bone mineralization, viability Flashcards

0
Q

amount of Ca released from bone daily?

A

400mg

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1
Q

percent body calcium in bones?

A

99%

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2
Q

primary regulators of Ca?

A

PTH, Vit. D

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3
Q

daily Ca dietary requirement?

A

children 600mg

adults 1300mg

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4
Q

percent body phosphate in bone?

A

85%

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5
Q

synthetic form of PTH?

A

Teriparatide

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6
Q

produces OPPOSITE effect of PTH?

A

Calcitonin

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7
Q

age range of peak bone mass?

A

16-25 years old

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8
Q

rate of bone loss after peak?

A

0.3-0.5% per year (2-3% menopausal), affects trabecular > cortical

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9
Q

most common cause of hyperCa?

A

malignancy

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10
Q

rickets/ osteomalacia

A

failure of mineralization

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11
Q

most common form of rickets?

A

familial hypophosphatemic rickets (vitamin D resistance)

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12
Q

osteoporosis WHO definition?

A

L2-L4 density 2.5 stdev less

mean density 1.0-2.5 stdev less

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13
Q

brown tumors in bone?

A

hypercalcemia

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14
Q

hypercalcemia histologic changes?

A

osteoblasts/clasts active on both sides of trabeculae (Paget’s)

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15
Q

ortho tx of hypercalcemia?

A

mobilization, bisphosphonates, vit. D (5000 IU daily)

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16
Q

rickets

A

failure of mineralization

17
Q

rickets signs

A

rachitic rosary

codfish vertebrae

18
Q

osteoporosis type of defect?

A

quantitative

19
Q

most affected bone type of osteoporosis?

A

cancellous

20
Q

type I osteoporosis

A

postmenopausal

21
Q

type II osteoporosis

A

age-related

22
Q

osteoporosis abnormal labs

A

none (xrays only for bone loss >30%)

23
Q

most accurate ‘special study’ for osteoporosis?

A

DEXA

24
Q

osteoporosis tx?

A

Ca 1000-1500mg

vit. D 400-800IU

25
Q

osteoporosis prophylaxis?

A

apt Ca intake, weight bearing, estrogen therapy

26
Q

osteomalacia type of defect?

A

qualitative (defect of mineralization)

27
Q

required for diagnosis of osteomalacia

A

transiliac biopsy (finding: widened osteoid seams)

28
Q

osteomalacia tx?

A

‘large doses’ of vit. D

29
Q

scurvy definition

A

vit. C deficiency (decrease in chondroitin sulfate - collagen - synthesis)

30
Q

scurvy clinical features

A

fatigue, gum bleeding, ecchymosis, joint effusions, iron deficiency

31
Q

scurvy histologic feature

A

calcification zone widening in physis

32
Q

pathophysiology of osteogenesis imperfecta

A

GLYCINE SUBSTITUTION in procollagen - failure in cross-linking

33
Q

effect of lead poisoning

A

alters chondrocyte response to PTH, TGF-beta (reduced bone density, short stature)

34
Q

osteopetrosis

A

failure of bone resorption; osteoclasts lack normal ruffled border

35
Q

malignant osteopetrosis (infantile)

A

‘bone within a bone’ on xray (no marrow)

36
Q

Paget’s disease etiology?

A

virus-like inclusion bodies in osteoclasts

37
Q

Paget’s disease ACTIVE phases

A

lytic, mixed, sclerotic

38
Q

Chandler’s disease

A

osteonecrosis of the femoral head in adults

39
Q

earliest study to yield positive results, highest specificity/sensitivity in osteonecrosis?

A

MRI

40
Q

osteochondrosis

A

traction apophyses (e.g., osgood-schlatter, legg-calve-perthes)