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Ann Rheum Dis 2003;62:1083-1087 doi:10.1136/ard.62.11.1083
  • Extended report

Endothelial nitric oxide synthase gene polymorphisms in Behçet’s disease and rheumatic diseases with vasculitis

  1. J U Kim1,
  2. H K Chang2,
  3. S S Lee3,
  4. J W Kim4,
  5. K T Kim5,
  6. S W Lee6,
  7. W T Chung6
  1. 1Department of Laboratory Medicine, Ulsan University, Kangnung, South Korea
  2. 2Division of Rheumatology, Department of Internal Medicine, Dankook University, Cheonan, South Korea
  3. 3Division of Rheumatology, Department of Internal Medicine, Chonnam National University Medical School, Kwangju, South Korea
  4. 4Department of Laboratory Medicine, Dankook University, Cheonan, South Korea
  5. 5Department of Emergency Medicine, Dankook University, Cheonan, South Korea
  6. 6Division of Rheumatology, Department of Internal Medicine, Dong-A University, Busan, South Korea
  1. Correspondence to:
    Dr H K Chang, Division of Rheumatology, Department of Internal Medicine, College of Medicine, Dankook University, 16-5 Anseo-Dong, Cheonan, Chungcheongnamdo, 330-715, South Korea; hanks22dankook.ac.kr
  • Accepted 12 March 2003

Abstract

Objective: To assess potential associations between Korean Behçet’s disease (BD) or other rheumatic diseases with vasculitis and two polymorphisms of the endothelial nitric oxide synthase (eNOS) gene, which include the Glu298Asp polymorphism in exon 7 and a variable number of tandem repeats (VNTR) polymorphism in intron 4.

Methods: 65 patients with BD, 27 with rheumatic diseases with vasculitis, and 80 controls were studied. Analyses of the Glu298Asp polymorphism in exon 7 and VNTR polymorphism in intron 4 of the eNOS gene were made by the polymerase chain reaction (PCR)-restriction fragment length polymorphism technique and PCR genotyping, respectively. Additionally, HLA-B51 typing was performed in the BD group and controls by a two step PCR sequence-specific primers method.

Results: Significant differences in Glu298Asp genotype frequencies were found between the BD or vasculitis groups and the controls (BD group v controls: pcorr=0.006; vasculitis group v controls: p<0.001). The Asp298 frequency was much higher in the BD and vasculitis groups than in the controls. Even after stratification of the BD group based on the results of HLA-B51 testing, a significant association of the Glu298Asp polymorphism was still found (p=0.002, Mantel-Haenszel weighted odds ratio 4.3, 95% confidence interval 1.7 to 10.9). Distribution of the genotype frequencies in two eNOS gene polymorphisms was similar in connective tissue diseases-associated vasculitis and primary vasculitic syndromes. In contrast, distribution of alleles and genotypes of VNTR polymorphism did not differ between BD or vasculitis groups and the controls.

Conclusion: The Glu298Asp polymorphism in exon 7 of the eNOS gene seems to be a susceptibility gene for Korean BD and other rheumatic diseases.

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