|Year : 2016 | Volume
| Issue : 1 | Page : 48-50
Exercise-induced urticaria, cholinergic urticaria, and Kounis syndrome
Nicholas G Kounis1, George N Kounis2, George D Soufras3
1 Department of Medical Sciences, Western Greece Highest Institute of Education and Technology, Patras, Greece
2 Department of General Practice, University of Patras Medical School, Patras, Greece
3 Department of Cardiology, Saint Andrew's State General Hospital, Patras, Greece
|Date of Submission||29-Aug-2015|
|Date of Acceptance||11-Dec-2015|
|Date of Web Publication||29-Mar-2016|
Nicholas G Kounis
Department of Medical Sciences, Western Greece Highest Institute of Education and Technology, Queen Olgas Square, 7 Aratou Street, Patras 26221, Achaia
Source of Support: None, Conflict of Interest: None
|How to cite this article:|
Kounis NG, Kounis GN, Soufras GD. Exercise-induced urticaria, cholinergic urticaria, and Kounis syndrome. J Pharmacol Pharmacother 2016;7:48-50
|How to cite this URL:|
Kounis NG, Kounis GN, Soufras GD. Exercise-induced urticaria, cholinergic urticaria, and Kounis syndrome. J Pharmacol Pharmacother [serial online] 2016 [cited 2020 Mar 29];7:48-50. Available from: http://www.jpharmacol.com/text.asp?2016/7/1/48/179355
Physical exercise may provoke the onset of clinical symptoms that are usually associated with an allergic reaction. Distinct forms of recognized physical allergies are exercise-induced anaphylaxis (EIA), food-dependent EIA cholinergic urticaria, exercise-induced bronchospasm, and rhinitis.
In a report, the authors described a 26-year-old male with 3-year history of exercise-induced rash accompanied by flushing, feeling unwell and warm, eyelid angioedema, pruritus, and headache. His symptoms were relieved with discontinuation of exercise.
No history of any specific food, drink, or medication intake before exercise was apparent, but the patient described nonspecific allergic rhinitis episodes to dust. He subsequently underwent extensive investigation including skin prick tests to numerous food items including meat and vegetables as well as specific immunoglobulin E (IgE) for wheat, most of which proved to be negative. The only positive skin prick tests were for mites and grasses. His symptoms subsided with antihistamine and antileukotriene therapy with montelukast that enabled him to start exercising again without symptoms.
EIA is an unpredictable and potentially fatal syndrome affecting pediatric individuals also  with a prevalence of 0.048% and can seriously damage the patient's quality of life. This condition may occur independently or may require the ingestion of a food allergen either pre- or post-exercise. Atopic individuals are specifically prone to this condition.
Therefore, this report raises several important questions concerning the etiology, pathophysiology, associations and treatment of EIA.
The authors have correctly speculated on mediators from degranulation of mast cells, lowering of degranulation threshold and increased sympathetic activity, but additional causes should be taken into consideration as has been emphasized in a recent position paper.
The consumption of substances such as alcohol or aspirin that damage the gastric mucosa may significantly increase the risk of food allergic patients developing anaphylaxis. On the other hand, the inhibitory effect of exercise on gastric acid secretion decreases the digestion of oral allergens and preserves the structural integrity that leads to continued systemic absorption of the allergens whether it be profilins, lipid transfer proteins, or other antigenic determinants.
Increased IgE cross-linking may be the result in tissue transglutaminase enzyme alterations causing peptide aggregation during exercise. Sudden redistribution of blood during exercise transports allergens away from the gut to the skin and/or skeletal muscle, where phenotypically different mast cells reside.
During exercise, a fall in pH takes place creating an acidic state that may promote mast cell degranulation.In vitro studies have shown that during exercise, plasma osmolarity is raised and this can increase basophil activation and histamine release.
In the described patient, there was no history of any specific food or medication intake before exercise, but there are several kinds of commonly used foods drugs and environmental exposures [Table 1] that should be always tested for. For example, tomato salad is a commonly used food which can induce exercise anaphylaxis and should be always tested. Although tomatoes have become one of the most consumed vegetables worldwide, unfortunately, tomatoes are accompanied by an increasing risk of tomato allergy via five proteins with putative clinical relevance as tomato allergens.
|Table 1: Causes associated with food dependent exercise-induced anaphylaxis|
Click here to view
Another effort-induced anaphylactic condition is the so-called cholinergic urticaria known as stress urticaria, allergy to effort and aquagenic urticaria. Cholinergic urticaria is a type of physical urticaria characterized by a number of short–lasting, highly pruritic weals. This kind of urticaria has been attributed to water in sweat (aquagenic), during exercise, which reacts with sebum forming a compound acting as an allergen that induces the release of histamine. This condition can be accompanied by systemic manifestations such as abdominal pain, nausea, vomiting and diarrhea. The humanized monoclonal IgG anti-IgE antibody omalizumab that binds specifically to circulating IgE molecules and interrupting the allergic cascade has been used to treat cholinergic urticaria.
