Obesity is a complicated condition that is poorly understood. The aim of this study is to increase our knowledge of how the condition may arise, and what makes obese people remain obese. We will be investigating 12 people who are overweight and comparing them to 12 people who are lean, to look at how quickly food empties out of the stomach (gastric emptying) and travels through the gut, what the blood flow to the gut is, and also to examine the hormones which are involved in determining how full people feel after eating. In order to do this, we will be using a magnetic resonance imaging (MRI) scanner, and performing blood tests. The rate of gastric emptying may have an impact on satiety (how full one feels) and has been implied in the development of obesity. This effect has been shown to impact on subsequent meal intake to a greater degree in overweight subjects, and may be due to a difference in gastric emptying of food in overweight individuals, or to hormones such as ghrelin, glucagon-like peptide 1, and Peptide YY.
The World Health Organisation (WHO) has deemed being overweight or obese as the fifth leading cause for global deaths, with more than 1.9 billion adults being defined as overweight, and 600 million defined as being obese. Conditions associated with obesity, such as stroke, type 2 diabetes, certain cancers, cardiovascular, fatty liver and airway disease can lead to premature death. Obesity results from an imbalance in energy intake versus expenditure, and fat mass accumulates. Studies have indicated that obese animals have a faster gastric emptying time, a weaker contraction of the duodenum, but a stronger contraction and relaxation of the ileum, with associated changes in gastrointestinal neurohormonal levels. The rate of gastric emptying may have an impact on feelings of satiety and has been implied in the pathogenesis of obesity. Moreover, mesenteric blood flow increases 3-fold following a meal and in a swine experimental model, a reduction in weight gain was seen when blood flow was intentionally limited to the gut using flow-restricting endovascular stenting. The authors concluded that this intervention may play a role in the treatment of obesity where other interventions have failed or are inappropriate; however the role of blood flow to the gut in obese individuals is important to elucidate. We hypothesize that nutrient absorption in obese and healthy weight individuals after a standardized meal is determined by differences in gastric emptying and mesenteric blood flow which give rise to different insulin, glucose and gut hormone responses. These may be contributory mechanisms to the evolution or maintenance of obesity. The aim of this study is to establish the effects of food ingestion on gastric emptying, gallbladder emptying, small bowel water content and splanchnic blood flow as measured by serial magnetic resonance imaging (MRI) in the context of changes in plasma gastrointestinal hormone secretion in human subjects who are obese or healthy weight. In addition, this pilot study will provide the data necessary to power a larger study investigating methods of dietary manipulation in the treatment of obesity. Method: In order to normalize the pre-study diet, volunteers will have consumed a standard diet for the 3 days immediately before the study visit, which will be based on foods in their normal diet and will be designed to meet their estimated energy requirements and provide 15% of total daily energy intake as protein, 35% as fat and 50% as carbohydrate. Participants will report at 0800 hours following a fast from midnight and after having abstained from alcohol, nicotine, and caffeine from 1800 hours the day before. On arrival, participants will be given a drink of water (200ml). A retrograde cannula will be inserted into a dorsal foot vein after prior intradermal infiltration of 1% lidocaine, with the foot placed in a magnetic resonance (MR) compatible warming box that we have developed, for arterialized-venous blood sampling. Prior to baseline blood sampling, participants will undergo a magnetic resonance imaging (MRI) scan to determine baseline values for superior mesenteric artery (SMA) blood flow, small bowel water content and gastric fluid and gas volumes. Liver fat, visceral fat and subcutaneous fat volumes will also be assessed at this time. Subsequently, a blood sample will be drawn for analysis of concentrations of hemoglobin, glucose, insulin, glucagon-like peptide 1 (GLP-1), glucagon-like peptide 2 (GLP-2), ghrelin and peptide YY (PYY). Serum osmolality will also be measured and subjective appetite assessed using visual analogue scales. The participants will then be given the test meal (in an upright, seated position) and asked to consume it within 15 minutes. The test meal will be comprised of pasta, cheese and tomato sauce, and provides 13% of total energy (E) from protein, 39%E fat, and 48%E carbohydrate. Following the test meal (time = 0 minutes), subjective appetite will be measured as before, then participants will be scanned at 30 minute intervals for 4 hours to assess gastric emptying, gastric accommodation, gastric motility and small bowel water content, as well as SMA blood flow. Blood samples will be drawn at 15 minutes, then every half hour until 240 minutes after the test meal, with a final blood sample taken at 300 minutes. Subjective appetite will be assessed every hour over the 300 minute study.
