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DOI: 10.1055/s-0043-115208
Zöliakie, Getreideallergie, Weizensensitivität: Glutenfreie Ernährungstherapie
Celiac Disease, Cereal Allergy, Wheat Sensitivity: Gluten-Free Nutrition TherapyVerantwortlicher Herausgeber dieser Rubrik: Wissenschaftlich verantwortlich gemäß Zertifizierungsbestimmungen für diesen Beitrag ist Prof. Dr. med. Christian Löser, Kassel
Publikationsverlauf
Publikationsdatum:
03. Januar 2018 (online)
Die 3 wichtigsten Krankheitsbilder einer Getreideunverträglichkeit stellen die Zöliakie, Getreideallergie und Nicht-Zöliakie-Nicht-Weizenallergie-Weizensensitivität (NZNWWS) dar. Dieser Beitrag grenzt diese voneinander ab, zeigt Beschwerden auf und stellt jeweils die differenzierte Diagnostik sowie Ernährungstherapie vor.
Abstract
Glutensensitivity represents celiac disease, wheat allergy and non-celiac glutensensitivity (NCGS). Gastrointestinal complaints, e. g. abdominal pain, diarrhea, obstipation, flatulence, nausea and vomiting, as well as extra intestinal problems, e. g. headache, muscle and joint pain, fatigue or skin disorders, are common symptoms in these diseases. A correct diagnosis is mandatory for an appropriate individually adapted therapy.
Celiac disease is triggered by gluten from wheat, rye and barley, as well as related cereals e. g. spelt, Einkorn or Emmer. In genetically predisposed individuals dietary gluten ingestion causes an activation of the immune system and the destruction of the intestinal mucosa that results in a generalized nutrient malabsorption and -digestion. For diagnosis the celiac specific IgA anti-transglutaminase 2/IgA anti-endomysium antibodies are determined and mucosal damage is evaluated according Marsh-Oberhuber criteria. In case of reduced serum IgA the detection of IgG antibodies against transglutaminase 2 is recommended. A lifelong strict glutenfree diet is the only available therapy.
Cereal allergy represents different forms. The respiratory wheat allergy is mainly caused by inhalation of cereal flour, contact urticaria by contact with wheat, and gastrointestinal complaints after oral food intake. Both, IgE triggered immediate hypersensitivity reactions and T cell induced late-phase or delayed-type hypersensitivity reactions may cause clinical symptoms. Several cereal components were identified as triggers for allergy and are able to induce cross reactions with other cereal proteins or inhaled substances. The diagnosis for immediate hypersensitivity response is based on a skin-prick-test and determination of total IgE and specific IgE against cereal proteins. Since wheat is the most frequently cultivated and processed cereal, wheat allergy possesses high therapeutic relevance. Patients with wheat allergy must avoid wheat products. However, rye or barley is well tolerated in most patients.
Patients with NCGS complain about intestinal and extra intestinal symptoms soon after consumption of wheat or other gluten containing products. Besides of gluten other wheat components, like amylase-trypsin-inhibitor or FODMAPs, are discussed for disease trigger. The diagnosis of NCGS is done by exclusion of other diseases and improvement of symptoms under glutenfree diet. The therapy is based on a glutenfree diet that can be less restrictive after some weeks.
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Die 3 wichtigsten Krankheitsbilder einer Getreideunverträglichkeit stellen die Zöliakie, Weizenallergie und NZNWWS dar.
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Alle 3 Krankheitsbilder können mit gastrointestinalen Symptomen einhergehen.
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Die Diagnostik der Zöliakie besteht im Nachweis der Serum-IgA-Antikörper gegen Transglutaminase 2 oder Endomysium und dem histologischen Nachweis einer Schädigung der Dünndarmmukosa. Die Diagnostik muss unbedingt unter glutenhaltiger Kost durchgeführt werden.
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Die Therapie bei Zöliakie besteht in einer lebenslangen, strikten glutenfreien Diät. Bereits kleinste Mengen Gluten können eine Schädigung der Mukosa zur Folge haben.
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Bei der Weizenallergie werden je nach Allergenexposition und immunologischer Reaktion verschiedene Formen unterschieden.
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Die Diagnostik einer Weizenallergie besteht aus einer ausführlichen Anamnese in Kombination mit einem Skin-Prick-Test und dem Nachweis von Gesamt- und spezifischem IgE gegen Weizenproteine.
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Weizenallergiker sollten eine weizenfreie Diät einhalten. Roggen und Gerste werden meist toleriert.
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Bei einer NZNWWS klagen die Patienten vorwiegend nach Verzehr von weizenhaltiger Kost über gastrointestinale und extraintestinale Symptome. Eine rasche Besserung erfahren die Patienten bei Einhalten einer glutenfreien Diät. Neben Gluten werden jedoch ebenfalls andere Bestandteile des Weizens als auslösende Agenzien diskutiert.
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Bisher liegen für die NZNWWS keine diagnostischen Parameter vor, sodass die Diagnose auf einer Ausschlussdiagnostik beruht.
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Die Therapie der NZNWWS beruht auf der Einhaltung einer glutenfreien Diät. Nach anfänglich strikter Diät kann hier meist wieder eine geringe Menge an Gluten aufgenommen werden. Ein persönlicher Schwellenwert muss ermittelt werden.
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Literatur
- 1 Dubé C, Rostom A, Sy R. et al. The prevalence of celiac disease in average-risk and at-risk Western European populations: a systematic review. Gastroenterology 2005; 128,4 (Suppl. 01) S57-S67
- 2 Fasano A, Catassi C. Clinical practice. Celiac disease. N Engl J Med 2012; 367: 2419-2426
- 3 Kratzer W, Kibele M, Akinli A. et al. Prevalence of celiac disease in Germany: a prospective follow-up study. World J Gastroenterol 2013; 19: 2612-2620
- 4 Felber J, Aust D, Baas S. et al. Results of a S2k-Consensus Conference of the German Society of Gastroenterolgy, Digestive- and Metabolic Diseases (DGVS) in conjunction with the German Coeliac Society (DZG) regarding coeliac disease, wheat allergy and wheat sensitivity. Z Gastroenterol 2014; 52: 711-743
- 5 Catassi C, Gatti S, Fasano A. The new epidemiology of celiac disease. J Pediatr Gastroenterol Nutr 2014; 59 (Suppl. 01) S7-S9
- 6 Sollid LM, Lundin KE. Diagnosis and treatment of celiac disease. Mucosal Immunol 2009; 2: 3-7
- 7 Qiao SW, Sollid LM, Blumberg RS. Antigen presentation in celiac disease. Curr Opin Immunol 2009; 21: 111-117
- 8 Tack GJ, Verbeek WH, Schreurs MW. et al. The spectrum of celiac disease: epidemiology, clinical aspects and treatment. Nat Rev Gastroenterol Hepatol 2010; 7: 204-213
- 9 Tosco A, Salvati VM, Auricchio R. et al. Natural history of potential celiac disease in children. Clin Gastroenterol Hepatol 2011; 9: 320-325; quiz e36
- 10 Oberhuber G, Granditsch G, Vogelsang H. The histopathology of coeliac disease: time for a standardized report scheme for pathologists. Eur J Gastroenterol Hepatol 1999; 11: 1185-1194
- 11 Hayat M, Cairns A, Dixon MF. et al. Quantitation of intraepithelial lymphocytes in human duodenum: what is normal?. J Clin Pathol 2002; 55: 393-394
- 12 Dieterich W, Ehnis T, Bauer M. et al. Identification of tissue transglutaminase as the autoantigen of celiac disease. Nat Med 1997; 3: 797-801
- 13 Molberg O, McAdam SN, Korner R. et al. Tissue transglutaminase selectively modifies gliadin peptides that are recognized by gut-derived T cells in celiac disease. Nat Med 1998; 4: 713-717
- 14 van der Windt DA, Jellema P, Mulder CJ. et al. Diagnostic testing for celiac disease among patients with abdominal symptoms: a systematic review. JAMA 2010; 303: 1738-1746
