Skip to main content

MINI REVIEW article

Front. Nutr., 13 June 2024
Sec. Nutrition and Food Science Technology
This article is part of the Research Topic Health, Science and Innovation for the Future of Food System View all 9 articles

Food allergies around the world

  • Department of Paediatrics, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, China

The increase in the prevalence of food allergy has been considered as the second wave in the allergy epidemic following the first wave of increase in asthma and allergic rhinitis. It is well known that the prevalence of allergic conditions would follow economic development and urbanization in many countries or regions. In developed countries, one in three children suffered from at least one allergic disorder and these conditions include food allergy, eczema, allergic rhinitis and asthma. Food allergy is very often the first allergic manifestation affecting infants and young children. The exact etiologies are not known. The clinical manifestations ranged from a simple rash or an itch around the mouth, to the more severe manifestations of angioedema and potentially fatal anaphylaxis. Among all cases of childhood anaphylaxis, food is the most common cause. The common allergens resulting in food allergies in developed countries include egg, milk, fish, wheat, peanuts and tree nuts. However, there are marked variations in the patterns of food allergens in developing countries. In line with the epidemiology of asthma, food allergy is also much less common in rural areas. Clear understanding of reasons explaining the disparity of food allergies between urban and rural population would pave the way to the development of effective primary prevention for food allergy.

Introduction

The first wave of the allergy epidemic began more than 50 years ago with the increase in the prevalence of asthma and allergic rhinitis. Food allergy has been considered as the second wave of the allergy epidemic started about 20 years ago. Similar to the epidemiology of asthma, countries with high prevalence rates of asthma were also found to have higher prevalence of food allergy (1, 2). Although there have been many epidemiology studies of food allergies around the world, accurate determination of the true prevalence of food allergies is very difficult. Most published studies have only used questionnaires to ascertain possible allergic symptoms related to food allergies, and only a small proportion of studies included objective testing such as skin prick test, serum specific IgE measurements or food challenge (3). The lack of objective testing and use of different methodologies make comparison of the data from different published epidemiology studies very difficult. Nevertheless, the patterns of food allergies appeared to be different across the world (2). Early guidelines from many countries recommended dietary avoidance or delayed introduction of allergenic foods especially in high risk infants. However, there have been several prospective randomized trials showing that early introduction of allergenic foods may be beneficial in preventing food allergies (4, 5). Subsequently, guidelines from around the world now recommend early introduction rather than avoidance of allergenic foods in infancy (6, 7). The continuing changes in the environment including dietary changes will shape the epidemiology of food allergies around the world. Clear understanding of how these environmental factors interact with the immune system resulting in the manifestations of food allergies will lead to development of effective primary preventive strategies.

Epidemiology of food allergy

Food allergy is defined as an adverse health effect due to a specific immune response that reproducibly occurs upon exposure to a specific food. Such adverse effects can be sub-divided in to two major types, IgE-mediated or non-IgE-mediated. Over the past few decades, there have been many epidemiology studies of food allergy around the world, and most of these studies evaluated the IgE-mediated type of food allergy using non-standardized methodologies (3, 8). Due to the complexity of evaluation of serum IgE in large-scale population studies, most published studies have only used questionnaires to evaluate the symptoms of food allergy without objective testing. However, many other diseases may have symptoms mimicking those of true food allergies. Studies using only questionnaires frequently overestimated the true prevalence of food allergy. Furthermore, the lack of standardization of various studies made comparison of the results difficult, if not impossible. Nevertheless, the prevalence rates and the patterns of food allergens appeared to be widely different across the world (2, 9, 10).

The most common food allergens include cow’s milk, wheat, egg, peanuts, shellfish, fish, soy, and tree nuts. In some parts of the world such as some Asian countries, other exotic allergens such as insects and bird’s nest can also induce food allergies (2). A telephone survey conducted across 10 European countries revealed a wide variation in the prevalence of food allergy among children in these countries. In this study, parents or guardians were interviewed to ascertain possible symptoms of food allergies of their children (11). Finland was found to have the highest reported prevalence of 11.7% while Austria was lowest at 1.7%. Cow’s milk, fruits, and egg were the top three most common offending foods. The European Community Respiratory Health Survey also revealed a wide variation of symptoms of adverse food reactions in European adults. The highest rate was reported in Melbourne, Australia, while it was lowest at 4.6% in Spain (12). A meta-analysis of 51 studies across the world revealed marked variations of the prevalence of food allergies ranging from 3 to 35% (3). However, the average prevalence rate of food allergy was only 3% if only studies with objective testing were included. These findings suggest marked over-estimation of the true prevalence by studies using questionnaires only. Food allergy has been reported to be common in the United States, affecting up to 8% of children and 10% adults. These studies were based on questionnaires only and might potentially overestimated the true prevalence (13, 14). The HealthNuts study from Melbourne, Australia used food challenge to document true food allergies. These Australian infants had a very high prevalence of food allergies (3% to peanuts, 8.9% to raw egg) (15).

