HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

The role of glutathione S-transferase and claudin-1 gene polymorphisms in contact sensitization: a cross-sectional study.

AbstractBACKGROUND:
Contact sensitization is frequent in the general population and arises from excessive or repeated skin exposure to chemicals and metals. However, little is known about its genetic susceptibility.
OBJECTIVES:
To determine the role of polymorphisms of glutathione S-transferase (GST) genes and the claudin-1 gene (CLDN1) on the risk of contact sensitization, taking common filaggrin gene (FLG) mutations into account.
METHODS:
In total, 3471 adult Danes from the general population were standard patch tested and filled out a questionnaire on their general health. They were genotyped for the following polymorphisms: GSTM1 and GSTT1 deletion, GSTP1 single nucleotide polymorphism (SNP) rs1695, four CLDN1 SNPs (rs893051, rs9290927, rs9290929 and rs17501010) and the FLG null mutations R501X and 2282del4.
RESULTS:
In individuals without ear piercings, a higher prevalence of nickel sensitization was found in those with the minor allele of CLDN1 SNP rs9290927 (P(trend)=0·013). For CLDN1 rs17501010, contact sensitization to organic compounds was associated with the major allele (P(trend)=0·031). The risk pattern was also identified for self-reported nickel dermatitis (P(trend)=0·011). The fragrance sensitization prevalence differed in a pairwise comparison of the CLDN1 rs893051 SNP genotypes (P=0·022), with the minor allele being associated with a higher prevalence. The associations were confirmed in logistic regression analyses.
CONCLUSIONS:
The CLDN1 polymorphisms rs9290927, rs893051 and rs17501010 were associated, respectively, with nickel contact sensitization in individuals without ear piercings, contact sensitization to fragrances, and with both organic compounds and nickel contact dermatitis. We could not find associations between GST gene polymorphisms and contact sensitization. FLG mutations did not affect the observed associations.
AuthorsK Ross-Hansen, A Linneberg, J D Johansen, L-G Hersoug, C Brasch-Andersen, T Menné, J P Thyssen
JournalThe British journal of dermatology (Br J Dermatol) Vol. 168 Issue 4 Pg. 762-70 (Apr 2013) ISSN: 1365-2133 [Electronic] England
PMID23136956 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2012 The Authors. BJD © 2012 British Association of Dermatologists.
Chemical References
  • Allergens
  • CLDN1 protein, human
  • Claudin-1
  • FLG protein, human
  • Filaggrin Proteins
  • Intermediate Filament Proteins
  • glutathione S-transferase T1
  • GSTP1 protein, human
  • Glutathione S-Transferase pi
  • Glutathione Transferase
  • glutathione S-transferase M1
Topics
  • Adult
  • Allergens (genetics, immunology)
  • Claudin-1 (genetics)
  • Cross-Sectional Studies
  • Dermatitis, Contact (genetics)
  • Filaggrin Proteins
  • Gene Deletion
  • Genetic Predisposition to Disease
  • Genotype
  • Glutathione S-Transferase pi (genetics)
  • Glutathione Transferase (genetics)
  • Humans
  • Intermediate Filament Proteins (genetics)
  • Mutation (genetics)
  • Patch Tests
  • Polymorphism, Single Nucleotide (genetics)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: