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| Name | Class |
|---|---|
| National Hellenic Research Foundation | OTHER |
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It is well proven that the intestinal microbe regulates bone metabolism by the absorption of calcium and other metallic trace elements. Studies also show that regulation of the intestine and its microbe can affect bone density and resistance to a variety of animal models and humans. At the same time, interest in polyphenol-intestinal microbial interactions and in particular flavonoids and catechins has increased. Indeed, it has been observed that they are transformed via the microbe into bioactive compounds, and polyphenols themselves can modify the synthesis of the intestinal microbe.
OSTEOME aspires to design and develop a novel dietary supplement for osteoporosis, activating the intestinal microbiome. At the same time companion biomarkers will be studied related to the efficacy and tolerability of the new supplement. The selection of flavonoids will take place through in vitro and in silico studies focusing on their interaction with pathways that regulate the activity of osteoclasts and osteoblasts. The efficacy and tolerability of the dietary supplement will be evaluated through a randomized clinical intervention.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Calcium and vitamin D supplement | Active Comparator | In this arm, 50 women will receive calcium and vitamin D supplement once per day. |
|
| Calcium, vitamin D and prebiotic supplement | Active Comparator | In this arm, 50 women will receive calcium, vitamin D and prebiotic supplement once per day. |
|
| Calcium, vitamin D, prebiotic and flavonoid supplement | Active Comparator | In this arm, 50 women will receive calcium, vitamin D, prebiotic and flavonoid supplement once per day. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Calcium and vitamin D supplement | Dietary Supplement | One hundred fifty postmenopausal women with osteopenia will be randomly and blindly allocated to receive in of the 3 different dietary supplements once per day. Patients of group A will receive orally 600 mg calcium and 2400 IU vitamin D3, group B will receive the same dose of calcium and vitamin D3 plus prebiotics once per day and group C will receive the same dose of calcium, vitamin D3 plus flavonoids once per day. |
| Measure | Description | Time Frame |
|---|---|---|
| Bone geometry | The primary endpoint is the within and between group change of bone geometry after 12 months of supplementation assessed by peripheral quantitative computed tomography (pQCT) of the tibia | 0 to 12 months |
| Measure | Description | Time Frame |
|---|---|---|
| Areal bone mineral density (aBMD), trabecular bone score (TBS), adverse effects (tolerability) and adherence to dietary supplement after 12 months | The secondary endpoints is the within- and between-groups differences of the areal BMD (aBMD) at the lumbar spine (LS) and the total hip (TH) using dual-energy X-ray absorptiometry (DXA) and trabecular bone score (TBS) at LS, and the between-group comparison of the adverse effects (tolerability) and adherence to dietary supplement after 12 months. |
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Inclusion Criteria:
Exclusion Criteria:
Postmenopausal women with osteopenia
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Laboratory for Research of the Musculoskeletal System | Kifissia | Athens | 14561 | Greece |
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|
| Calcium, vitamin D and prebiotic supplement | Dietary Supplement | One hundred fifty postmenopausal women with osteopenia will be randomly and blindly allocated to receive in of the 3 different dietary supplements once per day. Patients of group A will receive orally 600 mg calcium and 2400 IU vitamin D3, group B will receive the same dose of calcium and vitamin D3 plus prebiotics once per day and group C will receive the same dose of calcium, vitamin D3 and flavonoids once per day. |
|
| Calcium, vitamin D and flavonoid supplement | Dietary Supplement | One hundred fifty postmenopausal women with osteopenia will be randomly and blindly allocated to receive in of the 3 different dietary supplements once per day. Patients of group A will receive orally 600 mg calcium and 2400 IU vitamin D3, group B will receive the same dose of calcium and vitamin D3 plus prebiotics once per day and group C will receive the same dose of calcium, vitamin D3 and flavonoids once per day. |
|
| 12 months |
| Bone turnover markers, PINP and CTX | Secondary endpoint is the within- and between-group comparison change of bone turnover markers after 3, 6 and 12 months of supplementation. | 3, 6 and 12 months |
| Change of serum TNF-α, IL-1, OPG, RANKL and IGF-1 | Secondary endpoint is the within- and between-group comparison change of TNF-α, IL-1, OPG, RANKL and IGF-1 after 3, 6 and 12 months of supplementation. | 3, 6 and 12 months |
| Change of microMR1 Change of serum miRNAs | Secondary endpoint is the within- and between-group comparison change of miRNAs after 3, 6 and 12 months of supplementation. | 3, 6 and 12 months |
| Change of gut microbiota | Secondary endpoint is the within- and between-group comparison change of gut microbiota after 12 months of supplementation. | 12 months |
| ID | Term |
|---|---|
| D001851 | Bone Diseases, Metabolic |
| ID | Term |
|---|---|
| D001847 | Bone Diseases |
| D009140 | Musculoskeletal Diseases |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
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| ID | Term |
|---|---|
| D002118 | Calcium |
| D014807 | Vitamin D |
| ID | Term |
|---|---|
| D008673 | Metals, Alkaline Earth |
| D004602 | Elements |
| D007287 | Inorganic Chemicals |
| D008670 | Metals |
| D001779 | Blood Coagulation Factors |
| D001685 | Biological Factors |
| D012632 | Secosteroids |
| D013256 | Steroids |
| D000072473 | Fused-Ring Compounds |
| D011083 | Polycyclic Compounds |
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