Pharmacology of Osteoporosis and Gout (Wolff) Flashcards

1
Q

Calcitonin-salmon is similar in structure and function to human calcitonin synthesized by thyroid, but?

A

It has a longer half-life and greater potency

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2
Q

Calcitonin-salmon inhibits the activity of?

A

Osteoclasts in order to decrease bone resorption

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3
Q

What is the clinical application for Calcitonin-salmon?

A

Treatment of established osteoporosis but not prevention

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4
Q

Bisphosphonates such as alendronate (and other -nate) are structural analogs of what normal constituent of bone?

A

Pyrophosphate

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5
Q

What affect do Bisphosphonates have?

A

Inhibits bone resorption

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6
Q

What is the clinical application for Bisphosphonates?

A

Drugs of first choice for postmenopausal osteoporosis, osteoporosis in men, and glucocorticoid induced osteoporosis

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7
Q

What toxicities are noted with bisphosphonates?

A

1) Esophagitis
2) Osteonecrosis of jaw
3) Atypical femur fractures

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8
Q

Which bisphosphonates is given by IV and it avoids the GI problems associated with other bisphosphonates?

A

Zoledronic acid

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9
Q

What class of drug is raloxifene?

A

Selective Estrogen Receptor Modulator (SERM)

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10
Q

Raloxifene exerts its agonist estrogen effects at?

It blocks theses effects at?

A

1) Bone

2) Breast and uterus

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11
Q

What is the clinical application of raloxifene?

A

Prevents and treat postmenopausal osteoporosis

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12
Q

Like estrogen, raloxifene increases the risk of?

A

1) Deep venous thrombosis
2) Pulmonary embolism
3) Stroke

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13
Q

What is a truncated version of endogenous 1-84

PTH made by recombinant DNA technology that retains activity of full length PTH?

A

teriparatide (PTH 1-34)

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14
Q

What is the clinical application of teriparatide?

A

Treat all forms of osteoporosis

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15
Q

Teriparatide is the only drug for osteoporosis that has what effect?

A

Increases bone formation

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16
Q

When teriparatide is given as a daily pulsed therapy, what predominates?

How is it administered?

A

1) Osteoblast responses

2) Once daily by using pre-filled injectors

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17
Q

Denosumab is a monoclonal antibody that has what MOA?

A

RANKL inhibitor

18
Q

RANKL is a receptor activator of?

A

Nuclear factor kappa-B ligand

19
Q

By binding to RANKL, denosumab decreases the formation and function of?

A

Osteoclasts

20
Q

What is the clinical application of denosumab?

A

Treatment of osteoporosis in postmenopausal women at high risk for fracture

21
Q

How is denosumab administered?

A

Injected every 6 months SubQ

22
Q

What toxicities are noted with denosumab?

A

1) Delays fracture healing
2) Increases risk of new fractures
3) Osteonecrosis of jaw

23
Q

What is a natural antagonist of RANKL?

A

Osteoprotegerin (OPG)

24
Q

What is a major risk factor for osteoporosis in men?

So what is an important part of therapy?

A

1) Hypogonadism

2) Testosterone replacement

25
Q

What are contributors of osteoporosis in men with prostate cancer?

A

Glucocorticoids and androgen-deprivation therapy

26
Q

What are the agents of choice for osteoporosis in men?

What is the alternative?

A

1) Bisphosphonates

2) Denosumab

27
Q

What is a “calcimimetic” drug that binds to the calcium sensing receptors on the PTH gland?

A

cinacalcet

28
Q

What are the clinical applications of cinacalcet?

A

1) Primary hyperparathyroidism

2) Secondary hyperparathyroidism due to CKD

29
Q

What therapy can be utilized for the initial treatment of acute gout?

A

NSAID therapy such as naproxen, indomethacin, and celecoxib

30
Q

If NSAID therapy is contraindicated then what is the next course of therapy to be considered in the treatment of acute gout?

A

Colchicine

31
Q

If colchicine is contraindicated then what is the next course of therapy to be considered in the treatment of acute gout?

A

Glucocorticoids

32
Q

Colchicine diffuses into cells to bind to?

This blocks the formation of?

A

1) Tubulin

2) Microtubules

33
Q

What is the therapy used to prevent recurrent gout that causes frequent attacks (more than twice a year)?

A

Urate-lowering therapy with allopurinol

34
Q

If allopurinol is not tolerated what should be used instead as an alternative urate-lowering therapy?

A

Febuxostat

35
Q

In patients with chronic/severe tophaceous gout, what is the last resort biological monotherapy used?

A

Pegloticase

36
Q

Allopurinol and Febuxostat are inhibitors of?

They cause what to be excreted?

A

1) Xanthine oxidase

2) Hypoxanthine and xanthine

37
Q

Pegloticase is a recombinant mammalian?

It covalently attaches to?

It converts uric acid to the far more solubule?

A

1) Uricase
2) Methoxy polyethylene glycol
3) Allantoin

38
Q

Rasburicase is a nonpegylated recombinant uricase for prevention of?

A

Acute uric acid nephropathy due to tumor lysis syndrome

39
Q

Probenecid is an organic acid that blocks?

This has what effect?

A

1) Urate reabsorption more than urate secretion

2) Increases excretion of urate

40
Q

Probenecid can be used to reduce urate levels in underexcreters with?

A

1) GFR > 60 ml/min

2) No stones