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Polymorphisms of the eNOS gene are associated with disease activity in rheumatoid arthritis.
Bunjevacki, Vera; Maksimovic, Nela; Jekic, Biljana; Milic, Vera; Lukovic, Ljiljana; Novakovic, Ivana; Damjanov, Nemanja; Radunovic, Goran; Damnjanovic, Tatjana.
Afiliação
  • Bunjevacki V; Faculty of Medicine, Institute of Human Genetics, University of Belgrade, 26 Visegradska Str., Belgrade, 11000, Serbia.
  • Maksimovic N; Faculty of Medicine, Institute of Human Genetics, University of Belgrade, 26 Visegradska Str., Belgrade, 11000, Serbia.
  • Jekic B; Faculty of Medicine, Institute of Human Genetics, University of Belgrade, 26 Visegradska Str., Belgrade, 11000, Serbia.
  • Milic V; Faculty of Medicine, Institute of Rheumatology, University of Belgrade, Resavska 69 Str., Belgrade, Serbia.
  • Lukovic L; Faculty of Medicine, Institute of Human Genetics, University of Belgrade, 26 Visegradska Str., Belgrade, 11000, Serbia.
  • Novakovic I; Faculty of Medicine, Institute of Human Genetics, University of Belgrade, 26 Visegradska Str., Belgrade, 11000, Serbia.
  • Damjanov N; Faculty of Medicine, Institute of Rheumatology, University of Belgrade, Resavska 69 Str., Belgrade, Serbia.
  • Radunovic G; Faculty of Medicine, Institute of Rheumatology, University of Belgrade, Resavska 69 Str., Belgrade, Serbia.
  • Damnjanovic T; Faculty of Medicine, Institute of Human Genetics, University of Belgrade, 26 Visegradska Str., Belgrade, 11000, Serbia. tatjanadamnjanovic@yahoo.com.
Rheumatol Int ; 36(4): 597-602, 2016 Apr.
Article em En | MEDLINE | ID: mdl-26612436
Nitric oxide (NO) is a mediator in autoimmune responses and thus involved in the pathogenesis of a variety of rheumatic diseases. Genetic factors that influence the expression of the enzyme endothelial nitric oxide synthase (eNOS) that catalyzes NO synthesis are important for the control of NO level and consequently its activity. We have analyzed three functionally relevant polymorphisms of eNOS gene: T-786C, G894T and VNTR (4a/b), to investigate whether they are predisposing factors in pathogenesis of RA in Serbian population and to evaluate their role in clinical manifestations of RA. We performed genotyping of 196 patients with RA and the control group of 132 healthy individuals from Serbian population, using PCR and polymerase chain reaction-restriction fragment length polymorphism methods. Disease activity was prospectively assessed using number of tender joints, number of swollen joints and 28-joints disease activity score (DAS28). There were no differences between the patients and control groups in the genotypes and alleles frequencies of the three analyzed SNPs. Our results showed statistically significant differences in all three analyzed parameters of disease severity between 786TT/786CT and 786CC genotypes and between 894GG/894GT and 894TT genotypes. In the case of 4a/b polymorphism, carriers of minor allele had significantly lower DAS28 values. In conclusion, our results do not support the implication of analyzed eNOS gene polymorphisms in susceptibility to RA but associate them with the disease activity and give assumption that minor alleles are indicators of better clinical course.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Artrite Reumatoide / Polimorfismo de Nucleotídeo Único / Óxido Nítrico Sintase Tipo III Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Rheumatol Int Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Artrite Reumatoide / Polimorfismo de Nucleotídeo Único / Óxido Nítrico Sintase Tipo III Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Rheumatol Int Ano de publicação: 2016 Tipo de documento: Article