Geographic Distribution of Suspected Alpha-gal Syndrome Cases

United States, January 2017-December 2022

Julie M. Thompson, DVM, PhD; Ann Carpenter, DVM; Gilbert J. Kersh, PhD; Tyler Wachs; Scott P. Commins, MD; Johanna S. Salzer, DVM, PhD

Disclosures

Morbidity and Mortality Weekly Report. 2023;72(30):815-820. 

In This Article

Abstract and Introduction

Abstract

Alpha-gal syndrome (AGS) is an emerging, tick bite–associated allergic condition characterized by a potentially life-threatening immunoglobulin E (IgE)–mediated hypersensitivity to galactose-alpha-1,3-galactose (alpha-gal), an oligosaccharide found in most nonprimate mammalian meat and products derived from these mammals. Specific symptoms and severity of AGS vary among persons, and no treatment or cure is currently available. During 2010–2018, more than 34,000 suspected cases of AGS were identified in the United States, but current knowledge of where cases occur is limited. This study examined alpha-gal–specific IgE (sIgE) antibody testing results submitted to the commercial laboratory responsible for nearly all testing in the United States before 2022 to assess the geographic distribution and magnitude of this emerging condition. During January 1, 2017–December 31, 2022, a total of 357,119 tests were submitted from residences in the United States, corresponding to 295,400 persons. Overall, 90,018 (30.5%) persons received a positive test result in the study period, and the number of persons with positive test results increased from 13,371 in 2017 to 18,885 in 2021. Among 233,521 persons for whom geographic data were available, suspected cases predominantly occurred in counties within the southern, midwestern, and mid-Atlantic U.S. Census Bureau regions. These data highlight the evolving emergence of AGS and can be used to help state and local health agencies initiate surveillance and target public health outreach and health care provider education to high-risk localities.

Introduction

Alpha-gal syndrome (AGS) is an emerging, tick bite–associated allergic condition characterized by a potentially life-threatening immunoglobulin E (IgE)–mediated hypersensitivity to galactose-alpha-1,3-galactose (alpha-gal), an oligosaccharide found in most nonprimate mammalian tissue and products derived from these mammals, such as milk, other dairy products, and some pharmaceutical products.[1] Specific signs and symptoms and severity of AGS vary among persons,[2] and no treatment or cure is currently available.[1] More than 34,000 suspected AGS cases* were identified in the United States during 2010–2018,[3] but knowledge of where cases occurred is limited. This study examined alpha-gal–specific IgE (sIgE) antibody testing results submitted to the commercial laboratory responsible for nearly all testing in the United States before 2022 to describe the geographic distribution and magnitude of this emerging condition in the United States.

*The national standardized case definition accepted in 2021 by the Council of State and Territorial Epidemiologist defined a confirmed case of AGS as being in a person who met the clinical criteria and had confirmatory laboratory evidence (serum or plasma sIgE to alpha-gal ≥0.1 international unit per milliliter or ≥0.1 kU/L). A suspected case of AGS was defined as being in a person who had confirmatory laboratory evidence with no clinical information available. https://ndc.services.cdc.gov/case-definitions/alpha-gal-syndrome-ags/
Until August 2021, Eurofins Viracor was the primary commercial laboratory offering alpha-gal sIgE testing. Few academic institutions and specialty allergy clinics offered testing before August 2021. Several commercial laboratories began offering alpha-gal sIgE testing in August 2021.

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