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Publicação:
Brazilian individuals with impaired glucose tolerance are characterized by impaired insulin secretion

dc.contributor.authorPimenta, W. P. [UNESP]
dc.contributor.authorSantos, M. L. [UNESP]
dc.contributor.authorCruz, N. S. [UNESP]
dc.contributor.authorAragon, F. F. [UNESP]
dc.contributor.authorPadovani, C. R. [UNESP]
dc.contributor.authorGerich, J. E.
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniv. of Rochester Sch. of Medicine
dc.date.accessioned2022-04-28T19:55:38Z
dc.date.available2022-04-28T19:55:38Z
dc.date.issued2002-12-01
dc.description.abstractBackground: To better understand the pathogenesis of type 2 diabetes mellitus, insulin secretion and insulin sensitivity (IS) were evaluated in white Brazilians with impaired glucose tolerance (IGT), using the oral glucose tolerance test (OGTT) and the hyperglycemic clamp technique. Methods: Twenty-five IGT subjects were individually matched with normal glucose-tolerant (NGT) subjects for demographic characteristics. At first, they were submitted to the OGTT and plasma glucose and insulin were measured. Of the 25 pairs, 20 could participate in the hyperglycemic clamp procedures, at a second visit. All participants had their plasma glucose levels equally increased to 180 mg/dl; this was maintained for three hours by variable glucose infusion. During the procedure, plasma glucose and insulin were measured at established intervals. Results: In the postabsorptive state, the IGT subjects presented higher levels of plasma glucose, blood HbA1, and serum triglycerides, but similar plasma insulin levels. After the oral glucose load, early and total insulin release, in relation to glucose levels, were respectively, 43 and 67% lower in the IGT individuals. The index of whole-body IS was increased in the IGT individuals (4.36 ± 1.71 vs 3.61 ± 1.28 mg-1·μU-1·100·ml2; p < 0.05). By the hyperglycemic clamp technique first- (82 ± 26 vs 215 ± 88 μU/ml; p < 0.001) and second- (36 ± 19 vs 73 ± 44 μU/ml; p < 0.05) phases of insulin secretion was decreased in the IGT individuals, especiallythe first one. However, the groups did not differ in relation to the IS: IGT = 13.52 ± 7.27 and NGT = 9.96 ± 6.70 mg·ml/kg·μU·min-1; p > 0.05. Functional relationship of IS (y) on first-phase insulin release (x) showed a smaller (p < 0.05) regression coefficient for the IGT group. Conclusion: Brazilians with IGT well-matched with NGT ones were characterized by impaired first- and second-phase insulin secretion (mainly the former), while defects in IS were not evident.en
dc.description.affiliationDepartment of Internal Medicine School of Medicine São Paulo State University, Botucatu, São Paulo
dc.description.affiliationDepartment of Biostatistics Institute of Biosciences São Paulo State University, Botucatu, São Paulo
dc.description.affiliationDepartment of Medicine Univ. of Rochester Sch. of Medicine, Rochester, New York
dc.description.affiliationDepartamento de Clinica Medica Faculdade de Medicina de Botucatu UNESP, Caixa Postal, 584 Botucatu, São Paulo
dc.description.affiliationUnespDepartment of Internal Medicine School of Medicine São Paulo State University, Botucatu, São Paulo
dc.description.affiliationUnespDepartment of Biostatistics Institute of Biosciences São Paulo State University, Botucatu, São Paulo
dc.description.affiliationUnespDepartamento de Clinica Medica Faculdade de Medicina de Botucatu UNESP, Caixa Postal, 584 Botucatu, São Paulo
dc.format.extent468-476
dc.identifier.citationDiabetes and Metabolism, v. 28, n. 6 I, p. 468-476, 2002.
dc.identifier.issn1262-3636
dc.identifier.scopus2-s2.0-0036944156
dc.identifier.urihttp://hdl.handle.net/11449/224291
dc.language.isoeng
dc.relation.ispartofDiabetes and Metabolism
dc.sourceScopus
dc.subjectHyperglycemic clamp
dc.subjectImpaired glucose tolerance
dc.subjectInsulin secretion
dc.subjectInsulin sensitivity
dc.subjectOral glucose stimulus
dc.titleBrazilian individuals with impaired glucose tolerance are characterized by impaired insulin secretionen
dc.typeArtigo
dspace.entity.typePublication
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.departmentClínica Médica - FMBpt
unesp.departmentBioestatística - IBBpt

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