Calcium and phosphate regulation Flashcards
Paget’s disease
accelerated, localised and disorganised remodelling of bone
Paget’s disease pathophysiology
excessive resorption followed by compensatory increase in bone formation, which is woven bone (structurally disorganised and mechanically weaker) - leads to bone frailty, hypertrophy and deformity
Paget’s disease aetiology
usually FHx, and evidence of viral origin, although most patients are asymptomatic
Paget’s disease biochemical features
xs numbers of abnormal and large osteoclasts; normal calcium but plasma alkaline phosphatase (bone and liver isotopes also exist)
Paget’s disease clinical features
most commonly affects skull, T/L spine, pelvis, femur and tibia
Arthritis
Fractures
Pain
Deformity
Increased vascularity
Deafness (cochlear involvement)
Paget’s disease radiological features
lytic lesions on plain XRs, with thickened, enlarged and deformed bones in later stages
Paget’s disease treatment
bisphosphonates to reduce bone pain and disease activity
Osteoporosis
loss of bony trabeculae causing reduced bone mass and weaker bones that are predisposed to fracture after minimal trauma
Osteoporosis diagnosis
bone mineral density >2.5sd below average (T score
Osteoporosis risk factors
Postmenopausal oestrogen deficiency: oestrogen deficiency leads to loss of bone matrix and increased risk of fracture
Iatrogenic: heparin / glucocorticoid use
Endocrine: Cushing’s, hyperthyroidism, primary hyperparathyroidism
Hypogonadism
Age: leads to deficiency in bone homeostasis e.g. Osteoblast senescence