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Geographical differences in food allergy

Geographische Unterschiede bei Nahrungsmittelallergien

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Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz Aims and scope

Abstract

Background

Food allergy represents a health problem worldwide and leads to life-threatening reactions and even impairs quality of life. Epidemiological data during the past decades is very heterogeneous because of the use of different diagnostic procedures, and most studies have only been performed in specific geographical areas.

Objectives

The aim of this article is to review the available data on the geographical distribution of food allergies at the food source and molecular level and to link food allergy patterns to the aeroallergen influence in each area.

Methods

Systematic reviews, meta-analysis, studies performed within the EuroPrevall Project and EAACI position papers regarding food allergy were analysed.

Conclusions

The prevalence of food allergy sensitization differs between geographical areas, probably as a consequence of differences among populations, their habits and the influence of the cross-reactivity of aeroallergens and other sources of allergens. Geographical differences in food allergy are clearly evident at the allergenic molecular level, which seems to be directly influenced by the aeroallergens of each region and associated with specific clinical patterns.

Zusammenfassung

Hintergrund

Nahrungsmittelallergien stellen ein weltweites Gesundheitsproblem dar, sie führen zu lebensbedrohlichen Reaktionen und selbst zur Beeinträchtigung der Lebensqualität. Die epidemiologischen Daten aus den vergangenen Jahrzehnten sind wegen des Einsatzes unterschiedlicher diagnostischer Verfahren sehr heterogen, außerdem sind die meisten Studien nur in spezifischen geographischen Regionen durchgeführt worden.

Ziel

Ziel des vorliegenden Beitrags ist es, einen Überblick über die verfügbaren Daten zur geographischen Verteilung von Nahrungsmittelallergien auf der Ebene der Nahrungsquellen und auf molekularer Ebene zu geben und Muster von Nahrungsmittelallergien mit dem Einfluss von Aeroallergenen in der jeweiligen Region zu verknüpfen.

Methoden

Systematische Übersichtsarbeiten, Metaanalysen, innerhalb des EuroPrevall-Projekts durchgeführte Studien und Positionspapiere der EAACI (Europäische Akademie für Allergologie und klinische Immunologie) in Bezug auf Nahrungsmittelallergien wurden ausgewertet.

Schlussfolgerung

Die Prävalenz der Sensibilisierung bei Nahrungsmittelallergie ist zwischen geographischen Regionen unterschiedlich, wahrscheinlich als Folge von Unterschieden zwischen den jeweiligen Bevölkerungsgruppen, ihren Gewohnheiten und dem Einfluss der Kreuzreaktivität von Aeroallergenen und anderen Allergenquellen. Auf molekularer Ebene der Allergene sind geographische Unterschiede bei Nahrungsmittelallergien deutlich nachweisbar; dies scheint unmittelbar durch Aeroallergene der jeweiligen Region beeinflusst und mit spezifischen klinischen Mustern verknüpft zu sein.

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References

  1. Johansson SG, Bieber T, Dahl R, Friedmann PS et al (2004) Revised nomenclature for allergy for global use: Report of the Nomenclature Review Committee of the World Allergy Organization, October 2003. J Allergy Clin Immunol 113:832–836

    Article  CAS  PubMed  Google Scholar 

  2. Allen JK, Koplin JJ (2012) The epidemiology of IgE-mediated food allergy and anaphylaxis. Immunol Allergy Clin North Am 32:35–50

    Article  PubMed  Google Scholar 

  3. Rona RJ, Keil T, Summers C, Gislason D et al (2007) The prevalence of food allergy: a meta-analysis. J Allergy Clin Immunol 120:638–646

    Article  PubMed  Google Scholar 

  4. Zuidmeer L, Goldhahn K, Rona RJ et al (2008) The prevalence of plant food allergies: a systematic review. J Allergy Clin Immunol 121:1210–1218

    Article  CAS  PubMed  Google Scholar 

  5. Bunyavanich S, Rifas-Shiman SL, Platts-Mills TA et al (2014) Peanut allergy prevalence among school-age children in a US cohort not selected for any disease. J Allergy Clin Immunol 134:753–755