- 15 Volta U, Fabbri A, Parisi C. et al. Old and new serological tests for celiac disease screening. Expert Rev Gastroenterol Hepatol 2010; 4: 31-35
- 16 Ojetti V, Nucera G, Migneco A. et al. High prevalence of celiac disease in patients with lactose intolerance. Digestion 2005; 71: 106-110
- 17 Terjung B, Lammert F. Lactose intolerance: new aspects of an old problem. Dtsch Med Wochenschr 2007; 132: 271-275
- 18 Catassi C, Fabiani E, Iacono G. et al. A prospective, double-blind, placebo-controlled trial to establish a safe gluten threshold for patients with celiac disease. Am J Clin Nutr 2007; 85: 160-166
- 19 Akobeng AK, Thomas AG. Systematic review: tolerable amount of gluten for people with coeliac disease. Aliment Pharmacol Ther 2008; 27: 1044-1052
- 20 Daum S, Cellier C, Mulder CJ. Refractory coeliac disease. Best Pract Res Clin Gastroenterol 2005; 19: 413-424
- 21 Zuidmeer L, Goldhahn K, Rona RJ. et al. The prevalence of plant food allergies: a systematic review. J Allergy Clin Immunol 2008; 121: 1210-1218, e4
- 22 Nwaru BI, Hickstein L, Panesar SS. et al. Prevalence of common food allergies in Europe: a systematic review and meta-analysis. Allergy 2014; 69: 992-1007
- 23 Sander I, Flagge A, Merget R. et al. Identification of wheat flour allergens by means of 2-dimensional immunoblotting. J Allergy Clin Immunol 2001; 107: 907-913
- 24 Mittag D, Niggemann B, Sander I. et al. Immunoglobulin E-reactivity of wheat-allergic subjects (baker's asthma, food allergy, wheat-dependent, exercise-induced anaphylaxis) to wheat protein fractions with different solubility and digestibility. Mol Nutr Food Res 2004; 48: 380-389
- 25 Chinuki Y, Morita E. Wheat-dependent exercise-induced anaphylaxis sensitized with hydrolyzed wheat protein in soap. Allergol Int 2012; 61: 529-537
- 26 Inomata N. Wheat allergy. Curr Opin Allergy Clin Immunol 2009; 9: 238-243
- 27 Hofmann SC, Fischer J, Eriksson C. et al. IgE detection to alpha/beta/gamma-gliadin and its clinical relevance in wheat-dependent exercise-induced anaphylaxis. Allergy 2012; 67: 1457-1460
- 28 Matsuo H, Kohno K, Niihara H. et al. Specific IgE Determination to Epitope Peptides of omega-5 Gliadin and High Molecular Weight Glutenin Subunit Is a Useful Tool for Diagnosis of Wheat-Dependent Exercise-Induced Anaphylaxis. J Immunol 2005; 175: 8116-8122
- 29 Palacin A, Bartra J, Munoz R. et al. Anaphylaxis to wheat flour-derived foodstuffs and the lipid transfer protein syndrome: a potential role of wheat lipid transfer protein Tri a 14. Int Arch Allergy Immunol 2010; 152: 178-183
- 30 Pahr S, Selb R, Weber M. et al. Biochemical, biophysical and IgE-epitope characterization of the wheat food allergen, Tri a 37. PloS one 2014; 9: e111483
- 31 Matsukura S, Aihara M, Sugawara M. et al. Two cases of wheat-dependent anaphylaxis induced by aspirin administration but not by exercise. Clin Exp Dermatol 2010; 35: 233-237
- 32 Fiedler EM, Zuberbier T, Worm M. A combination of wheat flour, ethanol and food additives inducing FDEIA. Allergy 2002; 57: 1090-1091
- 33 Brockow K, Kneissl D, Valentini L. et al. Using a gluten oral food challenge protocol to improve diagnosis of wheat-dependent exercise-induced anaphylaxis. J Allergy Clin Immunol 2015; 135: 977-984
- 34 Morita E, Matsuo H, Chinuki Y. et al. Food-dependent exercise-induced anaphylaxis – importance of omega-5 gliadin and HMW-glutenin as causative antigens for wheat-dependent exercise-induced anaphylaxis. Allergol Int 2009; 58: 493-498
- 35 Nilsson N, Sjolander S, Baar A. et al. Wheat allergy in children evaluated with challenge and IgE antibodies to wheat components. Pediatr Allergy Immunol 2015; 26: 119-125
