Diet low in advanced glycation end products increases insulin sensitivity in healthy overweight individuals: A double-blind, randomized, crossover trial

Barbora de Courten, Maximilian P J de Courten, Georgia Soldatos, Sonia L. Dougherty, Nora Straznicky, Markus Schlaich, Karly C. Sourris, Vibhasha Chand, Jean LJM Scheijen, Bronwyn A. Kingwell, Mark E. Cooper, Casper G. Schalkwijk, Karen Z. Walker, Josephine M. Forbes

Research output: Contribution to journalArticleResearchpeer-review

Abstract

Background: The consumption of advanced glycation end products (AGEs) has increased because of modern food processing and has been linked to the development of type 2 diabetes in rodents. Objective: We determined whether changing dietary AGE intake could modulate insulin sensitivity and secretion in healthy, overweight individuals. Design: We performed a double-blind, randomized, crossover trial of diets in 20 participants [6 women and 14 men; mean ± SD body mass index (in kg/m2): 29.8 ± 3.7]. Isoenergetic- and macronutrient matched diets that were high or low in AGE content were alternately consumed for 2 wk and separated by a 4-wk washout period. At the beginning and end of each dietary period, a hyperinsulinemic euglycemic clamp and an intravenous glucose tolerance test were performed. Dietary, plasma and urinary AGEs NV-(carboxymethyl) lysine (CML), NV-(carboxyethyl)lysin (CEL), and methylglyoxal derived hydroimadazolidine (MG-H1) were measured with the use of mass spectrometry. Results: Participants consumed less CML, CEL, and MG-H1 during the low-AGE dietary period than during the high-AGE period (all P < 0.05), which was confirmed by changes in urinary AGE excretion. There was an overall difference in insulin sensitivity of 22.1 mg · kg-1 · min-1 between diets (P = 0.001). Insulin sensitivity increased by 1.3 mg · kg-1 · min-1 after the low-AGE diet (P = 0.004), whereas it showed a tendency to decrease by 0.8 mg · kg-1 · min-1 after the high-AGE diet (P = 0.086). There was no difference in body weight or insulin secretion between diets (P = NS). Conclusions: A diet that is low in AGEs may reduce the risk of type 2 diabetes by increasing insulin sensitivity. Hence, a restriction in dietary AGE content may be an effective strategy to decrease diabetes and cardiovascular disease risks in overweight individuals.

Original languageEnglish
Pages (from-to)1426-1433
Number of pages8
JournalAmerican Journal of Clinical Nutrition
Volume103
Issue number6
DOIs
Publication statusPublished - 1 Jun 2016

Keywords

  • Glycotoxin
  • Insulin resistance
  • Insulin secretion
  • Obesity
  • Receptors for AGEs

Cite this

de Courten, Barbora ; de Courten, Maximilian P J ; Soldatos, Georgia ; Dougherty, Sonia L. ; Straznicky, Nora ; Schlaich, Markus ; Sourris, Karly C. ; Chand, Vibhasha ; Scheijen, Jean LJM ; Kingwell, Bronwyn A. ; Cooper, Mark E. ; Schalkwijk, Casper G. ; Walker, Karen Z. ; Forbes, Josephine M. / Diet low in advanced glycation end products increases insulin sensitivity in healthy overweight individuals : A double-blind, randomized, crossover trial. In: American Journal of Clinical Nutrition. 2016 ; Vol. 103, No. 6. pp. 1426-1433.
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title = "Diet low in advanced glycation end products increases insulin sensitivity in healthy overweight individuals: A double-blind, randomized, crossover trial",
abstract = "Background: The consumption of advanced glycation end products (AGEs) has increased because of modern food processing and has been linked to the development of type 2 diabetes in rodents. Objective: We determined whether changing dietary AGE intake could modulate insulin sensitivity and secretion in healthy, overweight individuals. Design: We performed a double-blind, randomized, crossover trial of diets in 20 participants [6 women and 14 men; mean ± SD body mass index (in kg/m2): 29.8 ± 3.7]. Isoenergetic- and macronutrient matched diets that were high or low in AGE content were alternately consumed for 2 wk and separated by a 4-wk washout period. At the beginning and end of each dietary period, a hyperinsulinemic euglycemic clamp and an intravenous glucose tolerance test were performed. Dietary, plasma and urinary AGEs NV-(carboxymethyl) lysine (CML), NV-(carboxyethyl)lysin (CEL), and methylglyoxal derived hydroimadazolidine (MG-H1) were measured with the use of mass spectrometry. Results: Participants consumed less CML, CEL, and MG-H1 during the low-AGE dietary period than during the high-AGE period (all P < 0.05), which was confirmed by changes in urinary AGE excretion. There was an overall difference in insulin sensitivity of 22.1 mg · kg-1 · min-1 between diets (P = 0.001). Insulin sensitivity increased by 1.3 mg · kg-1 · min-1 after the low-AGE diet (P = 0.004), whereas it showed a tendency to decrease by 0.8 mg · kg-1 · min-1 after the high-AGE diet (P = 0.086). There was no difference in body weight or insulin secretion between diets (P = NS). Conclusions: A diet that is low in AGEs may reduce the risk of type 2 diabetes by increasing insulin sensitivity. Hence, a restriction in dietary AGE content may be an effective strategy to decrease diabetes and cardiovascular disease risks in overweight individuals.",
keywords = "Glycotoxin, Insulin resistance, Insulin secretion, Obesity, Receptors for AGEs",
author = "{de Courten}, Barbora and {de Courten}, {Maximilian P J} and Georgia Soldatos and Dougherty, {Sonia L.} and Nora Straznicky and Markus Schlaich and Sourris, {Karly C.} and Vibhasha Chand and Scheijen, {Jean LJM} and Kingwell, {Bronwyn A.} and Cooper, {Mark E.} and Schalkwijk, {Casper G.} and Walker, {Karen Z.} and Forbes, {Josephine M.}",
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Diet low in advanced glycation end products increases insulin sensitivity in healthy overweight individuals : A double-blind, randomized, crossover trial. / de Courten, Barbora; de Courten, Maximilian P J; Soldatos, Georgia; Dougherty, Sonia L.; Straznicky, Nora; Schlaich, Markus; Sourris, Karly C.; Chand, Vibhasha; Scheijen, Jean LJM; Kingwell, Bronwyn A.; Cooper, Mark E.; Schalkwijk, Casper G.; Walker, Karen Z.; Forbes, Josephine M.

