- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02654925
Myeloid to Adipocyte Transdifferentiation in Human Cells (MYTH)
June 23, 2021 updated by: University of Colorado, Denver
In order to design new programs to help prevent weight gain, promote successful and sustainable weight loss, and help treat diseases related to obesity, the investigators need a better understanding of why accumulating fat in certain regions of the body is bad for health.
It is known that not all fat cells are the same, but it was recently discovered that some fat cells may arise from stem cells that come from the bone marrow (bone marrow progenitors), a previously unrecognized origin.
This discovery has been paradigm shifting, because dogma has long held that all white fat cells arise from fat tissue resident mesenchymal stem cells.
This is also important because fat cells arising from the bone marrow lineage may be linked to worse health outcomes.
The aim of this study is to determine if cells that were not previously believed to contribute to fat generation in humans are indeed capable of becoming fat cells.
To answer this question the investigators will take samples of cells from the blood and the fat tissue of younger and older men and women, isolate the cells that came from the bone marrow and grow them in culture to determine if they will turn into fat cells.
The results of this investigation may reveal potential mechanistic targets for future therapies to reduce the negative health outcomes associated with obesity related chronic diseases.
Study Overview
Study Type
Observational
Enrollment (Actual)
59
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Colorado
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Aurora, Colorado, United States, 80045
- University of Colorado Anschutz Medical Campus
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
21 years to 100 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Community sample
Description
Inclusion Criteria:
- Men and women age 21-40 y or 55-100 y;
- Older women will be postmenopausal who are at least 12 months past the final menstrual period (FMP);
- Young women will be premenopausal and eumenorrheic, not on hormonal contraceptive therapy;
- Body Mass Index (BMI) 22-35 kg/m2;
- Non-active to moderately active (vigorous exercise ≤ 3 days/wk lasting < 30 min).
Exclusion Criteria:
- Immunosuppression therapy;
- On blood thinners, aspirin, or NSAIDs that cannot be withheld for the biopsy;
- Prior history of allergies to local anesthetics;
- Current use of hormones, or glucose lowering medication;
- Currently engaged in a vigorous exercise or diet program;
- Currently gaining or losing weight or using weight loss drugs;
- Type 2 diabetes (past/current diagnosis or treatment);
- Diagnosis of uncontrolled metabolic disorders (e.g., thyroid);
- History of severe obesity BMI ≥ 40 or significant weight loss (≥ 50 lbs);
- Postmenopausal - hormonal menopausal therapy use currently or in the previous 6 months;
- Premenopausal - irregular menstrual cycles defined as 2 or more missed cycles in the previous year, pregnant or planning to become pregnant during the study timeline (urine pregnancy test will be performed before DEXA [dual energy x-ray absorptiometry] scan is completed).
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Young Men
men 21-40 years of age
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Young Women
women 21-40 years of age; young women will be premenopausal and eumenorrheic, not on hormonal contraceptive therapy.
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Older Men
men 55-100 years of age
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Older Women
women 55-100 years of age; older women will be postmenopausal who are at least 12 months past the final menstrual period (FMP).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Adipogenic potential as measured by Oil Red-O staining (quantification by absorbance).
Time Frame: Within 60 days of biopsy
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Within 60 days of biopsy
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Adipocyte specific gene expression will be measured by qPCR (quantitative polymerase chain reaction) to confirm adipocyte status.
Time Frame: Sample collection within 60 days of biopsy, batched analysis completed depending on enrollment.
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Sample collection within 60 days of biopsy, batched analysis completed depending on enrollment.
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Assessment of the fraction of myeloid cells that become 'mesenchymal-like' (CD45-/CD14-/CD34+) (CD: cluster of differentiation) after fibrin culture by flow cytometry.
Time Frame: Within 2 weeks of biopsy
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Within 2 weeks of biopsy
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Progenitor cell proliferation capacity as measured by BrdU (bromodeoxyuridine) incorporation
Time Frame: Within 60 days of biopsy
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Within 60 days of biopsy
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In vivo adipogenesis in the Matrigel plug will be assessed by immunohistochemistry (IHC) for adipocyte (e.g., adiponectin) and nuclear markers (e.g., DAPI).
Time Frame: Samples will be collected within 60 days of biopsy, batched sample analysis will occur dependent on subject enrollment
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Samples will be collected within 60 days of biopsy, batched sample analysis will occur dependent on subject enrollment
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Kathleen M Gavin, PhD, University of Colorado Denver Anschutz Medical Campus
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2016
Primary Completion (Actual)
June 15, 2021
Study Completion (Actual)
June 15, 2021
Study Registration Dates
First Submitted
January 7, 2016
First Submitted That Met QC Criteria
January 11, 2016
First Posted (Estimate)
January 13, 2016
Study Record Updates
Last Update Posted (Actual)
June 24, 2021
Last Update Submitted That Met QC Criteria
June 23, 2021
Last Verified
June 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- 15-1779
- UL1TR001082 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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