cholesterol Flashcards

1
Q

cholesterol ester and Tg make up what part of apolipoproteins

A

nonpolar core

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2
Q

phospholipid and free cholesterol make up what part of apolipoproteins

A

polar surface coat

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3
Q

between VLDL and chylomicrons, which is atherogenic

A

VLDL is somewhat atherogenic while chylomicrons are NOT

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4
Q

name 2 atherogenic lipoproteins? which one is the main one?

A
  • IDL
  • LDL– main one
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5
Q

what regulates hepatic cholesterol synthesis

A

HMG-CoA reductase

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6
Q

autosomal dominant condition where there is deficient or defective hepatic LDL receptors causing elevated total & LDL from birth

A

familial hypercholesterolemia (FH)

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7
Q

which familial lipid d/o do you see tendon xanthoma, xanthelasmas, arcus corneus

A

FH (familial hypercholesterolemia)

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8
Q

which familial d/o do you see cardiac events in the 3-4th decade of life in heterozygous

A

familial hypercholesterolemia

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9
Q

varying LDL and VLDL in families w/ high apo B-100 levels

A

familial combined hyperlipidemia

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10
Q

why is familal combined hyperlipidemia hard to diagnose

A

because 1/3 hs increased LDL, 1/3 has increased TG and 1/3 has both

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11
Q

why does familial combined hyperlipidemia have increased atherogenicity (3)

A

small & dense LDL (can get through vessels and can block path)
cholesterol enriched VLDL
low less anti-inflammatory HDL

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12
Q

arcus corneus common and lipid abnormalities AFTER ADOLESCENCE

A

familal combined hyperlipidemia

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13
Q

which familial d/o is commonly associated with HTN, T2DM, obesity?

A

familial combined hyperlipidemia

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14
Q

hypothyroidism, obstructive liveer dz and diuretic use are 3 unique causes of what secondary lipid d/o?

A

secondary hypercholesterolemia

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15
Q

alcohol, estrogen, beta blockers & diuretics are 4 unique causes of what secondary lipid d/o?

A

secondary hypertriglyceridemia

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16
Q

beta blockers, progestin, anabolic steroid use are 3 unique causes of what secondary lipid d/o?

A

secondary hypoalphalipoproteinemia

17
Q

TG >500-1000; usually acquired but can be genetic

A

chylomicronemia syndrome

18
Q

main risk of chylomicronemia syndrome? why?

A

pancreatitis d/t hyperviscosity

19
Q

fatigue, impaired cognition and memory, paresthesias, hepatosplenomegaly are sx of what lipid d/o?

A

chylomicronemia syndrome

20
Q

finding eruptive xanthomata, lipemia retinalis on PE is associated with which lipid d/o?

A

chylomicronemia syndrome

21
Q

you do a NON-fasting lipid panel and TG comes back over 400, what do you do?

A

repeat as fasting

22
Q

4 dietary recommendations to reduce LDL

A
  1. reduce cholesterol to < 200mg/day
  2. reduce SFA and TFA to < 5-6% calories
  3. add psyllium/soluble fiber
  4. add plant stanol/sterol margarines
23
Q

first line action to reduce TG

A

achieve healthy weight to reduce insulin resistance

24
Q

2 things that inhibits LPL

A
  • alcohol (acutely)
  • simple carbs & sweets (also increases VLDL production)
25
Q

effect of omega-3 PUFAs (DHA, EPA) on lipids

A

less TG synthesis

26
Q

what is normal LDL in gen pop vs high risk/ASCVD

A
  • LDL < 130 general population
  • goal often < 70 for those with ASCVD or high risk
27
Q

what is normal HDL for men vs women

A
  • HDL >40 for men
  • > 50 for women
28
Q

what is normal TG goal?

A

TGs < 150