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Association between eNOS polymorphisms and risk of coronary artery disease in a Korean population: a meta-analysis.
Sung, J H; Lee, B E; Kim, J O; Jeon, Y J; Kim, S H; Lim, S W; Moon, J Y; Cha, D H; Kim, O J; Kim, I J; Kim, N K.
Afiliación
  • Sung JH; Department of Cardiology, CHA Bundang Medical Center, CHA University, Seongnam, South Korea.
  • Lee BE; Department of Biomedical Science, College of Life Science, CHA University, Seongnam, South Korea.
  • Kim JO; Department of Biomedical Science, College of Life Science, CHA University, Seongnam, South Korea.
  • Jeon YJ; Department of Biomedical Science, College of Life Science, CHA University, Seongnam, South Korea.
  • Kim SH; Department of Cardiology, CHA Bundang Medical Center, CHA University, Seongnam, South Korea.
  • Lim SW; Department of Cardiology, CHA Bundang Medical Center, CHA University, Seongnam, South Korea.
  • Moon JY; Department of Cardiology, CHA Bundang Medical Center, CHA University, Seongnam, South Korea.
  • Cha DH; Department of Cardiology, CHA Bundang Medical Center, CHA University, Seongnam, South Korea.
  • Kim OJ; Department of Neurology, CHA Bundang Medical Center, CHA University, Seongnam, South Korea.
  • Kim IJ; Department of Cardiology, CHA Bundang Medical Center, CHA University, Seongnam, South Korea.
  • Kim NK; Department of Biomedical Science, College of Life Science, CHA University, Seongnam, South Korea nkkim@cha.ac.kr.
Genet Mol Res ; 14(4): 16508-20, 2015 Dec 09.
Article en En | MEDLINE | ID: mdl-26662450
ABSTRACT
Coronary artery disease (CAD), a multifactorial disease, is a common cause of mortality in humans. Polymorphisms in the endothelial nitric oxide synthase (eNOS) gene (-786T>C, 4a4b, and 894G>T) have been previously associated with increased CAD risk. However, the sample size of this previous study was too small and limited to comprehensively define an association between eNOS polymorphisms and CAD; therefore, this analysis was duplicated with a larger population. The study was conducted on 559 patients with CAD and 574 healthy controls. Genetic DNA was extracted using the commercial G-DEX blood extraction kit and statistical analyses were performed on the GraphPad prism 4.0 and MedCalc 12.0 statistical software platforms. No single variant of the eNOS polymorphism was associated with CAD risk. The combination genotypes of eNOS -786TT/4a4b+4a4a [adjusted odds ratio (AOR) = 0.122; 95% confidence interval (CI) 0.042-0.358] and eNOS -786TC+CC/4b4b (AOR = 0.379; 95%CI 0.147-0.979) were associated with decreased CAD incidence. Haplotype analysis revealed that the T-4a haplotype of eNOS -786T>C and 4a4b exerted a protective effect against CAD. The association between eNOS -786T>C and increased CAD risk was not replicated in this (larger) population. However, some combined genotypes showed a meaningful association with CAD risk.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 6_ODS3_enfermedades_notrasmisibles Problema de salud: 6_cardiovascular_diseases / 6_ischemic_heart_disease Asunto principal: Polimorfismo Genético / Enfermedad de la Arteria Coronaria / Predisposición Genética a la Enfermedad / Pueblo Asiatico / Óxido Nítrico Sintasa de Tipo III / Estudios de Asociación Genética Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Aged / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Genet Mol Res Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA Año: 2015 Tipo del documento: Article País de afiliación: Corea del Sur

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 6_ODS3_enfermedades_notrasmisibles Problema de salud: 6_cardiovascular_diseases / 6_ischemic_heart_disease Asunto principal: Polimorfismo Genético / Enfermedad de la Arteria Coronaria / Predisposición Genética a la Enfermedad / Pueblo Asiatico / Óxido Nítrico Sintasa de Tipo III / Estudios de Asociación Genética Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Aged / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Genet Mol Res Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA Año: 2015 Tipo del documento: Article País de afiliación: Corea del Sur
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