Background And Aims: Alpha-gal allergy causes a delayed reaction to mammalian meats and has been reported worldwide. Patients with the allergy may present with isolated gastrointestinal (GI) symptoms, but this phenotype is poorly understood.
Methods: We pooled and analyzed symptoms and demographics of patients from two prospective cohorts of patients with a diagnosis of alpha-gal allergy who reacted after eating mammalian meat under observation. We compared the characteristics of patients who demonstrated GI-isolated symptoms on a challenge with those who exhibited symptoms outside the GI tract (skin, respiratory, and circulatory).
Results: Among the 91 children and adult alpha-gal allergic patients who exhibited symptoms after oral challenge with mammalian meat, 72.5% experienced GI distress with one or more GI symptoms, which was the most frequent class of symptoms, compared with skin changes in 57.1% and respiratory distress in 5.5%. The most common GI symptoms were abdominal pain (71%) and vomiting (22.0%). GI-isolated symptoms occurred in 37 patients (40.7%) who reacted, and those patients reacted more quickly than patients who exhibited systemic symptoms (median onset of symptoms in GI-isolated group 90 min vs 120 min) and were more likely to be children than adults (relative risk=1.94, 95% CI: 1.04-3.63).
Conclusions: Isolated-GI distress occurred in 4 in every 10 alpha-gal allergic individuals who developed symptoms on oral food challenge with mammalian meat. Alpha-gal allergic patients, particularly children, may exhibit GI distress alone, and adult and pediatric gastroenterologists should be aware of the diagnosis and management of the allergy.
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http://dx.doi.org/10.1097/MCG.0000000000001827 | DOI Listing |
Crit Care Nurs Q
December 2024
Author Affiliations: Atlantic Health System, Morristown Medical Center, Morristown, New Jersey (Silbernagel); and Novant Health New Hanover Regional Medical Center, Wilmington, North Carolina (Bullard).
Alpha-gal syndrome is a serious, potentially life-threatening allergic reaction to mammalian products that has been linked to the lone star tick. Early recognition and management of alpha-gal syndrome is key for desirable patient outcomes and informed nursing care can make all the difference. The purpose of this article is to provide background information regarding alpha-gal syndrome, review common sources of potential reaction triggers including food and medications, and discuss strategies to detect and avoid allergic reactions from occurring.
View Article and Find Full Text PDFCureus
October 2024
Allergy and Immunology, Keesler Medical Center, Biloxi, USA.
Alpha-gal syndrome is an acquired disease ranging from gastrointestinal discomfort to anaphylaxis, an acute, life-threatening allergic reaction. Susceptible individuals have high-risk vocations or hobbies that involve outdoor activities where tick populations are overabundant. Potential exposure increases if located in the southeastern United States where , or the lone star tick, carryingα-gal glycoprotein is prevalent.
View Article and Find Full Text PDFJ Investig Allergol Clin Immunol
November 2024
Department of Infection and Immunity, Luxembourg Institute of Health, Esch-sur-Alzette, Luxembourg.
Background And Objectives: α-Gal syndrome is characterized by specific IgE (sIgE) antibodies to the carbohydrate galactose-α-1,3-galactose (α-Gal) and delayed onset of allergic symptoms after ingestion of mammalian meat. While tick bites are assumed to mediate sensitization, the immune response to tick bites has not yet been investigated. To investigate the peripheral immune response to tick bites in humans over time.
View Article and Find Full Text PDFClin Transl Allergy
October 2024
Department of Infection and Immunity, Luxembourg Institute of Health, Esch-sur-Alzette, Luxembourg.
Turkiye Parazitol Derg
October 2024
Ege University, Graduate School of Natural and Applied Sciences, Department of Biology, İzmir, Türkiye.
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