Journal List > Allergy Asthma Immunol Res > v.5(5) > 1052341

Wong, Leung, and Ko: Changing Prevalence of Allergic Diseases in the Asia-Pacific Region

Abstract

Asia-Pacific is one of the most densely populated regions of the world and is experiencing rapid economic changes and urbanization. Environmental pollution is a significant problem associated with the rapid modernization of many cities in South Asia. It is not surprising that the prevalences of asthma and allergies are increasing rapidly, although the underlying reasons remain largely unknown. Many studies from this region have documented the changing prevalence of allergic diseases in various parts of the world. However, the methodologies used were neither standardized nor validated, making the results difficult to evaluate. The International Study of Asthma and Allergies in Childhood (ISAAC) has provided a global epidemiology map of asthma and allergic diseases, as well as the trend of changes in the prevalence of these diseases. Allergic sensitization is extremely common in many Asian communities. However, the prevalence of allergic diseases remains relatively rare. The rapid urbanization in the region, which increases environmental pollution and can affect the rural environment, will likely increase the prevalence of asthma and allergies in Asia.

INTRODUCTION

Recently, many studies have shown that the prevalence of asthma and allergic conditions have increased in various regions of the world.1-3 Comparative studies have demonstrated that asthma and related allergic disorders are more common in westernized or urbanized societies than in rural or developing countries.3-5 Despite intensive and extensive studies within a number of populations, the etiologies of these "atopic" conditions remain poorly understood. Nevertheless, epidemiological studies have played an important role in generating hypotheses regarding possible causative and protective factors.6-8
Asia is the world's most populous continent, and the region is undergoing rapid economic development and westernization. Common chronic childhood diseases such as asthma and related allergic diseases have become a major health priority in Asia.9 Many studies from this region have reported an increasing prevalence of childhood asthma, but the use of different methodologies and lack of precise definitions of asthma make reliable comparison of the reported prevalence from different regions difficult. Over the past decade, there use of standardized protocols to study asthma prevalence has increased. ISAAC attempted to study global variations of asthma and atopic disorders in children using standardized questionnaires, skin-prick testing and assessment of bronchial hyperresponsiveness.3-5,10 ISAAC was a multi-country cross-sectional survey of 2 age-groups of school children (6-7 years and 13-14 years). The study instruments included standardized questionnaires related to symptoms of asthma, allergic rhinoconjunctivitis, and eczema.10 A number of validation studies have confirmed that the ISAAC written and video questionnaires had excellent sensitivity and specificity for predicting asthma-associated bronchial hyperreactivity.11-13 The questions on eczema and allergic rhinitis have also been validated in a variety of settings with variable sensitivities and specificities depending on their gold standard for diagnosis.14-16 ISAAC Phase Three was a repetition of ISAAC Phase One that aimed to evaluate the possible trend of disease prevalence after a period of 5-10 years.

TRENDS IN ASTHMA AND ALLERGIES IN THE ASIA-PACIFIC REGION

ISAAC Phases 1 and 3 have provided a comprehensive world map of asthma prevalence and related atopic conditions using standardized and validated instruments. As shown by Phase 3, within a period of 6-7 years there have been significant changes in the prevalences of asthma and rhinoconjunctivitis across the region. Similar to Phase 1, the highest rates of asthma symptoms were found in English-speaking developed countries such as the United Kingdom, Australia and New Zealand. The regions with the lowest prevalence were areas in Africa and the Indian subcontinent. No further increase was observed among countries with high prevalence when compared to Phase 1 results.17-21 For both adolescents (13-14 years) and children (6-7 years), the prevalence of asthma in the Asia-Pacific region ranked in the middle on a global scale, while the prevalence of "current wheeze" and "severe attacks" were relatively low. However, the proportion of subjects with severe asthma was similar to locations with a much higher prevalence.22 Rhinoconjunctivitis was only modestly common in adolescents, but was quite prevalent in the younger children in Asia-Pacific (Tables 1 and 2).
In the adolescent group, the Asia-Pacific region was in the mid-range for reported current symptoms of rhinoconjunctivitis at a global scale. However, the prevalences in Hong Kong and Bangkok were among the highest recorded worldwide. In the 6-7-year-old group, Asia-Pacific had a fairly high prevalence of "current rhinoconjunctivitis", ranking as the third highest region globally.4 Asthma prevalence appears to have peaked or reached a plateau in countries with a high prevalence, while it is still rising in many Asian cities. Despite their very high degree of urbanization, the prevalence of asthma in cities such as Singapore, Seoul, and Hong Kong remains lower than those in the UK and Australia. Urbanization and economic development cannot explain such discrepancies. Furthermore, the known risk factors for asthma cannot explain the increased global prevalence, the international variations, or the recent decreases in prevalence in some Western countries.22-24 It is highly likely that these changes are related to the complex interplay between genetic factors and changing environmental exposure.25 A better understanding of these complex interactions could lead to the development of primary preventive strategies that may prevent further increases in the prevalence of allergies among Asian countries.
Similar to the global patterns of allergic diseases, asthma and rhinoconjunctivitis were more prevalent in well-developed areas, such as Korea, Japan, Hong Kong, and Singapore.26-28 The lowest prevalences of asthma symptoms were reported in the more underdeveloped countries or regions, such as Indonesia, several centers in Malaysia, and cities in mainland China (Tables 1 and 2).26-28 Nearly all the Asia-Pacific centers showed an annual increase in the prevalence of "current rhinoconjunctivitis" for both age groups.
An important aspect for asthma care is the level of control among asthmatic patients, since the most expensive component of asthma care is related to acute care, including emergency visits and hospitalization. The Asthma in Reality in Asia-Pacific (AIRIAP) study has been conducted twice in Asia, and centers from mainland China, Hong Kong, Korea, Malaysia, Philippines, Taiwan, and Vietnam participated.29 In the first survey, more than 3,000 adults and children were studied. More than 40% of the asthmatics had at least one hospitalization or visit to the emergency department for acute exacerbation. Inhaled corticosteroid use was reported by only 13.6% of the respondents. Another study was performed 10 years after the first survey, which applied the same methodology and recruited 4,805 subjects. Using the latest classification of the level of control derived from GINA, less than 5% of subjects achieved a level of complete control while more than one third of the subjects were in the uncontrolled asthma category. Similar to asthmatics in other parts of the world, patients in Asia tend to overestimate their level of control and tolerate a high degree of impairment of their daily activities.29-32

ASIA-PACIFIC-VARIATIONS AMONG POPULATIONS FROM DIFFERENT COUNTRIES OR CITIES

One of the most interesting findings of the ISAAC was the striking difference in asthma prevalence in populations with similar genetic or ethnic backgrounds from different environments.33-35 There are marked variations of asthma prevalence among different cities within the same countries such as those in Thailand, Malaysia, and China.36,37 Among Chinese cities, Hong Kong is the most developed and westernized while Guangzhou is located approximately 200 km north-west of Hong Kong and experiences a similar subtropical climate.38 The prevalence of asthma among children and adolescents was 2 times higher in Hong Kong than in Guangzhou. Furthermore, children recruited from Hong Kong (if they were born and raised in Hong Kong) had an asthma prevalence 2-3 times higher than those born in China who migrated to Hong Kong subsequently.39 These differences illustrated the importance of early or even in utero environmental exposure and the subsequent development of asthma. Although various factors such as cooking with gas, foam pillows, and exposure to house dampness were associated with an increased prevalence of asthma in Hong Kong,40 mechanistic studies are required to determine if these factors have a true pathogenetic role in causing asthma.

ALLERGIC RHINITIS IN THE ASIA-PACIFIC REGION

In addition to data on asthma, the ISAAC studies (Tables 1 and 2) have provided extensive global data on the prevalence of allergic rhinitis in children.4,5,41 Compared with children, adult epidemiology data are more difficult to obtain. For children, random populations can easily be obtained from primary or secondary schools. Therefore, community data of atopic diseases in adults are usually not from random populations. Nevertheless, such data are useful to establish the standard of care, perception, and control of asthma and related atopic diseases in adults. One of the largest studies performed on the impact of allergic rhinitis on adults and children in Asia is the Allergies in Asia-Pacific Survey.42 This survey recruited over 1,200 adults and children with physician diagnosis of allergic rhinitis after screening over 33,000 families in Australia, mainland China, Hong Kong, Malaysia, Philippines, Singapore, Taiwan, and Vietnam. Overall, the prevalence of allergic rhinitis was 8.7%. The rates varied from 13.2% in Australia to 4.2% in Hong Kong. Close to half of the subjects reported interference of their work or have missed work in the past year because of their allergic rhinitis. However, only 21% of the subjects were taking nasal inhalation steroids for their disease, despite the recommendation for such treatment based on evidence-based international guidelines.43

