Dementia Flashcards

1
Q

Define ‘dementia’

A

A syndrome that may be caused by a number of illnesses in which there is a progressive decline in multiple areas of function, including memory, reasoning, communication and ability to carry out daily activities

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2
Q

What are the non-modifiable risk factors for dementia?

A

Age, genetic predisposition, family history and Down’s syndrome

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3
Q

What are the modifiable risk factors for dementia?

A

High cholesterol, hypertension, diabetes, cognitive inactivity, head injury and depression

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4
Q

What are the main types of depression?

A

Parkinsons, vascular dementia, Alzheimers, dementia with Lewy bodies, frontal temporal dementia and mixed

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5
Q

What are the two components implicated in Alzheimer’s disease?

A

Neurofibrillary tangles (from hyperphosphorylated Tau protein) and amyloid plaques (B-amyloid peptide)

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6
Q

What are the consequences of neurofibrillary tangles?

A

These hyperphosphorylated Tau protein segments present in cell bodies and neuritis which causes synaptic loss and dystrophy which leads to significant loss of cholinergic cells

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7
Q

What is ‘early-onset’ Alzheimer’s disease?

A

When it occurs around 35 years of age

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8
Q

What genes are involved in the development of early-onset Alzheimer’s disease?

A

Amyloid precursor protein (APP) on chromosome 21, PSEN1 (chromosome 14) and PSEN2 (chromosome 1)

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9
Q

Which chromosome is APP on?

A

Chromosome 21

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10
Q

Why is there a greater risk of developing Alzheimer’s disease in those with Down Syndrome?

A

Down syndrome is a trisomy 21 condition, APP (conveys greater risk of early-onset AD) is present on chromosome 21, so there is a greater likelihood of it’s influence

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11
Q

Which chromosome is PSEN1 found on?

A

Chromosome 14

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12
Q

Which chromosome is PSEN2 found on

A

Chromosome 1

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13
Q

What is the function of PSEN1/2?

A

To cleave APP (amyloid precursor protein).

A subunit of gamma-secretase (aspartyl protease) for cleaving APP to Ab peptides

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14
Q

What type of mutation is present in APP/PSEN1/PSEN2 to give rise to early onset Alzheimers?

A

Missense mutation

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15
Q

Outline the pathogenesis of early-onset Alzheimers disease

A

Genetic mutation in APP/PSEN1/PSEN2 –> increased proteolysis of APP to Ab peptides or increased production of APP –> accumulation of A-beta peptides in interstitium –> deposition and aggregation to form plaques –> inflammatory response –> microglial activation and astryocytosis –> altered metabolism, damage, oxidative stress and altered kinase/phosphatase activity –> hyperphosphorylation of Tau –> tangles –>neuronal dysfunction and death in hippocampus and cerebral cortex

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16
Q

What is ‘late onset’ Alzheimer’s?

A

Occurs in those aged 60

17
Q

What gene is associated with late-onset Alzheimers disease?

A

Apolipoprotein E on chromosome 19

18
Q

By what two pathways may APP be cleaved?

A

Non-amyloidogenic: by alpha or gamma secretes

Amyloidogenic: by beta and gamma secretase to make amyloid peptides (Abeta)

19
Q

How does the presence of ApoE4 affect a persons chance of developing Alzheimers?

A

ApoE4 increases risk for late-onset AD as it decreases the clearance of extracellular amyloidogenic Ab peptides which contribute to plaque formation

20
Q

Which iso form of ApoE may be neuroprotective against late-onset Alzheimers disease?

A

ApoE2

21
Q

How may Alzheimers disease be diagnosed from CSF?

A

Amyloid decreases in CSF and more hyperphosphorylated tau in the CSF

22
Q

Explain how acetylcholinesterase inhibitors may be used in the treatment of Alzheimers disease

A

Increase cholinergic stimulation in the forebrain –> stimulates cortical and limbic structures

23
Q

What type of drugs are donepezil, galantamine and rivastigmine?

A

Acetylcholinesterase inhibitors

24
Q

What type of drug is memantine?

A

NMDA receptor antagonist

25
Q

Explain how NMDA receptor antagonists be used in the treatment of Alzheimers disease

A

AD may be associated with slow excitotoxicity from increased glutamate causing excess calcium influx causing production of free radicals and ROS which can cause mitochondrial dysfunction. Therefore by blocking the NMDA glutamate receptor it may prevent this from happening

26
Q

Which pathways degenerate in Alzheimers disease?

A

Cholinergic pathways in the forebrain which innervate the cortical and limbic structures

27
Q

What is the normal function of tau protein?

A

Stabilises microtubules through four tubular binding domains

28
Q

Why is the phosphorylation of tau a problem for it’s function?

A

When phosphorylated it cannot bind to the microtubules to stabilise them