- 36 Wang J. Management of the patient with multiple food allergies. Curr Allergy Asthma Rep 2010; 10: 271-277
- 37 DiGiacomo DV, Tennyson CA, Green PH. et al. Prevalence of gluten-free diet adherence among individuals without celiac disease in the USA: results from the Continuous National Health and Nutrition Examination Survey 2009–2010. Scand J Gastroenterol 2013; 48: 921-925
- 38 Sapone A, Bai JC, Ciacci C. et al. Spectrum of gluten-related disorders: consensus on new nomenclature and classification. BMC Med 2012; 10: 13
- 39 Guandalini S, Polanco I. Nonceliac gluten sensitivity or wheat intolerance syndrome?. J Pediatr 2015; 166: 805-811
- 40 Francavilla R, Cristofori F, Castellaneta S. et al. Clinical, serologic, and histologic features of gluten sensitivity in children. J Pediatr 2014; 164: 463-467, e1
- 41 Volta U, Tovoli F, Cicola R. et al. Serological tests in gluten sensitivity (nonceliac gluten intolerance). J Clin Gastroenterol 2012; 46: 680-685
- 42 Brottveit M, Beitnes AC, Tollefsen S. et al. Mucosal cytokine response after short-term gluten challenge in celiac disease and non-celiac gluten sensitivity. The Am J Gastroenterol 2013; 108: 842-850
- 43 Zevallos VF, Raker V, Tenzer S. et al. Nutritional Wheat Amylase-Trypsin Inhibitors Promote Intestinal Inflammation via Activation of Myeloid Cells. Gastroenterol 2017; 152: 1100-1113 e12
- 44 Sapone A, Lammers KM, Casolaro V. et al. Divergence of gut permeability and mucosal immune gene expression in two gluten-associated conditions: celiac disease and gluten sensitivity. BMC Med 2011; 9: 23
- 45 Uhde M, Ajamian M, Caio G. et al. Intestinal cell damage and systemic immune activation in individuals reporting sensitivity to wheat in the absence of coeliac disease. Gut 2016; 65: 1930-1937
- 46 Vazquez-Roque MI, Camilleri M, Smyrk T. et al. A controlled trial of gluten-free diet in patients with irritable bowel syndrome-diarrhea: effects on bowel frequency and intestinal function. Gastroenterol 2013; 144: 903-911, e3
- 47 Barmeyer C, Schumann M, Meyer T. et al. Long-term response to gluten-free diet as evidence for non-celiac wheat sensitivity in one third of patients with diarrhea-dominant and mixed-type irritable bowel syndrome. Int J Colorectal Dis 2016; 32: 29-39
- 48 de Roest RH, Dobbs BR, Chapman BA. et al. The low FODMAP diet improves gastrointestinal symptoms in patients with irritable bowel syndrome: a prospective study. Int J Clin Pract 2013; 67: 895-903
- 49 Halmos EP, Power VA, Shepherd SJ. et al. A diet low in FODMAPs reduces symptoms of irritable bowel syndrome. Gastroenterol 2014; 146: 67-75 e5
- 50 Biesiekierski JR, Peters SL, Newnham ED. et al. No effects of gluten in patients with self-reported non-celiac gluten sensitivity after dietary reduction of fermentable, poorly absorbed, short-chain carbohydrates. Gastroenterol 2013; 145: 320-328 e1-3
- 51 Carroccio A, Mansueto P, D’Alcamo A. et al. Non-celiac wheat sensitivity as an allergic condition: personal experience and narrative review. Am J Gastroenterol 2013; 108: 1845-1852; quiz 53
- 52 Catassi C, Elli L, Bonaz B. et al. Diagnosis of Non-Celiac Gluten Sensitivity (NCGS): The Salerno Expertsʼ Criteria. Nutrients 2015; 7: 4966-4977
- 53 Biesiekierski JR, Newnham ED, Irving PM. et al. Gluten causes gastrointestinal symptoms in subjects without celiac disease: a double-blind randomized placebo-controlled trial. Am J Gastroenterol 2011; 106: 508-514; quiz 15
- 54 Zanini B, Basche R, Ferraresi A. et al. Randomised clinical study: gluten challenge induces symptom recurrence in only a minority of patients who meet clinical criteria for non-coeliac gluten sensitivity. Aliment Pharmacol Ther 2015; 42: 968-976
