BMJ Open (Sep 2011)

A possible association between a dysfunctional skin barrier (filaggrin null-mutation status) and diabetes: a cross-sectional study

  • Allan Linneberg,
  • Torben Hansen,
  • Jacob P Thyssen,
  • Steen Stender,
  • Oluf Pedersen,
  • Berit C Carlsen,
  • Jeanne D Johansen,
  • Kåre Engkilde,
  • Flemming Pociot,
  • Michael Meldgaard,
  • Pal B Szecsi,
  • Torkil Menné

DOI
https://doi.org/10.1136/bmjopen-2011-000062
Journal volume & issue
Vol. 1, no. 1

Abstract

Read online

Background Filaggrin proteins are located in the skin and prevent epidermal water loss and impede the entry of micro-organisms, allergens and chemicals. Filaggrin null mutations are strongly associated with ichthyosis vulgaris and atopic dermatitis.Objective The authors aimed to investigate the association between filaggrin null mutations, atopic dermatitis and diabetes.Design A random sample of 3335 adults from the general population in Denmark was filaggrin-genotyped for R501X and 2282del4 null-mutations and questioned about atopic dermatitis and diabetes. Furthermore, two independent study populations of patients with type 1 (n=104) or 2 (n=774) diabetes were genotyped.Results In a crude data analysis, a positive association was detected between the filaggrin null genotype and, respectively, subjects from the general population who reported diabetes (p=0.04) and patients with established type 2 diabetes (p=0.073). Adjustment for age and gender resulted in significant associations for patients with type 2 diabetes (p=0.048) and subjects with self-reported diabetes (p=0.032).Conclusions Adult Danes with a filaggrin null genotype had a significantly increased prevalence of self-reported diabetes. This finding was replicated when an independent sample of Danish patients with established type 2 diabetes was compared with control subjects from the general population.