Study Type
OBSERVATIONAL
Enrollment
20
Queens Medical Centre
Nottingham, Notts, United Kingdom
Gastric emptying rate
time taken for a standard meal to empty from the stomach, assessed by serial volume measurements of the stomach using magnetic resonance imaging
Time frame: 240 minutes after feeding
Stomach volume in the fasted state
volume of the stomach measured by magnetic resonance imaging
Time frame: baseline
Superior mesenteric artery (SMA) blood flow in the fasted state
blood flow in the SMA assessed using magnetic resonance imaging
Time frame: baseline
superior mesenteric artery (SMA) blood flow response to feeding
blood flow response to feeding, determined in the SMA every half hour using magnetic resonance imaging
Time frame: 240 minutes after feeding
Fasting blood glucose concentration
whole blood glucose concentration assessed using a Hemocue glucose analyser
Time frame: before feeding
Blood glucose response to feeding
whole blood glucose concentration response to feeding, assessed by serial sampling using a Hemocue glucose analyser
Time frame: 300 minutes after feeding
Fasting insulin concentration
serum insulin concentration in the fasted state measured at a later date using a radio-immunoassay (RIA)
Time frame: baseline
serum insulin response to feeding
serum insulin concentration response to feeding, assessed by serial sampling and measured at a later date using a RIA
Time frame: 300 minutes after feeding
Fasting plasma GLP-1 concentration
Plasma GLP-1 concentration in the fasted state, measured at a later date using an enzyme-linked immunosorbent assay (ELISA)
Time frame: baseline
Plasma GLP-1 response to feeding
Plasma GLP-1 concentration response to feeding, assessed by serial sampling and measured at a later date using an ELISA
Time frame: 300 minutes after feeding
Fasting plasma GLP-2 concentration
Plasma GLP-2 concentration in the fasted state, measured at a later date using an enzyme-linked immunosorbent assay (ELISA)
Time frame: baseline
Plasma GLP-2 response to feeding
Plasma GLP-2 concentration response to feeding, assessed by serial sampling and measured at a later date using an ELISA
Time frame: 300 minutes after feeding
Fasting plasma Ghrelin
Plasma Ghrelin concentration in the fasted state measured at a later date using a RIA
Time frame: baseline
Plasma Ghrelin response to feeding
Plasma Ghrelin concentration response to feeding assessed by serial sampling and measured at a later date using a RIA
Time frame: 300 minutes after feeding
Fasting plasma peptide YY (PYY)
Plasma PYY concentration in the fasted state measured at a later date using a RIA
Time frame: baseline
Plasma peptide YY (PYY) response to feeding
Plasma PYY concentration response to feeding assessed by serial sampling and measured at a later date using a RIA
Time frame: 300 minutes after feeding
Subjective satiety in the fasted state
Satiety of individuals in the fasted state will be assessed using 4 visual analogue scales ('How hungry do you feel', 'how much food do you think that you could eat', how strong is your desire to eat' and how full do you feel')
Time frame: baseline
Subjective satiety after eating
Satiety immediately after eating the standard meal will be assessed using 4 visual analogue scales ('How hungry do you feel', 'how much food do you think that you could eat', how strong is your desire to eat' and 'how full do you feel')
Time frame: immediately after eating the standard meal
Subjective satiety response to eating
The satiety response to the standard meal will be assessed over the 300 minute study period using hourly collection of 4 visual analogue scales ('How hungry do you feel', 'how much food do you think that you could eat', how strong is your desire to eat' and 'how full do you feel')
Time frame: 300 minutes after eating
visceral adiposity
amount of visceral fat present, determined by MRI of the torso
Time frame: baseline
subcutaneous adiposity
thickness of the subcutaneous fat layer on the torso, determined by MRI
Time frame: before feeding
hepatic lipid content
liver triacylglyceride content will be estimated using proton magnetic resonance spectroscopy
Time frame: baseline
Attrition rate
Number of participants completing the protocol as a proportion of those who were recruited to the study
Time frame: 1 year
Recruitment rate
number of people volunteering to take part in the study as a proportion of those expressing initial interest
Time frame: 1 year
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