Dementia Flashcards

1
Q

What is dementia

A

Dementia is a syndrome with cognitive and behavioural symptoms

Has an insidious onset

Is a chronic condition with slow deterioration

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2
Q

Name some congitive symptoms seen in dementia

A

Impairment of memory

Impariment of orientation

Impariment of learning capacity

Impairment of judgement

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3
Q

Name some non-congitive symptoms seen in dementia

A

Behavioural symptoms - fear of unknown, agitation, aggression, wandering, sexual disinhibition

Depression and anxiety

Psychotic symptoms - visual and auditory hallucinations, persecutory delusions

Sleep symptoms - insomnia, daytime drowsiness

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4
Q

Name some differential diagnoses for dementia

A

Hypothyroidism

Hypercalcaemia

Vit B12 deficiency

Normal pressure hydrocephalus

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5
Q

What triad is seen in normal pressure hydrocephalus

A

Abnormal gait

Incontinence

Reduced cognition

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6
Q

What are the types of dementia

A

Alzheimer’s disease

Vascular dementia

Dementia with Lewy Bodies

Frontotemporal dementia

AIDs dementia complex

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7
Q

Describe the changes seen in alzheimer’s disease

A

Global atrophy of cerebral cortex -> sulcal widening and enlarged ventricles

Senile plaques (alpha-beta protein) - amyloid precursor protein broken down abnormally to alpha-beta protein that aggregates together to cause neuronal damage. Occur in foci of enlarged axons, synaptic terminals and dendrites

Neurofibrillary tangles - hyperphosphorylated Tau proteins that become deranged. Tau proteins normally bind and stabilise microtubules

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8
Q

What are the risk factors for vascular dementia/Alzheimer’s

A

Stroke

Hypertension

Hypercholesterolaemia

Diabetes

Smoking

AF

TIAs

Obesity

Coronary heart disease

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9
Q

How does vascular dementia present and how does it progress

A

Vascular dementia either has a sudden onset or comes on slowly over time

Patient progresses in a step-wise manner - suffer deterioration in cognition -> stable -> deteriorate

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10
Q

Describe dementia with lewy bodies including where the bodies are deposited and how it is defined in relation to Parkinson’s

A

Dementia with lewy bodies is caused by aggregations of alpha-synuclein protein within the neurone cytoplasm

In DLB the bodies are deposited in substantia nigra, frontal lobe, temporal lobe, cingulate gyrus amoung others

If patient has Parkinson’s -> develops dementia they have Parkinson’s with dementia

If patient has congitive features first (i.e. dementia) -> develop Parkinson’s then it is dementia with lewy bodies

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11
Q

Describe the presentation of DLB

A

Fluctuating cognition and alertness

Vivid visual hallucinations

Spontaneous features of Parkinson’s

Repeated falls due to festinating gait

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12
Q

What syndrome are patients with DLB susceptible to and what are the signs

A

Neuroleptic malignant syndrome - side effect of anti-psychotics caused by a sudden drop in dopamine. Signs:

Fever

Encephalopathy

Vital signs instability - tachycarida, tachypnoea, fluctuating BP

Elevated enzyme - creatinine phosphokinase

Rigidity

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13
Q

Describe frontotemporal dementia and the main syndromes of frontotemporal dementia

A

Have lobar atrophy of frontal and temporal lobes with symptoms based on lobe dysfunction

Three main syndromes:

  • Behavioural varient
  • Progressive non-fluent aphasia
  • Semantic
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14
Q

Name some symptoms of frontotemporal dementia

A

Loss of inhibition

Inappropraite social behaviour

Loss of motivation without depression

Repetitive/ritualistic behaviours

Non-fluent aphasia

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15
Q

Desribe AIDs dementia complex and the clinical features seen with it

A

AIDs dementia complex - HIV infected macrophages enter brain where HIV causes indirect damage to neurones

Rapid progression

Features: cognitive impairment, psychomotor retardation, tremor, ataxia, dysarthria, incontinence

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16
Q

Name some pharmacological methods of treating dementia

A

Acetylcholinesterase inhibitors - decrease ACh breakdwon to increase ACh for transmission. Good for improving cognition. E.g. donepezil, rivastigmine

NMDA antagonists - reduce overstimulation of NMDA and are used in patients who are agitated or aggressive (caused by overstimulation of NMDA). E.g. memantine

17
Q

Deposition of which protein is central to the pathogenesis of Alzheimer’s and which gene mutations increase the deposition of this protein

A

Amyloid deposition is key to pathogenesis of Alzheimer’s - seen in Down’s syndrome as well

Mutations of amyloid precursor protein gene or presenilin genes 1 and 2 can lead to incomplete breakdown of amyloid precursor protein and amyloid deposition