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The RepEAT study: Individual differences in postprandial glucose responses and the relation with diet and phenotype

The RepEAT study: Individual differences in postprandial glucose responses and the relation with diet and phenotype - RepEAT

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON51464
Enrollment
63
Registered
2022-06-17
Start date
2022-06-27
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

diabetes Impaired glucose tolerance

Interventions

Participants will consume test products that fall in the same food category, but differ in glycaemic index/carbohydrate content. Part of these products is provided by industrial partners, of which t

Sponsors

Wageningen Universiteit
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: • Apparently healthy men and women; • BMI of 25 - 40 kg/m2; • Age 45-75 years; • Weight stable (±

Exclusion criteria

Exclusion criteria: • Diagnosed with type 1 or type 2 diabetes; • Diseases or prior surgeries affecting the stomach, liver, or intestines; • Food allergies/intolerances for products used in the study design; • Receiving medication or supplements interfering with glucose metabolism (as judged by our research physician); • Regular use of medication interfering with immune function (e.g. corticosteroids, immune blockers, as judged by our research physician); • Donated blood within 2 months prior to the screening; • Anaemia defined as Hb concentrations =14 alcoholic beverages per week for women and >=21 alcoholic beverages per week for men; • Being pregnant or lactating; • Use of soft and/or hard drugs; • Unable/unwilling to download a research application on the mobile phone; • Participation in another study that involves an intervention within two months prior to the intervention; • Working at the division of Human Nutrition and Health of Wageningen University and Research or the Food, Health and Consumer research group of Wageningen University and Biobased Research.

Design outcomes

Primary

MeasureTime frame
The main study parameter is glucose concentration as measured by continuous glucose monitoring.

Secondary

MeasureTime frame
Short-term well-being, as assessed by questionnaires, and meal timing will be related to glucose responses. In addition, glucose responses will be related to phenotype, as measured by an array of different outcome parameters: • Anthropometrics: weight, height, waist and hip circumference, body composition (MRI/MRS), body fat distribution (MRI/MRS) • Fasting plasma glucose parameters: HbA1c, glucose concentration, insulin concentration • Immune function: PBMC RNA expression, Monocyte RNA expression, Monocyte response upon TLR activation • Oxidative stress: Plasma and urinary biomarkers • Advanced glycation end-products: AGE accumulation (AGE reader), plasma concentrations of a-dicarbonyls and AGEs • Cognitive performance (CANTAB) • Microbiota and gut health: Microbiota composition (faeces and saliva), transit time, stool frequency (Bristol stool chart), stool consistency (Bristol stool chart) • Amylase: concentration and activity (saliva samples) • Genetic variation: SNPs in amylase genes and in genes relevant for metabolism and metabolic responses to food (mouth swap) • Circulating metabolites: Fasting and following a high-fat mixed meal challenge

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)