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

Bibliographic Details
Main Author: Pimenta, W. P. [UNESP]
Publication Date: 2002
Other Authors: Santos, M. L. [UNESP], Cruz, N. S. [UNESP], Aragon, F. F. [UNESP], Padovani, C. R. [UNESP], Gerich, J. E.
Format: Article
Language: eng
Source: Repositório Institucional da UNESP
Download full: http://hdl.handle.net/11449/224291
Summary: Background: 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.
id UNSP_bcf4404fb637b9b7afd7972e18b6db9b
oai_identifier_str oai:repositorio.unesp.br:11449/224291
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling Brazilian individuals with impaired glucose tolerance are characterized by impaired insulin secretionHyperglycemic clampImpaired glucose toleranceInsulin secretionInsulin sensitivityOral glucose stimulusBackground: 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.Department of Internal Medicine School of Medicine São Paulo State University, Botucatu, São PauloDepartment of Biostatistics Institute of Biosciences São Paulo State University, Botucatu, São PauloDepartment of Medicine Univ. of Rochester Sch. of Medicine, Rochester, New YorkDepartamento de Clinica Medica Faculdade de Medicina de Botucatu UNESP, Caixa Postal, 584 Botucatu, São PauloDepartment of Internal Medicine School of Medicine São Paulo State University, Botucatu, São PauloDepartment of Biostatistics Institute of Biosciences São Paulo State University, Botucatu, São PauloDepartamento de Clinica Medica Faculdade de Medicina de Botucatu UNESP, Caixa Postal, 584 Botucatu, São PauloUniversidade Estadual Paulista (UNESP)Univ. of Rochester Sch. of MedicinePimenta, W. P. [UNESP]Santos, M. L. [UNESP]Cruz, N. S. [UNESP]Aragon, F. F. [UNESP]Padovani, C. R. [UNESP]Gerich, J. E.2022-04-28T19:55:38Z2022-04-28T19:55:38Z2002-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article468-476Diabetes and Metabolism, v. 28, n. 6 I, p. 468-476, 2002.1262-3636http://hdl.handle.net/11449/2242912-s2.0-0036944156Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengDiabetes and Metabolisminfo:eu-repo/semantics/openAccess2022-04-28T19:55:38Zoai:repositorio.unesp.br:11449/224291Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462022-04-28T19:55:38Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Brazilian individuals with impaired glucose tolerance are characterized by impaired insulin secretion
title Brazilian individuals with impaired glucose tolerance are characterized by impaired insulin secretion
spellingShingle Brazilian individuals with impaired glucose tolerance are characterized by impaired insulin secretion
Pimenta, W. P. [UNESP]
Hyperglycemic clamp
Impaired glucose tolerance
Insulin secretion
Insulin sensitivity
Oral glucose stimulus
title_short Brazilian individuals with impaired glucose tolerance are characterized by impaired insulin secretion
title_full Brazilian individuals with impaired glucose tolerance are characterized by impaired insulin secretion
title_fullStr Brazilian individuals with impaired glucose tolerance are characterized by impaired insulin secretion
title_full_unstemmed Brazilian individuals with impaired glucose tolerance are characterized by impaired insulin secretion
title_sort Brazilian individuals with impaired glucose tolerance are characterized by impaired insulin secretion
author Pimenta, W. P. [UNESP]
author_facet Pimenta, W. P. [UNESP]
Santos, M. L. [UNESP]
Cruz, N. S. [UNESP]
Aragon, F. F. [UNESP]
Padovani, C. R. [UNESP]
Gerich, J. E.
author_role author
author2 Santos, M. L. [UNESP]
Cruz, N. S. [UNESP]
Aragon, F. F. [UNESP]
Padovani, C. R. [UNESP]
Gerich, J. E.
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
Univ. of Rochester Sch. of Medicine
dc.contributor.author.fl_str_mv Pimenta, W. P. [UNESP]
Santos, M. L. [UNESP]
Cruz, N. S. [UNESP]
Aragon, F. F. [UNESP]
Padovani, C. R. [UNESP]
Gerich, J. E.
dc.subject.por.fl_str_mv Hyperglycemic clamp
Impaired glucose tolerance
Insulin secretion
Insulin sensitivity
Oral glucose stimulus
topic Hyperglycemic clamp
Impaired glucose tolerance
Insulin secretion
Insulin sensitivity
Oral glucose stimulus
description Background: 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.
publishDate 2002
dc.date.none.fl_str_mv 2002-12-01
2022-04-28T19:55:38Z
2022-04-28T19:55:38Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv Diabetes and Metabolism, v. 28, n. 6 I, p. 468-476, 2002.
1262-3636
http://hdl.handle.net/11449/224291
2-s2.0-0036944156
identifier_str_mv Diabetes and Metabolism, v. 28, n. 6 I, p. 468-476, 2002.
1262-3636
2-s2.0-0036944156
url http://hdl.handle.net/11449/224291
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Diabetes and Metabolism
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 468-476
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
_version_ 1797789266363809792