In: American Journal of Clinical Nutrition, Vol. 103, No. 6, 01.06.2016, p. 1426-1433.

Research output: Contribution to journalArticleResearchpeer-review

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T1 - Diet low in advanced glycation end products increases insulin sensitivity in healthy overweight individuals

T2 - A double-blind, randomized, crossover trial

AU - de Courten, Barbora

AU - de Courten, Maximilian P J

AU - Soldatos, Georgia

AU - Dougherty, Sonia L.

AU - Straznicky, Nora

AU - Schlaich, Markus

AU - Sourris, Karly C.

AU - Chand, Vibhasha

AU - Scheijen, Jean LJM

AU - Kingwell, Bronwyn A.

AU - Cooper, Mark E.

AU - Schalkwijk, Casper G.

AU - Walker, Karen Z.

AU - Forbes, Josephine M.

PY - 2016/6/1

Y1 - 2016/6/1

N2 - Background: The consumption of advanced glycation end products (AGEs) has increased because of modern food processing and has been linked to the development of type 2 diabetes in rodents. Objective: We determined whether changing dietary AGE intake could modulate insulin sensitivity and secretion in healthy, overweight individuals. Design: We performed a double-blind, randomized, crossover trial of diets in 20 participants [6 women and 14 men; mean ± SD body mass index (in kg/m2): 29.8 ± 3.7]. Isoenergetic- and macronutrient matched diets that were high or low in AGE content were alternately consumed for 2 wk and separated by a 4-wk washout period. At the beginning and end of each dietary period, a hyperinsulinemic euglycemic clamp and an intravenous glucose tolerance test were performed. Dietary, plasma and urinary AGEs NV-(carboxymethyl) lysine (CML), NV-(carboxyethyl)lysin (CEL), and methylglyoxal derived hydroimadazolidine (MG-H1) were measured with the use of mass spectrometry. Results: Participants consumed less CML, CEL, and MG-H1 during the low-AGE dietary period than during the high-AGE period (all P < 0.05), which was confirmed by changes in urinary AGE excretion. There was an overall difference in insulin sensitivity of 22.1 mg · kg-1 · min-1 between diets (P = 0.001). Insulin sensitivity increased by 1.3 mg · kg-1 · min-1 after the low-AGE diet (P = 0.004), whereas it showed a tendency to decrease by 0.8 mg · kg-1 · min-1 after the high-AGE diet (P = 0.086). There was no difference in body weight or insulin secretion between diets (P = NS). Conclusions: A diet that is low in AGEs may reduce the risk of type 2 diabetes by increasing insulin sensitivity. Hence, a restriction in dietary AGE content may be an effective strategy to decrease diabetes and cardiovascular disease risks in overweight individuals.

AB - Background: The consumption of advanced glycation end products (AGEs) has increased because of modern food processing and has been linked to the development of type 2 diabetes in rodents. Objective: We determined whether changing dietary AGE intake could modulate insulin sensitivity and secretion in healthy, overweight individuals. Design: We performed a double-blind, randomized, crossover trial of diets in 20 participants [6 women and 14 men; mean ± SD body mass index (in kg/m2): 29.8 ± 3.7]. Isoenergetic- and macronutrient matched diets that were high or low in AGE content were alternately consumed for 2 wk and separated by a 4-wk washout period. At the beginning and end of each dietary period, a hyperinsulinemic euglycemic clamp and an intravenous glucose tolerance test were performed. Dietary, plasma and urinary AGEs NV-(carboxymethyl) lysine (CML), NV-(carboxyethyl)lysin (CEL), and methylglyoxal derived hydroimadazolidine (MG-H1) were measured with the use of mass spectrometry. Results: Participants consumed less CML, CEL, and MG-H1 during the low-AGE dietary period than during the high-AGE period (all P < 0.05), which was confirmed by changes in urinary AGE excretion. There was an overall difference in insulin sensitivity of 22.1 mg · kg-1 · min-1 between diets (P = 0.001). Insulin sensitivity increased by 1.3 mg · kg-1 · min-1 after the low-AGE diet (P = 0.004), whereas it showed a tendency to decrease by 0.8 mg · kg-1 · min-1 after the high-AGE diet (P = 0.086). There was no difference in body weight or insulin secretion between diets (P = NS). Conclusions: A diet that is low in AGEs may reduce the risk of type 2 diabetes by increasing insulin sensitivity. Hence, a restriction in dietary AGE content may be an effective strategy to decrease diabetes and cardiovascular disease risks in overweight individuals.

KW - Glycotoxin

KW - Insulin resistance

KW - Insulin secretion

KW - Obesity

KW - Receptors for AGEs

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