| Literature DB >> 33440636 |
Annalisa Astolfi1, Francesca Cipriani2, Daria Messelodi2, Matilde De Luca3, Valentina Indio3, Costanza Di Chiara2, Arianna Giannetti2, Lorenza Ricci4, Iria Neri4, Annalisa Patrizi5, Giampaolo Ricci2, Andrea Pession6.
Abstract
Atopic dermatitis is frequently associated with the onset of other allergic conditions, such as asthma, rhino-conjunctivitis and food allergy. The etiology of atopic dermatitis is marginally understood in spite of the number of predisposing factors, above all, mutations in the Filaggrin gene (FLG). In this study, the association between loss-of-function variants in the FLG gene and other allergic manifestations, in particular food allergy, was evaluated in an Italian pediatric population affected by atopic dermatitis. The 10 more frequently mutated loci in the FLG gene were genotyped in 238 children affected by atopic dermatitis and tested for association with clinical features of allergic disorders by a multivariate logistic regression model. R501X and 2282del4 were the only two mutations identified; 12.2% of children carry one of these variants, corresponding to an allelic frequency of 6.5%. According to multivariate statistical analysis, loss-of-function variants in the FLG gene represent a risk factor for the onset of severe manifestations of food allergy (OR = 8.9; CI: 3.1-28.3). Peanut and hazelnut were identified as high-risk foods in patients with FLG mutations. This study demonstrates that atopic children carrying FLG mutations represent a high-risk population due to their predisposition to develop severe food allergy reactions, such as anaphylaxis.Entities:
Keywords: Filaggrin; atopic dermatitis; food allergy
Year: 2021 PMID: 33440636 DOI: 10.3390/jcm10020233
Source DB: PubMed Journal: J Clin Med ISSN: 2077-0383 Impact factor: 4.241