GLP-1 Therapy for Weight Loss and Improved Glucose Tolerance in Obese Children

University of Minnesota (UMN)

Status and phase

Completed

Phase 2

Conditions

Obesity, Morbid

Treatments

Drug: Exenatide

Study type

Interventional

Funder types

Other

Identifiers

NCT00886626

0902M59181

Details and patient eligibility

About

The prevalence of severely obese children is on the rise. Behavioral therapies for weight loss are successful in some, but others need more aggressive approaches such as drug therapy. In addition, up to 25% of severely obese children have impaired glucose tolerance (IGT), which places them at significantly elevated risk of developing type 2 diabetes mellitus and cardiovascular disease. Although various drug therapies for weight loss and IGT have been explored in adults, few have been evaluated in children.

Recently, a new drug class has emerged that targets deficiencies of GLP-1. One of the main glycemic mechanisms of action of the GLP-1 agonists such as exenatide is to enhance glucose disposal in the postprandial setting and improve glucose tolerance. In addition, exenatide can induce weight loss by decreasing appetite and slowing gastric motility.

Full description

This will be a randomized, open-label, controlled, crossover clinical trial in 12 patients. All patients will receive exenatide and undergo the control phase. Following baseline testing, participants will be randomly assigned to treatment order: therapy (exenatide) or control (lifestyle modification). Half (n = 6) will receive exenatide first (3-months) then cross over to control (no drug therapy for 3-months). Half (n = 6) will be assigned to control first (3-months) then cross over to exenatide (3-months). All efforts will be made to stratify randomization based on gender of the participants. Treatment and control conditions will be three months each. Because of the route of administration of exenatide (subcutaneous injection), placebo will not be utilized for the control phase of the study.

Participants in this study will engage in background intensive lifestyle modification offered by the University of Minnesota Pediatric Weight Management Clinic for the entire study, even during the active drug treatment phase. Intensive lifestyle modification will be purely clinical in nature in which children and their families receive continuing counseling from a team of trained professionals including physicians, dieticians, and psychologists to reduce weight by making healthier eating choices and increasing physical activity.

The screening visit will take place in the Pediatric Weight Management Clinic and will include a complete medical history and physical examination. Screening will include review of medical records for previous clinical and laboratory data (including clinically-ordered glucose tolerance test results). All research testing will take place in the University of Minnesota General Clinical Research Center (GCRC). Subjects will undergo testing at the following intervals: baseline, immediately after the first 3-month phase (whether exenatide or control), and immediately after the second 3- month phase (whether exenatide or control). The following measures will be collected after the subject has been fasting for at least twelve hours:

Height, weight, body mass index, waist and hip circumference
Fat and lean mass (dual energy x-ray absorptiometry: DXA)
Tanner stage determination (performed during screening physical exam or may be obtained from medical chart)
Fasting lipid profile (total-, LDL-, and HDL-cholesterol, triglycerides)
Systolic and diastolic blood pressure
Oral glucose tolerance test (glucose and insulin measured every 30 minutes for 2 hours)
Endothelial function (digital reactive hyperemia: EndoPAT 2000, Itamar Medical) - in addition to the baseline measure, endothelial function testing will occur at hours one and two of the oral glucose tolerance test
Frozen plasma for storage - in addition to the baseline blood draw, blood for endothelial biomarkers will be obtained at hours one and two of the oral glucose tolerance test
Arterial stiffness (pulse wave velocity; augmentation index: Sphygmocor, AtCor Medical)
Frozen plasma for pharmacokinetic determination of exenatide in children

Enrollment

12 patients

Sex

All

Ages

8 to 19 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age 8-19 years old
Subject able to give assent, and parent/guardian capable of giving consent on behalf of the child
Body mass index (BMI) ≥ 99th percentile (based on gender and age)

Exclusion criteria

Type 1 or 2 diabetes mellitus
Initiation of a new drug therapy within the past 30 days prior to the screening visit
BMI ≥ 55
History of weight loss surgery
Obesity from a genetic cause (e.g., Prader-Willi)
Central nervous system injury or severe neurological impairment
Known systolic or diastolic dysfunction or heart failure
Females who are currently pregnant or planning to become pregnant
Liver enzymes > 2.5 times upper limit of normal
Severe renal impairment (defined as creatinine clearance <30 mL/min)
Gastrointestinal disease