AM L4 Risk Flashcards

1
Q

How do population studies help us see genetic link?

A

If a population have a greater risk look at the particular genes in the populaiton

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2
Q

3 proposed genetic targes

A

Toll receptors
Inflammatory mediators
Homocysteine

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3
Q

How many genes are thought to influence predisposition to ATS?

A

400

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4
Q

2 reasons genetic studies are difficult for ATS?

A

heterogeneity of the population

complexity of a polygenic multifactorial disease

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5
Q

Non-modifiable risk factors (12)

A
MI
Stroke
Total chol
HDL
Total triglycerides
BMI
Systolic BP
Homocysteine levels
T2DM
Fibrinogen
C-reactive component
Gender
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6
Q

What is a polymorphism?

A

a common genetic variation, affecting at least 1% of the population - results in different phenotypes

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7
Q

2 examples of different phenotypes

A

Blood groups

Major histocompatibility complex

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8
Q

Population studies show results if (3)

  • we must consider all these options
A

True increase in susceptibility
Allele closely linked to real allele of pathogenesis
Coincidental

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9
Q

Population migration, where in the world has high risk and where low of CAD?

A

Japan has low risk compared to USA
BUT
Japanese-american = other americans

so is this genetic or environmental?

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10
Q

2 Monogenetic disorders that revolutionised understanding?

A

Tangiers disease

Familial hypercholesterolemia

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11
Q

Tangiers disease is a genetic disorder of….

A

cholesterol transport

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12
Q

Which gene is mutated in Tangiers?

on which chromosome?

A

ABCA1 gene mutation in chromosome 9q31

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13
Q

Tangiers disease results in mutant ………. and therefore reduced….

A

mutant ACBA1 transporter = reduced ability to transport chol out of cells. Cholesterol accumulates in the cell

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14
Q

Chol combines with …. to form HDL

A

apoA1

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15
Q

Tangiers disease results in reduced circulating

A

HDL

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16
Q

Tangiers provided the theory that….

A

low HDL increases CVD

17
Q

HDL can pick up more lipids from ……… & ….. and take them …..

A

VLDL and LDL

back to the liver

18
Q

What happens to ApoA1 lipoprotein in Tangiers?

A

it is cleared from the plasma

19
Q

Conditions associated with Tangiers

A

Thrombocytopenia
corneal opacity
orange tonsils (build-up of cholesterol droplets)
premature MI

20
Q

Familial Hypercholesterolemia is a loss of function of ….. receptor

A

LDL receptor (absent or deficient)

21
Q

Familial Hypercholesterolemia results in decreased…..

A

LDL uptake by the liver

22
Q

How does Familial Hypercholesterolemia clinically manifest?

A

elevated plasma LDL

23
Q

What happens to the cholesterol in Familial Hypercholesterolemia?

A

deposited in tissues, forms nodules.

24
Q

What are nodules of cholesterol called?

A

Xanthoma

25
Q

Where do chole nodules appear in Familial Hypercholesterolemia? (2)

A

Skin and tendons

26
Q

If someone is homozygous for Familial Hypercholesterolemia what happens?

A

death from CHD in childhood

27
Q

What is the only treatment for Familial Hypercholesterolemia?

A

Liver transpolant

28
Q

What happens to people who are heterozygous for Familial Hypercholesterolemia?

A

Milder more variable course of disease

29
Q

What proportion of people are heterozygous for Familial Hypercholesterolemia

A

1 in 500