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Individual Variability of Appetite Responses to a Standardised Meal

A Replicated Crossover Study to Explore Individual Variability of Appetite Responses to a Standardised Meal and Any Moderating Influence of the FTO Gene

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03771690
Enrollment
18
Registered
2018-12-11
Start date
2018-01-11
Completion date
2018-05-01
Last updated
2018-12-11

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

Conditions

Appetitive Behavior, Genetic Predisposition to Disease, Obesity

Keywords

Appetite, FTO, Ghrelin, Individual variability, Meal intake, Peptide YY

Brief summary

The aim of this study is to examine the interindividual variability of subjective and hormonal appetite responses to a standardised meal in healthy men and explore any moderating influence of the fat mass and obesity associated gene (FTO). Participants homozygous for the obesity risk A allele (AA) or low risk T allele (TT) of FTO rs9939609 will complete two fasted control and two standardised meal (5025 kJ energy, 47% carbohydrate, 9% protein, 44% fat) conditions in randomised sequences. Ratings of perceived appetite and venous blood samples will be taken before and after the interventions. Interindividual differences in appetite responses and the potential moderating influence of the FTO gene will be examined using bivariate correlations and linear mixed modelling.

Detailed description

Meal ingestion initiates a series of co-ordinated subjective and hormonal appetite responses. However, it is not known whether interindividual variability in appetite exists in response to a standardised meal. A recent approach proposed to quantify individual differences in the intervention response involves quantifying the participant-by-response interaction from replicated intervention and comparator arms. Using this approach (a replicated crossover study), the current study will (1) investigate whether the perceived appetite and appetite-related hormone responses to a standardised meal are reproducible on repeated occasions; (2) examine whether there is true individual variability in appetite responses to a standardised meal; and (3) determine whether the fat mass and obesity associated gene (FTO) moderates the magnitude of appetite responses to a standardised meal. A total of 18 healthy men will be recruited according to their FTO rs9939609 genotype: 9 homozygous minor allele (AA) and 9 homozygous major allele (TT). Participants will complete four main experimental conditions each separated by an interval of at least three days: two fasted control and two standardised meal conditions. Participants will arrive at the laboratory at 09:00 after a 13 h overnight fast and a cannula will be inserted into an antecubital vein for blood sampling. After 60 min rest, a fasting venous blood sample and rating of perceived appetite will be taken (0 h; 10:00). Participants will rest throughout all four conditions but will be provided with a standardised breakfast meal after the fasting measurements during the two meal conditions. Breakfast will be consumed within 15 min and consist of croissants, butter, chocolate spread, cereal biscuits and milkshake which will provide 5025 kJ energy (47% carbohydrate, 9% protein, 44% fat). Subsequent venous blood samples will be taken at 0.5 h (10:30) and 1 h (11:00), and appetite perceptions will be assessed at 1 h (11:00). Interindividual differences will be explored by correlating the two sets of response differences between meal and control conditions. Within-participant covariate-adjusted linear mixed models will be used to quantify participant-by-condition and FTO genotype-by-condition interactions.

Interventions

A standardised meal will be consumed at 10:00 which will provide 5025 kJ energy (47% carbohydrate, 9% protein, 44% fat).

Sponsors

Teesside University
CollaboratorOTHER
Loughborough University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Homozygous minor allele (AA) or major allele (TT) FTO rs9939609 genotype; * Non-smoker; * Weight stable for the previous 3 months.

Exclusion criteria

* Heterozygous FTO rs9939609 genotype (i.e., AT); * Any medical conditions (e.g., diabetes, coagulation or bleeding disorders); * Taking any medication that might influence appetite, fat metabolism or blood glucose; * Dieting or restrained eating behaviours; * Any food allergies.

Design outcomes

Primary

MeasureTime frameDescription
Acylated ghrelin concentration1 hour (Plasma samples will be collected at 0 hour (pre) and 1 hour (post))Control adjusted pre-to-post change in plasma acylated ghrelin concentration

Secondary

MeasureTime frameDescription
Total peptide YY concentration1 hour (Plasma samples will be collected at 0 hour (pre) and 1 hour (post))Control adjusted pre-to-post change in plasma total peptide YY concentration
Insulin concentration0.5 hour (Plasma samples will be collected at 0 hour (pre) and 0.5 hour (post))Control adjusted pre-to-post change in plasma insulin concentration
Glucose concentration0.5 hour (Plasma samples will be collected at 0 hour (pre) and 0.5 hour (post))Control adjusted pre-to-post change in plasma glucose concentration
Rating of perceived satisfaction1 hour (Visual analogue scales will be completed at 0 hour (pre) and 1 hour (post))Control adjusted pre-to-post change in rating of perceived satisfaction. Perceived satisfaction will be measured using a 100 mm visual analogue scale anchored at 0, 'I am completely empty', and 100, 'I cannot eat another bite'.
Rating of perceived fullness1 hour (Visual analogue scales will be completed at 0 hour (pre) and 1 hour (post))Control adjusted pre-to-post change in rating of perceived fullness. Perceived fullness will be measured using a 100 mm visual analogue scale anchored at 0, 'Not full at all', and 100, 'Totally full'.
Rating of perceived prospective food consumption1 hour (Visual analogue scales will be completed at 0 hour (pre) and 1 hour (post))Control adjusted pre-to-post change in rating of perceived prospective food consumption. Perceived prospective food consumption will be measured using a 100 mm visual analogue scale anchored at 0, 'Nothing at all', and 100, 'A lot'. consumption
Rating of perceived hunger1 hour (Visual analogue scales will be completed at 0 hour (pre) and 1 hour (post))Control adjusted pre-to-post change in rating of perceived hunger. Perceived hunger will be measured using a 100 mm visual analogue scale anchored at 0, 'I am not hungry at all', and 100, 'I have never been more hungry'.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026