Journal
CLINICAL AND EXPERIMENTAL DERMATOLOGY
Volume 46, Issue 8, Pages 1462-1470Publisher
WILEY
DOI: 10.1111/ced.14766
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Funding
- TUBITAK [SBAG-2388, 113S163]
- Pamukkale University Research Fund [2001TPF020]
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This study found that the CXCR2 rs2230054 TT genotype and the CXCL5 rs352046 polymorphism might be associated with Behcet disease. However, no association was found between the development of BD and the four CXCR1 polymorphisms or the other two CXCR2 SNPs. Haplotype analysis results also indicated differences in haplotypes of the CXCR2 and CXCR1-CXCR2 polymorphic loci between BD and HC groups.
Background Behcet disease (BD) is associated with the immune system, especially neutrophilic activity. The CXCR1, CXCR2 and CXCL5 genes mediate the activation and migration of neutrophils. Aim To investigate CXCR1, CXCR2 and CXCL5 single nucleotide polymorphisms (SNPs) and examine their association with BD. Methods We studied polymorphic sites in CXCR1 (four sites: rs16858811, rs9282752, rs16858809 and rs16858808), CXCR2 (three sites: rs2230054, rs1126579 and rs1126580) and CXCL5 (one site: rs352046) in 87 patients with BD and 111 healthy controls (HCs), using a PCR restriction-fragment length polymorphism-based approach for genotyping. Results We found that the CXCR2 rs2230054 TT genotype and the CXCL5 rs352046 polymorphism might be possible genetic factors responsible for BD. We did not find any association between the development of BD and any of the four CXCR1 polymorphisms or the other two CXCR2 SNPs. In addition, our haplotype analysis results indicated that the haplotypes of the CXCR2 and CXCR1-CXCR2 polymorphic loci were different between the BD and HC groups. Conclusion Our study suggests that polymorphisms of CXCR1, CXCR2 and CXCL5 may affect susceptibility to BD and increase the risk of developing the disease. These loci need to be studied in larger groups of patients from different geographical areas around the world in order to clarify the genetic background for BD pathogenesis.
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