Endothelial nitric oxide synthase gene Glu298Asp polymorphism is associated with Behçet's disease

Clin Exp Rheumatol. 2006 Sep-Oct;24(5 Suppl 42):S79-82.

Abstract

Objective: The 894 G-->T (Glu298Asp) polymorphism in exon 7 of the endothelial nitric oxide synthase (eNOS) gene was previously reported to be associated with Behçet's Disease (BD) susceptibility in Italian origin and Korean patients, but not in a group of unrelated Turkish patients. We analyzed whether this polymorphism is associated with BD, in another group of Turkish patients.

Methods: We studied 132 consecutive Turkish BD patients being followed up by Ege University Rheumatology Department and 91 healthy controls. All individuals were genotyped by PCR-RFLP for 894 G-->T in exon 7 (Glu298Asp).

Results: The frequency of the T allele in BD group (101/264) was significantly higher than in healthy controls (OR 1.88, %95 CI 1.27-2.49, p < 0.001). The frequency of the homozygote (TT) Glu298Asp polymorphism in BD (27/132) was also significantly higher than in healthy controls (5/91) (OR 3.72, %95 CI 3.44-4.0, p < 0.001). However, no association was found between the Glu298Asp polymorphism and clinical parameters in BD.

Conclusion: In this study, we found that Glu298Asp polymorphism of the eNOS gene was associated with BD in Turkish patients.

MeSH terms

  • Adult
  • Aspartic Acid
  • Behcet Syndrome / ethnology
  • Behcet Syndrome / genetics*
  • Case-Control Studies
  • Female
  • Genetic Predisposition to Disease
  • Glutamic Acid
  • Humans
  • Male
  • Middle Aged
  • Nitric Oxide Synthase Type III / genetics*
  • Polymorphism, Genetic*
  • Turkey

Substances

  • Aspartic Acid
  • Glutamic Acid
  • NOS3 protein, human
  • Nitric Oxide Synthase Type III