Abstract |
ED-71 is a new vitamin D receptor ligand, bearing a hydroxypropoxy substituent at the 2β-position of 1α, 25 ( OH) (2)D(3). In ovariectomized rats, ED-71 increased vertebral bone mass and bone strength by inhibiting bone resorption and maintaining bone formation. In randomized, placebo-controlled, double-blinded clinical trial for osteoporotic subjects, ED-71 increased lumber vertebral and hip bone mineral density independently vitamin D status. Furthermore, ED-71 may have a better osteoprotective effect than alfacalcidol and suggest that ED-71 may serve as a new generation of active vitamin D with anti-fracture efficacy in osteiporotic subjects.
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Authors | Itsuro Endo, Toshio Matsumoto |
Journal | Clinical calcium
(Clin Calcium)
Vol. 21
Issue 1
Pg. 53-8
(Jan 2011)
ISSN: 0917-5857 [Print] Japan |
PMID | 21187594
(Publication Type: Journal Article, Review)
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Chemical References |
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Topics |
- Animals
- Bone Density
(drug effects)
- Bone Resorption
(drug therapy)
- Dose-Response Relationship, Drug
- Female
- Fractures, Bone
(etiology, prevention & control)
- Humans
- Lumbar Vertebrae
(metabolism)
- Osteogenesis
(drug effects)
- Osteoporosis
(complications, drug therapy, metabolism)
- Randomized Controlled Trials as Topic
- Rats
- Stimulation, Chemical
- Vitamin D
(administration & dosage, analogs & derivatives, pharmacology)
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