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Effect of Oral Feeding on Gastric Emptying, Gut Blood Flow, and Hormone Responses in Obese and Healthy Weight Subjects

The Effect of Oral Feeding on Gastric Emptying, Small Bowel Water Content, Superior Mesenteric Artery Blood Flow, Plasma Hormone Concentrations and Blood Volume in Obese and Healthy Weight Subjects.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03860623
Enrollment
20
Registered
2019-03-04
Start date
2018-11-07
Completion date
2022-10-28
Last updated
2025-12-04

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

Conditions

Obesity

Keywords

satiety, gut blood flow, gastric emptying, obesity, incretin hormones

Brief summary

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.

Detailed description

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.

Interventions

None listed

Sponsors

University of Nottingham
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

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

Inclusion criteria

* BMI 30-40 kg/m2 * BMI 18-25 kg/m2; those with BMI up to 28kg/m2 will be included if waist circumference is \<96cm. * Males * Aged 18-60yrs

Exclusion criteria

* Acute illness in the preceding 6 weeks * Taking regular medication * History of deep vein thrombosis or clotting disorders * Hypertension * Diabetes * Any clinically significant findings at screening * History of substance abuse * Demonstrating factors precluding safe MRI * History of gastrointestinal motility disorders (e.g. gastroesophageal reflux disease -irritable bowel syndrome, gastroparesis, sphincter of Oddi dysfunction, etc.) * Previous thoracic or abdominal surgery. * Those who report having ≤3 bowel movements/week or \>2/day.

Design outcomes

Primary

MeasureTime frameDescription
Gastric emptying rate240 minutes after feedingtime taken for a standard meal to empty from the stomach, assessed by serial volume measurements of the stomach using magnetic resonance imaging

Secondary

MeasureTime frameDescription
Stomach volume in the fasted statebaselinevolume of the stomach measured by magnetic resonance imaging
Superior mesenteric artery (SMA) blood flow in the fasted statebaselineblood flow in the SMA assessed using magnetic resonance imaging
superior mesenteric artery (SMA) blood flow response to feeding240 minutes after feedingblood flow response to feeding, determined in the SMA every half hour using magnetic resonance imaging
Fasting blood glucose concentrationbefore feedingwhole blood glucose concentration assessed using a Hemocue glucose analyser
Blood glucose response to feeding300 minutes after feedingwhole blood glucose concentration response to feeding, assessed by serial sampling using a Hemocue glucose analyser
serum insulin response to feeding300 minutes after feedingserum insulin concentration response to feeding, assessed by serial sampling and measured at a later date using a RIA
Fasting plasma GLP-1 concentrationbaselinePlasma GLP-1 concentration in the fasted state, measured at a later date using an enzyme-linked immunosorbent assay (ELISA)
Plasma GLP-1 response to feeding300 minutes after feedingPlasma GLP-1 concentration response to feeding, assessed by serial sampling and measured at a later date using an ELISA
Fasting plasma GLP-2 concentrationbaselinePlasma GLP-2 concentration in the fasted state, measured at a later date using an enzyme-linked immunosorbent assay (ELISA)
Plasma GLP-2 response to feeding300 minutes after feedingPlasma GLP-2 concentration response to feeding, assessed by serial sampling and measured at a later date using an ELISA
Fasting plasma GhrelinbaselinePlasma Ghrelin concentration in the fasted state measured at a later date using a RIA
Fasting insulin concentrationbaselineserum insulin concentration in the fasted state measured at a later date using a radio-immunoassay (RIA)
Fasting plasma peptide YY (PYY)baselinePlasma PYY concentration in the fasted state measured at a later date using a RIA
Plasma peptide YY (PYY) response to feeding300 minutes after feedingPlasma PYY concentration response to feeding assessed by serial sampling and measured at a later date using a RIA
Subjective satiety in the fasted statebaselineSatiety 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')
Subjective satiety after eatingimmediately after eating the standard mealSatiety 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')
Subjective satiety response to eating300 minutes after eatingThe 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')
visceral adipositybaselineamount of visceral fat present, determined by MRI of the torso
subcutaneous adipositybefore feedingthickness of the subcutaneous fat layer on the torso, determined by MRI
hepatic lipid contentbaselineliver triacylglyceride content will be estimated using proton magnetic resonance spectroscopy
Attrition rate1 yearNumber of participants completing the protocol as a proportion of those who were recruited to the study
Recruitment rate1 yearnumber of people volunteering to take part in the study as a proportion of those expressing initial interest
Plasma Ghrelin response to feeding300 minutes after feedingPlasma Ghrelin concentration response to feeding assessed by serial sampling and measured at a later date using a RIA

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026