Tolerance to a new free amino acid-based formula in children with IgE or non-IgE-mediated cows milk allergy a randomized controlled clinical trial 英文参考文献.docVIP
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Tolerance to a new free amino acid-based formula in children with IgE or non-IgE-mediated cows milk allergy a randomized controlled clinical trial 英文参考文献
BerniCananietal.BMCPediatrics2013,13:24
/1471-2431/13/24
RESEARCH ARTICLE
OpenAccess
Tolerancetoanewfreeaminoacid-basedformula
inchildrenwithIgEornon-IgE-mediatedcow’s
milkallergy:arandomizedcontrolledclinicaltrial
RobertoBerniCanani1,2*,RitaNocerino1,LudovicaLeone1,MargheritaDiCostanzo1,GianlucaTerrin1,2,
AnnalisaPassariello1,3,LindaCosenza1andRiccardoTroncone1,2
Abstract
Background:Amino acid-based formulas (Aaf) are increasingly used in children with cow’s milk allergy (CMA).
To be labeled hypoallergenic these formulas must demonstrate in clinical studies that they don’ t provoke
reactions in 90% of subjects with confirmed CMA with 95% confidence when given in prospective randomized,
double-blind, placebo-controlled challenge (DBPCFC) trials. The majority of available safety data on Aaf derived
from patients with IgE-mediated CMA. Considering substantial differences in the immunologic mechanism and
clinical presentation of non-IgE-mediated CMA it’s important to investigate the hypoallergenicity of these
formulas also in these patients. We prospectively assessed the tolerance to a new commercially available Aaf in
children affected by IgE- or non-IgE-mediated CMA.
Methods: Consecutive patients affected by IgE- or non-IgE-mediated CMA, aged ≤ 4 years, were enrolled.
DBPCFC was carried out with increasing doses of the new Aaf (Sineall, Humana, Milan, Italy), using validated Aaf
as placebo. Faecal concentrations of calprotectin (FC) and eosinophilic cationic protein (ECP) were monitored.
Results: Sixty patients (44 male, 73.3%, median age 37, 95%CI 34.5–39.6 months, IgE-mediated CMA 29, 48.3%)
were enrolled. At the diagnosis clinical symptoms were gastrointestinal (46.6%), cutaneous (36.6%), respiratory
(23.3%), and systemic (10.0%). After DBPCFC with the new Aaf, no patient presented early or delayed clinical
reactions. Faecal concentration of calprotectin and of ECP remained stable after the exposure to the new Aaf.
Conclusions: The new Aaf is well tolerated in
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