dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:47:48Z
dc.date.accessioned2022-10-05T14:17:26Z
dc.date.available2014-05-20T13:47:48Z
dc.date.available2022-10-05T14:17:26Z
dc.date.created2014-05-20T13:47:48Z
dc.date.issued2009-03-01
dc.identifierBrazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 42, n. 3, p. 279-288, 2009.
dc.identifier0100-879X
dc.identifierhttp://hdl.handle.net/11449/17040
dc.identifier10.1590/S0100-879X2009000300009
dc.identifierS0100-879X2009000300009
dc.identifierWOS:000264200100009
dc.identifierS0100-879X2009000300009.pdf
dc.identifier8727897080522289
dc.identifier4369996017190767
dc.identifier0000-0002-6716-1170
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3891862
dc.description.abstractWe evaluated changes in glucose tolerance of 17 progressors and 62 non-progressors for 9 years to improve our understanding of the pathogenesis of type 2 diabetes mellitus. Changes in anthropometric measurements and responses to an oral glucose tolerance test (OGTT) were analyzed. We identified 14 pairs of individuals, one from each group, who were initially normal glucose tolerant and were matched for gender, age, weight, and girth. We compared initial plasma glucose and insulin curves (from OGTT), insulin secretion (first and second phases) and insulin sensitivity indices (from hyperglycemic clamp assay) for both groups. In the normal glucose tolerant phase, progressors presented: 1) a higher OGTT blood glucose response with hyperglycemia in the second hour and a similar insulin response vs non-progressors; 2) a reduced first-phase insulin secretion (2.0 ± 0.3 vs 2.3 ± 0.3 pmol/L; P < 0.02) with a similar insulin sensitivity index and a lower disposition index (3.9 ± 0.2 vs 4.1 ± 0.2 µmol·kg-1·min-1 ; P < 0.05) vs non-progressors. After 9 years, both groups presented similar increases in weight and fasting blood glucose levels and progressors had an increased glycemic response at 120 min (P < 0.05) and reduced early insulin response to OGTT (progressors, 1st: 2.10 ± 0.34 vs 2nd: 1.87 ± 0.25 pmol/mmol; non-progressors, 1st: 2.15 ± 0.28 vs 2nd: 2.03 ± 0.39 pmol/mmol; P < 0.05). Theses data suggest that β-cell dysfunction might be a risk factor for type 2 diabetes mellitus.
dc.languageeng
dc.publisherAssociação Brasileira de Divulgação Científica (ABRADIC)
dc.relationBrazilian Journal of Medical and Biological Research
dc.relation1.492
dc.rightsAcesso aberto
dc.sourceSciELO
dc.subjectImpaired glucose tolerance
dc.subjectImpaired insulin secretion
dc.subjectNormal glucose tolerance
dc.subjectHyperglycemic clamp
dc.subjectOral glucose tolerance test
dc.titleDemographic and metabolic characteristics of individuals with progressive glucose tolerance
dc.typeArtigo


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