Unit 05: Hyperlipidemia Flashcards

1
Q

what is hyperlipidemia

A

increased amount of lipids and/or lipoproteins in the blood- risk factor for cardiovascular diseaselike atherosclerosis

*most deaths in westernized world are related to atherosclerosis which si due to cholesterol and/or lipid plaques that form in arterial blood

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2
Q

What increased plasma lipoproteins are associated with atherosclerosis

A

low density lipoprotein (LDL), intermediate density lipoprotein (IDL), and very low density lipoprotein (VLDL), as well as decreased high density lipoprotein (HDL) levels.

* a decrease in plasma LDL is associated with a decrease in atherosclerosis

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3
Q

what condiitons result from atherosclerosis

A

Coronary artery disease, stroke and peripheral artery disease are sequelae (pathological condition resulting from disease, injury or trauma) to atherosclerosis.

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4
Q

what is thoguht to cause development of atherosclerotic lesions

A
  • thought to originate and develop in variety of ways - including from an intimal cell mass
  • Tunica intima which is the innermost layer of an artery or vein is composed of a layer of endothelial cells (endothelium) and is supported by an internal elastic membrane
  • below that is the tuna media consisting of several alyers fo smooth muscle cells and connective tissue
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5
Q

what can occur upon smooth muscle proliferation in layers of vessels

A

can result in a cell mass

  • LDLs cross the endothelium and make their way into mass where they can accumulate
  • macrophages then enguld the LDL and become activated which prouces “foam cells” resulting in an early lesion
  • damage to endothelium ensues, platelets adhere nd growth factors stimulate further vascular smooth muscle proliferation
  • eventually results in fibrous plaque formation along with more lipid accumulation
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6
Q

what are statins

A

structural analogs to 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA)

HMG- CoA = liver enzyme that is responsibel for producing cholesterol - statins used to lower cholesterol by inhibiting HMG CoA

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7
Q

what is lovastatin and simvastatin

A

part of statin drug class

  • most effective and best tolerated therapy for hyperlipidemias
  • can be used as monotherapy due to high efficacy but also in combination with other drug classes
  • in regards to metabolism they have a high hepatic first pass effect
  • partially inhibit HMG-CoA reducing cholesterol levels but also inc LDL receptors

*result is an increase in LDL clearance and decrease ni plasma LDL

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8
Q
A
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9
Q

adverse effects of statins

A
  • increase in liver enzymes and risk of teratogenic effects (statinsa re contraindicted in pregnancy_
  • drug interactions may be possile due to altered CYP45- enzymes
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10
Q

what are VLDL secretion inhibitors?

A
  • ex: niacin
  • one of oldest drugs to treat hyperlipidemias
  • naicin or nicotinic acid acts as a vitamin (vit B3) when converted to nicotamide adenine dibulceotide (NAD)
  • unconverted niacin produces lipid lowering effects, inhibit VLDL productiona nd secretion -> thus inhibits LDL levels via effects on liver
  • also inc lipoprotein lipase activity resulting in increased clearance of VLDL
  • noted as best agent for raising HDLs
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11
Q
A
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12
Q

formulation of niacin and adverse effects

A
  • comes in rapid and slow release ablets
  • those taking it may experience cutaneous flushing and pruritus (itching), mediated by prostaglandin release
  • aspirin can be used to alleviate these symptoms
  • elevated liver enzymes might occur although not a major concern
  • GI distress and ulcers also possible
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13
Q

what are bile acid sequestrants

A

cholestryamine and colestipl (colestid)

  • large and highly positively charged resins that bidn to neg charged bile acids in GI tract lumen - prevents reuptake in jejunum and ileum

0 throughr eduction of bile acids, bile production increases in the liver from cholesterol -> inc in cholesterol turnover and overall increase in LDL uptake and clearance form the plasma

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14
Q

when are bile acid sequestrants used? how are they formulated? what are side effects?

A
  • used as second agents if statins are inffective
  • available as granule packets or tabs that can be taken orally and are insolible in water and not abs by GI tract
  • should eb taken with meals when bile secretion is at its highest
  • constipation and bloating are common adverse effects - drug interactions may also occur due to poritive charges
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15
Q

what are fibrates

A

class of amphipathic carboxylic acid sued to treat hypercolesterolemia or high colesterol

  • peroxisome proliferator- activated receptors (PPARs) are pharmacologically related to fibrates and can be seud to lower lipid levels
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16
Q

What is Gemfibrozil

A

Activator of PPAR

MOA unclear but thoguht to act as ligand for the nuclear transcription receptor PPAR-α.

The PPAR-α.gene receptor is found alrely in the liver and activation results in an increase in lipoprotein lipase levels which yields a decrease in VLDLs

Also decreases VLDL secretion in the liver and a modest dec in LDL often occurs as well

17
Q

what can happen following activation of PPARs

A

moderate increase in HDLs is possible

  • agents are considered safe and can be used in combination with lother lipid loering agents
  • should eb aovided in patietns with liver disease and their use has been shown to inc risk of cholesterol callstones
18
Q

what is Ezetimibe

A

aka zetia

  • sterol absorption inhibitor
  • inhibts interestinal absorption of phytosterols and cholesterol whcih decreases LDL levels
  • sterol absorption inhibits target or inhibt a transport protein called NPC1L1 found in the jejuna enterocytes and is used to uptake cholesterol
  • hepatic LDL receptors are also inc as is removal of LDLs from plasma
  • ezetimibe is excreted in bile following ab and met and used primarily as an adjuncy with statins - appears to be very safe
19
Q

what should exetimble not be taken with

A
  • do not take in combination with bile aid sequestrants bc they inhibit absorption of ezetimbe
20
Q

overview of drugs used in hyperlipidemias

A