Omics Profiling of Weight Loss With Bariatric Surgery (Bariatric)
Obesity, Surgery

About this trial
This is an interventional supportive care trial for Obesity
Eligibility Criteria
Inclusion criteria obese subjects:
- Diagnosed with morbid obesity (defined as BMI > 40 kg/m2 or BMI > 35 kg/m2 with at least one serious comorbidity (1991 NIH compendium guidelines))
- Scheduled for bariatric surgery
- Age 18 years and older
- Ability to lie in supine or elevated position for 9 hours
- Willingness and ability to comply with the protocol
Inclusion criteria healthy subjects:
- Healthy male or female according to the investigator's or appointed staff's judgment
- Ability to walk, sit down and stand up independently
- Age 18 years or older
- Ability to lie in supine or elevated position for 9 hours
- Willingness and ability to comply with the protocol
Exclusion Criteria
- Any condition that may interfere with the definition 'healthy subject' according to the investigator's judgment (for healthy control group only)
- Presence of fever within the last 3 days
- Untreated metabolic diseases including hepatic or renal disorder unrelated to the primary disease
- Presence of acute illness or metabolically unstable chronic illness unrelated to the primary disease
- (Possible) pregnancy
- Any other condition according to the PI or nurse that would interfere with the study or safety of the patient
- Failure to give informed consent
- Use of protein or amino acid containing nutritional supplements within 3 days of first test day
Sites / Locations
- Texas A&M University-CTRAL
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Healthy matched controls
Obese subjects
screening visit: body weight and composition by DXA, height, and vital signs will be assessed. Subjects may sign a medical release form to obtain medical and psychological information about them that will help determine study eligibility or can be used for later coding. study day: muscle mass and function tests, resting energy expenditure, stable isotope infusions with blood draws, and questionnaires regarding quality of life, mood and depression, diet.
screening visit: body weight and composition by DXA, height, and vital signs will be assessed. Subjects may sign a medical release form to obtain medical and psychological information about them that will help determine study eligibility or can be used for later coding. 3 study days (one baseline, one pre-surgery, one post-surgery): muscle mass and function tests, resting energy expenditure, stable isotope infusions with blood draws, and questionnaires regarding quality of life, mood and depression, diet.