Investigation of the genetic overlap between rheumatoid arthritis and psoriatic arthritis in a Greek population

Scand J Rheumatol. 2017 May;46(3):180-186. doi: 10.1080/03009742.2016.1199734. Epub 2016 Jul 20.

Abstract

Objectives: Several rheumatoid arthritis (RA) susceptibility loci have also been found to be associated with psoriatic arthritis (PsA), demonstrating that there is a degree of genetic overlap between various autoimmune diseases. We sought to investigate whether single nucleotide polymorphisms (SNPs) mapping to previously reported RA and/or PsA susceptibility loci, including PLCL2, CCL21, REL, STAT4, CD226, PTPN22, and TYK2, are associated with risk for the two diseases in a genetically homogeneous Greek population.

Method: This study included 392 RA patients, 126 PsA patients, and 521 healthy age- and sex-matched controls from Greece. Genotyping of the SNPs was performed with Taqman primer/probe sets. Bioinformatic analysis was performed using BlastP, PyMOL, and Maestro and Desmond.

Results: A significant association was detected between the GC genotype of rs34536443 (TYK2) in both the PsA and RA cohorts. The C allele of this SNP was associated with PsA only. Evidence for association with PsA was also found for the GG genotype and G allele of the rs10181656 SNP of STAT4. The TC genotype of the rs763361 SNP of CD226 was associated with PsA only.

Conclusions: Genetic overlap between PsA and RA was detected for the rs34536443 SNP of the TYK2 gene within a Greek population. An association of STAT4 (rs10181656) with PsA was confirmed whereas CD226 (rs763361) was associated with PsA but not with RA, in contrast to previous reports. The different findings of this study compared to previous ones highlights the importance of comparative studies that include various ethnic or racial populations.

MeSH terms

  • Adult
  • Aged
  • Alleles
  • Antigens, Differentiation, T-Lymphocyte / genetics
  • Arthritis, Psoriatic / genetics*
  • Arthritis, Rheumatoid / genetics*
  • Case-Control Studies
  • Chemokine CCL21 / genetics
  • Cohort Studies
  • Female
  • Genetic Predisposition to Disease
  • Genotype
  • Genotyping Techniques
  • Greece
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics
  • Male
  • Middle Aged
  • Models, Molecular
  • Oncogene Proteins v-rel / genetics
  • Polymorphism, Single Nucleotide
  • Protein Tyrosine Phosphatase, Non-Receptor Type 22 / genetics
  • STAT4 Transcription Factor / genetics
  • T Lineage-Specific Activation Antigen 1
  • TYK2 Kinase / genetics
  • White People / genetics*

Substances

  • Antigens, Differentiation, T-Lymphocyte
  • CCL21 protein, human
  • T Lineage-Specific Activation Antigen 1
  • Chemokine CCL21
  • Intracellular Signaling Peptides and Proteins
  • Oncogene Proteins v-rel
  • PLCL2 protein, human
  • STAT4 Transcription Factor
  • STAT4 protein, human
  • TYK2 Kinase
  • TYK2 protein, human
  • PTPN22 protein, human
  • Protein Tyrosine Phosphatase, Non-Receptor Type 22