In the past two decades, exposure to rural environments has been persistently documented to be a major protective factors against the development of allergies (16). Food allergy is no exception. A comparative study using both questionnaire and skin prick test were conducted in South Africa to evaluate the prevalence of allergic diseases in both urban and rural children (17). A total of 1,185 urban and 398 rural toddlers aged 12–36 months were recruited for this study. The prevalence of food allergy was 2.3% in the urban population while it was only 0.5% in the rural population. The recent EuorPrevall-INCO study evaluate a large sample of 35,549 school children from China, Russia, and India using standardized questionnaires along with skin prick test and serum specific IgE measurement demonstrated that children from the highly urbanized city of Hong Kong had a prevalence of food allergy 3 times higher than those of children from mainland China (10). Furthermore, among children recruited from Hong Kong, those born and raised in Hong Kong had a prevalence of food allergy three times higher than those children born in mainland China and subsequently migrated to Hong Kong. Given the same genetic background of these two groups of children, early life exposures most likely have affected the early development of the immune system leading to differences in the subsequent manifestations of food allergy. A recent comparative study also demonstrated that Asians born in Australia had markedly higher prevalence of food allergy when compared to Asians from Singapore (18, 19). Many factors may potentially be important in explaining the disparity, and the potential factors are summarized in Table 1. Further studies are needed to evaluate how various environmental exposures and dietary factors might influence the early maturation of the immune system resulting in protection against the development of food allergy.

Table 1
www.frontiersin.org

Table 1. Potential factors associated with the development of food allergy.

Spectrum of food allergic reactions

The manifestations of food allergy vary widely from a very mild itch or redness on the skin, urticaria affecting a large area on the body, sneezing, itchy and watery eyes to the more severe symptoms such as difficulty with breathing and hypotension (19). Pollen-food allergy syndrome is a specific type of food allergy when the primary sensitizer is pollen such as birch pollen (20).

Due to similarity to other allergens found in fruits and vegetables, binding of the food allergens with the cross-reacting IgE would result in various symptoms of food allergy. The mildest form of pollen-food allergy syndrome typically associated with symptoms including itchy mouth, swelling of the lips and tongue. Such mild reaction is termed oral allergy syndrome, but more severe reactions including anaphylaxis can occur in patients with pollen-food allergy syndrome. Anaphylaxis is the most severe manifestation of food allergy, and appropriate treatment must be provided promptly to prevent mortality. Hospital admission data from across the world in the past 2 decades revealed significant increase in the number of food induced anaphylaxis admitted to hospitals in the United Kingdom, USA, Australia and Hong Kong (2124). The increase was found to be highest in Australian children under 4 years of age. From 1998 to 2012, the Australian hospital admission rate due to food induced anaphylaxis in children under 4 years has increased from 7.3 to 21.7 per 100,000 per year (21). Hospital admission data from Hong Kong also showed a doubling of anaphylaxis admission in 2019 when compared with data in 2009 (24). In order to optimize the clinical care of patients with food allergy, appropriate counseling of patients at risk for development of severe food allergic reactions is extremely important. However, there are no reliable features that can accurately predict the severity of food allergy. Many studies have showed that prior anaphylaxis was not a good predictor of the future risk. In fact, fatality associated with food induced anaphylaxis often occurred in patients with only prior mild reactions. Many co-factors are known to be associated with more severe reactions, such as concomitant poorly controlled asthma, medications (ACE inhibitor, beta-blockers), febrile illness, and menstruation (25, 26). Exercise is a well-known trigger typically associated with wheat allergy due to IgE sensitization to omega-5-gliadin (27). These patients usually can tolerate a small dose of wheat, but exercise would dramatically reduce the threshold and result in severe reactions. Due to the limitation of accurate prediction of severe reactions, all patients with food allergy should be educated to recognize and manage severe food allergic reactions. Although many different foods can result in food allergic reactions, they tend to differ in different regions of the world. In Europe, North America, and Australia, peanut, tree nuts, and cow’s milk are the most common foods resulting in food induced anaphylaxis while shellfish and seafood are more common in Asia and Latin America (2, 25). The exact reasons explaining such differences in the pattern of food allergens are not clear. In Hong Kong, shrimp has been found to be the most common food resulting in anaphylaxis seen in the emergency department (28). However, variations of environmental factors and dietary exposures are likely important in causing some of the differences. In rural China, cockroach has been found to be a major cross-reactive allergen source in shrimp-sensitized children (29). Further studies are needed to clearly understand how environmental exposures may influence the manifestations of food allergy in different parts of the world.

