Review article

FILAGGRIN GENE NULL-MUTATIONS AND ATOPIC DISEASES

IVANA SABOLIĆ PIPINIĆ ; Institute for Medical Research and Occupational Health, Zagreb, Croatia
JELENA MACAN ; Institute for Medical Research and Occupational Health, Zagreb, Croatia

Abstract

Null-mutations which cause loss of function of the gene encoding filaggrin (FLG) have been strongly linked to the development of atopic disorders, predominantly atopic eczema/dermatitis syndrome (AEDS). Filaggrin plays a key role in epidermal barrier function by upholding epidermal structure and moisturization. Up to now, around 40 variants of FLG nullmutations have been genotyped among different world populations. FLG null-mutations are present in up to 10% of the Caucasian population in Western Europe and North America, with R05X and 2282del4 as the most common null-mutations. Epidemiological studies conducted in Europe indicate a latitude dependent distribution of common FLG null-mutations with a decreasing north-south gradient of R501X and 2282del4 mutation frequencies. FLG null-mutation carriers are prone to develop unspecific skin symptoms related to atopic and non-atopic skin disorders due to their defect of epidermal barrier function, which allows greater skin penetration of various hazards. Epidemiological studies indicate an association of FLG null-mutations with AEDS, whereas results regarding an association of FLG null-mutations with sensitization to common inhalant allergens and development of rhinitis and asthma are incoherent. A study conducted in Croatia found a low frequency of FLG null-mutations in general population (2.6%) and did not confi rm FLG null-mutations as an etiological factor for atopy and atopic disease in the studied population.

Keywords

eczema/dermatitis syndrome; rhinitis; asthma; gene-environment interaction

Hrčak ID:

154199

URI

https://hrcak.srce.hr/154199

Publication date:

13.3.2016.

Article data in other languages: croatian

Visits: 1.755 *