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Effect of Smoking on Postprandial Gastric Emptying, Glucose Tolerance and Secretion of Gut and Pancreatic Hormones

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02497651
Acronym
SmokinGLP-1
Enrollment
24
Registered
2015-07-14
Start date
2015-05-31
Completion date
2016-06-30
Last updated
2017-08-07

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

Conditions

Diabetes Mellitus

Keywords

Smoking, Diabetes, Incretin hormones, Glucose tolerance

Brief summary

The study aims to evaluate the effect of smoking on postprandial responses such as plasma glucose, secretion of gut - and pancreatic hormones and gastric emptying in healthy, heavy smoking men.

Detailed description

Epidemiological studies show that active smoking increases the risk of type 2 diabetes in a dose-dependent fashion. Smokers seem to be characterized by central obesity, increased inflammatory markers and oxidative stress, which may lead to insulin resistance and irregularities in glucose metabolism. The current study is a meal test study, in which the aim is to examine a number of variables during a liquid mixed meal test (including gastric emptying, glucose tolerance, gut and pancreatic hormone responses, gall bladder emptying, appetite and food intake) performed in healthy non-smoking subjects and in healthy smokers with or without concomitant cigarette smoking. The investigators hypothesize that smoking-induced increases in circulating nicotine levels and simultaneous activation of nicotinic receptors in the gastrointestinal tract and in the autonomic nervous system would have detrimental effect on postprandial glucose metabolism and, thus, constitute an important link between smoking and the risk of type 2 diabetes. The current study will help to clarify this hypothesis and improve our general understanding of the association between smoking and gut hormone secretion, gastric emptying and glucose metabolism.

Interventions

DIETARY_SUPPLEMENTLiquid mixed meal

The subjects will ingest a 400 ml chocolate drink, rich on carbohydrates, fat and lipids. In the following 4 hours, blood samples will be drawn from a PVC for the measurement of plasma glucose, gut- and pancreatic hormones, acetaminophen etc. After the 4 hours, the subjects will be offered an ad libitum meal.

OTHERSkin Biopsy

All subjects will undergo a skin biopsy procedure. Two small (3 mm) biopsies will be taken from the hip area under local anaesthesia. Standard wound treatment will follow.

Sponsors

University of Copenhagen
CollaboratorOTHER
European Foundation for the Study of Diabetes
CollaboratorOTHER
University Hospital, Gentofte, Copenhagen
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Both groups * Caucasian ethnicity * Healthy males * Normal haemoglobin * Age above 18 years * Informed and written consent * BMI \>20 kg/m2 Smokers • Minimum 20 cigarettes pr. day for at least 1 year Non-smokers • No smoking on a regular basis

Exclusion criteria

* Both groups * Diabetes or prediabetes (fasting plasma glucose levels \>6.5 mM or HbA1c \>6.0%) * First- or second-degree relatives with diabetes * Liver disease (alanine aminotransferase (ALAT) and/or serum aspartate aminotransferase (ASAT) \>2 times normal values) or history of hepatobiliary disorder * Gastrointestinal disease, previous intestinal resection, cholecystectomy or any major intra-abdominal surgery * Hypo- or hyperphosphataemia * Nephropathy (serum creatinine \>150 µM and/or albuminuria * Treatment with medicine that cannot be paused for 12 hours * Hypo- or hypercalcaemia * Hypo- and hyperthyroidism * Treatment with oral anticoagulants * Active or recent malignant disease * Any treatment or condition requiring acute or sub-acute medical or surgical intervention * Any condition considered incompatible with participation by the investigators

Design outcomes

Primary

MeasureTime frameDescription
Postprandial response of glucagon-like peptide-1 (GLP-1)-30, -20, -10, 0, 10, 20, 30, 50, 70, 90, 120, 150, 180, 240 minutes (meal tests start at 0 min)Incremental and total area under the Concentration-Time Curve (AUC 0-240 min)

Secondary

MeasureTime frameDescription
Postprandial response of Glukagon-30, -20, -10, 0, 10, 20, 30, 50, 70, 90, 120, 150, 180, 240 minutes (meal tests start at 0 min)Incremental and total area under the Concentration-Time Curve (AUC 0-240 min)
Postprandial response of CCK-30, -20, -10, 0, 10, 20, 30, 50, 70, 90, 120, 150, 180, 240 minutes (meal tests start at 0 min)Incremental and total area under the Concentration-Time Curve (AUC 0-240 min)
Postprandial response of Gastrin-30, -20, -10, 0, 10, 20, 30, 50, 70, 90, 120, 150, 180, 240 minutes (meal tests start at 0 min)Incremental and total area under the Concentration-Time Curve (AUC 0-240 min)
Postprandial response of GIP-30, -20, -10, 0, 10, 20, 30, 50, 70, 90, 120, 150, 180, 240 minutes (meal tests start at 0 min)Incremental and total area under the Concentration-Time Curve (AUC 0-240 min)
Postprandial response of insulin-30, -20, -10, 0, 10, 20, 30, 50, 70, 90, 120, 150, 180, 240 minutes (meal tests start at 0 min)Incremental and total area under the Concentration-Time Curve (AUC 0-240 min)
Blood Inflammatory and metabolic markers (composite)-30, -20, -10, 0, 10, 20, 30, 50, 70, 90, 120, 150, 180, 240 minutes (meal tests start at 0 min)
Gall bladder volume-30, 20, 40, 80, 240 minutes (meal tests start at 0 min)Assessment of gall bladder volume will be mediated by ultrasound
Gastric emptying-30, -20, -10, 0, 10, 20, 30, 50, 70, 90, 120, 150, 180, 240 minutes (meal tests start at 0 minMeasurement of acetaminophen is taken as a measure of gastric emptying
GLP-1 receptor expression in the skinAfter the 240 minutesAnalysis of the skin cells from the biopsies.
Postprandial increment in plasma glucose-30, -20, -10, 0, 10, 20, 30, 50, 70, 90, 120, 150, 180, 240 minutes (meal tests start at 0 min)Incremental and total area under the Concentration-Time Curve (AUC 0-240 min)

Countries

Denmark

Outcome results

None listed

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