Single-Nucleotide Polymorphisms in IL23R-IL12RB2 (rs1495965) Are Highly Prevalent in Patients with Behcet's Uveitis and Vary Between Populations.
Michal KramerMurat HasanreisogluShirel WeissDeniz KumovaMichal Schaap-FoglerSezen Guntekin-ErgunSengul OzdekGokhan GurelikMehmet Ali ErgünNitza Goldenberg-CohenYoram CohenPublished in: Ocular immunology and inflammation (2018)
Purpose: To test the frequency of single-nucleotide polymorphisms in the IL-10, IL23R-IL12RB2 genes in patients with Behcet's uveitis. Methods: Blood samples were collected from 89 Israeli and Turkish patients, and from healthy control subjects of different origins. Genomic DNA was extracted from peripheral blood leukocytes and genotyped. Results: The risk allele, A, in rs1800871, of IL-10 gene was highly prevalent in Behcet's uveitis and healthy control samples alike; highest among the Turkish groups. Prevalence of G allele, in rs1495965, in the IL23R-IL12RB2 gene was high in Behcet's uveitis patients, and among healthy Turkish and Israelis of Middle Eastern origin, while lower among the other Israeli control group (77.9%, 78.9%, 27.8%, respectively, P < 0.001). Conclusion: Our findings highlight the differences between populations and may account for the increased prevalence of the disease among Turkish and Israelis of Middle Eastern origin. Further studies are required to map other healthy and affected populations.
Keyphrases
- end stage renal disease
- peripheral blood
- juvenile idiopathic arthritis
- chronic kidney disease
- newly diagnosed
- ejection fraction
- ankylosing spondylitis
- risk factors
- genome wide
- south africa
- prognostic factors
- peritoneal dialysis
- gene expression
- genome wide identification
- patient reported
- genetic diversity
- circulating tumor cells
- circulating tumor