Aani CP: Lipoprotein Metabolism Flashcards

1
Q

Which protein is used to transport Cholesterol across the intestinal brush border into blood?

A

NPC 1L1

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2
Q

Which proteins bring Cholesterol back into intestine from blood?

A

ABC G5 and ABC G8

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3
Q

How to reduce LDL cholesterol?

A

Statins

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4
Q

Which lipoproteins are good: HDL or LDL?

A

HDL

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5
Q

What are the 4 categories of dyslipidaemia?

A

Primary Hypercholestremia
Primary Hypertriglyceridemia
Mixed Hyperlipidaemia
Hypolipidaemia

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6
Q

What are the 3 conditions in Primary Hypertriglyeridemia

A

Familial 1
Familial 4
Familial 5

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7
Q

What is deficient in Familial 1 Hypertriglyceridemia?

A

ApoC or lipoprotien lipase

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8
Q

What is wrong in Familial 4 Hypertriglyeridemia?

A

High triglycerides

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9
Q

What is deficient in Familial Hypertriglyceridemia 5?

A

ApoA 5

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10
Q

PCSK9 is seen in which lipid metabolism disorder?

A

Familial Hypercholesterolaemia (autosomal dominant type)

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11
Q

Dominant Homozygous Familial Hyeprcholesteroleamia is caused by which mutations?

A

PCSK9, ApoB, LDL R mutation

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12
Q

Heterozygous Familial Hypercholesterolaemia is caused by which mutations?

A

LDLRAP1

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13
Q

What features do you get in heterozygous Familial Hypercholesterolaemia ?

A

Tendon Xanthoma, Xanthelasma, Corneal Arcus

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14
Q

Which lipoprotein disorder gives you eruptive xanthoma papules?

A

Familial Hypertriglyceridemia Type 1

and Familial Dys-beta-lipoproteinaemia

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15
Q

What is the mutation in Hyper alpha lipoprotein?

A

CEPT

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16
Q

What is the mutation(s) you get in Phytosterolaemia?

A

ABC G5 and G8

17
Q

What are the causes of Mixed Hyperlipidaemia?

A
  • Familial Hepatic lipase deficiency
  • Familial combined Hyperlipidaemia
  • Familial dys-Beta-lipoprotinaemia
18
Q

Which type of fatty acids are good?

19
Q

Which type of fatty acids are bad?

20
Q

Which chylomicron protein increases risk of Alzheimer’s?

A

ApoE E4 (watch Alzheimer shows on E4)

21
Q

What symptoms do you get in ApoE E2 Type 3 deficiency? (Familial dys-beta- lipoproteinaemia?

A

Yellow palmar crease and fatty liver and eruptive xanthoma on skin

22
Q

What is the mutation in Tangier Disease?

A

ABC A1 - HDL deficiency

23
Q

What is the mutation in Hypo-beta-lipoproteinaemia?

A

Truncated apoB protein

24
Q

Which lipoprotein can be high in untreated diabetes?

25
Familial combined hyperlipidaemia is thought to involve an increase in synthesis of which apolipoprotein?
Apo B 100
26
The most common cause in the Western world for secondary hyperlipidaemia?
Diabetes Mellitus
27
There is high-density lipoprotein (HDL) deficiency as a result of ABC AI mutations?
Tangier Disease
28
This inborn error of metabolism is tested for universally, across the United Kingdom a few days after birth?
MCADD (medium chain co-A dehydrogenase deficiency)
29
A form of inherited disease that causes high levels of VLDL and chylomicrons in the plasma. It is sometimes due to apoA V deficiency?
Familial Hypertriglyceridaemia V
30
Cause hydrolysis of chylomicron remnants and release glycerol and fatty acids into the cell, which may be used for energy or stored for later use
Lisosomes
31
Activate lipoprotein lipase via apolipoprotein C-II
Chylomicrons
32
Particles formed when triacylglycerol and cholesterol are assembled with apolipoprotein B-100?
VLDL
33
Encoded by the APOC2 gene?
Apo C II
34
What does PCSK9 do?
Binds to LDLR and promotes its degradation (therefore increases LDL)
35
Novel form of LDL therapy?
Anti-PCSK9 MAb