    Article  PubMed  PubMed Central  Google Scholar 

  6. Beyer K, Morrow E, Li XM et al (2001) Effects of cooking methods on peanut allergenicity. J Allergy Clin Immunol 107:1077–1081

    Article  CAS  PubMed  Google Scholar 

  7. Du Toit G, Roberts G, Sayre P et al (2015) Randomized trial of peanut consumption in infants at risk for peanut allergy. N Engl J Med 372:803–813

    Article  PubMed  PubMed Central  Google Scholar 

  8. Werfel T, Asero R, Ballmer-Weber BK et al (2015) Position paper of the EAACI: food allergy due to immunological cross-reactions with common inhalant allergens. Allergy 70:1079–1090

    Article  CAS  PubMed  Google Scholar 

  9. Hong X, Hao K, Ladd-Acosta et al (2015) Genome-wide association study identifies peanut allergy-specific loci and evidence of epigenetic mediation in US children. Nat Commun 6:6304

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Nwaru BI, Hickstein L, Panesar SS et al (2014) Prevalence of common food allergies in Europe: a systematic review and meta-analysis. Allergy 69:992–1007

    Article  CAS  PubMed  Google Scholar 

  11. Burney PGJ, Potts J, Kummeling I et al (2014) The prevalence and distribution of food sensitization in European adults. Allergy 69:365–371

    Article  CAS  PubMed  Google Scholar 

  12. Schoemaker AA, Sprikkelman AB, Grimshaw KE et al (2015) Incidence and natural history of challenge-proven cow’s milk allergy in European children – EuroPrevall birth cohort. Allergy 70:963–972

    Article  CAS  PubMed  Google Scholar 

  13. Canonica GW, Ansotegui IJ, Pawankar R et al (2013) A WAO – ARIA – GA2LEN consensus document on molecular-based allergy diagnostics. World Allergy Organ J 6:1–17

    Article  Google Scholar 

  14. Asero R, Ballmer-Weber BK, Beyer K et al (2006) IgE-mediated food allergy diagnosis: current status and new perspectives. Mol Nutr Food Res 51:135–147

    Article  Google Scholar 

  15. Jansen JJ, Kardinaal AF, Huijbers G, Vlieg-Boerstra BJ, Martens BP, Ockhuizen T (1994) Prevalence of food allergy and intolerance in the adult Dutch population. J Allergy Clin Immunol 93:446–456

    Article  CAS  PubMed  Google Scholar 

  16. Osterballe M, Hansen TK, Mortz CG et al (2005) The prevalence of food hypersensitivity in an unselected population of children and adults. Pediatr Allergy Immunol 16:567–573

    Article  CAS  PubMed  Google Scholar 

  17. Zuberbier, Edenharter G, Worm M et al (2004) Prevalence of adverse reactions to food in Germany – a population study. Allergy 59:338–345

    Article  CAS  PubMed  Google Scholar 

  18. Roehr CC, Edenharter G, Reimann S et al (2004) Food allergy and non-allergic food hypersensitivity in children and adolescents. Clin Exp Allergy 34:1534–1541

    Article  CAS  PubMed  Google Scholar 

  19. Keil T, McBride D, Grimshaw K et al (2010) The multinational birth cohort of EuroPrevall: background, aims and methods. Allergy 65:482–490

    Article  CAS  PubMed  Google Scholar 

  20. Kummeling I, Mills EN, Clausen M et al (2009) The EuroPrevall surveys on the prevalence of food allergies in children and adults: background and study methodology. Allergy 64:1493–1497

    Article  CAS  PubMed  Google Scholar 

  21. Fernández-Rivas M, Barreales L, Mackie AR et al (2015) The EuroPrevall outpatient clinic study on food allergy: background and methodology. Allergy 70:576–584

    Article  PubMed  Google Scholar 

  22. Wong GWK, Mahesh PA, Ogorodova L (2010) The EuroPrevall-INCO surveys on the prevalence of food allergies in children from China, India and Russia: the study methodology. Allergy 65:385–390

