lipid lowering drugs Flashcards

1
Q

Lipid lowering drugs

A
  • HMG-CoA inhibitor - STATINS
  • PCSK9 inhibitor - EVOLOCUMAB, ALIROCUMAB
  • fibrates - GEMFIBROZIL, FENOFIBRATE
  • OMACOR
  • bile acid binding resins - CHOLESTYRAMINE
  • inhibitors of intestinal sterol absorption - EZETIMIBE
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2
Q

MOA of statins

A
  • inhibit HMG-CoA reductase (inhibit rate limiting step in cholesterol synthesis)
  • upregulate LDL receptors on cell surface due to cholesterol depletion -> receptors bind and internalize circulation LDLs
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3
Q

statins PK

A

oral, taken in evening (endogenous cholesterol synthesis rates higher as less food eaten)

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4
Q

is statins contraindicated in pregnancy?

A

yes, cholesterol is important for fetal development

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5
Q

statins adverse effects

A
  • rhabdomyolysis (tea coloured urine)
  • liver impairment
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6
Q

MOA PCSK9 inhibitor

A
  • inhibit to PCSK9, prevents PCSK9 from binding to LDL receptors and endocytosis -> increase LDL receptors on cell surface to internalize circulation LDL
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7
Q

PCSK9 inhibitor mode of administration and Thalf

A
  • IV
  • 10-20 days (very long)
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8
Q

indications for PCSK9 inhibitor

A
  • high LDL-C in familial hypercholestrolaemias if intolerant to statins
  • together with statin in additional LDL lowering
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9
Q

Fibrates MOA

A
  • interact with PPAR
    -alpha to increase activity of lipoprotein lipase (breaks down VLDL) -> VLDL levels decrease, HDL levels rise
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10
Q

PCSK9 inhibitor adverse effects

A
  • hypersensitivity in some patients
  • inflammatory reaction at site of injection
  • nasopharyngitis
  • sinusitis
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11
Q

Fibrates clinical indications

A
  • hypertriglyceridemias with VLDL elevation, especialy for dysbetalipoproteinemia
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12
Q

Fibrates adverse effects

A
  • nausea
  • skin rashes
  • GALL STONES
  • MYOSITIS
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13
Q

Omacor MOA

A
  • reduce triglyceride (TG) production and increase TG clearance
  • inhibit diglyceride acyltransferase (responsible for TG synthesis)
  • increase free fatty acid breakdown by beta oxidation
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14
Q

omacor PK

A
  • oral, taken with food
  • metabolized by liver
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15
Q

omacor clinical indications

A
  • Type IV
  • Type IIb along with statins
  • NOT FOR Type I
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16
Q

omacor adverse effects

A
  • contraindicated for ppl allergic to fish
  • GI
  • may increase LDL-C in some patients (counterproductive)
  • reduce production of TXA2, can increase bleeding time
17
Q

cholestyramine MOA

A
  • binds to bile acids & bile salts -> lower bile acid concentration -> hepatocytes increases conversion of cholesterol to bile acids -> increase uptake of LDL in hepatocyte
18
Q

cholestyramine clinical indications

A
  • hypercholesterolemia (IIa)
  • hyperlipidemia (IIb) -> combine with niacin
19
Q

cholestyramine dosage form

A
  • oral
20
Q

cholestyramine adverse effects

A
  • GI (nausea, constipation, flatulence)
  • impaired absorption of vitamins K, A, D, E
21
Q

Ezetimibe MOA

A
  • inhibit NPC1L1 at small intestine to reduce cholesterol absorption

**useful even in NO cholesterol diet -> body produces and excretes cholesterol into intestinal tract on its own as well

22
Q

Ezetimibe clinical indications

A
  • reduce LDL (more effective when combined with simvastatin -> vytorin)
23
Q

Ezetimibe adverse effects

A
  • diarrhoea, flatulence
  • rhabdomyolysis
  • reversible hepatotoxicity