Recent development and updates of food allergy guidelines

Allergen avoidance, whether during pregnancy or in early infancy, has been thought to be useful in reducing the risk of sensitization, and hence the risk of allergy. In the past, many guidelines from around the world recommended a variety of avoidance measures during pregnancy or in early infancy especially for high risk infants (3032). For example, it was recommended that infants should avoid egg and milk for the first year of life, and peanuts, tree nuts, shellfish till 2–4 years of age. However, recent randomized controlled trials have documented that avoidance of food allergens during pregnancy could not reduce the risk of food allergy in their offspring. Furthermore, there have been several prospective randomized clinical trials testing whether food avoidance in early infancy was effective in preventing subsequent food allergies (4, 5). The Learning Early About Peanut (LEAP) trial recruited 640 high risk infants and randomized them to consume 6 g of peanut protein weekly or to avoid peanuts for the first 5 years of life (4). At 5 years of age, peanut allergy documented by food challenge in the avoidance group was 17.2% as compared with the 3.2% in the intervention group. In the Enquiry About Tolerance (EAT) study, more than 1,300 infants were recruited and randomized to introduction of six allergenic foods (peanut, egg, cow’s milk, sesame, fish, and wheat) starting at 6 month of age (5). The children were followed up till 3 years of age for assessment of possible food allergy to the six allergenic foods. In the per-protocol analysis, the primary outcome was significantly lower in the early introduction group (2.4%) than in the standard-introduction group (7.3%), but the difference was not significantly different in the intention-to-treat analysis. Adherence to this challenging protocol was very low at 42.8% as many parents found it very difficult to feed so many different types of solid foods to their young infants. These clinical trials clearly demonstrated that early consumption rather than delayed introduction was likely more beneficial as primary preventive strategy. Since the publication of these clinical trials, guidelines from around the world have been updated to recommend early introduction of allergenic food at around 6 months of age, and maternal dietary restrictions during pregnancy are no longer recommended (6, 7).

The remaining question is how to translate these trial findings into the real world. A recent study from Australia has been conducted comparing the prevalence of peanut allergy in one-year-old infants before and 2 years after the guideline recommendation was changed (33). A total of 7,209 infants were recruited with 1933 in 2018–2019 and 5,276 in 2007–2011. Despite earlier introduction of peanut in the later cohort, there was no significant change in the prevalence of peanut allergy across this population. Further studies are needed to determine how to introduce allergenic foods early in infants in the community level, and evaluate other potential environmental factors which may affect the manifestation of food allergy. One should also note that the prevalence of peanut allergy is extremely rare in many Asian countries such as Thailand and China (10). A birth cohort from Singapore documented a very low prevalence of food allergy despite rather late introduction of allergenic foods (34). Therefore, a consensus statement from the Asia Pacific Academy of Pediatric Allergy, Respirology & Immunology recommends that it is not necessary to delay introduction of solids, but more studies are needed to determine the role of early introduction of various allergenic foods in populations with a very low background prevalence of food allergy (35).

Discussion

There is no doubt that food allergy is becoming a major problem especially in the developed countries such as United Kingdom, United States, and Australia in the past two decades. The exact reasons driving the increase in the prevalence are not clear. Evidence is building up that early consumption as opposed to delayed introduction may be a more effective approach to prevent the subsequent development of food allergy. On the other hand, there are potentially many lessons we can learn from countries where the background prevalence of food allergy is very low, and yet early introduction of allergenic foods in these countries is not the norm. Similar to the manifestations of other atopic conditions such as asthma or allergic rhinitis, the development of food allergy is the result of the complex interactions between environmental exposures and genetic influences. The disparity of food allergy in populations with the same genetic background brought up in different environments clearly illustrates the importance of environmental exposures which include dietary variations in shaping the development of food allergy. Clear understanding of the underlying reasons explaining the variations of food allergy epidemiology around the world will provide clues for developing effective primary preventive strategies.

Author contributions

GW-KW: Conceptualization, Formal analysis, Funding acquisition, Methodology, Writing – original draft, Writing – review & editing.

Funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.

Conflict of interest

The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Sigurdardottir, ST, Jonasson, K, Clausen, M, Lilja Bjornsdottir, K, Sigurdardottir, SE, Roberts, G, et al. Prevalence and early-life risk factors of school-age allergic multimorbidity: the euro Prevall-iFAAM birth cohort. Allergy. (2021) 76:2855–65. doi: 10.1111/all.14857

PubMed Abstract | Crossref Full Text | Google Scholar

2. Sampath, V, Abrams, EM, Adlou, B, Akdis, C, Akdis, M, Brough, HA, et al. Food allergy across the globe. J Allergy Clin Immunol. (2021) 148:1347–64. doi: 10.1016/j.jaci.2021.10.018

PubMed Abstract | Crossref Full Text | Google Scholar

3. Rona, RJ, Keil, T, Summers, C, Gislason, D, Zuidmeer, L, Sodergren, E, et al. The prevalence of food allergy: a meta-analysis. J Allergy Clin Immunol. (2007) 120:638–46. doi: 10.1016/j.jaci.2007.05.026

Crossref Full Text | Google Scholar

4. Du Toit, G, Roberts, G, Sayre, PH, Bahnson, HT, Radulovic, S, Santos, AF, et al. Randomized trial of peanut consumption in infants at risk for peanut allergy. N Engl J Med. (2015) 372:803–13. doi: 10.1056/NEJMoa1414850

PubMed Abstract | Crossref Full Text | Google Scholar

5. Perkin, MR, Logan, K, Tseng, A, Raji, B, Ayis, S, Peacock, J, et al. Randomized trial of introduction of allergenic foods in breast-fed infants. N Engl J Med. (2016) 374:1733–43. doi: 10.1056/NEJMoa1514210

PubMed Abstract | Crossref Full Text | Google Scholar

6. Halken, S, Muraro, A, de Silva, D, Khaleva, E, Angier, E, Arasi, S, et al. European academy of allergy and clinical immunology food allergy and anaphylaxis guidelines group. EAACI guideline: preventing the development of food allergy in infants and young children (2020 update). Pediatr Allergy Immunol. (2021) 32:843–58. doi: 10.1111/pai.13496

PubMed Abstract | Crossref Full Text | Google Scholar

7. Fleischer, DM, Sicherer, S, Greenhawt, M, Campbell, D, Chan, E, Muraro, A, et al. Consensus communication on early peanut introduction and the prevention of peanut allergy in high risk infants. J Allergy Clin Immunol. (2015) 136:258–61. doi: 10.1016/j.jaci.2015.06.001

PubMed Abstract | Crossref Full Text | Google Scholar

8. Wong, GW, Mahesh, PA, Ogorodova, L, Leung, TF, Fedorova, O, Holla, AD, et al. The euro Prevall-INCO surveys on the prevalence of food allergies in children from China, India and Russia: the study methodology. Allergy. (2010) 65:385–90. doi: 10.1111/j.1398-9995.2009.02214.x

PubMed Abstract | Crossref Full Text | Google Scholar

9. Fu, W, Zheng, Z, Zhao, J, Feng, M, Xian, M, Wei, N, et al. Allergic disease and sensitization disparity in urban and rural China: a euro Prevall-INCO study. Pediatr Allergy Immunol. (2022) 33:e13903. doi: 10.1111/pai.13903

PubMed Abstract | Crossref Full Text | Google Scholar

10. Li, J, Ogorodova, LM, Mahesh, PA, Wang, MH, Fedorova, OS, Leung, TF, et al. Comparative study of food allergies in children from China, India, and Russia: the euro Prevall-INCO surveys. J Allergy Clin Immunol Pract. (2020) 8:1349–1358.e16. doi: 10.1016/j.jaip.2019.11.042

PubMed Abstract | Crossref Full Text | Google Scholar

11. Steinke, M, Fiocchi, A, Kirchlechner, V, Ballmer-Weber, B, Brockow, K, Hischenhuber, C, et al. Perceived food allergy in children in 10 European nations. A randomized telephone survey. Int Arch Allergy Immunol. (2007) 143:290–5. doi: 10.1159/000100575

PubMed Abstract | Crossref Full Text | Google Scholar

12. Woods, RK, Abramson, M, Bailey, M, and Walters, EH. International prevalences of reported food allergies and intolerances. Comparisons arising from the European Community respiratory health survey (ECRHS) 1991-1994. Eur J Clin Nutr. (2001) 55:298–304. doi: 10.1038/sj.ejcn.1601159

