Skip to main content
OpenTrials
Completed

NCT Number: NCT03369145

High-fat Overfeeding, Hepatokines and Appetite Regulation

The present study will investigate the effect of high-fat overfeeding on a group of liver-secreted proteins linked to worsened blood sugar control, as well as proteins involved in appetite control. Participants will consume both a high-fat diet, consisting of 50% extra calories above their daily required intake, and a control diet, consisting of their normal 'habitual' diet, with each diet lasting seven days. The diets will be undertaken in a randomised order, with a period of three weeks separating the two diets. Blood samples will be taken before and after each diet to measure blood sugar control. Further blood samples will also be taken 24 hours and 72 hours into each diet to see how levels of the liver and appetite-regulating proteins change over the course of the seven days.

It is expected that blood sugar control will be worsened by the high-fat diet and this will be accompanied by increases in levels of the liver-secreted proteins and an impaired release of the appetite-regulating proteins into the blood.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–40 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

National Centre for Sport and Exercise Medicine, Loughborough University, Loughborough, Leicestershire, United Kingdom

Loading trial locations.

About this study

In recent years, researchers have identified a number of liver-secreted proteins, termed "hepatokines", which are thought to play an important role in inter-organ crosstalk between the liver and other metabolically active tissues such as skeletal muscle and adipose tissue. Specifically, previous studies have demonstrated that hepatokines contribute to whole body glucose and lipid homeostasis through acting in an endocrine-like fashion. Understanding how circulating concentrations of these hepatokines can be manipulated in humans is essential, as impaired blood glucose and lipid control is a key feature of metabolic diseases, such as type 2 diabetes and non-alcoholic fatty liver disease.

Previous research at Loughborough University has found that acute high-fat overfeeding for up to seven days can impair glycaemic control; however, the exact mechanisms responsible for these detrimental changes are not fully understood. Based upon previous evidence that hepatokine production is nutritionally modulated, the investigators believe that changes in hepatokine production may play a role in the detrimental metabolic effects seen following short-term, high-fat overfeeding which has implications for long-term metabolic health.

Appetite regulation is also thought to play a role in the pathophysiology of obesity and insulin resistance, as the impaired secretion of several appetite regulatory hormones in both fasting and postprandial conditions has been observed in obesity, which is characterised by an chronic excessive energy intake. Therefore, the investigators are also interested to examine the appetite regulatory hormone response to short-term, high-fat overfeeding.

The present study is a randomised, controlled, crossover study in which twelve recreationally active, healthy males will consume both a hypercaloric, high-fat diet (consisting of 50% extra energy above the daily requirement, 65% of which is fat) and a control diet (the participants' habitual diet) in a randomised fashion. A three-week washout period will separate the two diets in order to remove any lasting effects confounding the subsequent diet.

Following a prescreening session in which anthropometric data will be collected, participants will commence their first dietary condition. An oral glucose tolerance test will be performed before and after the two diets to measure changes in glycaemic control/whole body insulin sensitivity. Further blood samples will be taken 24 hours and 72 hours after commencing the diets in order to observe the time course of any changes in circulating hepatokine and appetite hormone concentrations. Physical activity will also be monitored for the duration of the two dietary conditions to ensure that habitual physical activity levels are maintained.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Recreationally active - ≤ 2 structured exercise sessions per week
  • BMI between 18.5 - 27.9 kg/m2
  • Body fat percentage < 20%
  • Metabolically healthy - No known cardiovascular or metabolic disease such as diabetes, respiratory or heart disease.
  • Non-smoker
  • Weight stable in the past 6 months
  • Normal fasting blood glucose levels (3.6 - 5.5 mmol/l)

Exclusion criteria

  • Contraindications to exercise
  • Needle Phobia

Treatment and study plan

High-fat diet

Dietary Supplement

The high-fat diet will provide 7 days of overfeeding comprising of: +50% extra calories above the daily required intake, 65% of which is fat.