- 55 Junker Y, Zeissig S, Kim SJ. et al. Wheat amylase trypsin inhibitors drive intestinal inflammation via activation of toll-like receptor 4. J Exp Med 2012; 209: 2395-2408
- 56 Fric P, Gabrovska D, Nevoral J. Celiac disease, gluten-free diet, and oats. Nutr Rev 2011; 69: 107-115
- 57 Deutsche Zöliakie-Gesellschaft e. V.. Hafer in der glutenfreien Ernährung. Stellungnahme der Deutschen Zöliakie-Gesellschaft e. V. 2016. Im Internet: https://www.dzg-online.de/files/2016_05_stellungnahme_hafer_dzg.pdf (Stand: 05.07.2017)
- 58 Kinsey L, Burden ST, Bannerman E. A dietary survey to determine if patients with coeliac disease are meeting current healthy eating guidelines and how their diet compares to that of the British general population. Eur J Clin Nutr 2008; 62: 1333-1342
- 59 Wild D, Robins GG, Burley VJ. et al. Evidence of high sugar intake, and low fibre and mineral intake, in the gluten-free diet. Aliment Pharmacol Ther 2010; 32: 573-581
- 60 Shepherd SJ, Gibson PR. Nutritional inadequacies of the gluten-free diet in both recently-diagnosed and long-term patients with coeliac disease. J Hum Nutr Diet 2013; 26: 349-358
- 61 Lee AR, Ng DL, Dave E. et al. The effect of substituting alternative grains in the diet on the nutritional profile of the gluten-free diet. J Hum Nutr Diet 2009; 22: 359-363
- 62 Muir JG RR, Rosella O, Liels K. et al. Measurement of short-chain carbohydrates in common Australian vegetables and fruits by high-performance liquid chromatography (HPLC). J Agric Food Chem 2009; 57: 554-565
- 63 Muir JG SS, Rosella O, Rose R. et al. Fructan and free fructose content of common Australian vegetables and fruit. J Agric Food Chem 2007; 55: 6619-6627
- 64 Nilsson U, Dahlqvist A, Nilsson B. Cereal fructosans: Part 2 – characterization and structure of wheat fructosans. Food Chemistry 1986; 22: 95-106
- 65 Barrett JS, Gearry RB, Muir JG. et al. Dietary poorly absorbed, short-chain carbohydrates increase delivery of water and fermentable substrates to the proximal colon. Aliment Pharmacol Ther 2010; 31: 874-882
- 66 Gibson PR, Shepherd SJ. Evidence-based dietary management of functional gastrointestinal symptoms: The FODMAP approach. J Gastroenterol Hepatol 2010; 25: 252-258
- 67 Barrett JS, Irving PM, Shepherd SJ. et al. Comparison of the prevalence of fructose and lactose malabsorption across chronic intestinal disorders. Aliment Pharmacol Ther 2009; 30: 165-174
- 68 Hyams JS. Sorbitol intolerance: an unappreciated cause of functional gastrointestinal complaints. Gastroenterol 1983; 84: 30-33
- 69 Teuri U, Vapaatalo H, Korpela R. Fructooligosaccharides and lactulose cause more symptoms in lactose maldigesters and subjects with pseudohypolactasia than in control lactose digesters. Am J Clin Nutr 1999; 69: 973-979
- 70 Gibson PR, Newnham E, Barrett JS. et al. Review article: fructose malabsorption and the bigger picture. Aliment Pharmacol Ther 2007; 25: 349-363
- 71 Staudacher HM, Lomer MC, Anderson JL. et al. Fermentable carbohydrate restriction reduces luminal bifidobacteria and gastrointestinal symptoms in patients with irritable bowel syndrome. J Nutr 2012; 142: 1510-1518
- 72 van Gils T, Nijeboer P, CE IJ. et al. Prevalence and Characterization of Self-Reported Gluten Sensitivity in The Netherlands. Nutrients 2016; 8, pii: E714
- 73 Biesiekierski JR, Rosella O, Rose R. et al. Quantification of fructans, galacto-oligosacharides and other short-chain carbohydrates in processed grains and cereals. J Hum Nutr Diet 2011; 24: 154-176