Insight Into Subcutaneous Adipose Tissue Disorders

Lipedema Clinical Trial

— INSIGHT  

Official title:

Insight Into Subcutaneous Adipose Tissue Disorders As Part of The TREAT Program (Treatment, Research, Education, Adipose Tissue) at the University of Arizona

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02838277
• Other study ID #: 1602399502A001
• Status: Recruiting
• Phase: N/A
• First received: June 28, 2016
• Last updated: September 14, 2017
• Start date: June 2016
• Est. completion date: December 2018

Study information

• Verified date: September 2017
• Source: University of Arizona
• Contact: Karen L Herbst, PhD, MD
• Phone: 5206267689
• Email: karenherbst[@]deptofmed.arizona.edu
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The INSIGHT study aims to phenotype individuals with subcutaneous adipose tissue (SAT) disorders specifically lipedema and Dercum's disease with an aim to find a cure for the SAT in these disorders that is resistant to diet and exercise.

Description:

Lipedema is a syndrome of painful fatty enlargement of the buttocks, hips and thighs primarily in women which cannot be lost by diet, exercise or bariatric surgery. Arms are affected in 80% of women with lipedema to varying degrees. The etiology of lipedema is not known and there are no evidence-based treatments that work for a majority of individuals except for excision of the subcutaneous adipose tissue (SAT) by liposuction which has risks. Millions of women are affected with lipedema yet they are grossly under-diagnosed, have mobility issues and can develop lymphedema. The goal of this project is to better understand the etiology of lipedema SAT, find out how it is different from non-lipedema SAT, to improve our ability to identify the abnormal SAT and determine the response of the tissue to therapeutics by imaging and biomarkers. People with diffuse Dercum's disease (DD) appear to have lipedema plus a tissue inflammation that causes illness and pain. People with SAT disorders that have similarities to lipedema will also be included in this protocol. More research is needed to determine how these fatty disorders are similar and different from each other and from obesity so they can be distinguished clinically and by laboratory testing and imaging. Since these painful fatty disorders are associated with SAT growth, research focused on these disorders may provide unique insight into mechanisms of obesity.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 500
• Est. completion date: December 2018
• Est. primary completion date: June 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 19 Years to 70 Years

Eligibility

Inclusion Criteria:

1. Ambulatory males and/or females of any race able to understand the consent process.

2. 19-70 years of age.

3. Diagnosis of lipedema, Dercum's disease or familial multiple lipomatosis or other similar fat disorder.

4. Individuals without a fat disorder (will be matched by age, sex, race and body mass index to individuals in "2").

5. Weight stable for past three months within a 10 pound range per personal report of the subject.

6. Overweight or obese (BMI > 26 kg/m2) in order to be able to get enough SAT for the biopsy.

7. Individuals with BMI < 26 kg/m2 may participate in all aspects of the study protocol except the SAT biopsy.

8. Thyroid levels in the normal range as confirmed by a TSH level. May have treated hypothyroidism that is stable over 6 months.

Exclusion Criteria:

1. HIV infection (because of the associated lipodystrophy and fatty growths [lipomas]).

2. Subjects will be excluded from having a SAT biopsy with any history of scleroderma, keloid formation or other skin condition that would result in substantial scarring after biopsy, a history of recurrent cellulitis, any history of bleeding diathesis that would place the subject at great risk for persistent bleeding after a biopsy/liposuction, any history of major complication after a previous biopsy including requirement of a blood transfusion, hospitalization, failure to heal, or major infection, requiring intravenous antibiotics, or anyone whose skin and tissue would put them at risk for an infection after the biopsy per the assessment of study staff and the principal investigator. These individuals may participate in the remainder of the protocol, just not the SAT biopsy.

3. Use of any immunosuppressant or corticosteroid medication.

4. Use of any anti-inflammatory medication such as NSAIDs, aspirin, histamine (H) 1 blocker, H2 blocker, tetracycline or corticosteroids within five days of the study procedure visit.

5. Use of medications that might cause weight gain (e.g., second generation anti-psychotics).

6. Blood donation less than 56 days prior to screening visit.

7. Tobacco or marijuana use which may alter inflammation in the body.

8. Any antibiotics within the last month.

9. Barium enema in the last week which would affect gut bacteria and the MRI.

10. Pregnancy due to the risks associated with the fat biopsy in the area of the fetus and because pregnancy will alter hormone levels.

Related Conditions & MeSH terms

• Dercum's Disease
• Familial Multiple Lipomatosis
• Lipedema
• Madelung's Disease

Locations

Country	Name	City	State
United States	University of Arizona College of Medicine (South Campus)	Tucson	Arizona

Sponsors (2)

Lead Sponsor	Collaborator
University of Arizona	Lipedema Foundation

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Transcriptomics of all enrolled subjects from a single timepoint to assess for changes in gene expression in lipedema tissue compared to controls	This is a phenotyping study that collects data as a single time point though studies may occur on different days.	Single time point study with imaging, blood draw, exam and biopsies over multiple days for a total of approximately 8 hours time.
Primary	Metabolomics of all enrolled subjects from a single timepoint to assess for changes in metabolites in lipedema tissue compared to controls	This is a phenotyping study that collects data as a single time point though studies may occur on different days.	Single time point study with imaging, blood draw, exam and biopsies over multiple days for a total of approximately 8 hours time.
Primary	Lipidomics of all enrolled subjects from a single timepoint to assess for changes in lipid particles in lipedema tissue and blood compared to controls	This is a phenotyping study that collects data as a single time point though studies may occur on different days.	Single time point study with imaging, blood draw, exam and biopsies over multiple days for a total of approximately 8 hours time.
Primary	Cytokines of all enrolled subjects from a single timepoint to assess for changes in cytokine arrays in lipedema tissue and blood compared to controls	This is a phenotyping study that collects data as a single time point though studies may occur on different days.	Single time point study with imaging, blood draw, exam and biopsies over multiple days for a total of approximately 8 hours time.
Primary	Myostatin of all enrolled subjects from a single timepoint to assess for levels of myostatin in lipedema tissue and blood compared to controls	This is a phenotyping study that collects data as a single time point though studies may occur on different days.	Single time point study with imaging, blood draw, exam and biopsies over multiple days for a total of approximately 8 hours time.