Lecture 39: Aging, MCI and Non-Alzheimer's Disease Dementia Syndromes Flashcards

1
Q

What is the unifying hypothesis for cognitive aging?

A

Localization to the premotor frontal cortex

- deficit of executive control	
- evidence shown in imaging of atrophy in prefrontal brain regions
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2
Q

What are normal cognitive problems?

A

Relative preservation of vocab and world knowledge (semantic memory)

  • however, there is forgetfulness
    • decreased information retrieval, word-finding difficulty (with names)
    • slower info processing
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3
Q

What is mild cognitive impairment?

A

More cognitive decline than memory but DAILY ACTIVITIES ARE NORMAL

  • so more like mild cognitive unimpairment lol
  • does not meet criteria for dementia
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4
Q

What must you exclude when you see somebody with MCI or dementia?

A

Impairment from depression

- anxiety
- medications
- B12 deficiency
- vascular disease
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5
Q

What are two types of MCI? And what is the significance?

A

A. Amnestic MCI
-single domain
-multiple domain
Significance: leads to AD

B. Non-amnestic MCI
-single domain
-multiple domain
Significance: leads to non-AD dementia

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6
Q

What are risk factors for MCI progression?

A
  1. increasing age
  2. amnestic component
  3. APOE genotype
  4. vascular risk factors (clotting)
  5. Amyloid imaging (Pittsburgh Compound B elevated = PiB)
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7
Q

What is treatment for MCI?

A

AChE inhibitor but there no treatment shown to definitively improve MCI outcome

  • stay physically and mentally active
  • treat vascular risk factors
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8
Q

What are the three general types of Non-AD dementias (that we have to know for this test lol)

A
  1. Frontotemporal Dementia
  2. Dementia with Lewy Bodies
  3. Vascular Dementia
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9
Q

What is Frontotemporal dementia? And what impairments are to be expected in general?

A

Focal degeneration of the frontal and temporal lobes (with cognitive and behavioral disturbances)
Young onset (45-65)
a. Behavioral/emotional disinhibition (anterior cingulate/orbitofrontal cortex degeneration)
b. Decreased executive function (prefrontal motor cortex)
c. Broca’s aphasia
d. Loss of semantic knowledge
-words/concepts on left
-emotions/faces on right
-associated with temporal lobe degeneration

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10
Q

What are the three types of frontotemporal dementias (FTD)?

A
  1. Behavioral Variant FTD
  2. Progressive nonfluent aphasia (PNFA)
  3. Semantic dementia
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11
Q

Delineating factor for behavioral variant FTD

A
Think of Phineas Gage
Loss of empathy
Personality change
-socially inappropriate behavior
-overeating/preference for sweet foods
Poor executive function
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12
Q

Delineating factor of Progressive nonfluent aphasia (PNFA)

A

Broca’s aphasia

  • agrammatic, language apraxia, decreased total verbal output for words
  • they can find the CORRECT label for an object…just can say it
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13
Q

What is semantic memory?

A

General knowledge of objects, word meanings, facts WITHOUT connection to any particular time or place

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14
Q

Delineating factor of Semantic dementia

A

Loss of semantic memory (words lose their meaning)
Example: forget how to spell a word, the fact that Cows make a “moo” sound, that milk is consumed by humans, etc.
Localized on the temporal lobe

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15
Q

What are the two types of proteins involved in pathology of FTDs?

A
  1. Tauopathy (Pick bodies)
    PNFA is majority Pick bodies while BehavioralFTD is 50/50
  2. TDP-43 proteinopathy
    Semantic dementia is majority TDP-43
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16
Q

Delineating factor of dementia with Lewy bodies (DLB)

A

Benign hallucinations (kitten on the couch or kids running around)
PD like motor symptoms (shuffling steps when turning)
-autonomic dysfunction
-REM sleep behavior disorder (RBD)

17
Q

What is REM sleep behavior disorder (RBD)? And what is its significance?

A

When you are acting out your dream
-your muscles should be paralyzed during sleep…but not so in these patients
Predictor for DLB/Parkinson’s disease with dementia

18
Q

How do you treat dementia with lewy bodies (DLB)?

A
  1. Acetylcholinesterase improves cognition

2. Low levels of levodopa (too much can worsen hallucinations)

19
Q

What are the three types of vascular dementia?

A
  1. Multi-infarct dementia
  2. Subcortical vascular dementia
  3. Strategic infarct dementia
20
Q

Delineating factors for multi-infarct dementia:

A

Person has vascular risk factors and stepwise declien
Corresponds with arterial territories
anterior cerebral artery: apathy, abulia (loss of initiative), kinetic features, akinetic mutism
MCA: aphasia, neglect (right and left respectively)
PCA: amnesia, agnosia (cant interpret sensation), anomia (cant name shit)

21
Q

Delineating factors for Subcortical vascular dementia

A

-psycho-motor slowing
-impaired concentration
-forgetfulness
Absence of focal cortical deficits (like no aphasia, no apraxia)

22
Q

Delineation of strategic infarct dementia

A

Impairs a critical frontal-subcortical connection by lesioning a key relay pathway
Example:
1. Thalamic dementia from dorsomedial nucleus lesion
-thiamine deficiency
-loss of memory
-stroke from paramedian artery (branch of PCA)
2. infarct to anterior thalamic nuclei
-amnesia with apathy and reduced emotional expression (loss of Papez circuit)
-loss of tuberothalamic artery (from PCOMM)

  1. Infarct of genu of internal capsule
23
Q

How do you treat?

A

Prevent stroke
-vascular dementia cant be treated once don
Primary prevention: managing risk factor
Secondary prevention: management of risk factors after initial episode of vascular brain injury
Tertiary amelioration of symptoms: neurostimulants