Comparative Effects of Variations in Duodenal Glucose Load on Glycemic, Insulinemic, and Incretin Responses in Healthy Young and Older Subjects
Context:Aging is associated with deteriorating glucose tolerance. Studies assessing glucose tolerance and subsequent insulin and incretin hormone release often fail to take into account the rate of gastric emptying when evaluating these responses.Objective:Our objective was to determine the comparat...
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Published in | The journal of clinical endocrinology and metabolism Vol. 97; no. 3; pp. 844 - 851 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Bethesda, MD
Oxford University Press
01.03.2012
Copyright by The Endocrine Society Endocrine Society |
Subjects | |
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Abstract | Context:Aging is associated with deteriorating glucose tolerance. Studies assessing glucose tolerance and subsequent insulin and incretin hormone release often fail to take into account the rate of gastric emptying when evaluating these responses.Objective:Our objective was to determine the comparative effects of variations in the small intestinal glucose load on the glycemic, insulinemic, and incretin responses in healthy young and older subjects.Materials and Methods:Twelve healthy young (six males, six females; age 22.2 ± 2.3 yr) and 12 older (six males, six females; age 68.7 ± 1.0 yr) subjects had measurements of blood glucose, serum insulin and plasma incretin hormones [glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP)] and calculations of insulin resistance (homeostatic model assessment) and β-cell function corrected for insulin sensitivity, before and during intraduodenal infusions of glucose at 1, 2, or 3 kcal/min or saline for 60 minutes. The study was double-blinded and randomized, and performed in the Discipline of Medicine at the Royal Adelaide Hospital.Results:At baseline, blood glucose and serum insulin were slightly higher in the older subjects (P < 0.001), whereas GLP-1 and GIP were comparable between groups. In both groups, the glycemic, insulinemic, and GLP-1 responses were dependent on the duodenal glucose load in a nonlinear fashion (P < 0.001). The glycemic response was greater (P < 0.001) in the older subjects, whereas GLP-1 and GIP responses were comparable between groups. The older subjects were more insulin resistant (P < 0.001) and had impaired β-cell function, particularly at higher glucose loads (P < 0.05).Conclusion:When glucose is infused into the small intestine at equal rates in healthy young and older subjects, GLP-1 and GIP responses are comparable, indicating that impaired incretin secretion does not account for age-related glucose intolerance. |
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AbstractList | Context:Aging is associated with deteriorating glucose tolerance. Studies assessing glucose tolerance and subsequent insulin and incretin hormone release often fail to take into account the rate of gastric emptying when evaluating these responses.Objective:Our objective was to determine the comparative effects of variations in the small intestinal glucose load on the glycemic, insulinemic, and incretin responses in healthy young and older subjects.Materials and Methods:Twelve healthy young (six males, six females; age 22.2 ± 2.3 yr) and 12 older (six males, six females; age 68.7 ± 1.0 yr) subjects had measurements of blood glucose, serum insulin and plasma incretin hormones [glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP)] and calculations of insulin resistance (homeostatic model assessment) and β-cell function corrected for insulin sensitivity, before and during intraduodenal infusions of glucose at 1, 2, or 3 kcal/min or saline for 60 minutes. The study was double-blinded and randomized, and performed in the Discipline of Medicine at the Royal Adelaide Hospital.Results:At baseline, blood glucose and serum insulin were slightly higher in the older subjects (P < 0.001), whereas GLP-1 and GIP were comparable between groups. In both groups, the glycemic, insulinemic, and GLP-1 responses were dependent on the duodenal glucose load in a nonlinear fashion (P < 0.001). The glycemic response was greater (P < 0.001) in the older subjects, whereas GLP-1 and GIP responses were comparable between groups. The older subjects were more insulin resistant (P < 0.001) and had impaired β-cell function, particularly at higher glucose loads (P < 0.05).Conclusion:When glucose is infused into the small intestine at equal rates in healthy young and older subjects, GLP-1 and GIP responses are comparable, indicating that impaired incretin secretion does not account for age-related glucose intolerance. CONTEXT:Aging is associated with deteriorating glucose tolerance. Studies assessing glucose tolerance and subsequent insulin and incretin hormone release often fail to take into account the rate of gastric emptying when evaluating these responses. OBJECTIVE:Our objective was to determine the comparative effects of variations in the small intestinal glucose load on the glycemic, insulinemic, and incretin responses in healthy young and older subjects. MATERIALS AND METHODS:Twelve healthy young (six males, six females; age 22.2 ± 2.3 yr) and 12 older (six males, six females; age 68.7 ± 1.0 yr) subjects had measurements of blood glucose, serum insulin and plasma incretin hormones [glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP)] and calculations of insulin resistance (homeostatic model