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dc.contributor.authorGattás, G. J. F.-
dc.contributor.authorKato, M.-
dc.contributor.authorVieira, J. A. Soares-
dc.contributor.authorSiraque, M. S.-
dc.contributor.authorKohler, P.-
dc.contributor.authorGomes, L.-
dc.contributor.authorRêgo, Marco Antônio Vasconcelos-
dc.contributor.authorBydlowski, S. P.-
dc.creatorGattás, G. J. F.-
dc.creatorKato, M.-
dc.creatorVieira, J. A. Soares-
dc.creatorSiraque, M. S.-
dc.creatorKohler, P.-
dc.creatorGomes, L.-
dc.creatorRêgo, Marco Antônio Vasconcelos-
dc.creatorBydlowski, S. P.-
dc.date.accessioned2011-11-25T12:07:44Z-
dc.date.available2011-11-25T12:07:44Z-
dc.date.issued2004-
dc.identifier.issn0100-879X-
dc.identifier.urihttp://www.repositorio.ufba.br/ri/handle/ri/3874-
dc.descriptionp. 451-458.pt_BR
dc.description.abstractThe distribution of polymorphisms related to glutathione S-transferases (GST) has been described in different populations, mainly for white individuals. We evaluated the distribution of GST mu (GSTM1) and theta (GSTT1) genotypes in 594 individuals, by multiplex PCRbased methods, using amplification of the exon 7 of CYP1A1 gene as an internal control. In São Paulo, 233 whites, 87 mulattos, and 137 blacks, all healthy blood-donor volunteers, were tested. In Bahia, where black and mulatto populations are more numerous, 137 subjects were evaluated. The frequency of the GSTM1 null genotype was significantly higher among whites (55.4%) than among mulattos (41.4%; P = 0.03) and blacks (32.8%; P < 0.0001) from São Paulo, or Bahian subjects in general (35.7%; P = 0.0003). There was no statistically different distribution among any non-white groups. The distribution of GSTT1 null genotype among groups did not differ significantly. The agreement between self-reported and interviewer classification of skin color in the Bahian group was low. The interviewer classification indicated a gradient of distribution of the GSTM1 null genotype from whites (55.6%) to light mulattos (40.4%), dark mulattos (32.0%) and blacks (28.6%). However, any information about race or ethnicity should be considered with caution regarding the bias introduced by different data collection techniques, specially in countries where racial admixture is intense, and ethnic definition boundaries are loose. Because homozygous deletions of GST gene might be associated with cancer risk, a better understanding of chemical metabolizing gene distribution can contribute to risk assessment of humans exposed to environmental carcinogens.pt_BR
dc.language.isoenpt_BR
dc.subjectGlutathione S-transferase mu (GSTM1)pt_BR
dc.subjectGlutathione S-transferase theta (GSTT1)pt_BR
dc.subjectEnzyme polymorphismpt_BR
dc.subjectPopulation frequencypt_BR
dc.subjectEthnicitypt_BR
dc.subjectBrazilpt_BR
dc.titleEthnicity and glutathione S-transferase (GSTM1/GSTT1) polymorphisms in a Brazilian populationpt_BR
dc.title.alternativeBrazilian Journal of Medical and Biological Researchpt_BR
dc.typeArtigo de Periódicopt_BR
dc.identifier.number37(4)pt_BR
Aparece nas coleções:Artigo Publicado em Periódico (Faculdade de Medicina)

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