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:
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Authors | Yannik B Schönknecht, Silke Crommen, Birgit Stoffel-Wagner, Martin Coenen, Rolf Fimmers, Jens J Holst, Marie-Christine Simon, Peter Stehle, Sarah Egert |
Journal | Molecular nutrition & food research
(Mol Nutr Food Res)
Vol. 64
Issue 9
Pg. e1901035
(05 2020)
ISSN: 1613-4133 [Electronic] Germany |
PMID | 32223057
(Publication Type: Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Copyright | © 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. |
Chemical References |
- Antioxidants
- Biomarkers
- Blood Glucose
- Insulin
- Lipids
- Glucagon-Like Peptide 1
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Topics |
- Aged
- Antioxidants
(metabolism)
- Biomarkers
(blood)
- Blood Glucose
(analysis)
- Cross-Over Studies
- Diet
(adverse effects)
- Diet, Mediterranean
- Diet, Western
- Energy Intake
- Female
- Glucagon-Like Peptide 1
(blood)
- Humans
- Hyperglycemia
(blood, etiology)
- Hyperlipidemias
(blood, etiology)
- Inflammation
(blood, etiology)
- Insulin
(blood)
- Lipids
(blood)
- Male
- Middle Aged
- Postprandial Period
(physiology)
- Risk Factors
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