bone mineralization, viability Flashcards
amount of Ca released from bone daily?
400mg
percent body calcium in bones?
99%
primary regulators of Ca?
PTH, Vit. D
daily Ca dietary requirement?
children 600mg
adults 1300mg
percent body phosphate in bone?
85%
synthetic form of PTH?
Teriparatide
produces OPPOSITE effect of PTH?
Calcitonin
age range of peak bone mass?
16-25 years old
rate of bone loss after peak?
0.3-0.5% per year (2-3% menopausal), affects trabecular > cortical
most common cause of hyperCa?
malignancy
rickets/ osteomalacia
failure of mineralization
most common form of rickets?
familial hypophosphatemic rickets (vitamin D resistance)
osteoporosis WHO definition?
L2-L4 density 2.5 stdev less
mean density 1.0-2.5 stdev less
brown tumors in bone?
hypercalcemia
hypercalcemia histologic changes?
osteoblasts/clasts active on both sides of trabeculae (Paget’s)
ortho tx of hypercalcemia?
mobilization, bisphosphonates, vit. D (5000 IU daily)
rickets
failure of mineralization
rickets signs
rachitic rosary
codfish vertebrae
osteoporosis type of defect?
quantitative
most affected bone type of osteoporosis?
cancellous
type I osteoporosis
postmenopausal
type II osteoporosis
age-related
osteoporosis abnormal labs
none (xrays only for bone loss >30%)
most accurate ‘special study’ for osteoporosis?
DEXA
osteoporosis tx?
Ca 1000-1500mg
vit. D 400-800IU
osteoporosis prophylaxis?
apt Ca intake, weight bearing, estrogen therapy
osteomalacia type of defect?
qualitative (defect of mineralization)
required for diagnosis of osteomalacia
transiliac biopsy (finding: widened osteoid seams)
osteomalacia tx?
‘large doses’ of vit. D
scurvy definition
vit. C deficiency (decrease in chondroitin sulfate - collagen - synthesis)
scurvy clinical features
fatigue, gum bleeding, ecchymosis, joint effusions, iron deficiency
scurvy histologic feature
calcification zone widening in physis
pathophysiology of osteogenesis imperfecta
GLYCINE SUBSTITUTION in procollagen - failure in cross-linking
effect of lead poisoning
alters chondrocyte response to PTH, TGF-beta (reduced bone density, short stature)
osteopetrosis
failure of bone resorption; osteoclasts lack normal ruffled border
malignant osteopetrosis (infantile)
‘bone within a bone’ on xray (no marrow)
Paget’s disease etiology?
virus-like inclusion bodies in osteoclasts
Paget’s disease ACTIVE phases
lytic, mixed, sclerotic
Chandler’s disease
osteonecrosis of the femoral head in adults
earliest study to yield positive results, highest specificity/sensitivity in osteonecrosis?
MRI
osteochondrosis
traction apophyses (e.g., osgood-schlatter, legg-calve-perthes)