Metabolic Bone Disease Flashcards
What is Osteoprotegerin?
It is a decoy receptor that binds to RANK-L and
prevents it from attaching to RANK; it is therefore a major endogenous inhibitor of bone remodeling
What are Fragility fractures
Bone fractures that occur with low trauma (a fall from a standing height or less)
The most common fragility fractures are ______
vertebral fractures, hip fractures and wrist fractures
Using bone densitometry criteria,
osteoporosis is diagnosed when the lowest T-score is _____ and osteopenia is diagnosed when the lowest T-score is ______, whereas BMD is normal when T-scores at all sites are ______
< -2.5,
-1.0 to -2.4,
> -1.0.
Using the FRAX tool to calculate 10 year probability of a fragility fracture, treatment is generally
recommended if the fracture risk is ______ for hip fracture or _____for a major osteoporosis fracture.
> 3%,
> 20%
calcium carbonate absorption is significantly reduced in patients who have ______
deficient gastric acid production (atrophic gastritis and proton pump inhibitors).
How is new bone formed?
Osteoblasts migrate into pits (made by osteoclasts) and secrete osteoid (bone specific collagen) which subsequently become mineralized with calcium-phosphate (hydroxyapatite) crystals to form strong new bone
_______is defined as impaired bone mineralization resulting in soft, weak bones. It is caused by any
condition that results in a low extracellular fluid calcium x phosphate product that is insufficient to mineralize
bone osteoid.
Osteomalacia
What is Paget’s disease of bone?
idiopathic condition of bone characterized by excessive and unregulated bone resorption and formation.
The _____ gene has been found in 40-80% of families with Paget’s disease
Sequestosome I/P62
The most commonly affected bones in paget’s disease are the ___
pelvis, skull, vertebrae, tibia and fibula
What are the biomarkers of osteoclastic bone resorption
Ntelopeptides, C-telopeptides, Pyridinoline crosslinks
What are the biomarkers of bone formation
alkaline phosphatase, osteocalcin
Treatment options for pagets disease include _____
oral and intravenous bisphosphonates,
calcitonin, analgesics, non-steroidal anti-inflammatory drugs, and corrective surgery for deformities.
______ is the treatment for congenital 1 alpha hydroxylase deficiency (vitamin D dependent rickets type 1), and in very high doses for congenital vitamin D receptor deficiency (vitamin D dependent rickets type 2).
Calcitriol