assessment) and β-cell function corrected for insulin sensitivity, before and during intraduodenal infusions of glucose at 1, 2, or 3 kcal/min or saline for 60 minutes. The study was double-blinded and randomized, and performed in the Discipline of Medicine at the Royal Adelaide Hospital. RESULTS:At baseline, blood glucose and serum insulin were slightly higher in the older subjects (P < 0.001), whereas GLP-1 and GIP were comparable between groups. In both groups, the glycemic, insulinemic, and GLP-1 responses were dependent on the duodenal glucose load in a nonlinear fashion (P < 0.001). The glycemic response was greater (P < 0.001) in the older subjects, whereas GLP-1 and GIP responses were comparable between groups. The older subjects were more insulin resistant (P < 0.001) and had impaired β-cell function, particularly at higher glucose loads (P < 0.05). CONCLUSION:When glucose is infused into the small intestine at equal rates in healthy young and older subjects, GLP-1 and GIP responses are comparable, indicating that impaired incretin secretion does not account for age-related glucose intolerance. Aging is associated with deteriorating glucose tolerance. Studies assessing glucose tolerance and subsequent insulin and incretin hormone release often fail to take into account the rate of gastric emptying when evaluating these responses. Our objective was to determine the comparative effects of variations in the small intestinal glucose load on the glycemic, insulinemic, and incretin responses in healthy young and older subjects. Twelve healthy young (six males, six females; age 22.2±2.3 yr) and 12 older (six males, six females; age 68.7±1.0 yr) subjects had measurements of blood glucose, serum insulin and plasma incretin hormones [glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP)] and calculations of insulin resistance (homeostatic model assessment) and β-cell function corrected for insulin sensitivity, before and during intraduodenal infusions of glucose at 1, 2, or 3 kcal/min or saline for 60 minutes. The study was double-blinded and randomized, and performed in the Discipline of Medicine at the Royal Adelaide Hospital. At baseline, blood glucose and serum insulin were slightly higher in the older subjects (P<0.001), whereas GLP-1 and GIP were comparable between groups. In both groups, the glycemic, insulinemic, and GLP-1 responses were dependent on the duodenal glucose load in a nonlinear fashion (P<0.001). The glycemic response was greater (P<0.001) in the older subjects, whereas GLP-1 and GIP responses were comparable between groups. The older subjects were more insulin resistant (P<0.001) and had impaired β-cell function, particularly at higher glucose loads (P<0.05). When glucose is infused into the small intestine at equal rates in healthy young and older subjects, GLP-1 and GIP responses are comparable, indicating that impaired incretin secretion does not account for age-related glucose intolerance. Aging is associated with deteriorating glucose tolerance. Studies assessing glucose tolerance and subsequent insulin and incretin hormone release often fail to take into account the rate of gastric emptying when evaluating these responses.CONTEXTAging is associated with deteriorating glucose tolerance. Studies assessing glucose tolerance and subsequent insulin and incretin hormone release often fail to take into account the rate of gastric emptying when evaluating these responses.Our objective was to determine the comparative effects of variations in the small intestinal glucose load on the glycemic, insulinemic, and incretin responses in healthy young and older subjects.OBJECTIVEOur objective was to determine the comparative effects of variations in the small intestinal glucose load on the glycemic, insulinemic, and incretin responses in healthy young and older subjects.Twelve healthy young (six males, six females; age 22.2±2.3 yr) and 12 older (six males, six females; age 68.7±1.0 yr) subjects had measurements of blood glucose, serum insulin and plasma incretin hormones [glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP)] and calculations of insulin resistance (homeostatic model assessment) and β-cell function corrected for insulin sensitivity, before and during intraduodenal infusions of glucose at 1, 2, or 3 kcal/min or saline for 60 minutes. The study was double-blinded and randomized, and performed in the Discipline of Medicine at the Royal Adelaide Hospital.MATERIALS AND METHODSTwelve healthy young (six males, six females; age 22.2±2.3 yr) and 12 older (six males, six females; age 68.7±1.0 yr) subjects had measurements of blood glucose, serum insulin and plasma incretin hormones [glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP)] and calculations of insulin resistance (homeostatic model assessment) and β-cell function corrected for insulin sensitivity, before and during intraduodenal infusions of glucose at 1, 2, or 3 kcal/min or saline for 60 minutes. The study was double-blinded and randomized, and performed in the Discipline of Medicine at the Royal Adelaide Hospital.At baseline, blood glucose and serum insulin were slightly higher in the older subjects (P<0.001), whereas GLP-1 and GIP were comparable between groups. In both groups, the glycemic, insulinemic, and GLP-1 responses were dependent on the duodenal glucose load in a nonlinear fashion (P<0.001). The glycemic response was greater (P<0.001) in the older subjects, whereas GLP-1 and GIP responses were comparable between groups. The older subjects were