TY - JOUR
T1 - Phenotypic characterization of childhood- and adult-onset food allergy among adults in the United States
AU - Hultquist, Haley
AU - Dyer, Ashley Anne
AU - Jiang, Jialing
AU - Gupta, Ruchi
AU - Warren, Christopher Michael
N1 - Funding Information:
Disclosure of potential conflict of interest: C. Warren reports institutional research funding from Food Allergy Research & Education ( FARE ) and the National Institutes of Health ( NIH ). R. Gupta reports receipt of research support from the NIH (R21 ID no. AI135705; R01 ID no. AI130348; U01 ID no. AI138907), FARE , Melchiorre Family Foundation , Sunshine Charitable Foundation , The Walder Foundation , UnitedHealth Group , Thermo Fisher Scientific , and Genentech ; reports service as medical consultant/advisor for Genentech, Novartis, Aimmune LLC, Allergenis LLC, and FARE; and has ownership interest in Yobee Care Inc. The rest of the authors declare that they have no relevant conflicts of interest.
Funding Information:
Supported by grant R21AI135702 from the National Institute of Allergy and Infectious Diseases .
Publisher Copyright:
© 2022 The Authors
PY - 2022/11
Y1 - 2022/11
N2 - Background: Food allergy (FA) affects ∼10% of adults; however, little is known about the extent to which FA phenotypes and psychosocial burden vary depending on timing of allergy onset, whether in childhood or as an adult. Objective: This study explored FA characteristics according to timing of FA onset in US adults. Methods: Between 2015 and 2016, a cross-sectional survey was administered to 40,443 US adults. Complex survey–weighted results were tabulated across key demographic and clinical strata. Linear regression models explored covariate-adjusted variability in FA-related psychosocial burden across 3 groups: (1) adults solely with childhood-onset FA, (2) adults solely with adult-onset FA, and (3) adults with both childhood- and adult-onset FA. Results: Adults with both childhood- and adult-onset FAs, compared to adults with solely childhood- or adult-onset FAs, are significantly more likely to have severe FAs (57.3%, 52.6%, 43.2%), physician-diagnosed FAs (54.2%, 52.4%, 33.0%), and multiple FAs (74.8%, 41.0%, 30.3%) (P <.001). Adults solely with childhood-onset FA, compared to adults solely with adult-onset FA, had significantly lower rates of environmental allergies (27.6% vs 39.2%; P <.001) and medication allergies (17.3% vs 25.9%; P <.001). Adults with both childhood- and adult-onset FAs reported highest rates of all comorbidities. Adults solely with adult-onset FA reported significantly lower FA-related psychosocial burden (P <.05). Conclusion: Differences exist in reaction severity, health care utilization, atopic comorbidities, and psychosocial burden according to the timing of FA onset. Future research exploring the heterogeneity of phenotypic expressions of adult FA may inform underlying mechanisms.
AB - Background: Food allergy (FA) affects ∼10% of adults; however, little is known about the extent to which FA phenotypes and psychosocial burden vary depending on timing of allergy onset, whether in childhood or as an adult. Objective: This study explored FA characteristics according to timing of FA onset in US adults. Methods: Between 2015 and 2016, a cross-sectional survey was administered to 40,443 US adults. Complex survey–weighted results were tabulated across key demographic and clinical strata. Linear regression models explored covariate-adjusted variability in FA-related psychosocial burden across 3 groups: (1) adults solely with childhood-onset FA, (2) adults solely with adult-onset FA, and (3) adults with both childhood- and adult-onset FA. Results: Adults with both childhood- and adult-onset FAs, compared to adults with solely childhood- or adult-onset FAs, are significantly more likely to have severe FAs (57.3%, 52.6%, 43.2%), physician-diagnosed FAs (54.2%, 52.4%, 33.0%), and multiple FAs (74.8%, 41.0%, 30.3%) (P <.001). Adults solely with childhood-onset FA, compared to adults solely with adult-onset FA, had significantly lower rates of environmental allergies (27.6% vs 39.2%; P <.001) and medication allergies (17.3% vs 25.9%; P <.001). Adults with both childhood- and adult-onset FAs reported highest rates of all comorbidities. Adults solely with adult-onset FA reported significantly lower FA-related psychosocial burden (P <.05). Conclusion: Differences exist in reaction severity, health care utilization, atopic comorbidities, and psychosocial burden according to the timing of FA onset. Future research exploring the heterogeneity of phenotypic expressions of adult FA may inform underlying mechanisms.
KW - adult food allergy
KW - adult-onset
KW - comorbidities
KW - Food allergy
KW - health care utilization
KW - prevalence
KW - quality of life
KW - severity
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U2 - 10.1016/j.jacig.2022.05.011
DO - 10.1016/j.jacig.2022.05.011
M3 - Article
C2 - 36425303
AN - SCOPUS:85160281200
SN - 2772-8293
VL - 1
SP - 257
EP - 264
JO - Journal of Allergy and Clinical Immunology: Global
JF - Journal of Allergy and Clinical Immunology: Global
IS - 4
ER -