PubMed Abstract | Crossref Full Text | Google Scholar

13. Gupta, RS, Warren, CM, Smith, BM, Jiang, J, Blumenstock, JA, Davis, MM, et al. Prevalence and severity of food allergies among US adults. JAMA Netw Open. (2019) 2:e185630. doi: 10.1001/jamanetworkopen.2018.5630

PubMed Abstract | Crossref Full Text | Google Scholar

14. Gupta, RS, Warren, CM, Smith, BM, Blumenstock, JA, Jiang, J, Davis, MM, et al. The public health impact of parent-reported childhood food allergies in the United States. Pediatrics. (2018) 142:e20181235. doi: 10.1542/peds.2018-1235

PubMed Abstract | Crossref Full Text | Google Scholar

15. Osborne, NJ, Koplin, JJ, Martin, PE, Gurrin, LC, Lowe, AJ, Matheson, MC, et al. Health nuts investigators. Prevalence of challenge-proven IgE-mediated food allergy using population-based sampling and predetermined challenge criteria in infants. J Allergy Clin Immunol. (2011) 127:668–676.e2. doi: 10.1016/j.jaci.2011.01.039

PubMed Abstract | Crossref Full Text | Google Scholar

16. Schröder, PC, Li, J, Wong, GW, and Schaub, B. The rural–urban enigma of allergy: what can we learn from studies around the world? Pediatr Allergy Immunol. (2015) 26:95–102. doi: 10.1111/pai.12341

PubMed Abstract | Crossref Full Text | Google Scholar

17. Botha, M, Basera, W, Facey-Thomas, HE, Gaunt, B, Genuneit, J, Gray, CL, et al. Nutrition and allergic diseases in urban and rural communities from the south African food allergy cohort. Pediatr Allergy Immunol. (2019) 30:511–21. doi: 10.1111/pai.13058

PubMed Abstract | Crossref Full Text | Google Scholar

18. Suaini, NHA, Loo, EX, Peters, RL, Yap, GC, Allen, KJ, Van Bever, H, et al. Children of Asian ethnicity in Australia have higher risk of food allergy and early-onset eczema than those in Singapore. Allergy. (2021) 76:3171–82. doi: 10.1111/all.14823

PubMed Abstract | Crossref Full Text | Google Scholar

19. Sicherer, SH, Warren, CM, Dant, C, Gupta, RS, and Nadeau, KC. Food allergy from infancy through adulthood. J Allergy Clin Immunol Pract. (2020) 8:1854–64. doi: 10.1016/j.jaip.2020.02.010

PubMed Abstract | Crossref Full Text | Google Scholar

20. Carlson, G, and Coop, C. Pollen food allergy syndrome (PFAS): a review of current available literature. Ann Allergy Asthma Immunol. (2019) 123:359–65. doi: 10.1016/j.anai.2019.07.022

PubMed Abstract | Crossref Full Text | Google Scholar

21. Mullins, RJ, Dear, KB, and Tang, ML. Time trends in Australian hospital anaphylaxis admissions in 1998-1999 to 2011-2012. J Allergy Clin Immunol. (2015) 136:367–75. doi: 10.1016/j.jaci.2015.05.009

PubMed Abstract | Crossref Full Text | Google Scholar

22. Dribin, TE, Motosue, MS, and Campbell, RL. Overview of allergy and anaphylaxis. Immunol Allergy Clin N Am. (2023) 43:435–51. doi: 10.1016/j.iac.2022.10.009

PubMed Abstract | Crossref Full Text | Google Scholar

23. Baseggio Conrado, A, Ierodiakonou, D, Gowland, MH, Boyle, RJ, and Turner, PJ. Food anaphylaxis in the United Kingdom: analysis of national data, 1998-2018. BMJ. (2021) 372:n251. doi: 10.1136/bmj.n251

Crossref Full Text | Google Scholar

24. Leung, ASY, Li, RMY, Au, AWS, Rosa Duque, JS, Ho, PK, Chua, GT, et al. Changing pattern of pediatric anaphylaxis in Hong Kong, 2010-2019. Pediatr Allergy Immunol. (2022) 33:e13685. doi: 10.1111/pai.13685

PubMed Abstract | Crossref Full Text | Google Scholar

25. Turner, PJ, Arasi, S, Ballmer-Weber, B, Baseggio Conrado, A, Deschildre, A, Gerdts, J, et al. Risk factors for severe reactions in food allergy: rapid evidence review with metaanalysis. Allergy. (2022) 77:2634–52. doi: 10.1111/all.15318

PubMed Abstract | Crossref Full Text | Google Scholar

26. Bartra, J, Turner, PJ, and Muñoz-Cano, RM. Cofactors in food anaphylaxis in adults. Ann Allergy Asthma Immunol. (2023) 130:733–40. doi: 10.1016/j.anai.2023.03.017

PubMed Abstract | Crossref Full Text | Google Scholar

27. Foong, RX, Giovannini, M, and du Toit, G. Food-dependent exercise-induced anaphylaxis. Curr Opin Allergy Clin Immunol. (2019) 19:224–8. doi: 10.1097/ACI.0000000000000531

Crossref Full Text | Google Scholar

28. Smit, DV, Cameron, PA, and Rainer, TH. Anaphylaxis presentations to an emergency department in Hong Kong: incidence and predictors of biphasic reactions. J Emerg Med. (2005) 28:381–8. doi: 10.1016/j.jemermed.2004.11.028

PubMed Abstract | Crossref Full Text | Google Scholar

29. Yang, Z, Zhao, J, Wei, N, Feng, M, Xian, M, Shi, X, et al. Cockroach is a major cross-reactive allergen source in shrimp-sensitized rural children in southern China. Allergy. (2018) 73:585–92. doi: 10.1111/all.13341

PubMed Abstract | Crossref Full Text | Google Scholar

30. Fiocchi, A, Assa'ad, A, and Bahna, SAdverse reactions to foods committee; American College of Allergy, asthma and immunology. Food allergy and the introduction of solid foods to infants: a consensus document. Adverse reactions to foods committee American College of Allergy, asthma and immunology. Ann Allergy Asthma Immunol. (2006) 97:10–21. doi: 10.1016/S1081-1206(10)61364-6

Crossref Full Text | Google Scholar

31. Prescott, SL, and Tang, ML. Australasian Society of Clinical Immunology and Allergy. The Australasian Society of Clinical Immunology and Allergy position statement: summary of allergy prevention in children. Med J Aust. (2005) 182:464–7. doi: 10.5694/j.1326-5377.2005.tb06787.x

PubMed Abstract | Crossref Full Text | Google Scholar

32. Kramer, MS, and Kakuma, R. Maternal dietary antigen avoidance during pregnancy or lactation, or both, for preventing or treating atopic disease in the child. Cochrane Database Syst Rev. (2012) 2012:CD000133. doi: 10.1002/14651858.CD000133.pub3

Crossref Full Text | Google Scholar

33. Soriano, VX, Peters, RL, Moreno-Betancur, M, Ponsonby, AL, Gell, G, Odoi, A, et al. Association between earlier introduction of Peanut and prevalence of Peanut allergy in infants in Australia. JAMA. (2022) 328:48–56. doi: 10.1001/jama.2022.9224

PubMed Abstract | Crossref Full Text | Google Scholar

34. Tham, EH, Lee, BW, Chan, YH, Loo, EXL, Toh, JY, Goh, A, et al. Low food allergy prevalence despite delayed introduction of allergenic foods-data from the GUSTO cohort. J Allergy Clin Immunol Pract. (2018) 6:466–475.e1. doi: 10.1016/j.jaip.2017.06.001

PubMed Abstract | Crossref Full Text | Google Scholar

35. Tham, EH, Shek, LP, Van Bever, HP, Vichyanond, P, Ebisawa, M, Wong, GW, et al. Asia Pacific Association of Pediatric Allergy, Respirology & Immunology (APAPARI) early introduction of allergenic foods for the prevention of food allergy from an Asian perspective-an Asia Pacific Association of Pediatric Allergy, Respirology & Immunology (APAPARI) consensus statement. Pediatr Allergy Immunol. (2018) 29:18–27. doi: 10.1111/pai.12820

PubMed Abstract | Crossref Full Text | Google Scholar

Keywords: food allergy, risk factor, anaphylaxis, epidemiology, global

Citation: Wong GW-K (2024) Food allergies around the world. Front. Nutr. 11:1373110. doi: 10.3389/fnut.2024.1373110

Received: 19 January 2024; Accepted: 03 April 2024;
Published: 13 June 2024.

Edited by:

Melanie Charron, Soremartec Italia Srl, Italy

Reviewed by:

Linda Monaci, National Research Council (CNR), Italy

Copyright © 2024 Wong. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Gary Wing-Kin Wong, wingkinwong@cuhk.edu.hk

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.