Osteoporosis
Conditions
Interventions
None listed
Sponsors
Erasmus MC, Universitair Medisch Centrum Rotterdam
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Postmenopausal women with a vertebral fracture and postmenopausal women without a vertebral fracture with high bone mineral density (T-score >-1 S.D.)
Exclusion criteria
Exclusion criteria: Medication influencing osteoclast function and formation (Bisphosphonates, Hormone Replacement Therapy, Strontium Ranelate, Teriparatide, Raloxifen)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Osteoclast formation will be studied by staining them with a Tartrate Resistant Acid Phosphatase staining. Bone resorption will be studied using a pit-assay to determine the surface and the number of resorption pits. | — |
Secondary
| Measure | Time frame |
|---|---|
| To study the expression of genetic markers of bone resorption and fractures, osteoclast will be seeded for RNA isolation. Furthermore, since osteoclast are derived from the hematopoietic line like lymfocytes, the PBMCs will be used to study the influence of lymfocytes and factors derived from lymfocytes on osteoclasts. Furhtermore blood will be collected as well to study biochemic and serum markers to be able to relate them to osteoporosis or other pathology. | — |
Countries
Netherlands
Outcome results
None listed