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Objective eliciting doses of peanut-allergic adults and children can be combined for risk assessment purposes.
Klemans, R J B; Blom, W M; van Erp, F C; Masthoff, L J N; Rubingh, C M; van der Ent, C K; Bruijnzeel-Koomen, C A F M; Houben, G F; Pasmans, S G M A; Meijer, Y; Knulst, A C.
Afiliação
  • Klemans RJ; Department of Dermatology and Allergology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Blom WM; The Netherlands Organisation for Applied Scientific Research (TNO), Zeist, The Netherlands.
  • van Erp FC; Department of Pediatric Pulmonology and Allergology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Masthoff LJ; Department of Dermatology and Allergology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Rubingh CM; The Netherlands Organisation for Applied Scientific Research (TNO), Zeist, The Netherlands.
  • van der Ent CK; Department of Pediatric Pulmonology and Allergology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Bruijnzeel-Koomen CA; Department of Dermatology and Allergology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Houben GF; The Netherlands Organisation for Applied Scientific Research (TNO), Zeist, The Netherlands.
  • Pasmans SG; Department of Dermatology and Allergology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Meijer Y; Department of Pediatric Dermatology and Allergology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Knulst AC; Department of Pediatric Pulmonology and Allergology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
Clin Exp Allergy ; 45(7): 1237-44, 2015 Jul.
Article em En | MEDLINE | ID: mdl-25900644
ABSTRACT

BACKGROUND:

To improve food labelling strategies, information regarding eliciting doses (EDs) and the effect of patient characteristics on these EDs is necessary.

OBJECTIVE:

To establish EDs for objective and subjective symptoms and analyse the effect of sensitization levels and other patient characteristics on threshold distribution curves (TDCs).

METHODS:

Threshold data from 100 adults and 262 children with a positive food challenge were analysed with interval-censoring survival analysis (ICSA) and fitted to a TDC from which EDs could be extracted. Possible influencing factors were analysed as covariates by ICSA. A hazard ratio (HR) was calculated in case of a significant effect.

RESULTS:

TDCs for both objective and subjective symptoms were significantly different between adults and children (P < 0.001). Objective ED05 values, however, were comparable (2.86 mg peanut protein in adults and 6.38 mg in children). Higher levels of sIgE to Ara h 2 and peanut extract were associated with a larger proportion of patient groups reacting to a dose increase with objective symptoms (adults and children) or subjective symptoms (adults, in children a trend). Age had a similar effect in children (HR 1.05 for objective symptoms and 1.09 for subjective symptoms). Gender had no effect on TDCs. CONCLUSION AND CLINICAL RELEVANCE Subjective and objective TDCs were different between adults and children, but objective ED05 values were comparable, meaning that threshold data from children and adults can be combined for elaboration of reference doses for risk assessment. Higher sIgE levels to Ara h 2 and peanut extract were associated with a larger proportion of both patient groups to react to a certain dose increase.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Arachis / Alérgenos / Medição de Risco / Hipersensibilidade a Amendoim / Antígenos de Plantas Tipo de estudo: Clinical_trials / Etiology_studies / Risk_factors_studies Limite: Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Arachis / Alérgenos / Medição de Risco / Hipersensibilidade a Amendoim / Antígenos de Plantas Tipo de estudo: Clinical_trials / Etiology_studies / Risk_factors_studies Limite: Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article