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Effects of Glucagon Like Peptide-1(GLP-1) and Liraglutide on Brain Satiety and Reward Circuits and Feeding Behavior in Diabetes

Not Applicable
Completed
Conditions
Obesity
Type 2 Diabetes
Interventions
Drug: insulin glargine treatment
Drug: GLP-1 receptor antagonist
Registration Number
NCT01363609
Lead Sponsor
Amsterdam UMC, location VUmc
Brief Summary

The aim of this study is to investigate if endogenous Glucagon Like Peptide -1 (GLP-1) has an effect on brain satiety and reward systems and if there are alterations in obese patients with type 2 diabetes (T2DM). Secondly, the aim is to investigate whether treatment with a GLP-1 analog, liraglutide, restores these signals in obese patients with type 2 diabetes. Finally, also the endogenous GLP-1 effects will be investigated in obese individuals before and after gastric bypass surgery on brain satiety and reward systems.

Detailed Description

First aim will be addressed in a cross-sectional randomized study. 20 healthy, lean and 20 obese individuals with type 2 diabetes (T2DM) will be exposed to food cues and with concomitant infusion of glucagon Like peptide-1 (GLP-1) receptor antagonist or saline, to assess the involvement of endogenous GLP-1, secreted in response to a meal. Measurements activation of CNS circuits involved in satiety and reward will be performed using blood oxygen level-dependent (BOLD) functional magnetic resonance imaging (fMRI).

The second aim will be addressed in cross-over randomized-controlled trial (RCT) in the T2DM patients only. Patients will be randomly assigned liraglutide vs insulin glargine treatment, during a treatment period of 12 weeks each with a 12-week washout period in between. The investigators will perform the same fMRI protocol.

The third aim will be addressed in a study with obese individuals who are scheduled for a gastric bypass surgery. The same protocol as for the first aim will be performed and this will be before and after the surgery in the same individuals.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
50
Inclusion Criteria
  • For the healthy, lean individuals:
  • Age 18-65 years
  • Women: post menopausal (excluding possible menstruation cycle effects)
  • Body-mass index (BMI) of <25 kg/m2,
  • Stable bodyweight (<5% reported change during the previous 3 months).
  • Normal fasting and 2h post load glucose as ascertained during a 75-g oral glucose tolerance test (OGTT) (34)
  • Right handed

For the obese T2DM individuals:

  • Age 18-65 years
  • Women: post menopausal (excluding possible menstruation cycle effects)
  • BMI 25-40 kg/m2
  • Stable bodyweight (<5% reported change during the previous 3 months).
  • Diagnosed with T2DM > 3 months prior to screening
  • HbA1C 6.5-8.5%
  • Treatment with metformin at a stable dose for at least 3 months.
  • Right handed

For the obese individuals scheduled for gastric bypass surgery:

  • Age 18-65 years
  • Women: preferably post menopausal (excluding possible menstruation cycle effects)
  • Body-mass index (BMI) of >30 kg/m2,
  • Stable bodyweight (<5% reported change during the previous 1 months).
  • Normal or impaired fasting and 2h post load glucose as ascertained during a 75-g oral glucose tolerance test (OGTT) (defined as glucose fasting < 7.1 mmol/l and after OGTT t=120min < 11.0 mmol/l) (39)
  • Right handed
Exclusion Criteria
  • GLP-1 based therapies, thiazolidinediones, sulphonylurea or insulin within 3 months before screening
  • Weight-lowering agents within 3 months before screening.
  • Congestive heart failure (NYHA II-IV)
  • Chronic renal failure (glomerular filtration rate < 60 mL/min/1.73m2 per Modification of Diet in Renal Disease (MDRD))
  • Liver disease
  • History of gastrointestinal disorders (including gastropareses, pancreatitis and cholelithiasis)
  • Neurological illness
  • Malignancy
  • Other type of bariatric surgery (Redo-GBP, sleeve, distal GBP, adj banding, Scopinaro)
  • History of major heart disease
  • History of major renal disease
  • Pregnancy or breast feeding
  • Implantable devices
  • Substance abuse
  • Addiction
  • Contra-indication for MRI, such as claustrophobia or pacemaker
  • Any psychiatric illness; including eating disorders and depression
  • Chronic use of centrally acting agents or glucocorticoids within 2 weeks immediately prior to screening.
  • Use of cytostatic or immune modulatory agents
  • History or known allergy for acetaminophen.
  • History of allergy for insulin analog
  • History of allergy for liraglutide
  • Participation in other studies
  • Individuals who have received treatment within the last 30 days with a drug that has not received regulatory approval for any indication at the time of study entry
  • Individuals who are investigator site personnel, directly affiliated with the study, or are immediate family

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
LiraglutideLiraglutide treatment 12 weeks12 week treatment with liraglutide in fixed dosage
Insulin glargineinsulin glargine treatment12 week treatment, once daily, with insulin glargine. Dosage based on fasting blood glucose measurements
before start of treatment periodGLP-1 receptor antagonistbefore start of the treatment period, one day with tests will be performed. During this test a GLP-1 receptor antagonist will be administered In the group with obesity and planned gastric bypass surgery, the GLP-1 receptor agonist will be administered during 1 test before and 1 test after the surgery
Primary Outcome Measures
NameTimeMethod
food-stimuli related neuronal activity in reward and satiety circuits as represented by BOLD fMRI signal change from baseline (%)approximately 3 years

* differences between obese T2DM patients and healthy lean subjects food-stimuli related neuronal activity in reward and satiety circuits as represented by BOLD fMRI signal change from baseline (%)

* the involvement of endogenous GLP-1 food-stimuli related neuronal activity in reward and satiety circuits as represented by BOLD fMRI signal change from baseline (%)

* Effects of treatment with the GLP-1 analog liraglutide in obese patients with type 2 diabetes in food-stimuli related neuronal activity in reward and satiety circuits as represented by BOLD fMRI signal change from baseline (%)

* - To investigate the involvement of the increased meal-related endogenous GLP-1 levels after gastric bypass surgery in these food-stimuli related CNS satiety and reward responses and to investigate whether pharmacological blocking of endogenous GLP-1 receptor activation, using a GLP-1 antagonist, differentially affects these responses before and after gastric bypass surgery in obese individuals.

Secondary Outcome Measures
NameTimeMethod
GLP-1 analog treatment related changes in obese patients with type 2 diabetes in microvascular function and vasomotionapproximately 3 years
GLP-1 analog treatment related changes in obese patients with type 2 diabetes in cardiovascular autonomic nervous balanceapproximately 3 years
Alterations in resting state brain activity networks in obese patients with type 2 diabetes compared to lean, healthy individuals and the involvement of endogenous GLP-1approximately 3 years
Alterations in brain arterial blood flow in obese patients with type 2 diabetes compared to lean, healthy individuals and the involvement of endogenous GLP-1approximately 3 years
GLP-1 analog treatment related changes in obese patients with type 2 diabetes in self-reported hunger, satiety, fullnessapproximately 3 years
GLP-1 analog treatment related changes in obese patients with type 2 diabetes in concomitant changes in metabolic and humoral markersapproximately 3 years
GLP-1 analog treatment related changes in obese patients with type 2 diabetes in basal metabolic rate and post-prandial energy expenditureapproximately 3 years
GLP-1 analog treatment related changes in obese patients with type 2 diabetes in resting state brain activity networks.approximately 3 years
GLP-1 analog treatment related changes in obese patients with type 2 diabetes in brain arterial blood flow.approximately 3 years

Trial Locations

Locations (1)

VU University Medical Center

🇳🇱

Amsterdam, Netherlands

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