NCD Alz Dz- 15D Flashcards

1
Q

In Major NCD due to Alz Dz, what is unusual about diagnostic criteria?

A

-decrease in cognitive function in TWO domains (as opposed to 1 domain)

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2
Q

Risk factors for Alz Disease

A
  • age
  • family history (increases risk for 2-3 fold)
  • ApoE epsillon 4 allele
  • female sex
  • high homocysteine levels
  • less education
  • usual cardiovascular/cerebrovascular risks
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3
Q

Protective factors for Alz Disease

A
  • physical activity
  • high n-3 fatty acids
  • ApoE episilon 2 allele
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4
Q

The average time to death from diagnosis in Alz Dz

A

-10 years

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5
Q

Most common cause of death in Alz Dz

A

-aspiration pneumonia

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6
Q

Features for severe Alz Dz

A
  • Folstein < 10
  • complete care and feeding needed
  • apathy, lack of recognition, disconnection from environment
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7
Q

Differences between senile plaques and neurofibrillary tangles

A

-senile plaques are extracellular; NFTs are intracellular
-senile plaques consist of AB42; NFT’s consist of tau and ubiquitin
-

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8
Q

List the pathologic findings in Alz Dz

A
  • senile plaques
  • neurofibrillary tangles
  • early neuronal loss in hippocampus
  • cerebral amyloid angiopathy- amyloid-B arterial plaques
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9
Q

The use of biomarkers is currently recommended for the diagnosis of Alz Dz. True or False

A

FALSE

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10
Q

What are the 2 genetic types of early onset (before age 65y) Alz Dz?

A
  • early onset familial AD (eFAD): AUTOSOMAL DOM (50%)

- non-familial: SPORATIC (50%)

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11
Q

Describe the gene mutations that cause eFAD

A
  • presenilin 1 (chromosome 14)-knife
  • presenilin 2 (chromosome 1)-knife
  • Amyloid precursor protein (chromosome 21)-mellon
  • NORMAL/UNMUTATED forms of these genes are responsible for creating the soluble/functional amyloid AB-40 protein
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12
Q

In eFAD, the genes produce products that results in production of:

A
  • Amyloid AB-42 insoluble protein that kills cells leading to formation of senile plaques
  • AB-42 causes extra influx of Ca++
  • therefore when cells are killed the plaques that remain contain AB-42, glial cells, abnormal neuronal axons
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13
Q

Describe the genetics that assigns RISK of developing Alz Dz

A
  • Alleles of Apoprotein E (Apo E)
  • ApoE2-is protective (2 t’s protective)
  • ApoE3-is neutral
  • ApoE4-increases risk (4 increases risk FOUR Alz Dz)
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14
Q

What do Apolipoproteins (Apo proteins) do?

A

-remove excess cholesterol and Amyloid-Beta from the brain

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15
Q

Describe the genetics of ApoE4

A
  • 25% of population has at least 1 E4 allele present
  • E4 allele is present in ~60% of pts with Alz Dz
  • increases risk of Alz Dz by 2.5 times compared to general population
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16
Q

Name the categories of cognitive enhancers used in the management of Alz Dz

A
  • cholinesterase inhibitors
  • NMDA-antagonists
  • Ketone diet
17
Q

Four rules of thumb for prescribing cholinesterase inhibitors

A
  • start treatment early
  • continue treatment long term
  • switch meds in class if med becomes ineffective or develops side effects
  • prescribe with memantine
18
Q

Name the cholinesterase inhibitors FDA approved for management of Alz Dz

A
  • Donepezil
  • Galantamine
  • Rivastigmine
  • all approved for the treatment of mild-moderate Alz Dz
19
Q

Which of the cholinesterase inhibitors is approved for the management of severe Alz Disease

A

-Donepezil, Rivastigmine

20
Q

Which of the cholinesterase inhibitors is also approved for management of NCD due to Parkinson’s Dz

A

-Rivastigmine

21
Q

Which of the cholinesterase inhibitors IS NOT hepatically metabolized

A

-RIVASTIGMINE

22
Q

Hepatically metabolized cholinesterase inhibitors are metabolized by CYP450

A

-2D6, 3A4

23
Q

Which of the cholinesterase inhibitors should be avoided in severe renal and hepatic disease and or require dose adjustments

A

-GALANTAMINE

24
Q

What is memantine?

A
  • NMDA antagonist

- treatment of moderate to severe Alz Dz

25
Q

What is Caprylidene?

A
  • FDA approved
  • nutritional management of Alz Dz
  • increases ketones in brain as alternative source of energy for neurons
  • no drug-drug interactions