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 contentchange 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
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