FOXP3 polymorphisms in type 1 diabetes and coeliac disease

• The FOXP3 gene encodes a transcription factor thought to be essential for the development and function of T regulatory cells. Two previous studies have tested common polymorphisms in FOXP3 for association with type 1 diabetes (T1D) with conflicting results. The aim of our study was to see whether there is any evidence of association between the FOXP3 polymorphisms previously reported to be associated with T1D, in a Caucasian population regarding T1D and coeliac disease (CD). We further looked for evidence of interaction between FOXP3 polymorphisms and HLA-DR3 in conferring susceptibility to T1D. Initially, we analysed two microsatellites in the FOXP3 gene in 363 T1D nuclear families. Our results indicated an association between FOXP3 and T1D (global p=0.004) and a possible interaction between FOXP3 and the HLA-DR3-DQ2 susceptibility haplotype. We then genotyped an additional independent set of 826 T1D patients and 1459 controls as well as one CD dataset consisting of 325 families. A similar tendency was revealed in the CD family material (pnc=0.055 for the associated allele). On the other hand, we were unable to reproduce our initial findings in the T1D case-control dataset (global p=0.6). Our results suggest that the tested FOXP3 markers do not have any major impact on susceptibility for these diseases.

Nyckelord

Adolescent

Celiac Disease/*genetics

Child

Child

Preschool

Diabetes Mellitus

Type 1/*genetics

Forkhead Transcription Factors/*genetics

*Genetic Predisposition to Disease

HLA-DR3 Antigen/genetics

Humans

Infant

Infant

Newborn

Linkage Disequilibrium/genetics

Microsatellite Repeats/genetics

Polymerase Chain Reaction

*Polymorphism

Genetic

Publikations- och innehållstyp

ref (ämneskategori)

art (ämneskategori)