    Article  CAS  PubMed  Google Scholar 

  23. Venter C, Pereira B, Grundy J et al (2006) Incidence of parentally reported and clinically diagnosed food hypersensitivity in the first year of life. J Allergy Clin Immunol 117:1118–1124

    Article  PubMed  Google Scholar 

  24. Schrander JJ, Bogart JP van den, Forget PP, Schrander-Stumpel CT, Kuijten RH, Kester AD (1993) Cow’s milk protein intolerance in infants under 1 year of age: a prospective epidemiological study. Eur J Pediatr 152:640–644

    Article  CAS  PubMed  Google Scholar 

  25. Burks AW, Tang M, Sicherer S, Muraro A, Eigenmann PA, Ebisawa M et al (2012) ICON: food allergy. J Allergy Clin Immunol 129:906–920

    Article  PubMed  Google Scholar 

  26. Smith M, Jager S, Berger U et al (2014) Geographical and temporal variations in pollen exposure across Europe. Allergy 69:913–923

    Article  CAS  PubMed  Google Scholar 

  27. Breiteneder H (2004) Thaumatin-like proteins – a new family of pollen and fruit allergens. Allergy 59:479–481

    Article  PubMed  Google Scholar 

  28. Salcedo G, Sanchez-Monge R, Diaz-Perales A (2004) Plant non-specific lipid transfer proteins as food and pollen allergens. Clin Exp Allergy 34:1336–1341

    Article  CAS  PubMed  Google Scholar 

  29. Kleine-Tebbe J, Vogel L, Crowell DN, Haustein UF, Vieths S (2002) Severe oral allergy syndrome and anaphylactic reactions caused by a Bet v 1‑ related PR-10 protein in soybean, SAM22. J Allergy Clin Immunol (110):797–804

  30. Van Ree R (2002) Clinical importance of nonspecific lipid transfer proteins as food allergens. Biochem Soc Trans 30:910–913

    Article  PubMed  Google Scholar 

  31. Lombardero M, Garcia-Selles FJ, Polo F et al (2004) Prevalence of sensitization to Artemisia allergens Art v 1, Art v 3 and Art v 60 kDa. Cross-reactivity among Art v 3 and other relevant lipid-transfer protein allergens. Clin Exp Allergy 34:1415–1421

    Article  CAS  PubMed  Google Scholar 

  32. Reuter A, Lidholm J, Andersson K et al (2006) A critical assessment of allergen component-based in vitro diagnosis in cherry allergy across Europe. Clin Exp Allergy 36:815–823

    Article  CAS  PubMed  Google Scholar 

  33. Enrique E, Cistero-Bahima A, Bartolome B et al (2002) Platanus acerifolia pollinosis and food allergy. Allergy 57:351–356

    Article  CAS  PubMed  Google Scholar 

  34. Florido LJF, Quiralte EJ, Arias de Saavedra Alias JM et al (2002) An allergen from Olea europaea pollen (Ole e 7) is associated with plant-derived food anaphylaxis. Allergy 57:53–59

    Article  Google Scholar 

  35. Sánchez-López J, Asturias JA, Enrique E, Suárez-Cervera M, Bartra J (2011) Cupressus arizonica pollen: A new pollen involved in the lipid transfer protein syndrome? J Investig Allergol Clin Immunol 21:522–526

    PubMed  Google Scholar 

  36. Valenta R, Duchene M, Ebner C et al (1992) Profilins constitute a novel family of functional plant pan-allergens. J Exp Med 175:377–385

    Article  CAS  PubMed  Google Scholar 

  37. Ruiz-García M, García del Potro M et al (2011) Profilin: a relevant aeroallergen? J Allergy Clin Immunol 128:416–418

    Article  PubMed  Google Scholar 

  38. Rodriguez-Perez R, Crespo JF, Rodriguez J, Salcedo G (2003) Profilin is a relevant melon allergen susceptible to pepsin digestion in patients with oral allergy syndrome. J Allergy Clin Immunol 111:634–639

    Article  CAS  PubMed  Google Scholar 

  39. Alvarado MI, Jimeno L, De La Torre F et al (2014) Profilin as a severe food allergen in allergic patients overexposed to grass pollen. Allergy 69:1610–1616

