Dementia Symposium Flashcards

1
Q

How many thousand people in the UK are affected by dementia?

A

700,000

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What percentage of over 65s and over 80s suffer from dementia?

A

over 65s - 5%

over 80s - 20%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

In a typical district general hospital what percentage of patients have dementia?

A

over 20%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Abnormality in the frontal lobe leads to what 5 defects?

A

1) Impaired judgement
2) Impaired abstract reasoning and strategic planning
3) Impaired emotional restraint
4) Impaired control over appetite
5) Incontinence

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Diseases of the parietal lobe give rise to what 2 things?

A

1) Impairment of visuospatial skills leading to apraxias

2) Impaired integration of sensory inputs leading to sensory agnosias

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Diseases of the medial temporal lobe, hippocampus, amygdala and limbic system leads to what 2 features?

A

1) Disorders of memory

2) Hallucinations

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Diseases of the temporal neocortex is associated with what 2 features?

A

1) Receptive dysphasia

2) Automatisms (performance of actions without concious thought)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Diseases of the occipital lobe leads typically to what?

A

Failure of the visual sensory systems

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What 8 ‘treatable’ conditions can cause dementia?

A

1) Depression
2) Iatrogenic (anticholinergics, sedatives, narcotics, H2 blockers, multiple meds)
3) Hypothyroidism
4) B12 deficiency
5) Neurosyhpilis
6) Normal pressure hydrocephalus
7) Subdural hematoma
8) Encephalitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Give the 4 main types of neurodegenerative dementias?

A

1) Alzheimer’s dementia
2) Lewy Body dementia
3) Frontotemporal dementia
4) Huntington’s disease (and many others)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are the other 2 main types of dementias which are not classed as neurodegenerative dementias?

A

1) Vascular dementia

2) Prion disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Can vascular dementia be treated?

A

Treatment can slow down progression but cannot cure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is the prognosis of prior disease?

A

Untreatable but with rapid progression

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

In addition to type how else can dementias be classified?

A

By site - ie anterior/posterior, cortical/subcortical

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

How do the symptoms of anterior dementia tend to differ from posterior dementia?

A

Anterior - behaviour changes - ie loss of inhibition, antisocial etc.
Posterior - disturbance of cognitive function (memory and language) without marked changes in behaviour

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is the common site of Alzheimer’s disease?

A

Posterior cortical

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Name 2 types of dementias which tend to be sub cortical?

A

1) Parkinson’s disease

2) AIDS dementia complex

18
Q

How do the symptoms of subcortical dementias tend to differ from cortical dementias?

A

Subcortical - apathetic, forgetful and slow, associated with other neurological signs and movement disorders
Cortical - Higher cortical abnormalities - dysphasia, agnosia, apraxia

19
Q

Traditionally, which 3 neurodegenerative disorders were classified as dementias (as opposed to movement disorders)?

A

1) Alzheimer’s disease
2) Frontotemproal dementia
3) Dementia with Lewy bodies

20
Q

Traditionally which 4 neurodegenerative disorders were classified as movement disorders (Rather than dementias)?

A

1) Parkinson’s disease
2) Parkinson plus syndromes (progressive supranuclear palsy, multiple system atrophy, corticobasal degeneration)
3) Huntington’s disease
4) Motor neuron disease

21
Q

What are the 3 current molecular-genetic classifications of neurodegenerative disorders?

A

1) Tauopathies
2) Synucleinopathies
3) Ubiquinopathies

22
Q

Which molecular genetic classification does Alzheimer’s disease fall into?

A

Tauopathies

23
Q

Which molecular genetic classification does Parkinson’s disease and Dementia with Lewy bodies fall into?

A

Synucleinopathies

24
Q

What 2 types of dementia fall under the classification of ubiquinopathies?

A

1) MND and MND/Dementia
2) Semantic dementia
(Both subtypes of frontotemporal dementia)

25
Q

Normal pressure hydrocephalus is a triad of which 3 symptoms occurring in conjunction with what?

A

1) Dementia
2) Gait disturbance
3) Urinary incontinence
Occurring in conjunction with hydrocephalus and normal CSF pressure

26
Q

What are the 2 types of normal pressure hydrocephalus (NPH)?

A

1) NPH with a preceding cause (SAH, meningitis, trauma, radiation induced)
2) NPH with no known preceding cause - idiopathic (50%)

27
Q

Why is CJD described as a transmissable spongiform encephalopathy?

A

Under a microscope, the affected brain tissue looks like a sponge

28
Q

How would an EEG appear in a person with CJD?

A

Triphasic waves - on repeat testing

29
Q

What would be the 2 typical symptoms of someone with CJD?

A

1) Rapid cognitive decline

2) Myoclonic jerks (quick involuntary muscle jerks)

30
Q

What would be the main feature of an MRI of a patient with sporadic CJD?

A

Non specific changes in the basal ganglia

31
Q

What is the characteristic abnormality in MRI in patient with variant CJD?

A

Abnormality in the posterior thalamic region - called pulvinar sign which is highly sensitive and specific for vCJD

32
Q

Corticobasal degeneration falls into which molecular genetic classfication?

A

Tauopathy

33
Q

What is the main feature corticobasal degeneration on electron microscopy?

A

Phospho-tau filaments with the neurons (also cytoplasmic tangles, neuropil threads)

34
Q

If a patient presents with fitting and ongoing confusion what is the most likely diagnosis?

A

Encephalitis

35
Q

Encephalitis due to Voltage gated postassium channel Ab (VGKC Ab LE) is what kind of encephalitis?

A

Autoimmune encephalitis

36
Q

What are the 4 common signs and symptoms of VGKC Ab LE)

A

1) Subacute memory loss
2) Psychiatric/behavioural disturbances
3) Seizures - usually partial
4) Hyponatraemia in common

37
Q

What sign do 60% of people with VGKC Ab LE shown on MRI?

A

Medial temporal lobe high signal on MRI

38
Q

Does VGKC Ab LE cause treatable or untreatable dementia?

A

Treatable dementia - type of autoimmune enecephalitis which can be treated with steroid treatment

39
Q

What is the prognosis of VGKC Ab LE?

A

Thymoma/SCLC (Small cell lung cancer) may also be present but isnt commonly associated
If no tumour is present then the prognosis is very good with immuno modulation

40
Q

What kind of conditions are neurologists mainly concerned with in regards to dementia?

A

Treatable conditions

41
Q

Which specialty deals with dementias caused by untreatable conditions?

A

Psychiatry