THE FUTURE CHALLENGES OF ALLERGIC DISORDERS IN ASIA

Given the rapid economic development and urbanization in Asia, the prevalence of allergic disorders will continue to rise in the next 2 decades. The loss of protective factors associated with a traditional rural environment and the emergence of risk factors associated with modern urbanized living will increase the total burden of allergic diseases on the health care systems in Asia. The increasing prevalence and possible increasing severity of asthma and related allergic conditions will become an important issue for physicians. Many of the so-called established risk factors for the development of allergies cannot explain the international and intra-regional variations in asthma prevalence patterns.44 The results of the ISAAC study challenge the common belief of a strong deterministic association between atopy and asthma.45 Sensitization of the major indoor allergen, house dust mite (HDM), was considered an important risk factor for the development of asthma.46 However, HDM exposure was high in many regions in Asia with a relatively low asthma prevalence. Leung and Ho47 reported a study of Chinese schoolchildren from Mainland China, Hong Kong and Malaysia Kota Kinabalu, and the overall rate of atopic sensitization (49%-63%) across all 3 regions. The prevalence of asthma in Hong Kong was 2-6 times higher than in the other 2 cities.47 Allergic sensitization is a significant factor associated with asthma, and appears to be a marker rather than a causative factor for subsequent asthma development.48-50 Air pollution has been implicated as an important precipitant of asthma exacerbation, but it could not explain the observed patterns of asthma prevalence in Asia.51-53 For example, there was a two-to-three-fold higher prevalence of asthma from Chinese children in Hong Kong than Chinese children living in the far more polluted cities in Mainland China, such as Chongqing.38,39
Recent research has focused on factors that modulate the early immune system towards the development of allergic diseases.54-56 Many studies have documented the protective roles of the rural environment and farming exposure,57-59 daycare attendance,60,61 changes in T-helper cell compositions,62 endotoxin exposure,63 exposure to farm animals,64,65 consumption of unpasteurized farm milk,66,67 fruits or vegetables,68 and exposure to microbial diversity in the living environment.69,70 Many of these factors have not been investigated thoroughly in Asia and likely reduce the prevalence there when compared to the UK or Western Europe. Another emerging challenge is food allergies, which has been described as the second wave of allergies after the rise in the prevalence of asthma in the past few decades.71 Recent studies from Australia suggested a prevalence as high as 10% in infants.72 Little published data are available from Asia regarding the epidemiology of food allergies using standardized and validated tools. The Europrevall study has provided a standardized protocol for the study of food allergies in the community from China. Russia and India have also participated in this study, using the same standardized instrument.73 The prevalence of food allergies will continue to increase in parallel to the improvement of economic levels in Asia. Furthermore, we should not ignore important information regarding the genetic contribution to the development of asthma and allergies. A better understanding of how different genes interact with various environmental factors and the timing of exposure of these factors are all important for the advancement of effective primary preventive strategies against the development of allergies.25,74,75

CONCLUSION

Although the prevalences of asthma and allergies remain relatively low in Asia compared with other regions, they will likely increase. The Asian environment is highly diverse with significant variation in genetic backgrounds. Furthermore, populations with similar genetic backgrounds live in different environments, making Asia ideal for epidemiological and gene-environment interaction studies. Continuing epidemiological studies using standardized and validated tools are important for identification of factors that modulate the immune system towards the development of allergies. Meticulous documentation of environmental changes in Asia may facilitate identification of probable triggers, risk factors and protective factors for allergies. Also, the increasing number of patients with allergic conditions makes necessary changing how we educate our health-care workers and patients regarding achieving better control so as to minimize the morbidity and mortality related to asthma and allergies.

