Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Study terminated by study partners
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
This study aims to characterize the neurological basis of obesity and response to surgical and medical treatment by inducing adult pluripotent stem cells into neuronal cells from subjects that have demonstrated extreme response to bariatric surgery or pharmacological treatment for obesity.
The investigators will consent subjects who have achieved extreme response to either bariatric surgery or pharmacologic treatment for obesity and harvest fibroblasts from skin biopsies, which will be reprogrammed to induced pluripotent stem cells (iPSC). These iPSC's will then be differentiated into neural progenitor cells, neurons, astrocytes, and microglia to identify genetic and epigenetic pathways altered in disease-specific neural progenitor cells of the brain.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Bariatric Surgery | Subjects that have demonstrated extreme response to bariatric surgery. |
| |
| Anti Obesity Medications | Subjects that have demonstrated extreme response to anti obesity pharmacotherapy. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Bariatric Surgery | Procedure | Sleeve gastrectomy or Roux-en-Y Gastric Bypass |
| |
| Measure | Description | Time Frame |
|---|---|---|
| DNA sequencing | Perform DNA sequencing from skin biopsy progenitor cells | 4 months |
| Generate human cell based models of obesity | Fibroblasts will be expanded in culture and then reprogrammed to hiPSCs. | 4 months |
| Differentiation to human CNS cells | Disease specific hiPSCs cells will be differentiated into neural progenitor cells, neurons, astrocytes, and microglia | 4 months |
| Identification of genetic and epigenetic pathways | Identify genetic and epigenetic pathways altered in disease-specific neural progenitor cells, neurons, and non-neuronal cells of the brain | 4 months |
Not provided
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Subjects with obesity who are considered super responders to bariatric surgery or anti obesity pharmacotherapy.
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Eduardo Grunvald, MD | UCSD | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of California San Diego | La Jolla | California | 92037 | United States |
This is not an intervention trial
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D009767 | Obesity, Morbid |
| D009765 | Obesity |
| ID | Term |
|---|---|
| D050177 | Overweight |
| D044343 | Overnutrition |
| D009748 | Nutrition Disorders |
| D009750 | Nutritional and Metabolic Diseases |
Not provided
Not provided
| ID | Term |
|---|---|
| D050110 | Bariatric Surgery |
| D019440 | Anti-Obesity Agents |
| ID | Term |
|---|---|
| D049088 | Bariatrics |
| D000073319 | Obesity Management |
| D013812 | Therapeutics |
| D013514 | Surgical Procedures, Operative |
Not provided
Not provided
Not provided
Not provided
Not provided
Fibroblasts, iPSCs, and DNA sequencing information generated from skin biopsies will be expanded and stored for potential future use.
| Anti Obesity Drugs |
| Drug |
Response to FDA approved anti obesity medications |
|
| D001835 |
| Body Weight |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D045506 |
| Therapeutic Uses |
| D020228 | Pharmacologic Actions |
| D020164 | Chemical Actions and Uses |