Recent reports have associated food-dependent EIA with acute coronary syndrome and especially with the Kounis hypersensitivity-associated coronary syndrome., This syndrome is associated with anaphylactic or anaphylactoid reactions and is increasingly encountered in clinical practice. It can manifest as allergic angina, allergic myocardial infarction or stent thrombosis with thrombus infiltrated by eosinophils and mast cells.
As far as the treatment is concerned, physicians should be aware and mindful of the anaphylactic cardiovascular events during exercise, and treatment should include supine position, oxygen and antiallergic medications such as antihistamines, steroids, sodium cromoglycate, leukotriene modifiers, humanized monoclonal antibodies, and intravenous fluids. A personalized, written anaphylaxis emergency action plan should be readily available. Patients and caregivers must always keep self-injectable epinephrine available and should be educated about its indications and contraindications.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Povesi Dascola C, Caffarelli C. Exercise-induced anaphylaxis: A clinical view. Ital J Pediatr 2012;38:43.
Gajbhiye S, Agrawal RP, Atal S, Tiwari V, Phadnis P. Exercise-induced anaphylaxis and antileukotriene montelukast. J Pharmacol Pharmacother 2015;6:163-5.
Aihara Y, Takahashi Y, Kotoyori T, Mitsuda T, Ito R, Aihara M, et al.
Frequency of food-dependent, exercise-induced anaphylaxis in Japanese junior-high-school students. J Allergy Clin Immunol 2001;108:1035-9.
Shadick NA, Liang MH, Partridge AJ, Bingham III CO, Wright E, Fossel AH, et al.
The natural history of exercise-induced anaphylaxis: Survey results from a 10-year follow-up study. J Allergy Clin Immunol 1999;104:123-7.
Ansley L, Bonini M, Delgado L, Del Giacco S, Du Toit G, Khaitov M, et al.
Pathophysiological mechanisms of exercise-induced anaphylaxis: An EAACI position statement. Allergy 2015;70:1212-21.
Chen JY, Quirt J, Lee KJ. Proposed new mechanism for food and exercise induced anaphylaxis based on case studies. Allergy Asthma Clin Immunol 2013;9:11.
Welter S, Lehmann K, Dölle S, Schwarz D, Weckwerth W, Scheler C, et al.
Identification of putative new tomato allergens and differential interaction with IgEs of tomato allergic subjects. Clin Exp Allergy 2013;43:1419-27.
Kounis NG, MacMahon RG. Cholinergic urticaria with systemic manifestations. Ann Allergy 1975;35:243-5.
Kutlu A, Tanoglu A, Ozturk S. Healing effects of omalizumab in a patient with cholinergic urticaria associated severe dyspeptic complaints. Chin Med J (Engl) 2015;128:1559-60.
Yaegashi T, Nakamura Y, Sakagami S, Saeki T, Omi W, Ikeda K. Acute myocardial infarction following food-dependent exercise-induced anaphylaxis. Intern Med 2011;50:451-4.
Kounis NG, Almpanis G, Tsigkas G, Kounis GN, Mazarakis A. Kounis syndrome following food-dependent exercise-induced anaphylaxis. Intern Med 2011;50:1451.
|This article has been cited by|
||The EAACI/GA˛LEN/EDF/WAO guideline for the definition, classification, diagnosis and management of urticaria
| ||T. Zuberbier,W. Aberer,R. Asero,A. H. Abdul Latiff,D. Baker,B. Ballmer-Weber,J. A. Bernstein,C. Bindslev-Jensen,Z. Brzoza,R. Buense Bedrikow,G. W. Canonica,M. K. Church,T. Craig,I. V. Danilycheva,C. Dressler,L. F. Ensina,A. Giménez-Arnau,K. Godse,M. Gonçalo,C. Grattan,J. Hebert,M. Hide,A. Kaplan,A. Kapp,C. H. Katelaris,E. Kocatürk,K. Kulthanan,D. Larenas-Linnemann,T. A. Leslie,M. Magerl,P. Mathelier-Fusade,R. Y. Meshkova,M. Metz,A. Nast,E. Nettis,H. Oude-Elberink,S. Rosumeck,S. S. Saini,M. Sánchez-Borges,P. Schmid-Grendelmeier,P. Staubach,G. Sussman,E. Toubi,G. A. Vena,C. Vestergaard,B. Wedi,R. N. Werner,Z. Zhao,M. Maurer |
| ||Allergy. 2018; 73(7): 1393 |
|[Pubmed] | [DOI]|