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Nutrigenomics Investigation of the Body's Metabolic Response to 2 Different Meal Challenges

A Nutrigenomics Study of Post-prandial Metabolic Responses in Individuals of Varying Body Weight: An Assessment of the Body's Response to Meals Containing Different Levels of Fat and Carbohydrate

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01172951
Acronym
MECHE
Enrollment
200
Registered
2010-07-30
Start date
2008-12-31
Completion date
2010-12-31
Last updated
2011-01-11

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

Conditions

Healthy Subjects

Keywords

Post-prandial, Nutrigenomic, Test meal, Oral glucose tolerance test, Oral lipid tolerance test

Brief summary

The purpose of this study is to investigate the biological response to a metabolic stress, given in the form of a high carbohydrate or fat meal in normal weight, overweight and obese individuals and to further explore these responses using novel metabolomic, proteomic, transcriptomic and genotyping techniques.

Detailed description

The most recent statistics from the Department of Health in Ireland (2005) indicate that the leading causes of death are those in which nutrition can play a key preventative role. The proposed study will provide information on the metabolic stress from varying body weight overlaid by the additional metabolic stress of a test-meal challenge, in this case being delivered in the form of an oral glucose tolerance test (OGTT) and oral lipid tolerance test (OLTT), standard metabolic challenges in post-prandial research. Previous studies assessing metabolic risk factors associated with a disease have typically focused on information collected from individuals in a fasting state only. However, it is equally important to assess how the body responds when stressed. Employing an acute high fat or carbohydrate intake is sufficient to induce a mild stress in which time an individual's unique post-prandial response can be monitored. This study will combine traditional markers (dietary, anthropometric, lifestyle, clinical and physical activity) with nutrigenomics, a tool that attempts to describe the genome-wide influences of nutrition by examining the impact of diet on genes (genomics), mRNA (transcriptomics), proteins (proteomics) and metabolites (metabolomics).

Interventions

OTHEROral glucose tolerance test

75g anhydrous glucose powder mixed with 100mls water

OTHEROral lipid tolerance test

150ml drink composed of 2 commercially available high fat products

Sponsors

University College Dublin
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Aged 18 to 60 years * Not taking medication (other than contraceptive pill/HRT) * Irish resident and living in Dublin area

Exclusion criteria

* Known chronic/infectious disease * Pregnancy/lactation * Desire to conceive or lose weight during study * Athlete

Design outcomes

Primary

MeasureTime frame
Comprehensive analysis of the metabolic response to the acute ingestion of fat and glucose loads2-5 hours post test meal ingestion

Countries

Ireland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 20, 2026