    Article  CAS  PubMed  Google Scholar 

  40. Valenta R, Duchene M, Pettenburger K, Sillaber C, Valent P, Bettelheim P et al (1991) Identification of profilin as a novel pollen allergen: IgE autoreactivity in sensitized individuals. Science 253:557–560

    Article  CAS  PubMed  Google Scholar 

  41. Vieths S (1997) Allergenic cross-reactivity, food allergy and pollen. Environ Tox Pharm 4:61–70

    Article  CAS  Google Scholar 

  42. Breiteneder H, Ebner C (2000) Molecular and biochemical classification of plant-derived food allergens. J Allergy Clin Immunol 106:27–36

    Article  CAS  PubMed  Google Scholar 

  43. Egger M, Mutschlechner S, Wopfner N et al (2006) Pollen-food syndromes associated with weed pollinosis: an update from the molecular point of view. Allergy 61:461–476

    Article  CAS  PubMed  Google Scholar 

  44. Barber D, Torre F de la, Feo F, Florido F et al (2008) Understanding patient sensitization profiles in complex pollen areas: a molecular epidemiological study. Allergy 63:1550–1155

    Article  CAS  PubMed  Google Scholar 

  45. Palacín A, Tordesillas L, Gamboa P, Sánchez-Monge R, Cuesta-Herranz J et al (2010) Characterization of peach thaumatin-like proteins and their identification as major peach allergens. Clin Exp Allergy 40:1422–1430

    Article  PubMed  Google Scholar 

  46. Palacín A, Rivas LA, Gómez-Casado C, Aguirre J, Tordesillas L et al (2012) The involvement of Thaumatin-like proteins in plant food cross-reactivity: A multic enter study using a specific protein Microarray. PLoS ONE 7(9):e44088

    Article  PubMed  PubMed Central  Google Scholar 

  47. Fernandez-Rivas M, Bolhaar S, Gonzalez-Mancebo E et al (2006) Apple allergy across Europe: how allergen sensitization profiles determine the clinical expression of allergies to plant foods. J Allergy Clin Immunol 118:481–488

    Article  CAS  PubMed  Google Scholar 

  48. Vereda A, Hage M van, Ahlstedt S et al (2011) Peanut allergy: Clinical and immunologic differences among patients from 3 different geographical regions. J Allergy Clin Immunol 127:603–607

    Article  CAS  PubMed  Google Scholar 

  49. Datema M, Zuidmeer-Jongejan L, Asero R et al (2015) Hazelnut allergy across Europe dissected molecularly: A EuroPrevall outpatient clinic survey. J Allergy Clin Immunol 136:382–391

    Article  CAS  PubMed  Google Scholar 

  50. Le T‑M, Bublin M, Breiteneder M, Fernández-Rivas MR, Asero R, Ballmer-Weber B (2013) Kiwifruit allergy across Europe: Clinical manifestation and IgE recognition patterns to kiwifruit allergens. J Allergy Clin Immunol 131:164–171

    Article  CAS  PubMed  Google Scholar 

  51. Ayuso R, Reese G, Leong-Kee S, Plante M, Lehrer SB (2002) Molecular basis of arthropod cross-reactivity: IgE-binding cross-reactive epitopes of shrimp, house dust mite and cockroach tropomyosins. Int Arch Allergy Immunol 129:38–48

    Article  CAS  PubMed  Google Scholar 

  52. Villalta D, Pantarotto L, Da Re M et al (2015) Galactose-α1,3-galactose in rural pre-Alps area: a cross-sectional study. Clin Exp Allergy : doi:10.1111/cea.12655

    Google Scholar 

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Correspondence to Joan Bartra.

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J. Bartra, A. García-Moral and E Enrique state that there are no conflicts of interest.

The accompanying manuscript does not include studies on humans or animals.

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Bartra, J., García-Moral, A. & Enrique, E. Geographical differences in food allergy. Bundesgesundheitsbl 59, 755–763 (2016). https://doi.org/10.1007/s00103-016-2357-0

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