Acute Effects of Three Different Meal Patterns on Postprandial Metabolism in Older Individuals with a Risk Phenotype for Cardiometabolic Diseases: A Randomized Controlled Crossover Trial

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Acute Effects of Three Different Meal Patterns on Postprandial Metabolism in Older Individuals with a Risk Phenotype for Cardiometabolic Diseases : A Randomized Controlled Crossover Trial. / Schönknecht, Yannik B.; Crommen, Silke; Stoffel-Wagner, Birgit; Coenen, Martin; Fimmers, Rolf; Holst, Jens J.; Simon, Marie Christine; Stehle, Peter; Egert, Sarah.

In: Molecular Nutrition & Food Research, Vol. 64, No. 9, 1901035, 2020.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Schönknecht, YB, Crommen, S, Stoffel-Wagner, B, Coenen, M, Fimmers, R, Holst, JJ, Simon, MC, Stehle, P & Egert, S 2020, 'Acute Effects of Three Different Meal Patterns on Postprandial Metabolism in Older Individuals with a Risk Phenotype for Cardiometabolic Diseases: A Randomized Controlled Crossover Trial', Molecular Nutrition & Food Research, vol. 64, no. 9, 1901035. https://doi.org/10.1002/mnfr.201901035

APA

Schönknecht, Y. B., Crommen, S., Stoffel-Wagner, B., Coenen, M., Fimmers, R., Holst, J. J., Simon, M. C., Stehle, P., & Egert, S. (2020). Acute Effects of Three Different Meal Patterns on Postprandial Metabolism in Older Individuals with a Risk Phenotype for Cardiometabolic Diseases: A Randomized Controlled Crossover Trial. Molecular Nutrition & Food Research, 64(9), [1901035]. https://doi.org/10.1002/mnfr.201901035

Vancouver

Schönknecht YB, Crommen S, Stoffel-Wagner B, Coenen M, Fimmers R, Holst JJ et al. Acute Effects of Three Different Meal Patterns on Postprandial Metabolism in Older Individuals with a Risk Phenotype for Cardiometabolic Diseases: A Randomized Controlled Crossover Trial. Molecular Nutrition & Food Research. 2020;64(9). 1901035. https://doi.org/10.1002/mnfr.201901035

Author

Schönknecht, Yannik B. ; Crommen, Silke ; Stoffel-Wagner, Birgit ; Coenen, Martin ; Fimmers, Rolf ; Holst, Jens J. ; Simon, Marie Christine ; Stehle, Peter ; Egert, Sarah. / Acute Effects of Three Different Meal Patterns on Postprandial Metabolism in Older Individuals with a Risk Phenotype for Cardiometabolic Diseases : A Randomized Controlled Crossover Trial. In: Molecular Nutrition & Food Research. 2020 ; Vol. 64, No. 9.

Bibtex

@article{dccada5f397c453eaa3d610a36f6720f,
title = "Acute Effects of Three Different Meal Patterns on Postprandial Metabolism in Older Individuals with a Risk Phenotype for Cardiometabolic Diseases: A Randomized Controlled Crossover Trial",
abstract = "Scope: The aim of this study is to investigate acute postprandial responses to intake of meals typical for Mediterranean and Western diets. Methods: In a randomized crossover design, overweight and obese participants with a risk phenotype for cardiometabolic diseases consumed three different isoenergetic meals: Western diet-like high-fat (WDHF), Western diet-like high-carbohydrate (WDHC), and Mediterranean diet (MED) meal. Blood samples are collected at fasting and 1, 2, 3, 4, 5 h postprandially and analyzed for parameters of lipid and glucose metabolism, inflammation, oxidation, and antioxidant status. Results: Compared to MED and WDHF meals, intake of a WDHC meal results in prolonged and elevated increases in glucose and insulin. Elevations for triglycerides are enhanced after the WDHF meal compared to the MED and the WDHC meal. Glucagon-like peptide-1 and interleukin-6 increase postprandially without meal differences. Apart from vitamin C showing an increase after the MED meal and a decrease after WDHF and WDHC meals, antioxidant markers decrease postprandially without meal differences. Plasma interleukin-1β is not affected by meal intake. Conclusions: Energy-rich meals induce hyperglycemia, hyperlipemia, an inflammatory response, and a decrease in antioxidant markers. A meal typical for the Mediterranean diet results in favorable effects on glycemic, insulinemic, and lipemic responses.",
keywords = "glucose response, inflammation, Mediterranean diet, triglyceride response, Western diet",
author = "Sch{\"o}nknecht, {Yannik B.} and Silke Crommen and Birgit Stoffel-Wagner and Martin Coenen and Rolf Fimmers and Holst, {Jens J.} and Simon, {Marie Christine} and Peter Stehle and Sarah Egert",
year = "2020",
doi = "10.1002/mnfr.201901035",
language = "English",
volume = "64",
journal = "Molecular Nutrition & Food Research",
issn = "1613-4125",
publisher = "Wiley-VCH",
number = "9",

