DEMENTIA Flashcards

1
Q

what is dementia?

A

an umbrella term for a range of progressive conditions affecting the brain and disturbing higher cortical function without clouding conciousness

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2
Q

what are the 5 most common types of dementia?

A
alzheimers
vascular disease
dementia with lewy bodies
frontotemporal dementia
mixed dementia
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3
Q

how do we distinguish dementia from normal ageing?

A

the symptoms must be worse than normally expected in someone of their age in dementia and must be severe enough to impair ADLs

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4
Q

what is young onset dementia?

A

when it starts before the age of 65

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5
Q

what are the symptoms of dementia?

A

memory loss
difficulty communicating or finding words
difficulty with visual and spatial abilities
difficulty reasoning or problem solving
difficulty handling complex tasks
difficulty with planning and organization

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6
Q

whats the most common type of dementia?

A

alzheimers disease

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7
Q

whats the cause of alzheimers disease?

A

plaques - beta amyloid clumps together and disrupt cell to cell communciation
tangles - tau proteins change shape and organize themselves into neurofibrillary tangles which disrupt the transport system and are toxic to cells

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8
Q

whats it called when beta amyloid plaques deposit around blood vessels in the brain?
what is the result of this?

A

amyloid angiopathy

weakens blood vessel walls and increases risk of haemorrhage

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9
Q

what forms neurofibrillary tangles in alzheimer disease?

A

abnormal accumulations of tau protein inside neurones

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10
Q

what are the 2 types of alzheimers disease?

A

sporadic and familial

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11
Q

what is sporadic alzheimers?

A

late onset type where the exact cause isnt very well defined but is probably a combination of genetic and environmental risk factors

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12
Q

whats a gene thats been identified as possible contributing to an increased alzheimers risk?

A

APOE-e4 gene
APOE genes helps break down beta-amyloid but the e4 allele is less effective than other alleles so people are more likely to develop beta-amyloid plaques.

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13
Q

what is familial alzheimers disease?

A

cases where some dominant gene was inherited and speeds up the progression of the disease
its usually earlier onset w

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13
Q

what is familial alzheimers disease?

A

cases where some dominant gene was inherited and speeds up the progression of the disease
its usually earlier onset w

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14
Q

what is familial alzheimers disease?

A

cases where some dominant gene was inherited and speeds up the progression of the disease
its usually earlier onset w

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15
Q

which type of alzheimers is more common?

A

sporadic

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16
Q

what mutations have been linked to early onset alzheimers?

A

PSEn-1 and PSEN-2 on chromosomes 14 or 1
mutations in these can change the location where amyloid precursor protein gene is chopped, producing different length beta amyloid molecules which have a tendancy to clump and form plawues

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17
Q

why is trisomy 21 also a genetic cause of familial alzheimers?

A

the gene responsible for producing APP is on chromosome 21 so those with down syndrome have an extra APP gene and so increases the amount of amyloid plaque build up

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18
Q

what age does familial alzheimers disease often progress by?

A

40

19
Q

outline the symptoms of alzheimers?

A

starts with short-term memory loss
then loss of motor skills and language becomes difficulty
eventually they lose long term memory and become more and more disorientated

20
Q

what causes death in alzheimers?

A

often an infection such an pneumonia as they are bed ridden

21
Q

how do we diagnose alzheimers?

A

by excluding all other causes of dementia

22
Q

what are the treatment options of alzheimers?

A

acetylcholinesterase inhibitors e.g. donepezil, rivastigmine and galantamine
memantine

23
Q

how does memantine work at treating dementia?

A

memantine binds mmore effectively than Mg2+ ions at the NMDA receptor, effectively blocking the prolonged influx of Ca2+ through the channel whilst preserving transient phsyiological activation of the channels by higher concentrations of synaptically released glutamate. therefore it protects against chronically elevated glutamate concentrations

24
Q

how does donepezil work for treating dementia?

A

reversible inhibition of acetylcholinesterase, leading to an increase in ACh at cholinergic synapses, enhancing cholinergic function

25
Q

what are alzheimers risk factors?

A
age
family history
APOE e4 gene 
down syndrome
being female (only because they often live longer so prevalence is higher)
mild cognitive impairment 
head trauma
air pollution
excessive alcohol consumption
poor sleep patterns
heart disease risk factors
low education levels and low social engagement q
26
Q

what is mild cognitive impairment?

A

a decline in memory or other thinkng skills that is greater than normal for a persons age, but the decline doesnt prevent a person from functioning in social environments

27
Q

what is vascular dementia also known as?

A

multi-infarct dementia

28
Q

what is vascular dementia?

A

progressive loss of brain function caused by long term poor blood flow to the brain (typically because of a series of strokes)

29
Q

what are the symptoms of vascular dementia?

A

they depend on where the stroke occured in the brain e.g. if temporal lobe then they may have difficulty with memory or if parietal lobe they may have aphasia
Symptoms appear suddenly and brain function decreases with each stroke

30
Q

how do we diagnose vascular dementia?

A

neuropsychological tests

then brain imaging, usually CT or MRI which would show atrophy of the brain cortex, confirming ischaemia

31
Q

how do we treat vascular dementia?

A

focus on reducing risk of recurring strokes e.g. lowering bp, stopping smoking, controlling diabetes etc

32
Q

what causes lewy body dementia?

A

misfolded alpha synuclein which aggregates to form lewy bodies which accumulate

33
Q

what are the symptoms of lewy body dementia?

A

early signs are usually cognitive:
difficulty focussing, poor memory, visual hallucinations, disorganized speech and depression

later sigsn are usually motor:
resting tremors, stiff and slow movements, reduced facial expressions

note: some people have sleeping disorders too

34
Q

how do we diagnose lewy body dementia?

A

pattern of symptoms and confirmed with a brain autopsy which shows lewy bodies in neurones

35
Q

whats the treatment for lewy body dementia?

A

motor symptoms respond to drugs used to treat parkinsons e.g. levodopa
cognitive symptoms respond to drugs for alzheimers e.g. donepezil

36
Q

what is frontotemporal dementia?

A

a degeneration of frontal and temporal lobes of the brain which affects behaviour, personalty, language and movement

37
Q

what causes frontotemporal dementia?

A

abnormal tau protein inclusions form in the cytoplasm or nuclei of neurones. This damages the neurones so they undergo apoptosis. the brain now atrophies and the gyri get narrower and sulci get wider. The ventricles also expand as the brain shrinks.

38
Q

what are symptoms of frontotemporal dementia?

A

if frintal lobe is affeted we get personality and behaviour changes - most common
when temporal lobe is affected we may get semantic variant primry progressive aphasia or non-fluent variant primary progressive aphasia
as atrophy dveelops a person may struggle with memory, concentration and ability to learn neew things

39
Q

what is semantic variant primary progressive aphasia

A

difficulty finding the right words

40
Q

what is nonfluent variant primary progressive aphasia?

A

difficulty speaking while knowing the meanings of individual words

41
Q

how do we diagnose frontotemporal dmeentia?

A

mental status changes
imaging studies to see changes in frontal and temporal lobes
brain biopsy after death is the onyl real definitive test

42
Q

what are the types of frontotemporal dementia?

A

behavioral variant frontotemporal dementia (bvFTD), primary progressive aphasia (PPA), and movement disorders.

43
Q

what is picks disease?

A

behavioural variant frontotemporal dementia

44
Q

what are the symptoms of picks disease?

A

personality changes
apathy
proressive decline in socially appropriate behaviour, judgement, self control
and empathy

45
Q

at what age does frontotemporal dmeentia usually start showing symptoms?

A

between 40 and 65