Correlation of age-of-onset of Atopic Dermatitis with Filaggrin loss-of-function variant status

• Published in: Scientific reports 2020-02, Vol.10 (1), p.2721-2721, Article 2721
• Main Authors: Smieszek, S. P., Welsh, S., Xiao, C., Wang, J., Polymeropoulos, C., Birznieks, G., Polymeropoulos, M. H.
• Format: Article
• Language: English
• Subjects: 38; 45; 45/23; 45/43; 631/208/2489/144; 692/308/2056; 692/499; 692/699/4033; Adult; Age; Age of Onset; Atopic dermatitis; Child, Preschool; Chronic Disease; Dermatitis; Dermatitis, Atopic - genetics; Dermatitis, Atopic - metabolism; Dermatitis, Atopic - pathology; Eczema; Etiology; Female; Filaggrin; Gene Expression; Genetic Predisposition to Disease; Genomes; Humanities and Social Sciences; Humans; Loss of Function Mutation; Male; multidisciplinary; Permeability; Pruritus; Pruritus - genetics; Pruritus - metabolism; Pruritus - pathology; Risk factors; S100 Proteins - genetics; S100 Proteins - metabolism; Science; Science (multidisciplinary); Severity of Illness Index; Skin - metabolism; Skin - pathology; Whole Genome Sequencing
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-020-59627-7

The genetic background of Atopic Dermatitis (AD) with chronic pruritus is complex. Filaggrin ( FLG ) is an essential gene in the epidermal barrier formation s. Loss-of-function (LOF) variants in FLG associated with skin barrier dysfunction constitute the most well-known genetic risk factor for AD. In this study, we focused on the frequency and effect of FLG loss-of-function variants in association with self-reported age-of-onset of AD. The dataset consisted of 386 whole-genome sequencing (WGS) samples. We observe a significant association between FLG LOF status and age-of-onset, with earlier age of onset of AD observed in the FLG LOF carrier group (p-value 0.0003, Wilcoxon two-sample test). We first tested this on the two most prevalent FLG variants. Interestingly, the effect is even stronger when considering all detected FLG LOF variants. Having two or more FLG LOF variants associates with the onset of AD at 2 years of age. In this study, we have shown enrichment of rare variants in the EDC region in cases compared with controls. Age-of-onset analysis shows not only the effect of the FLG and likely EDC variants in terms of the heightened risk of AD, but foremost enables to predict early-onset, lending further credence to the penetrance and causative effect of the identified variants. Understanding the genetic background and risk of early-onset is suggestive of skin barrier dysfunction etiology of AD with chronic pruritus