Primary outcomes

  1. Leukocyte cell-derived chemotaxin 2 (LECT2)

    Time frame: Baseline, 1 day, 3 days, 7 days

    Time-course of LECT2 plasma concentrations across the 7-day dietary interventions

Secondary outcomes

  1. Fibroblast growth factor 21 (FGF21)

    Time frame: Baseline, 1 day, 3 days, 7 days

    Time-course of FGF21 plasma concentrations across the 7-day dietary interventions

  2. Fetuin-A

    Time frame: Baseline, 1 day, 3 days, 7 days

    Time-course of Fetuin-A plasma concentrations across the 7-day dietary interventions

  3. Acylated ghrelin

    Time frame: Baseline, 1 day, 3 days, 7 days

    Time-course of acylated ghrelin plasma concentrations across the 7-day dietary interventions

  4. Peptide YY (PYY)

    Time frame: Baseline, 1 day, 3 days, 7 days

    Time-course of PYY plasma concentrations across the 7-day dietary interventions

  5. C-Terminal Telopeptide of Type 1 Collagen (CTX)

    Time frame: Baseline, 1 day, 3 days, 7 days

    Time-course of CTX plasma concentrations across the 7-day dietary interventions

  6. N-Terminal Propeptide of Type 1 Procollagen (P1NP)

    Time frame: Baseline, 1 day, 3 days, 7 days

    Time-course of P1NP plasma concentrations across the 7-day dietary interventions

  7. Visual Analogue Scale for Subjective Ratings of Appetite

    Time frame: Baseline, 1 day, 3 days, 7 days

    Time-course of subjective ratings of hunger across the 7-day dietary interventions, measured using an appetite visual analogue scale. The scale is divided into subscales of different appetite perceptions including: hunger, fullness, satisfaction and prospective food consumption. Each subscale is rated on a 100mm scale (i.e. from 0 - 100), with a rating of 100 fully supporting the perception and a rating of 0 fully opposing the perception.

  8. Subjective food preference

    Time frame: Baseline, 1 day, 3 days, 7 days

    Time-course of subjective food preference across the 7-day dietary interventions, measured using the Leeds Food Preference Questionnaire.

  9. Whole-body insulin sensitivity

    Time frame: Baseline, 7 Days

    Changes in whole-body insulin sensitivity using the Matsuda Index, calculated from plasma glucose and insulin concentrations during the oral glucose tolerance test

  10. Homeostasis model assessment of insulin resistance (HOMA-IR)

    Time frame: Baseline, 1 day, 3 days, 7 days

    Changes in HOMA-IR (a marker of hepatic insulin resistance) using baseline concentrations of plasma glucose and insulin.

  11. Adipose tissue insulin resistance (ADIPO-IR)

    Time frame: Baseline, 1 day, 3 days, 7 days

    Changes in ADIPO-IR using baseline concentrations of plasma insulin and non-esterified free fatty acids.

  12. Physical activity and sedentary behaviour

    Time frame: 7 days (per diet)

    Amounts of sitting time, standing time, light activity and moderate-vigorous activity will be measured across the duration of each diets to compare between the two. This will be Measured using Acitgraph and ActivPAL monitors.

  13. Resting Metabolic Rate

    Time frame: Baseline, 7 Days

    Changes in resting metabolic rate in response to the diets will be measured using indirect calorimetry and estimated using the Haldane transformation.

  14. Fat Oxidation

    Time frame: Baseline, 7 Days

    Changes in fat oxidation in response to the diets will be measured using indirect calorimetry and estimated using the Haldane transformation.

  15. Blood pressure

    Time frame: Baseline, 1 day, 3 days, 7 days

    Changes in blood pressure (systolic and diastolic) across the two dietary interventions will be measured using an automated pressure cuff.

  16. Body weight

    Time frame: Baseline, 1 day, 3 days, 7 days

    Changes in body weight across the two dietary interventions.

  17. Body fat percentage

    Time frame: Baseline, 7 Days

    Changes in body fat percentage across the two dietary interventions using bioelectrical impedance analysis.

Sponsors and collaborators

Lead sponsor

Loughborough University

Other

Collaborators

  • Nottingham Trent University
  • Nottingham University Hospitals NHS Trust

Registry information

Official study title

Influence of High-fat Overfeeding on Circulating Hepatokine Concentrations: a Randomised Crossover Study

Acronym: OVEREAT

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Dec 11, 2017
Registry last updated
Feb 18, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.