Metabolic Bone Disease Flashcards

1
Q

What does PTH do to calcium and phosphate

A

always increases serum calcium

PTH:

Kidneys: phos. wasting
Bone: increases phos. release
Serum: deceases phosphate

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2
Q

What does Vitamin D do to calcium and phosphate?

A

always increases serum calcium and phosphate through mineralization, GUT and Kidneys

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3
Q

PTH mechanism of action

A

Binds to osteoblasts–> Osteoblasts bind to RANK on osteoclasts —> calcium release

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4
Q

what are effected in ext. bone diseases?

A

serum calcium usually affected

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5
Q

Primary HPTIism labs?

A

high calcium, high PTH, high/normal Alk phos (marker of bone turnover)

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6
Q

primary HPTism presentation?

A

kidney stones, gi issues, bone turn over, psychiaytric

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7
Q

Osteitis Fibrosa Cystica is cause by what?

A

Hyperparathyroidism

  • the bone is resorbed causing cystic bone lesion “Brown Tumor”
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8
Q

2nd hyperparathyroidism causes?

A

chronically high phosphate and/or low calcium

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9
Q

2nd HTPism lab findings?

A

low/normal calcium

very high PTH- trying to elevate calcium

Very high ALK phos- bone turn over

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10
Q

2nd HPTism presentation

A

serum calcium WILL NOT be elevated

high bone turnover rate

OFC and brown tunmor

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11
Q

Renal Osteodystrophy is seen with what?

A

chronic kidney disease , causes secondary hyperparathyroidism

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12
Q

High Turn over RO etiology?

A

Kidney failure

decreases kidney phosphate excretion–>
leads to increased serum phosphate—>

1) Phosphate binds to serum Calcium —> decreased calcium
2) Phosphate inhibits hydroxylation of D3–> calcium, goes down

BOTTOM LINE:
Decreased Calcium and Phosphate= 2nd HPTism

Deceased Vit D3 –> Osteomalacia

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13
Q

Late Renal Osteodystrophy shows what?

A

Will produce soft tissue calcification AND osteosclerosis

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14
Q

What is tertiary hyperparathyroidism

A

desensitization of pth receptors

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15
Q

How does low turn over renal OD work?

A

Aluminum is deposited in bone mineralization site —> impaired osteoclasts and blasts

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16
Q

treatment for low turn over RO?

A

Po4 binding agents, alum. chelators, vit d replacement

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17
Q

Hypothyroidism labs?

A

low calcium and high po4?

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18
Q

What is Albright Hereditary OD?

A

hypothyroidism…end organ resistance to PTH

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19
Q

Physical exam of Hypocalcemia?

A

Troussea’s Sign– hand spasm

Chvostek Sign– eye twitching

20
Q

Osteomalacia/ and Rickets pathogenesis

A

Defective mineralization of normal osteoid

  • bones are soft
  • Low serum calcium

CA X Po4 > 30—-> poor mineralization

21
Q

causes of rickets

A

vitamin d deficiency

malnutrition

renal failure

lack of sun

22
Q

Hereditary Vit D. Dependent Rickets Type 1

A

defect in hydroxylase enzyme

23
Q

Hereditary Vit D. Dependent Rickets Type 2?

A

Defect in intracellular receptor

24
Q

hypophasphatemic rickets?

A

kidneys cannot reabsord phosphate

25
Q

hypophosphatasia?

A

dont have enough alk phos.

26
Q

rickets presentation?

A

bone pain, limp (bow legs), rosary

27
Q

what is the ratio of osteoid to osteomalacia?

A

osteoid that doesn’t become mineralized with hydroxyapetite

28
Q

Describe the clinical presentation of osteomalacia?

A

bone pain, local tenderness, fractures

29
Q

What are pseudofractures associated with?

A

osteomalacia

consists of osteomalacic bone

30
Q

what is hall mark of intrinsic bone diseases?

A

do not present with serum calcium abnormalities

31
Q

What is osteoporosis?

A

normal calcium and bone
- NOT ENOUGH BONE

-Labs: Normal calcium and phosphate

32
Q

What is the osteoporosis level?

A
  1. 5 standard deviation below normal level

2. 5 t-score on a text scale

33
Q

What is osteoporosis?

A

normal calcium and bone
- NOT ENOUGH BONE

-Labs: Normal calcium and phosphate

34
Q

Clinical presentation of post-menopausal osteoporosis?

A

distal radius and vertebral fractures

high turn over!!

35
Q

What type of bone is affected in PM OP?

A

trabecular bone

36
Q

presentation of AR-OR?

A

proximal femur fractures and vertebral fractures

low turn over!!

37
Q

Etiology of AR-OP?

A

uncoupling of osteoblasts and osteoclasts

with equal trabecular and cortical involvement

38
Q

Causes of secondary osteoporosis?

A

hyperthyroidism

-steroid-induced (inhibits osteoblast precursor)

39
Q

Causes of secondary osteoporosis?

A
  • hyperthyroidism
  • steroid-induced (inhibits osteoblast precursor)
  • malignancies
40
Q

What is Osteogenesis imperfecta?

A

Disorder of bone formation

type 1 collagen defect —> multiple fractures

41
Q

Associated findings of OI?

A

Blue sclera, hearing loss, tooth abnormalitis

42
Q

Causes of osteopetrosis?

A

Resorption disorder–> osteoclast failure

Adult form- dominant
kids- recessive

43
Q

Osteoporisis buzzword?

A

erlenmeyer flask

44
Q

Cause of Pagets?

A

Disorder of bone remodeling – > high bone turnover from increased osteoclast function

45
Q

Paget clinical?

A

high output HF, bone pain, arthritis