The aim of the present study was to assess the level of glycaemic control by the measurement of 24 h blood glucose profiles and standard blood analyses under identical nutritional and physical activity conditions in patients with Type II diabetes and healthy normoglycaemic controls. A total of 11 male patients with Type II diabetes and 11 healthy matched controls participated in a 24 h CGMS (continuous subcutaneous glucose-monitoring system) assessment trial under strictly standardized dietary and physical activity conditions. In addition, fasting plasma glucose, insulin and HbA1c (glycated haemoglobin) concentrations were measured, and an OGTT (oral glucose tolerance test) was performed to calculate indices of whole-body insulin sensitivity, oral glucose tolerance and/or glycaemic control. In the healthy control group, hyperglycaemia (blood glucose concentration >10 mmol/l) was hardly present (2±1% or 0.4±0.2/24 h). However, in the patients with Type II diabetes, hyperglycaemia was experienced for as much as 55±7% of the time (13±2 h over 24 h) while using the same standardized diet. Breakfast-related hyperglycaemia contributed most (46±7%; P<0.01 as determined by ANOVA) to the total amount of hyperglycaemia and postprandial glycaemic instability. In the diabetes patients, blood HbA1c content correlated well with the duration of hyperglycaemia and the postprandial glucose responses (P<0.05). In conclusion, CGMS determinations show that standard measurements of glycaemic control underestimate the amount of hyperglycaemia prevalent during real-life conditions in Type II diabetes. Given the macro- and micro-vascular damage caused by postprandial hyperglycaemia, CGMS provides an excellent tool to evaluate alternative therapeutic strategies to reduce hyperglycaemic blood glucose excursions.
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August 2006
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Research Article|
July 13 2006
Glycaemic instability is an underestimated problem in Type II diabetes
Stephan F. E. Praet;
*Department of Movement Sciences, Nutrition and Toxicology Research Institute Maastricht (NUTRIM), Maastricht University, Maastricht, The Netherlands
Correspondence: Dr Stephan F. E. Praet (email [email protected]).
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Ralph J. F. Manders;
Ralph J. F. Manders
†Department of Human Biology, NUTRIM, Maastricht University, Maastricht, The Netherlands
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Ruth C. R. Meex;
Ruth C. R. Meex
†Department of Human Biology, NUTRIM, Maastricht University, Maastricht, The Netherlands
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A. G. Lieverse;
A. G. Lieverse
‡Department of Internal Medicine, Máxima Medical Center, Eindhoven, The Netherlands
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Coen D. A. Stehouwer;
Coen D. A. Stehouwer
§Department of Internal Medicine, University Hospital Maastricht, Maastricht, The Netherlands
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Harm Kuipers;
Harm Kuipers
*Department of Movement Sciences, Nutrition and Toxicology Research Institute Maastricht (NUTRIM), Maastricht University, Maastricht, The Netherlands
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Hans A. Keizer;
Hans A. Keizer
*Department of Movement Sciences, Nutrition and Toxicology Research Institute Maastricht (NUTRIM), Maastricht University, Maastricht, The Netherlands
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Luc J. C. van Loon
Luc J. C. van Loon
*Department of Movement Sciences, Nutrition and Toxicology Research Institute Maastricht (NUTRIM), Maastricht University, Maastricht, The Netherlands
†Department of Human Biology, NUTRIM, Maastricht University, Maastricht, The Netherlands
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Publisher: Portland Press Ltd
Received:
February 17 2006
Revision Received:
April 12 2006
Accepted:
April 13 2006
Accepted Manuscript online:
April 13 2006
Online ISSN: 1470-8736
Print ISSN: 0143-5221
The Biochemical Society
2006
Clin Sci (Lond) (2006) 111 (2): 119–126.
Article history
Received:
February 17 2006
Revision Received:
April 12 2006
Accepted:
April 13 2006
Accepted Manuscript online:
April 13 2006
Citation
Stephan F. E. Praet, Ralph J. F. Manders, Ruth C. R. Meex, A. G. Lieverse, Coen D. A. Stehouwer, Harm Kuipers, Hans A. Keizer, Luc J. C. van Loon; Glycaemic instability is an underestimated problem in Type II diabetes. Clin Sci (Lond) 1 August 2006; 111 (2): 119–126. doi: https://doi.org/10.1042/CS20060041
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