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The Effect of Glitazone Treatment on Bone Marrow and Bone Marrow Cells

Information source: University of Aarhus
Information obtained from ClinicalTrials.gov on February 12, 2009
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Change in Bone Mineral Density; Change in Bone Marrow Fat Content

Intervention: Rosiglitazone (Drug); Placebo pill (Drug)

Phase: Phase 2

Status: Recruiting

Sponsored by: University of Aarhus

Official(s) and/or principal investigator(s):
Torben Harsløf, Dr., Principal Investigator, Affiliation: Aarhus University Hospital

Overall contact:
Torben Harsløf, Dr, Phone: +4589497681, Email: torben.harslof@ki.au.dk

Summary

Osteoporosis is a generalised bone disease leading to an increased risk of fractures. The disease is caused partly by environmental and partly by genetic factors. It is well known that the fat content of the bone marrow is increased in osteoporotic patients. Animal studies suggest that stimulation of bone marrow stem cells through the molecule PPARgamma with the drug rosiglitazone converts the stem cells to fat cells instead of bone cells thereby decreasing bone strength. In a single study healthy volunteers were treated with rosiglitazone for 14 weeks and had a decrease in bone mineral density.

In the present study we wish to investigate the effect of this treatment on bone and fat tissue. 25 women above the age of 60 will be treated with rosiglitazone 8 mg/day for 14 weeks and compared with 25 women receiving placebo.

The effect will be evaluated as follows:

1. The effect on bone marrow density will be examined by a bone scan prior to and after treatment and again after 6 and 9 months.

2. The effect on bone turnover will be measured in blood- and urine samples at the same times.

3. The effect on fat distribution will be evaluated by an MRI scan after treatment.

4. The effect on bone marrow cells will be investigated bone marrow sampling immediately after treatment

5. The direct effect on fat will be examined by a biopsy immediately after treatment The study hypothesis is that rosiglitazone treatment decreases bone mineral density and increases bone marrow fat content. The causal molecular mechanisms will be investigated from the bone marrow and fat samples

Clinical Details

Official title: The Effect of Glitazone Treatment on Bone Marrow and Bone Marrow Cells

Study design: Basic Science, Randomized, Double Blind (Subject, Investigator), Placebo Control, Parallel Assignment, Pharmacodynamics Study

Primary outcome: Change in bone mineral density

Secondary outcome:

Change in bone marrow fat content

change in biochemical markers of bone turnover

Change in gene expression in bone marrow and fat cells

Eligibility

Minimum age: 60 Years. Maximum age: 75 Years. Gender(s): Female.

Criteria:

Inclusion Criteria:

- Postmenopausal women age 60-75 with no rosiglitazone allergy

Exclusion Criteria:

- Osteoporosis

- Diabetes

- Hyperthyroidism, untreated hypothyroidism, hyperparathyroidism

- Treatment with bone active drugs

- Low impact fracture

- Heart disease

- Kidney failure

- Liver failure

- Anaemia

- Ineligibility for MRI-scan

- Cancer within last 5 years

Locations and Contacts

Torben Harsløf, Dr, Phone: +4589497681, Email: torben.harslof@ki.au.dk

Aarhus University Hospital, Aarhus 8000 C, Denmark; Recruiting
Torben Harsløf, Dr, Phone: +4589497681, Email: torben.harslof@ki.au.dk
Bente L Langdahl, Dr., Ph.D., Phone: +4589497678, Email: bente.langdahl@as.aaa.dk
Torben Harsløf, Dr, Principal Investigator
Additional Information

Starting date: January 2008
Ending date: January 2010
Last updated: August 11, 2008

Page last updated: February 12, 2009

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