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The X-X-/E+E+ genotype of the XbaI/EcoRI polymorphisms of the apolipoprotein B gene as a marker of coronary artery disease in a Brazilian sample
Scartezini, M; Zago, M. A; Chautard-Freire-Maia, E. A; Pazin-Filho, A; Marin-Neto, J. A; Hotta, J. K. S; Nascimento, A. J; Dos-Santos, J. E.
  • Scartezini, M; Universidade Federal do Paraná. Departamento de Patologia Médica. Curitiba. BR
  • Zago, M. A; Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Clínica Médica. Ribeirão Preto. BR
  • Chautard-Freire-Maia, E. A; Universidade Federal do Paraná. Departamento de Genética. Curitiba. BR
  • Pazin-Filho, A; Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Clínica Médica. Ribeirão Preto. BR
  • Marin-Neto, J. A; Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Clínica Médica. Ribeirão Preto. BR
  • Hotta, J. K. S; Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Clínica Médica. Ribeirão Preto. BR
  • Nascimento, A. J; Universidade Federal do Paraná. Departamento de Bioquímica. Curitiba. BR
  • Dos-Santos, J. E; Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Clínica Médica. Ribeirão Preto. BR
Braz. j. med. biol. res ; 36(3): 369-375, Mar. 2003. tab
Article in English | LILACS | ID: lil-329463
RESUMO
Studies that consider polymorphisms within the apolipoprotein B (apo B) gene as risk factors for coronary artery disease (CAD) have reported conflicting results. The aim of the present study was to search for associations between two DNA RFLPs (XbaI and EcoRI) of the apo B gene and CAD diagnosed by angiography. In the present study we compared 116 Brazilian patients (92 men) with CAD (CAD+) to 78 control patients (26 men) without ischemia or arterial damage (CAD-). The allele frequencies at the XbaI (X) and EcoRI (E) sites did not differ between groups. The genotype distributions of CAD+ and CAD- patients were different (chi²(1) = 6.27, P = 0.012) when assigned to two classes (X-X-/E+E+ and the remaining XbaI/EcoRI genotypes). Multivariate logistic regression analysis showed that individuals with the X-X-/E+E+ genotype presented a 6.1 higher chance of developing CAD than individuals with the other XbaI/EcoRI genotypes, independently of the other risk factors considered (sex, tobacco consumption, total cholesterol, hypertension, and triglycerides). We conclude that the X-X-/E+E genotype may be in linkage disequilibrium with an unknown variation in the apo B gene or with a variation in another gene that affects the risk of CAD
Subject(s)
Full text: Available Index: LILACS (Americas) Main subject: Apolipoproteins B / Polymorphism, Genetic / Deoxyribonuclease EcoRI / Deoxyribonucleases, Type II Site-Specific / Coronary Disease Type of study: Etiology study / Observational study / Prevalence study / Risk factors Limits: Adult / Female / Humans / Male Country/Region as subject: South America / Brazil Language: English Journal: Braz. j. med. biol. res Journal subject: Biology / Medicine Year: 2003 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Federal do Paraná/BR / Universidade de São Paulo/BR

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Full text: Available Index: LILACS (Americas) Main subject: Apolipoproteins B / Polymorphism, Genetic / Deoxyribonuclease EcoRI / Deoxyribonucleases, Type II Site-Specific / Coronary Disease Type of study: Etiology study / Observational study / Prevalence study / Risk factors Limits: Adult / Female / Humans / Male Country/Region as subject: South America / Brazil Language: English Journal: Braz. j. med. biol. res Journal subject: Biology / Medicine Year: 2003 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Federal do Paraná/BR / Universidade de São Paulo/BR