Clinical and laboratory features of patients diagnosed with alpha‐gal syndrome—2010–2019. Issue 2 (14th October 2022)
- Record Type:
- Journal Article
- Title:
- Clinical and laboratory features of patients diagnosed with alpha‐gal syndrome—2010–2019. Issue 2 (14th October 2022)
- Main Title:
- Clinical and laboratory features of patients diagnosed with alpha‐gal syndrome—2010–2019
- Authors:
- Binder, Alison M.
Cherry‐Brown, Dena
Biggerstaff, Brad J.
Jones, Emma S.
Amelio, Claire L.
Beard, Charles B.
Petersen, Lyle R.
Kersh, Gilbert J.
Commins, Scott P.
Armstrong, Paige A. - Abstract:
- Abstract: Background: Alpha‐gal syndrome (AGS) is an IgE‐mediated allergy to galactose‐alpha‐1, 3‐galactose. Clinical presentation ranges from hives to anaphylaxis; episodes typically occur 2–6 h after exposure to alpha‐gal‐containing products. In the United States, lone star tick bites are associated with the development of AGS. To characterize features of AGS, we evaluated a cohort of patients presenting for care at the University of North Carolina, focusing on symptoms, severity, and identifying features unique to specific alpha‐gal‐containing product exposures. Methods: We performed a chart review and descriptive analysis of 100 randomly selected patients with AGS during 2010–2019. Results: Median age at onset was 53 years, 56% were female, 95% reported White race, 86% reported a history of tick bite, and 75% met the criteria for anaphylaxis based on the involvement of ≥2 organ systems. Those reporting dairy reactions were significantly less likely to report isolated mucocutaneous symptoms (3% vs. 24%; ratio [95% CI]: 0.1 [0.1, 0.3]) than those who tolerated dairy, and were more likely to report gastrointestinal symptoms (79% vs. 59%; ratio [95% CI]: 1.3 [0.7, 2.6]), although this difference was not statistically significant. Dairy‐tolerant patients demonstrated higher alpha‐gal sIgE titers (as a percentage of total IgE) than dairy‐reactive patients (GM 4.1 [95% CI: 2.7, 6.1] vs. GM 2.5 [95% CI: 1.3, 4.8], respectively; ratio −1.6 [95% CI: −1.0, 3.9]). Conclusion: WhileAbstract: Background: Alpha‐gal syndrome (AGS) is an IgE‐mediated allergy to galactose‐alpha‐1, 3‐galactose. Clinical presentation ranges from hives to anaphylaxis; episodes typically occur 2–6 h after exposure to alpha‐gal‐containing products. In the United States, lone star tick bites are associated with the development of AGS. To characterize features of AGS, we evaluated a cohort of patients presenting for care at the University of North Carolina, focusing on symptoms, severity, and identifying features unique to specific alpha‐gal‐containing product exposures. Methods: We performed a chart review and descriptive analysis of 100 randomly selected patients with AGS during 2010–2019. Results: Median age at onset was 53 years, 56% were female, 95% reported White race, 86% reported a history of tick bite, and 75% met the criteria for anaphylaxis based on the involvement of ≥2 organ systems. Those reporting dairy reactions were significantly less likely to report isolated mucocutaneous symptoms (3% vs. 24%; ratio [95% CI]: 0.1 [0.1, 0.3]) than those who tolerated dairy, and were more likely to report gastrointestinal symptoms (79% vs. 59%; ratio [95% CI]: 1.3 [0.7, 2.6]), although this difference was not statistically significant. Dairy‐tolerant patients demonstrated higher alpha‐gal sIgE titers (as a percentage of total IgE) than dairy‐reactive patients (GM 4.1 [95% CI: 2.7, 6.1] vs. GM 2.5 [95% CI: 1.3, 4.8], respectively; ratio −1.6 [95% CI: −1.0, 3.9]). Conclusion: While tick exposure is common in the southern United States, nearly all AGS patients reported a tick bite. Gastrointestinal symptoms were prominent among those reporting reactions to dairy. Anaphylaxis was common, underscoring the severity and need to raise awareness of AGS among patients and providers. Abstract : This report provides a comprehensive description of the epidemiology, clinical presentation, and laboratory testing trends among large cohort of patients diagnosed with alpha‐gal syndrome in the United States. Eighty six percent reported a history of tick bite, and 75% met the criteria for anaphylaxis based on the involvement of more than 2 organ systems. Patients reporting dairy reactions were significantly less likely to report isolated mucocutaneous symptoms (3% vs. 24%) than those who tolerated dairy and were more likely to report gastrointestinal symptoms (79% vs. 59%).Abbreviation: AGS, alpha‐gal syndrome … (more)
- Is Part Of:
- Allergy. Volume 78:Issue 2(2023)
- Journal:
- Allergy
- Issue:
- Volume 78:Issue 2(2023)
- Issue Display:
- Volume 78, Issue 2 (2023)
- Year:
- 2023
- Volume:
- 78
- Issue:
- 2
- Issue Sort Value:
- 2023-0078-0002-0000
- Page Start:
- 477
- Page End:
- 487
- Publication Date:
- 2022-10-14
- Subjects:
- alpha‐gal syndrome -- anaphylaxis -- galactose‐alpha‐1, 3‐galactose -- red meat allergy -- tick bite
Allergy -- Periodicals
616.97 - Journal URLs:
- http://estar.bl.uk/cgi-bin/sciserv.pl?collection=journals&journal=01054538 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1398-9995 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/all.15539 ↗
- Languages:
- English
- ISSNs:
- 0105-4538
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0790.945000
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