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Clinical factors associated with peanut allergy in a high-risk infant cohort.
Sicherer, Scott H; Wood, Robert A; Perry, Tamara T; Jones, Stacie M; Leung, Donald Y M; Henning, Alice K; Dawson, Peter; Burks, A Wesley; Lindblad, Robert; Sampson, Hugh A.
Afiliação
  • Sicherer SH; Department of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Wood RA; Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Perry TT; Department of Pediatrics, Arkansas Children's Hospital, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
  • Jones SM; Department of Pediatrics, Arkansas Children's Hospital, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
  • Leung DYM; Department of Pediatrics, National Jewish Health, Denver, Colorado.
  • Henning AK; The EMMES Company, LLC, Rockville, Maryland.
  • Dawson P; The EMMES Company, LLC, Rockville, Maryland.
  • Burks AW; Department of Pediatrics, University of North Carolina, Chapel Hill, North Carolina.
  • Lindblad R; The EMMES Company, LLC, Rockville, Maryland.
  • Sampson HA; Department of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, New York.
Allergy ; 74(11): 2199-2211, 2019 11.
Article em En | MEDLINE | ID: mdl-31120555
ABSTRACT

BACKGROUND:

Prognostication of peanut allergy (PNA) is relevant for early interventions. We aimed to determine baseline parameters associated with the development of PNA in 3- to 15-month-olds with likely egg and/or milk allergy, and/or moderate to severe atopic dermatitis (AD) and a positive egg/milk skin prick test (SPT), but no known PNA.

METHODS:

The primary endpoint was PNA [confirmed/convincing diagnosis or last classified as serologic PNA (<2 years, ≥5 kUA/L, otherwise ≥14 kUA/L, peanut IgE)] among 511 participants (median follow-up, 7.3 years). Associations were explored with univariate logistic regression; factors with P < 0.15 were analyzed by stepwise multiple logistic regression, using data stratified by PNA status and randomly assigned to development and validation datasets.

RESULTS:

205/511 (40.1%) had PNA. Univariate factors associated with PNA (P < 0.01) included increased AD severity, larger egg and peanut SPT, greater egg, milk, peanut, Ara h1-h3 IgE, higher peanut IgG and IgG4, and increased pregnancy peanut consumption. P-values were between 0.01 and 0.05 for younger age, non-white race, lack of breastfeeding, and increased lactation peanut consumption. Using a development dataset, the multivariate model identified younger age at enrollment, greater peanut and Ara h2 IgE, and lack of breastfeeding as prognosticators. The final model predicted 79% in the development and 75% in the validation dataset (AUC = 0.83 for both). Models using stricter or less strict PNA criteria both found Ara h2 as predictive.

CONCLUSIONS:

Key factors associated with PNA in this high-risk population included lack of breastfeeding, age, and greater Ara h2 and peanut-specific IgE, which can be used to prognosticate outcomes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Arachis / Alérgenos / Hipersensibilidade a Amendoim Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Infant / Male / Newborn Idioma: En Revista: Allergy Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Arachis / Alérgenos / Hipersensibilidade a Amendoim Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Infant / Male / Newborn Idioma: En Revista: Allergy Ano de publicação: 2019 Tipo de documento: Article