Figures and Tables

Table 1
Trends in self-reported symptoms of asthma and allergic rhinoconjunctivitis in 13-14-year-old Asian children from ISAAC Phases 1 and 3 results: average annual change in prevalence
aair-5-251-i001
Cities/Countries Asthma Ever Current Wheeze Rhinoconjunctivitis
Alor Setar 10.8 (+0.09%) 9.3 (+0.05%) 16.3 (-0.06%)
Bangkok 15.9 (+0.30%) 13.9 (+0.06%) 23.9 (+1.41%)
Beijing 6.3 (-0.08%) 7.2 (+0.30%) 10.2 (+0.33%)
Philippines 20.9 (+0.47%) 8.4 (-0.55%) 11.0 (-0.61%)
Chiang Mai 9.9 (+0.10%) 8.7 (-0.65%) 17.2 (+0.26%)
Guangzhou 4.6 (+0.09%) 4.8 (+0.20%) 10.7 (+0.33%)
Hong Kong 10.1 (-0.15%) 8.6 (-0.55%) 22.6 (-0.21%)
Indonesia 12.4 (+1.80%) 5.2 (+0.52%) 4.8 (-0.08%)
Japan 19.9 (+0.12%) 13.0 (-0.05%) 17.6 (+0.34%)
Klang Valley 16.1 (+0.37%) 11.6 (-0.11%) 19.8 (+0.87%)
Kota Bharu 9.0 (+0.04%) 5.8 (-0.20%) 12.5 (+0.46%)
Seoul 5.0 (+0.44%) 9.1 (+0.16%) 11.9 (+0.24%)
Singapore 26.5 (+0.79%) 11.4 (+0.24%) 16.5 (+0.20%)
Taiwan 17.0 (+1.28%) 7.0 (+0.26%) 17.8 (+1.02%)
Mean 12.6 (+0.39%) 8.8 (+0.07%) 15.1 (+0.32%)
Table 2
Trends in parental-reported symptoms of asthma and allergic rhinoconjunctivitis in 6-7-year-old Asian children from ISAAC Phases 1 and 3 results: average annual change in prevalence
aair-5-251-i002
Cities/Countries Asthma Ever Current Wheeze Rhinoconjunctivitis
Alor Setar 9.8 (-0.52%) 5.7 (-0.07%) 4.2 (+0.09%)
Bangkok 10.7 (+0.24%) 15.0 (+0.68%) 13.4 (+0.58%)
Chiang Mai 6.1 (+0.32%) 7.8 (+0.38%) 6.2 (+0.24%)
Hong Kong 7.9 (+0.04%) 9.4 (+0.03%) 17.7 (+0.67%)
Indonesia 4.8 (-0.33%) 2.8 (-0.22%) 3.6 (-0.04%)
Japan 23.0 (+0.59%) 18.2 (+0.10%) 10.6 (+0.35%)
Klang Valley 11.9 (+0.13%) 7.4 (-0.07%) 6.2 (+0.21%)
Kota Bharu 11.2 (+0.14%) 4.3 (-0.21%) 4.2 (+0.06%)
Seoul 9.9 (+0.18%) 6.5 (-1.71%) 9.0 (-0.38%)
Singapore 15.5 (-0.42%) 10.2 (-0.80%) 8.7 (+0.02%)
Taiwan 14.4 (+0.24%) 9.8 (+0.04%) 24.2 (+1.37%)
Mean 11.4 (+0.12%) 8.9 (-0.06%) 10.6 (+0.18%)

ACKNOWLEDGMENTS

The authors' research relevant to this article has been supported by Research Grants Council of the Hong Kong Special Administrative Region CUHK 4512/06M and CUHK 477110.

Notes

There are no financial or other issues that might lead to conflict of interest.

