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Glucose Effectiveness in Obese Children: Relation to Degree of Obesity and Dysglycemia

OBJECTIVE: Impaired glucose effectiveness (GE) plays a role in the deterioration of glucose metabolism. Our aim was to validate a surrogate of GE derived from an oral glucose tolerance test (OGTT) and to assess the impact of degrees of obesity and of glucose tolerance on it. RESEARCH DESIGN AND METH...

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Autores principales: Weiss, Ram, Magge, Sheela N., Santoro, Nicola, Giannini, Cosimo, Boston, Raymond, Holder, Tara, Shaw, Melissa, Duran, Elvira, Hershkop, Karen J., Caprio, Sonia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4370330/
https://www.ncbi.nlm.nih.gov/pubmed/25633663
http://dx.doi.org/10.2337/dc14-2183
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author Weiss, Ram
Magge, Sheela N.
Santoro, Nicola
Giannini, Cosimo
Boston, Raymond
Holder, Tara
Shaw, Melissa
Duran, Elvira
Hershkop, Karen J.
Caprio, Sonia
author_facet Weiss, Ram
Magge, Sheela N.
Santoro, Nicola
Giannini, Cosimo
Boston, Raymond
Holder, Tara
Shaw, Melissa
Duran, Elvira
Hershkop, Karen J.
Caprio, Sonia
author_sort Weiss, Ram
collection PubMed
description OBJECTIVE: Impaired glucose effectiveness (GE) plays a role in the deterioration of glucose metabolism. Our aim was to validate a surrogate of GE derived from an oral glucose tolerance test (OGTT) and to assess the impact of degrees of obesity and of glucose tolerance on it. RESEARCH DESIGN AND METHODS: The OGTT-derived surrogate of GE (oGE) was validated in obese adolescents who underwent an OGTT and an intravenous glucose tolerance test (IVGTT). We then evaluated anthropometric determinants of the oGE and its impact on the dynamics of glucose tolerance in a cohort of children with varying degrees of obesity. RESULTS: The correlation of oGE and IVGTT-derived GE in 98 obese adolescents was r = 0.35 (P < 0.001) as a whole and r = 0.51 (P < 0.001) in subjects with normal glucose tolerance. In a cohort of 1,418 children, the adjusted GE was associated with increasing obesity (P < 0.001 for each category of obesity). Quartiles of oGE and the oral disposition index were associated with 2-h glucose levels (P < 0.001 for both). Among 421 nondiabetic obese subjects (276 subjects with normal glucose tolerance/145 subjects with impaired glucose tolerance who repeated their OGTT after a mean time of 28 ± 16 months), oGE changes were tightly associated with weight (r = 0.83, P < 0.001) and waist circumference changes (r = 0.67, P < 0.001). Baseline oGE and changes in oGE over time emerged as significant predictors of the change in 2-h glucose levels (standardized B = −0.76 and B = −0.98 respectively, P < 0.001 for both). CONCLUSIONS: The oGE is associated with the degree of and changes in weight and waist circumference and is an independent predictor of glucose tolerance dynamics.
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spelling pubmed-43703302016-04-01 Glucose Effectiveness in Obese Children: Relation to Degree of Obesity and Dysglycemia Weiss, Ram Magge, Sheela N. Santoro, Nicola Giannini, Cosimo Boston, Raymond Holder, Tara Shaw, Melissa Duran, Elvira Hershkop, Karen J. Caprio, Sonia Diabetes Care Pathophysiology/Complications OBJECTIVE: Impaired glucose effectiveness (GE) plays a role in the deterioration of glucose metabolism. Our aim was to validate a surrogate of GE derived from an oral glucose tolerance test (OGTT) and to assess the impact of degrees of obesity and of glucose tolerance on it. RESEARCH DESIGN AND METHODS: The OGTT-derived surrogate of GE (oGE) was validated in obese adolescents who underwent an OGTT and an intravenous glucose tolerance test (IVGTT). We then evaluated anthropometric determinants of the oGE and its impact on the dynamics of glucose tolerance in a cohort of children with varying degrees of obesity. RESULTS: The correlation of oGE and IVGTT-derived GE in 98 obese adolescents was r = 0.35 (P < 0.001) as a whole and r = 0.51 (P < 0.001) in subjects with normal glucose tolerance. In a cohort of 1,418 children, the adjusted GE was associated with increasing obesity (P < 0.001 for each category of obesity). Quartiles of oGE and the oral disposition index were associated with 2-h glucose levels (P < 0.001 for both). Among 421 nondiabetic obese subjects (276 subjects with normal glucose tolerance/145 subjects with impaired glucose tolerance who repeated their OGTT after a mean time of 28 ± 16 months), oGE changes were tightly associated with weight (r = 0.83, P < 0.001) and waist circumference changes (r = 0.67, P < 0.001). Baseline oGE and changes in oGE over time emerged as significant predictors of the change in 2-h glucose levels (standardized B = −0.76 and B = −0.98 respectively, P < 0.001 for both). CONCLUSIONS: The oGE is associated with the degree of and changes in weight and waist circumference and is an independent predictor of glucose tolerance dynamics. American Diabetes Association 2015-04 2015-01-29 /pmc/articles/PMC4370330/ /pubmed/25633663 http://dx.doi.org/10.2337/dc14-2183 Text en © 2015 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered.
spellingShingle Pathophysiology/Complications
Weiss, Ram
Magge, Sheela N.
Santoro, Nicola
Giannini, Cosimo
Boston, Raymond
Holder, Tara
Shaw, Melissa
Duran, Elvira
Hershkop, Karen J.
Caprio, Sonia
Glucose Effectiveness in Obese Children: Relation to Degree of Obesity and Dysglycemia
title Glucose Effectiveness in Obese Children: Relation to Degree of Obesity and Dysglycemia
title_full Glucose Effectiveness in Obese Children: Relation to Degree of Obesity and Dysglycemia
title_fullStr Glucose Effectiveness in Obese Children: Relation to Degree of Obesity and Dysglycemia
title_full_unstemmed Glucose Effectiveness in Obese Children: Relation to Degree of Obesity and Dysglycemia
title_short Glucose Effectiveness in Obese Children: Relation to Degree of Obesity and Dysglycemia
title_sort glucose effectiveness in obese children: relation to degree of obesity and dysglycemia
topic Pathophysiology/Complications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4370330/
https://www.ncbi.nlm.nih.gov/pubmed/25633663
http://dx.doi.org/10.2337/dc14-2183
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