in Japan prohibited patients with AD from using soap. As a result, the bodies of these patients were covered with sweat, scales, crusts, and debris of medicaments. Subsequently, however, several studies have demonstrated that such unclean skin is accompanied by severe pruritus, especially during the summer months when it is hot and humid in Japan [18, 19]. Therefore, most dermatologists now recommend that patients with AD use skin cleansing agent (i.e., soaps, detergent, cleanser) while bathing to keep both involved and uninvolved skin areas clean. Instead of the decrease in seasonal deterioration, perennial deterioration of the symptoms of AD has increased. Although it is not clear what factors are responsible for the increase in the occurrence of perennial worsening, the increase could be attributable to changes in environmental factors. For example, housing in Japan has generally changed from houses with open wooden structures to airtight homes made of concrete and synthetic materials. As a result, many patients with AD are perennially exposed to house dust and molds, which may provoke aggravation of the disease. In another study performed to investigate the relationship between residential environments and AD, 1378 elementary school children were examined by dermatological specialists in October 1994 (first series) and April 1995 (second series). Half of the children with AD showed symptoms in only one of the two seasons, either the autumn or spring, so the drifting of symptoms of AD occurred largely by season. Multiple logistic regression analysis showed that more children who were diagnosed positive for AD twice (AD(+,+)) lived in damp and moldy homes than did children who were diagnosed negative for AD twice (AD(−,−)). Thus, damp and moldy houses may be risk factors for the occurrence of AD [20].
In a study that evaluated the relationship between month of birth and prevalence of AD, individuals born in autumn showed the highest (7.5%), and those born in spring showed the lowest (5.5%), prevalence of AD [21]. These findings lead us to speculate that the climate to which one is exposed in early infancy affects the condition of the skin and that those born in autumn have dry skin in early infancy, which may ultimately result in a higher prevalence of AD among young schoolchildren. In fact, a recent study showed that skin barrier function measured through transepidermal water loss (TEWL) of the forehead during the first week of life is associated with the development of AD [22].
29.3 Does Air Pollution Exacerbate Symptoms of AD?
A systematic review of 26 studies suggested that there was good evidence of a higher disease burden in cities compared with the countryside, suggesting that place of residence may have a role in the pathogenesis of AD. One theory to explain this rise in AD is an increase in exposure to air pollution [23]. Air pollution became a social concern in the era of rapid economic growth in Japan. Nowadays, air pollution continues to increase in East Asia, particularly in China, and is considered to cause health problems in Japan. Studies on the association between outdoor pollution and AD from Sweden and East Germany found that AD risk increased with living close to heavy traffic [24, 25]. In a more recent population-based cross-sectional survey among more than 300,000 Taiwanese schoolchildren, objective measurement of traffic-related air pollutants, including nitrogen dioxide (NO2) and carbon monoxide (CO), suggested that air pollution may contribute to the risk of AD [8]. Similarly, a cohort study among 3000 schoolchildren in West Germany with repeat objective pollutant measurements reported that NO2 exposure was positively associated with physician-diagnosed AD at age 6 [26]. In a study involving 4907 French children (9–11 years of age) residing at their current address for 3 years or longer, lifetime eczema was significantly associated with 3-year average concentrations of PM10, NO2, NOx, and CO; adjusted odds ratios (ORs) were 1.13, 1.23, 1.06, and 1.08, respectively [27].
In addition to its effects on the prevalence of AD, outdoor air pollution also influences the skin symptoms in AD patients. In a prospective study, the concentrations of outdoor PM10, PM2.5, toluene, and total volatile organic compounds were higher on days when the patients had symptoms of AD than on days when they reported no symptoms [28]. PM is a mixture of solid and liquid particles of different origins with various chemical and physical properties, including pollen grains and mold spores. PM with a diameter of 10 μm or less is known as PM10, and particulate matter with a diameter of 2.5 μm or less is known as PM2.5. Diesel exhaust particulate (DEP) accounts for most of the airborne PM in the atmosphere in large cities. A study found that an increase in the concentration of outdoor PM10 of 1 μg/m3 was significantly associated with a 0.44% increase in AD symptoms on the following day. The effect of PM on AD was also investigated in a study of 41 schoolchildren aged between 8 and 12 years [29]. In the study, daily symptom scores and daily PM concentrations were measured. The results showed that the pruritus score was significantly associated with the concentrations of PM with a diameter <0.1 μm, but not larger particles. In Japan, the very stringent restrictions on emission sources have resulted in a low level of PM2.5 mass concentration. Therefore, pollutants originating in China and arriving via long-range transport have a significant impact on the PM2.5 concentration. In the future, PM from China might be one of the major factors that exacerbate AD symptoms in Japan.
29.4 Do Bathing Habits Matter in AD?
29.4.1 Bathing Habits in Japan
Bathing is an important behavior for keeping the body clean and is one of the habits of Japanese daily life. Bathing styles involve a full bath (body immersed in water in bathtub) or whole-body bathing (shower bath). Japanese individuals are known for their “specific” bathing habits. People in Japan usually take a bath every day, and a full bath (with or without shower) is the most common type of home bathing in Japan. Many Japanese individuals like high water temperatures, and some take baths of a long duration. Most people use “skin cleansing agent (i.e., soaps, detergent, cleanser),” and some, particularly elderly individuals, enjoy scrubbing their skin when they wash and dry their body. For many Japanese people, bathing is not only for cleaning the body but also for relieving fatigue and attaining a relaxed state of mind.
In a recent report about bathing habits among 189 Japanese healthy people, 128 participants (67.7%) took ≥7 baths per week. The most common water temperature was 40–41 °C, reported by 70 participants (40.2%). The mean water temperature was 40.14 ± 1.14 °C. The most common bath duration was 10–15 min, reported by 58 participants (30.9%). The mean bathing duration was 11.95 ± 9.03 min. In terms of water level, 167 participants (83.3%) took a full bath [30]. Nishioka et al. previously reported the bathing habits of Japanese people with various skin diseases. About 80% of the participants took a bath every day, and the most common bath duration was 10–20 min. Over 80% took a full bath (with or without shower). Most of them used soap or detergent, and 85% used a towel when washing the body [31]. Hattori et al. also reported that about 85% of patients who have various skin diseases use implements such as towels or gauze, and 56.4% scrub their skin when they wash their body [32]. These data remind us of traditional bathing habits in Japanese daily life. Another report regarding bathing habits in Okinawa found that 36% of people bathe more than twice a day in the summer season. Interestingly, 81% of these individuals take only a shower bath [33].
29.4.2 Studies in Favor of Bathing
Although most dermatologists agree that the skin of patients with AD should be kept clean, there is no unanimity of opinion or good evidence regarding bathing technique or proper use of soap or detergent.