References

1. von Mutius E. The rising trends in asthma and allergic disease. Clin Exp Allergy. 1998; 28:Suppl 5. 45–49. discussion 50-1.
2. Chinn S, Jarvis D, Burney P, Luczynska C, Ackermann-Liebrich U, Antó JM, Cerveri I, De Marco R, Gislason T, Heinrich J, Janson C, Künzli N, Leynaert B, Neukirch F, Schouten J, Sunyer J, Svanes C, Vermeire P, Wjst M. Increase in diagnosed asthma but not in symptoms in the European Community Respiratory Health Survey. Thorax. 2004; 59:646–651.
3. Strachan D, Sibbald B, Weiland S, Aït-Khaled N, Anabwani G, Anderson HR, Asher MI, Beasley R, Björkstén B, Burr M, Clayton T, Crane J, Ellwood P, Keil U, Lai C, Mallol J, Martinez F, Mitchell E, Montefort S, Pearce N, Robertson C, Shah J, Stewart A, von Mutius E, Williams H. Worldwide variations in prevalence of symptoms of allergic rhinoconjunctivitis in children: the International Study of Asthma and Allergies in Childhood (ISAAC). Pediatr Allergy Immunol. 1997; 8:161–176.
4. The International Study of Asthma and Allergies in Childhood (ISAAC) Steering Committee. Worldwide variation in prevalence of symptoms of asthma, allergic rhinoconjunctivitis, and atopic eczema: ISAAC. Lancet. 1998; 351:1225–1232.
5. Worldwide variations in the prevalence of asthma symptoms: the International Study of Asthma and Allergies in Childhood (ISAAC). Eur Respir J. 1998; 12:315–335.
6. Lewis S. ISAAC--a hypothesis generator for asthma? International Study of Asthma and Allergies in Childhood. Lancet. 1998; 351:1220–1221.
7. Enarson DA. Fostering a spirit of critical thinking: the ISAAC story. Int J Tuberc Lung Dis. 2005; 9:1.
8. Burney PG, Luczynska C, Chinn S, Jarvis D. The European Community Respiratory Health Survey. Eur Respir J. 1994; 7:954–960.
9. Sterk PJ, Buist SA, Woolcock AJ, Marks GB, Platts-Mills TA, von Mutius E, Bousquet J, Frew AJ, Pauwels RA, Aït-Khaled N, Hill SL, Partridge MR. The message from the World Asthma Meeting. The Working Groups of the World Asthma Meeting, held in Barcelona, Spain, December 9-13, 1998. Eur Respir J. 1999; 14:1435–1453.
10. Asher MI, Keil U, Anderson HR, Beasley R, Crane J, Martinez F, Mitchell EA, Pearce N, Sibbald B, Stewart AW, Strachan D, Weiland SK, Williams HC. International Study of Asthma and Allergies in Childhood (ISAAC): rationale and methods. Eur Respir J. 1995; 8:483–491.
11. Jenkins MA, Clarke JR, Carlin JB, Robertson CF, Hopper JL, Dalton MF, Holst DP, Choi K, Giles GG. Validation of questionnaire and bronchial hyperresponsiveness against respiratory physician assessment in the diagnosis of asthma. Int J Epidemiol. 1996; 25:609–616.
12. Lai CK, Chan JK, Chan A, Wong G, Ho A, Choy D, Lau J, Leung R. Comparison of the ISAAC video questionnaire (AVQ3.0) with the ISAAC written questionnaire for estimating asthma associated with bronchial hyperreactivity. Clin Exp Allergy. 1997; 27:540–545.
13. Crane J, Mallol J, Beasley R, Stewart A, Asher MI. International Study of Asthma and Allergies in Childhood Phase I study group. Agreement between written and video questions for comparing asthma symptoms in ISAAC. Eur Respir J. 2003; 21:455–461.
14. Flohr C, Weinmayr G, Weiland SK, Addo-Yobo E, Annesi-Maesano I, Björkstén B, Bråbäck L, Büchele G, Chico M, Cooper P, Clausen M, El Sharif N, Martinez Gimeno A, Mathur RS, von Mutius E, Morales Suarez-Varela M, Pearce N, Svabe V, Wong GW, Yu M, Zhong NS, Williams HC. ISAAC Phase Two Study Group. How well do questionnaires perform compared with physical examination in detecting flexural eczema? Findings from the International Study of Asthma and Allergies in Childhood (ISAAC) Phase Two. Br J Dermatol. 2009; 161:846–853.
15. Strina A, Barreto ML, Cunha S, de Fátima S P de Oliveira M, Moreira SC, Williams HC, Rodrigues LC. Validation of epidemiological tools for eczema diagnosis in Brazilian children: the ISAAC's and UK Working Party's criteria. BMC Dermatol. 2010; 10:11.
16. Kim H, Levin L, LeMasters GK, Villareal M, Evans S, Lockey JE, Khurana Hershey GK, Bernstein DI. Validating childhood symptoms with physician-diagnosed allergic rhinitis. Ann Allergy Asthma Immunol. 2012; 108:228–231.
17. Beasley R, Ellwood P, Asher I. International patterns of the prevalence of pediatric asthma the ISAAC program. Pediatr Clin North Am. 2003; 50:539–553.
