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

Status

Completed

Conditions

Intervention / Treatment

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

    • Colorado
      • Aurora, Colorado, United States, 80045
        • University of Colorado Anschutz Medical Campus

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
Young Men
men 21-40 years of age
Young Women
women 21-40 years of age; young women will be premenopausal and eumenorrheic, not on hormonal contraceptive therapy.
Older Men
men 55-100 years of age
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
Adipogenic potential as measured by Oil Red-O staining (quantification by absorbance).
Time Frame: Within 60 days of biopsy
Within 60 days of biopsy
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.
Sample collection within 60 days of biopsy, batched analysis completed depending on enrollment.

Secondary Outcome Measures

Outcome Measure
Time Frame
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
Within 2 weeks of biopsy
Progenitor cell proliferation capacity as measured by BrdU (bromodeoxyuridine) incorporation
Time Frame: Within 60 days of biopsy
Within 60 days of biopsy
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
Samples will be collected within 60 days of biopsy, batched sample analysis will occur dependent on subject enrollment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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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