}

RIS

TY - JOUR

T1 - Acute Effects of Three Different Meal Patterns on Postprandial Metabolism in Older Individuals with a Risk Phenotype for Cardiometabolic Diseases

T2 - A Randomized Controlled Crossover Trial

AU - Schönknecht, Yannik B.

AU - Crommen, Silke

AU - Stoffel-Wagner, Birgit

AU - Coenen, Martin

AU - Fimmers, Rolf

AU - Holst, Jens J.

AU - Simon, Marie Christine

AU - Stehle, Peter

AU - Egert, Sarah

PY - 2020

Y1 - 2020

N2 - Scope: The aim of this study is to investigate acute postprandial responses to intake of meals typical for Mediterranean and Western diets. Methods: In a randomized crossover design, overweight and obese participants with a risk phenotype for cardiometabolic diseases consumed three different isoenergetic meals: Western diet-like high-fat (WDHF), Western diet-like high-carbohydrate (WDHC), and Mediterranean diet (MED) meal. Blood samples are collected at fasting and 1, 2, 3, 4, 5 h postprandially and analyzed for parameters of lipid and glucose metabolism, inflammation, oxidation, and antioxidant status. Results: Compared to MED and WDHF meals, intake of a WDHC meal results in prolonged and elevated increases in glucose and insulin. Elevations for triglycerides are enhanced after the WDHF meal compared to the MED and the WDHC meal. Glucagon-like peptide-1 and interleukin-6 increase postprandially without meal differences. Apart from vitamin C showing an increase after the MED meal and a decrease after WDHF and WDHC meals, antioxidant markers decrease postprandially without meal differences. Plasma interleukin-1β is not affected by meal intake. Conclusions: Energy-rich meals induce hyperglycemia, hyperlipemia, an inflammatory response, and a decrease in antioxidant markers. A meal typical for the Mediterranean diet results in favorable effects on glycemic, insulinemic, and lipemic responses.

AB - Scope: The aim of this study is to investigate acute postprandial responses to intake of meals typical for Mediterranean and Western diets. Methods: In a randomized crossover design, overweight and obese participants with a risk phenotype for cardiometabolic diseases consumed three different isoenergetic meals: Western diet-like high-fat (WDHF), Western diet-like high-carbohydrate (WDHC), and Mediterranean diet (MED) meal. Blood samples are collected at fasting and 1, 2, 3, 4, 5 h postprandially and analyzed for parameters of lipid and glucose metabolism, inflammation, oxidation, and antioxidant status. Results: Compared to MED and WDHF meals, intake of a WDHC meal results in prolonged and elevated increases in glucose and insulin. Elevations for triglycerides are enhanced after the WDHF meal compared to the MED and the WDHC meal. Glucagon-like peptide-1 and interleukin-6 increase postprandially without meal differences. Apart from vitamin C showing an increase after the MED meal and a decrease after WDHF and WDHC meals, antioxidant markers decrease postprandially without meal differences. Plasma interleukin-1β is not affected by meal intake. Conclusions: Energy-rich meals induce hyperglycemia, hyperlipemia, an inflammatory response, and a decrease in antioxidant markers. A meal typical for the Mediterranean diet results in favorable effects on glycemic, insulinemic, and lipemic responses.

KW - glucose response

KW - inflammation

KW - Mediterranean diet

KW - triglyceride response

KW - Western diet

UR - http://www.scopus.com/inward/record.url?scp=85083503697&partnerID=8YFLogxK

U2 - 10.1002/mnfr.201901035

DO - 10.1002/mnfr.201901035

M3 - Journal article

C2 - 32223057

AN - SCOPUS:85083503697

VL - 64

JO - Molecular Nutrition & Food Research

JF - Molecular Nutrition & Food Research

SN - 1613-4125

IS - 9

M1 - 1901035

ER -

ID: 244652043