18. Pearce N, Douwes J. The global epidemiology of asthma in children. Int J Tuberc Lung Dis. 2006; 10:125–132.
19. Robertson CF, Roberts MF, Kappers JH. Asthma prevalence in Melbourne schoolchildren: have we reached the peak? Med J Aust. 2004; 180:273–276.
20. García-Marcos L, Quirós AB, Hernández GG, Guillén-Grima F, Díaz CG, Ureña IC, Pena AA, Monge RB, Suárez-Varela MM, Varela AL, Cabanillas PG, Garrido JB. Stabilization of asthma prevalence among adolescents and increase among schoolchildren (ISAAC phases I and III) in Spain. Allergy. 2004; 59:1301–1307.
21. Anderson HR, Ruggles R, Strachan DP, Austin JB, Burr M, Jeffs D, Standring P, Steriu A, Goulding R. Trends in prevalence of symptoms of asthma, hay fever, and eczema in 12-14 year olds in the British Isles, 1995-2002: questionnaire survey. BMJ. 2004; 328:1052–1053.
22. Douwes J, Pearce N. Asthma and the westernization 'package'. Int J Epidemiol. 2002; 31:1098–1102.
23. Wong GW, von Mutius E, Douwes J, Pearce N. Environmental determinants associated with the development of asthma in childhood. Int J Tuberc Lung Dis. 2006; 10:242–251.
24. Pearce N, Pekkanen J, Beasley R. How much asthma is really attributable to atopy? Thorax. 1999; 54:268–272.
25. Le Souëf PN. Variations in genetic influences on the development of asthma throughout childhood, adolescence and early adult life. Curr Opin Allergy Clin Immunol. 2006; 6:317–322.
26. Asher MI, Montefort S, Björkstén B, Lai CK, Strachan DP, Weiland SK, Williams H. ISAAC Phase Three Study Group. Worldwide time trends in the prevalence of symptoms of asthma, allergic rhinoconjunctivitis, and eczema in childhood: ISAAC Phases One and Three repeat multicountry cross-sectional surveys. Lancet. 2006; 368:733–743.
27. Pearce N, Aït-Khaled N, Beasley R, Mallol J, Keil U, Mitchell E, Robertson C. the ISAAC Phase Three Study Group. Worldwide trends in the prevalence of asthma symptoms: phase III of the International Study of Asthma and Allergies in Childhood (ISAAC). Thorax. 2007; 62:758–766.
28. Björkstén B, Clayton T, Ellwood P, Stewart A, Strachan D. ISAAC Phase III Study Group. Worldwide time trends for symptoms of rhinitis and conjunctivitis: Phase III of the International Study of Asthma and Allergies in Childhood. Pediatr Allergy Immunol. 2008; 19:110–124.
29. Lai CK, De Guia TS, Kim YY, Kuo SH, Mukhopadhyay A, Soriano JB, Trung PL, Zhong NS, Zainudin N, Zainudin BM. Asthma Insights and Reality in Asia-Pacific Steering Committee. Asthma control in the Asia-Pacific region: the Asthma Insights and Reality in Asia-Pacific Study. J Allergy Clin Immunol. 2003; 111:263–268.
30. Rabe KF, Adachi M, Lai CK, Soriano JB, Vermeire PA, Weiss KB, Weiss ST. Worldwide severity and control of asthma in children and adults: the global asthma insights and reality surveys. J Allergy Clin Immunol. 2004; 114:40–47.
31. Nathan RA, Meltzer EO, Blaiss MS, Murphy KR, Doherty DE, Stoloff SW. Comparison of the Asthma in America and Asthma Insight and Management surveys: did asthma burden and care improve in the United States between 1998 and 2009? Allergy Asthma Proc. 2012; 33:65–76.
32. Zainudin BM, Lai CK, Soriano JB, Jia-Horng W, De Guia TS. Asthma Insights and Reality in Asia-Pacific (AIRIAP) Steering Committee. Asthma control in adults in Asia-Pacific. Respirology. 2005; 10:579–586.
33. Wong GW, Leung TF, Fok TF. ISAAC and risk factors for asthma in the Asia-Pacific. Paediatr Respir Rev. 2004; 5:Suppl A. S163–S169.
34. Leung TF, Wong GW. The Asian side of asthma and allergy. Curr Opin Allergy Clin Immunol. 2008; 8:384–390.
35. Hsieh KH, Shen JJ. Prevalence of childhood asthma in Taipei, Taiwan, and other Asian Pacific countries. J Asthma. 1988; 25:73–82.
36. Norzila MZ, Haifa AL, Deng CT, Azizi BH. Prevalence of childhood asthma and allergy in an inner city Malaysian community: intra-observer reliability of two translated international questionnaires. Med J Malaysia. 2000; 55:33–39.
37. Trakultivakorn M, Sangsupawanich P, Vichyanond P. Time trends of the prevalence of asthma, rhinitis and eczema in Thai children-ISAAC (International Study of Asthma and Allergies in Childhood) Phase Three. J Asthma. 2007; 44:609–611.