more insulin resistant (P<0.001) and had impaired β-cell function, particularly at higher glucose loads (P<0.05).RESULTSAt baseline, blood glucose and serum insulin were slightly higher in the older subjects (P<0.001), whereas GLP-1 and GIP were comparable between groups. In both groups, the glycemic, insulinemic, and GLP-1 responses were dependent on the duodenal glucose load in a nonlinear fashion (P<0.001). The glycemic response was greater (P<0.001) in the older subjects, whereas GLP-1 and GIP responses were comparable between groups. The older subjects were more insulin resistant (P<0.001) and had impaired β-cell function, particularly at higher glucose loads (P<0.05).When glucose is infused into the small intestine at equal rates in healthy young and older subjects, GLP-1 and GIP responses are comparable, indicating that impaired incretin secretion does not account for age-related glucose intolerance.CONCLUSIONWhen glucose is infused into the small intestine at equal rates in healthy young and older subjects, GLP-1 and GIP responses are comparable, indicating that impaired incretin secretion does not account for age-related glucose intolerance. |
Author | Gentilcore, Diana Horowitz, Michael Trahair, Laurence G. Lange, Kylie Rayner, Christopher K. Wishart, Judith M. Jones, Karen L. |
AuthorAffiliation | University of Adelaide (L.G.T., M.H., C.K.R., D.G., K.L., J.M.W., K.L.J.), Discipline of Medicine, Royal Adelaide Hospital; National Health and Medical Research Council Centre of Clinical Research Excellence in Nutritional Physiology, Interventions, and Outcomes (L.G.T., M.H., C.K.R., K.L., J.M.W., K.L.J.); and University of South Australia (D.G.), School of Health Sciences, Adelaide, Australia 5000 |
AuthorAffiliation_xml | – name: University of Adelaide (L.G.T., M.H., C.K.R., D.G., K.L., J.M.W., K.L.J.), Discipline of Medicine, Royal Adelaide Hospital; National Health and Medical Research Council Centre of Clinical Research Excellence in Nutritional Physiology, Interventions, and Outcomes (L.G.T., M.H., C.K.R., K.L., J.M.W., K.L.J.); and University of South Australia (D.G.), School of Health Sciences, Adelaide, Australia 5000 |
Author_xml | – sequence: 1 givenname: Laurence G. surname: Trahair fullname: Trahair, Laurence G. organization: 1University of Adelaide (L.G.T., M.H., C.K.R., D.G., K.L., J.M.W., K.L.J.), Discipline of Medicine, Royal Adelaide Hospital, Adelaide, Australia 5000 – sequence: 2 givenname: Michael surname: Horowitz fullname: Horowitz, Michael organization: 1University of Adelaide (L.G.T., M.H., C.K.R., D.G., K.L., J.M.W., K.L.J.), Discipline of Medicine, Royal Adelaide Hospital, Adelaide, Australia 5000 – sequence: 3 givenname: Christopher K. surname: Rayner fullname: Rayner, Christopher K. organization: 1University of Adelaide (L.G.T., M.H., C.K.R., D.G., K.L., J.M.W., K.L.J.), Discipline of Medicine, Royal Adelaide Hospital, Adelaide, Australia 5000 – sequence: 4 givenname: Diana surname: Gentilcore fullname: Gentilcore, Diana organization: 1University of Adelaide (L.G.T., M.H., C.K.R., D.G., K.L., J.M.W., K.L.J.), Discipline of Medicine, Royal Adelaide Hospital, Adelaide, Australia 5000 – sequence: 5 givenname: Kylie surname: Lange fullname: Lange, Kylie organization: 1University of Adelaide (L.G.T., M.H., C.K.R., D.G., K.L., J.M.W., K.L.J.), Discipline of Medicine, Royal Adelaide Hospital, Adelaide, Australia 5000 – sequence: 6 givenname: Judith M. surname: Wishart fullname: Wishart, Judith M. organization: 1University of Adelaide (L.G.T., M.H., C.K.R., D.G., K.L., J.M.W., K.L.J.), Discipline of Medicine, Royal Adelaide Hospital, Adelaide, Australia 5000 – sequence: 7 givenname: Karen L. surname: Jones fullname: Jones, Karen L. email: karen.jones@adelaide.edu.au organization: 1University of Adelaide (L.G.T., M.H., C.K.R., D.G., K.L., J.M.W., K.L.J.), Discipline of Medicine, Royal Adelaide Hospital, Adelaide, Australia 5000 |
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Snippet | Context:Aging is associated with deteriorating glucose tolerance. Studies assessing glucose tolerance and subsequent insulin and incretin hormone release often... CONTEXT:Aging is associated with deteriorating glucose tolerance. Studies assessing glucose tolerance and subsequent insulin and incretin hormone release often... Aging is associated with deteriorating glucose tolerance. Studies assessing glucose tolerance and subsequent insulin and incretin hormone release often fail to... |
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SubjectTerms | Age Factors Aged Aging Beta cells Biological and medical sciences Blood glucose Blood Glucose - metabolism Double-Blind Method Duodenum - drug effects Duodenum - metabolism Endocrinopathies Feeding. Feeding behavior Female Fundamental and applied biological sciences. Psychology Gastric emptying Gastric Emptying - drug effects Gastric Inhibitory Polypeptide - blood GIP protein Glucagon Glucagon-like peptide 1 Glucagon-Like Peptide 1 - blood Glucose Glucose - pharmacology Glucose tolerance Hormone release Humans Incretins - blood Insulin - blood Insulin resistance Insulin Resistance - physiology Male Medical sciences Postprandial Period - drug effects Small intestine Vertebrates: anatomy and physiology, studies on body, several organs or systems Vertebrates: endocrinology Young Adult |
Title | Comparative Effects of Variations in Duodenal Glucose Load on Glycemic, Insulinemic, and Incretin Responses in Healthy Young and Older Subjects |
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