B6.052 Prework 6: Osteoporosis Pharmacology Flashcards

1
Q

prevention and treatment of postmenopausal osteoporosis

A

appropriate calcium and vit D intake (esp prior to achieving PBM)
exercise
pharm agents

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2
Q

pharm agents for osteoporosis

A

bisphosphonates
denosumab
teriparatide
raloxifene

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3
Q

effectiveness of Ca and vit d in treating osteoporosis

A

beneficial effect on bone density in postmenopausal women and older men
benefit on reduction of fracture rates is variable

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4
Q

vit D and Ca guidelines

A

vit D supplements: 1000 IU/d
Ca diet + supplements: 1000 mg
for adults over 65

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5
Q

types of bisphosphonates

A

alendronate- weekly
risedronate- weekly, monthly
ibandronate- monthly, IV every 3 months
zolendronic acid- IV annually

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6
Q

mechanism of bisphosphonates

A

direct inhibition of bone resorption

  • concentrate at sites of active remodeling, remains in matrix until the bone is remodeled
  • released in acid environment of the resorption lacunae and induces apoptosis in osteoclasts
  • inhibits cholesterol biosynthetic pathway which contributes to anti-resorptive activty
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7
Q

adverse reactions with bisphosphonates

A

hypocalcemia
osteonecrosis of the jaw
atypical femur fractures
gastric symptoms

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8
Q

mechanism of denosumab

A

fully human monoclonal Ab to RANKL

binds/inhibits ability of RANKL to mature osteoclasts from osteoclast precursors (similar to OPG)

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9
Q

use of denosumab

A

twice yearly sc injection
if stopped, bone lost rapidly if another agent is not used
has applications in cancer treatment

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10
Q

adverse effects of denosumab

A
osteonecrosis of the jaw
atypical femur fractures
hypocalcemia
skin infection (usually cellulitis of the lower extremity)
derm reactions
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11
Q

raloxifene drug class

A

SERM

selective estrogen receptor modulator

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12
Q

how do SERMs work?

A

not “pure” agonists of estrogen receptor, have different effects in different tissues
-produce different structural changes in receptor upon binding, alters the co-factors with which ER interacts

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13
Q

mechanism of raloxifene

A

partially replaces missing estrogen post-menopause w respect to bone remodeling
less effect than seen with estrogens

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14
Q

effectiveness of raloxifene

A

reduces occurrence of vertebral fracture by 30-50%

no data for reduced risk of nonvertebral fractures over 8 years of observation

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15
Q

side effects of raloxifene

A

NO effect on heart disease, NOT associated with increased risk of uterine cancer/ benign uterine disease
65% reduction in invasive breast cancer (mainly decreased ER-positive)

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16
Q

effects of calcitonin

A
bone:
-stimulates osteoblasts
-inhibits osteoclasts
kidney:
-transient increase in Ca secretion
17
Q

what is teriparatide

A

recombinant human PTH

amino acids 1-34 of the 84 AA endogenous PTH

18
Q

mechanism of teriparatide

A

first approved anabolic agent
stimulates osteoblastic bone formation
with short duration of action, most likely activates osteoblasts without activating osteoclasts

19
Q

effectiveness of teriparatide

A

increases predominantly trabecular bone at lumbar spine and femoral neck (less significant at cortical sites)

20
Q

administration of teriparatide

A

administered once daily by subq injection in thigh or abdominal wall
use for 2 years in men and post menopausal women with osteoporosis
-followed w anti-resorptive agent to maintain BMD gain
-no fracture reduction benefit from second course of teriparatide

21
Q

calcitonin administration

A

injection or nasal spray

22
Q

what is calcitonin

A

32 ss peptide with sequence of calcitonin from salmon, 30x potency of human calcitonin

23
Q

effectiveness of calcitonin

A

effects assessed by high res MRI
benefit in maintaining trabecular microarchitecture at multiple skeletal sites
reduced incidence of vertebral compression fractures by about 40% in osteoporotic women

24
Q

on graph, drugs from best to worst

A
teriparatide
PTH + estradiol
alendronate
estradiol
raloxifene
calcitonin