38. Wong GW, Hui DS, Chan HH, Fok TF, Leung R, Zhong NS, Chen YZ, Lai CK. Prevalence of respiratory and atopic disorders in Chinese schoolchildren. Clin Exp Allergy. 2001; 31:1225–1231.
39. Fok AO, Wong GW. What have we learnt from ISAAC phase III in the Asia-Pacific rim? Curr Opin Allergy Clin Immunol. 2009; 9:116–122.
40. Wong GW, Ko FW, Hui DS, Fok TF, Carr D, von Mutius E, Zhong NS, Chen YZ, Lai CK. Factors associated with difference in prevalence of asthma in children from three cities in China: multicentre epidemiological survey. BMJ. 2004; 329:486.
41. Asher MI, Montefort S, Björkstén B, Lai CK, Strachan DP, Weiland SK, Williams H. ISAAC Phase Three Study Group. Worldwide time trends in the prevalence of symptoms of asthma, allergic rhinoconjunctivitis, and eczema in childhood: ISAAC Phases One and Three repeat multicountry cross-sectional surveys. Lancet. 2006; 368:733–743.
42. Katelaris CH, Lai CK, Rhee CS, Lee SH, Yun WD, Lim-Varona L, Quang VT, Hwang J, Singh H, Kim J, Boyle JM, Dhong HJ, Narayanan P, Vicente G, Blaiss M, Sacks R. Nasal allergies in the Asian-Pacific population: results from the Allergies in Asia-Pacific Survey. Am J Rhinol Allergy. 2011; 25:Suppl 1. S3–S15.
43. Brozek JL, Bousquet J, Baena-Cagnani CE, Bonini S, Canonica GW, Casale TB, van Wijk RG, Ohta K, Zuberbier T, Schünemann HJ. Global Allergy and Asthma European Network. Grading of Recommendations Assessment, Development and Evaluation Working Group. Allergic Rhinitis and its Impact on Asthma (ARIA) guidelines: 2010 revision. J Allergy Clin Immunol. 2010; 126:466–476.
44. Pearce N, Douwes J. Commentary: asthma time trends--mission accomplished? Int J Epidemiol. 2005; 34:1018–1019.
45. Janson C, Anto J, Burney P, Chinn S, de Marco R, Heinrich J, Jarvis D, Kuenzli N, Leynaert B, Luczynska C, Neukirch F, Svanes C, Sunyer J, Wjst M. European Community Respiratory Health Survey II. The European Community Respiratory Health Survey: what are the main results so far? European Community Respiratory Health Survey II. Eur Respir J. 2001; 18:598–611.
46. Sporik R, Chapman MD, Platts-Mills TA. House dust mite exposure as a cause of asthma. Clin Exp Allergy. 1992; 22:897–906.
47. Leung R, Ho P. Asthma, allergy, and atopy in three south-east Asian populations. Thorax. 1994; 49:1205–1210.
48. Zöllner IK, Weiland SK, Piechotowski I, Gabrio T, von Mutius E, Link B, Pfaff G, Kouros B, Wuthe J. No increase in the prevalence of asthma, allergies, and atopic sensitisation among children in Germany: 1992-2001. Thorax. 2005; 60:545–548.
49. Illi S, von Mutius E, Lau S, Nickel R, Niggemann B, Sommerfeld C, Wahn U. Multicenter Allergy Study Group. The pattern of atopic sensitization is associated with the development of asthma in childhood. J Allergy Clin Immunol. 2001; 108:709–714.
50. Cullinan P, MacNeill SJ, Harris JM, Moffat S, White C, Mills P, Newman Taylor AJ. Early allergen exposure, skin prick responses, and atopic wheeze at age 5 in English children: a cohort study. Thorax. 2004; 59:855–861.
51. Wong GW, Ko FW, Lau TS, Li ST, Hui D, Pang SW, Leung R, Fok TF, Lai CK. Temporal relationship between air pollution and hospital admissions for asthmatic children in Hong Kong. Clin Exp Allergy. 2001; 31:565–569.
52. Garty BZ, Kosman E, Ganor E, Berger V, Garty L, Wietzen T, Waisman Y, Mimouni M, Waisel Y. Emergency room visits of asthmatic children, relation to air pollution, weather, and airborne allergens. Ann Allergy Asthma Immunol. 1998; 81:563–570.
53. Wong GW, Li ST, Hui DS, Fok TF, Zhong NS, Chen YZ, Lai CK. Individual allergens as risk factors for asthma and bronchial hyperresponsiveness in Chinese children. Eur Respir J. 2002; 19:288–293.
54. Romagnani S. The increased prevalence of allergy and the hygiene hypothesis: missing immune deviation, reduced immune suppression, or both? Immunology. 2004; 112:352–363.
55. Strachan DP. Family size, infection and atopy: the first decade of the "hygiene hypothesis". Thorax. 2000; 55:Suppl 1. S2–S10.
56. Woodfolk JA, Platts-Mills TA. The immune response to intrinsic and extrinsic allergens: determinants of allergic disease. Int Arch Allergy Immunol. 2002; 129:277–285.
57. Wong GW, Chow CM. Childhood asthma epidemiology: insights from comparative studies of rural and urban populations. Pediatr Pulmonol. 2008; 43:107–116.
