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 inThe journal of clinical endocrinology and metabolism Vol. 97; no. 3; pp. 844 - 851
Main Authors Trahair, Laurence G., Horowitz, Michael, Rayner, Christopher K., Gentilcore, Diana, Lange, Kylie, Wishart, Judith M., Jones, Karen L.
Format Journal Article
LanguageEnglish
Published Bethesda, MD Oxford University Press 01.03.2012
Copyright by The Endocrine Society
Endocrine Society
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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.
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
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  givenname: Laurence G.
  surname: Trahair
  fullname: Trahair, Laurence G.
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  surname: Horowitz
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  givenname: Christopher K.
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  givenname: Kylie
  surname: Lange
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– 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
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  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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Issue 3
Keywords Human
Obesity
Incretin
Duodenum
Healthy subject
Nutrition
Digestive system
Nutrition disorder
Variations
Metabolic diseases
Glucose tolerance test
Small intestine
Elderly
Endocrinology
Nutritional status
Comparative study
Glycemia
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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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