Cardiology Biochem Flashcards

1
Q

Function of apoAI

A

Activates LCAT; structural HDL component

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2
Q

Function of apoB48

A

Assembly/secretion of chlyomicrons from small intestine

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3
Q

Function of apoB100

A

VLDL assembly/secretion (liver)

VLDL, IDL, LDL structural protein

LDL receptor ligand for extrahepatic cells

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4
Q

Function of apoCII

A

Cofactor activator of LPL

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5
Q

Function of apoE

A

VLDL and chlyomicron remnant uptake by the liver

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6
Q

Function of apo (a)

A

Unknown; linked by disulfide bond to apoB100

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7
Q

Cause of familial hyperchylomicronemia (type I)

A

LDP or apo-CII deficiency

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8
Q

Lipoprotein fractions seen in familial hyperchylomicronemia (type I)

A

Increased chylomicrons

Increased TGs

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9
Q

Cause of familial hypercholesterolemia (type IIa)

A

Defect in LDL receptor

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10
Q

Lipoprotein fractions seen in familial hypercholesterolemia (type IIa)

A

Increased LDL

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11
Q

Cause of familial mixed hyperlipidemia (type IIb)

A

Defect in internalization of LDL receptor

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12
Q

Lipoprotein fractions seen in familial mixed hyperlipidemia (type IIb)

A

Increased LDL, VLDL, and TGs

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13
Q

Cause of familial dysbetalipoproteinemia (type III)

A

Defect in apo-E

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14
Q

Lipoprotein fractions seen in familial dysbetalipoproteinemia (type III)

A
Increased IDL (beta VLDL)
Increased chlyomicron remnants
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15
Q

Cause of familial hypertriglyceridemia (type IV)

A

Multiple factors

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16
Q

Lipoprotein fractions seen in familial hypertriglyceridemia (type IV)

A

Increased VLDL and TG

17
Q

Cause of familial mixed hypertriglyceridemia (type V)

A

LPL deficiency plus increased VLDL production

18
Q

Lipoprotein fractions seen in familial mixed hypertriglyceridemia (type V)

A

Increased VLDL, chlyomicrons, and TGs