58. Von Ehrenstein OS, Von Mutius E, Illi S, Baumann L, Böhm O, von Kries R. Reduced risk of hay fever and asthma among children of farmers. Clin Exp Allergy. 2000; 30:187–193.
59. Kilpeläinen M, Terho EO, Helenius H, Koskenvuo M. Farm environment in childhood prevents the development of allergies. Clin Exp Allergy. 2000; 30:201–208.
60. Krämer U, Heinrich J, Wjst M, Wichmann HE. Age of entry to day nursery and allergy in later childhood. Lancet. 1999; 353:450–454.
61. Ball TM, Castro-Rodriguez JA, Griffith KA, Holberg CJ, Martinez FD, Wright AL. Siblings, day-care attendance, and the risk of asthma and wheezing during childhood. N Engl J Med. 2000; 343:538–543.
62. Salvi SS, Babu KS, Holgate ST. Is asthma really due to a polarized T cell response toward a helper T cell type 2 phenotype? Am J Respir Crit Care Med. 2001; 164:1343–1346.
63. von Mutius E, Braun-Fahrländer C, Schierl R, Riedler J, Ehlermann S, Maisch S, Waser M, Nowak D. Exposure to endotoxin or other bacterial components might protect against the development of atopy. Clin Exp Allergy. 2000; 30:1230–1234.
64. Braun-Fahrländer C, Gassner M, Grize L, Neu U, Sennhauser FH, Varonier HS, Vuille JC, Wüthrich B. Prevalence of hay fever and allergic sensitization in farmer's children and their peers living in the same rural community. SCARPOL team. Swiss Study on Childhood Allergy and Respiratory Symptoms with Respect to Air Pollution. Clin Exp Allergy. 1999; 29:28–34.
65. Ernst P, Cormier Y. Relative scarcity of asthma and atopy among rural adolescents raised on a farm. Am J Respir Crit Care Med. 2000; 161:1563–1566.
66. Waser M, Michels KB, Bieli C, Flöistrup H, Pershagen G, von Mutius E, Ege M, Riedler J, Schram-Bijkerk D, Brunekreef B, van Hage M, Lauener R, Braun-Fahrländer C. PARSIFAL Study team. Inverse association of farm milk consumption with asthma and allergy in rural and suburban populations across Europe. Clin Exp Allergy. 2007; 37:661–670.
67. Loss G, Apprich S, Waser M, Kneifel W, Genuneit J, Büchele G, Weber J, Sozanska B, Danielewicz H, Horak E, van Neerven RJ, Heederik D, Lorenzen PC, von Mutius E, Braun-Fahrländer C. GABRIELA study group. The protective effect of farm milk consumption on childhood asthma and atopy: the GABRIELA study. J Allergy Clin Immunol. 2011; 128:766–773.e4.
68. Ellwood P, Asher MI, Björkstén B, Burr M, Pearce N, Robertson CF. ISAAC Phase One Study Group. Diet and asthma, allergic rhinoconjunctivitis and atopic eczema symptom prevalence: an ecological analysis of the International Study of Asthma and Allergies in Childhood (ISAAC) data. Eur Respir J. 2001; 17:436–443.
69. Hanski I, von Hertzen L, Fyhrquist N, Koskinen K, Torppa K, Laatikainen T, Karisola P, Auvinen P, Paulin L, Mäkelä MJ, Vartiainen E, Kosunen TU, Alenius H, Haahtela T. Environmental biodiversity, human microbiota, and allergy are interrelated. Proc Natl Acad Sci U S A. 2012; 109:8334–8339.
70. Ege MJ, Mayer M, Normand AC, Genuneit J, Cookson WO, Braun-Fahrländer C, Heederik D, Piarroux R, von Mutius E. GABRIELA Transregio 22 Study Group. Exposure to environmental microorganisms and childhood asthma. N Engl J Med. 2011; 364:701–709.
71. Prescott S, Allen KJ. Food allergy: riding the second wave of the allergy epidemic. Pediatr Allergy Immunol. 2011; 22:155–160.
72. Koplin JJ, Tang ML, Martin PE, Osborne NJ, Lowe AJ, Ponsonby AL, Robinson MN, Tey D, Thiele L, Hill DJ, Gurrin LC, Wake M, Dharmage SC, Allen KJ. HealthNuts investigators. Predetermined challenge eligibility and cessation criteria for oral food challenges in the HealthNuts population-based study of infants. J Allergy Clin Immunol. 2012; 129:1145–1147.
73. Wong GW, Mahesh PA, Ogorodova L, Leung TF, Fedorova O, Holla AD, Fernandez-Rivas M, Clare Mills EN, Kummeling I, van Ree R, Yazdanbakhsh M, Burney P. The EuroPrevall-INCO surveys on the prevalence of food allergies in children from China, India and Russia: the study methodology. Allergy. 2010; 65:385–390.
74. Cookson W. Genetics and genomics of asthma and allergic diseases. Immunol Rev. 2002; 190:195–206.
75. Barnes KC. Genetic epidemiology of health disparities in allergy and clinical immunology. J Allergy Clin Immunol. 2006; 117:243–254. quiz 255-6.
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