Carriers of filaggrin gene (FLG) mutations avoid professional exposure to irritants in adulthood

Josefine Bandier, Katrine Ross-Hansen, Berit C. Carlsen, Torkil Menné, Allan Linneberg, Steen Stender, Pal B. Szecsi, Michael Meldgaard, Jacob P. Thyssen, Jeanne D. Johansen

    Publikation: Bidrag til tidsskriftArtikelForskningpeer review


    Summary Background Loss-of-function mutations in the filaggrin gene (FLG) are associated with xerosis, atopic dermatitis, and early onset of hand eczema. Irritant exposure is a risk factor for occupational hand eczema, and FLG mutations increase the risk of occupational irritant contact dermatitis on the hands in hospital cohorts. It is unknown whether FLG mutations affect the level of irritant exposure. Objectives To evaluate whether exposure to occupational irritants was dependent on FLG mutations, atopic dermatitis, and age at hand eczema onset. Methods Randomly chosen Danish adults completed a questionnaire on general health and occupational exposures. Genotyping for FLG mutations (R501X, 2282del4, and R2447X) and patch testing were performed. Results Overall, 38.7% of subjects reported present or previous occupational exposure to irritants. Among individuals who reported hand eczema onset before entering their work life, 50.6% (45/89) of FLG non-mutation carriers became exposed to irritants, as compared with 28.6% (4/14) of heterozygous and 0% (0/6) of homozygous mutation carriers (p = 0.006). Avoidance was conspicuous among mutation carriers reporting childhood hand eczema and atopic dermatitis (odds ratio 0.08, 95% confidence interval 0.01-0.65). Conclusions Carriers of FLG mutations who have had hand eczema onset in childhood avoid occupational exposure to irritants; the association is most marked with homozygous mutation status combined with atopic dermatitis.

    Sider (fra-til)355-362
    Antal sider8
    TidsskriftContact Dermatitis
    Udgave nummer6
    StatusUdgivet - 1 dec. 2013

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