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dc.contributor.authorCrispim, Daisypt_BR
dc.contributor.authorCanani, Luis Henrique Santospt_BR
dc.contributor.authorGross, Jorge Luizpt_BR
dc.contributor.authorTschiedel, Balduínopt_BR
dc.contributor.authorSouto, Kátia Elisabete Pirespt_BR
dc.contributor.authorRoisenberg, Israelpt_BR
dc.date.accessioned2011-01-15T05:58:59Zpt_BR
dc.date.issued2006pt_BR
dc.identifier.issn0003-4800pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/27436pt_BR
dc.description.abstractThe aims of this studywere to investigate the contributions of the mitochondrialDNAm.4216T>Cand m.4917A> Gvariants, and also of the European-specific mitochondrial cluster J/T, to the development of type 2 diabetes mellitus in Caucasian-Brazilian patients from Southern Brazil. We analyzed 347 type 2 diabetes patients and 350 control subjects. Variant frequencies in patients and control subjects were compared using χ2 tests or odds ratio. We also compared clinical and laboratory characteristics among patients with and without the variants. We found that the frequencies of the m.4216T > C and m.4917A > G variants are higher in diabetic patients than in control subjects. Moreover, haplogroups J (partially defined by the presence of the m.4216T > C variant only) and T (partially defined by the presence of both m.4216T > C and m.4917A > G variants) are more frequent in the type 2 diabetic group than in the control group. Patients belonging to the cluster J/T are more insulin resistant than patients of other haplogroups. In conclusion, our results indicate the association of the cluster J/T (as suggested by analyses of the m.4216T > C and m.4917A > G variants) with insulin resistance and type 2 diabetes.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofAnnals of human genetics. London. Vol. 70, no.4 (Jun. 2006), p. 488-495pt_BR
dc.rightsOpen Accessen
dc.subjectDiabetes mellitus tipo 2pt_BR
dc.titleThe european-specific mitochondrial cluster J/T could confer an increased risk of insulin-resistance and type 2 diabetes : an analysis of the m.4216T > C and m.4917A > G variantspt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb000535643pt_BR
dc.type.originEstrangeiropt_BR


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