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Nutrient sensing in response to starvation in obese and lean individuals.

Nutrient sensing in response to starvation in obese and lean individuals.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON29226
Enrollment
24
Registered
2010-07-01
Start date
2010-06-05
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

obesity

Interventions

In this study a group of 12 obese individuals and a group of 12 lean individuals (control group) will be exposed to 60 hours of starvation. Before and after this intervention we will obtain muscle bio

Sponsors

Leiden University Medical Center
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Healthy males and females; 2. Age 19-60 yrs; 3. Obese subjects: BMI >30 kg/m2; 4. Lean controls: BMI 19-25 kg/m2; 5. Stable weight for the last 3 months; 6. Caucasian; 7. FPG 7.5 mmol/l; 11. Negative family history (first degree) of DM2.

Exclusion criteria

Exclusion criteria: 1. Use of medication known to affect glucose metabolism (for example prednisone) or lipid metabolism; 2. History of genetic or psychiatric disease (e.g. fragile X syndrome, major depression) that affects the brain; 3. Significant chronic disease; 4. Renal or hepatic disease; 5. Pregnancy; 6. Smoking (current); 7. Alcohol consumption of more than 14 units per week at present or in the past; 8. Difficult accessible veins for insertion of an intravenous catheter; 9. Recent blood donation (within the last 3 months); 10. Recent participation in other research projects (within the last 3 months), participation in 2 or more projects in one year; 11. Contra-indication to MRI scanning: A. Claustrophobia; B. Pacemakers and defibrillators; C. Nerve stimulators; D. Intracranial clips; E. Intraorbital or intraocular metallic fragments; F. Cochlear implants; G. Ferromagnetic implants.

Design outcomes

Primary

MeasureTime frame
The primary outcome are biochemical parameters (eg AMPK, Sirtuins) measured in muscle biopsies. These will be obtained before and after 60 hours of starvation and for the obese group after the weight loss intervention as well.

Secondary

MeasureTime frame
Secondary outcomes are: Antropometrics, fMRI, heart rate variability, biometric impedance analysis, blood pressure and pulse, indirect calorimetry and blood samples. All will be obtained before and after 60 hours of starvation and for the obese group after the weight loss intervention as well.

Contacts

Public ContactM.A. Wijngaarden
m.a.wijngaarden@lumc.nl+31715265304

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)