ch. 12: cortical dementias Flashcards

1
Q

What are common myths about aging and cognition?

A

Memory and intelligence decline drastically, learning becomes more difficult, and nothing can counteract these deficits (all myths).

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2
Q

What types of memory decline with age?

A

Episodic memory, free recall, and nonverbal memory (fluid intelligence).

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3
Q

What types of memory remain stable with age?

A

Semantic memory, short-term memory, long-term memory, and recognition memory.

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4
Q

What is the main cause of memory decline with aging - retention or retrieval?

A

Retrieval issues, not retention

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5
Q

What type of intelligence declines with age?

A

Fluid intelligence (problem-solving, speeded thinking)

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6
Q

What type of intelligence is spared with age?

A

Crystallized intelligence (facts, memory, and semantic memory)

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7
Q

Name three ways to slow cognitive decline.

A

Exercise, a healthy diet, and continued education.

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8
Q

How does an enriched environment help reduce cognitive decline?

A

Activities like reading, traveling, and engaging in cultural activities stimulate the brain.

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9
Q

What is dementia?

A

A decline in cognitive abilities that interferes with daily living (ADLs and IADLs)

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10
Q

What is the difference between ADLs and IADLs?

A
  • ADLs: basic tasks (bathing, dressing, eating)
  • IADLs: higher cognitive tasks (managing money, medication, cooking)
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11
Q

How is dementia diagnosed?

A

Significant cognitive decline in one or more domains that interferes with independence, not caused by delirium or psychiatric disorders.

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12
Q

Name two cortical dementias.

A

Alzheimer’s disease and frontotemporal dementia.

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13
Q

Name two subcortical dementias.

A

Parkinson’s disease and Huntington’s disease.

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14
Q

What are two mixed dementias?

A

Vascular dementia and dementia with Lewy bodies.

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15
Q

Is Alzheimer’s disease reversible?

A

No, it is irreversible and progressive.

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16
Q

What are the hallmark pathological features of AD?

A

Beta-amyloid plaques and neurofibrillary tangles

17
Q

What is the greatest risk factor for AD?

A

age (especially over 60)

18
Q

What genes are associated with early-onset AD?

A

Chromosomes 1, 14, and 21.

19
Q

What gene is associated with late-onset AD?

A

APOE gene on chromosome 19.

20
Q

What are the two major toxic processes in AD?

A

Amyloid-beta accumulation and tau protein misfolding.

21
Q

What happens to microtubules in AD?

A

Tau protein misfolding leads to neurofibrillary tangles, disrupting neuronal transport.

22
Q

Name three newer theories of AD pathology.

A

Glutamate dysregulation, inflammation, oxidative stress.

23
Q

What type of memory is most impaired in early AD?

A

Delayed episodic recall.

24
Q

How does language change in AD?

A

Early anomic aphasia (word-finding difficulty), later comprehension problems and reduced conversation fluency.

25
Q

What is one of the earliest signs of visual-spatial deficits in AD?

A

Difficulty drawing a clock or navigating familiar spaces.

26
Q

How does attention change in AD?

A

Simple attention is intact until later stages, but complex attention declines early.

27
Q

How is executive function affected in AD?

A

Disorganization, task incompletion, repetition, loss of problem-solving skills.

28
Q

What is the only definitive way to diagnose AD?

A

Brain biopsy (post-mortem)

29
Q

How often should cognitive assessments be done for AD?

A

Every 9-12 months.

30
Q

What medications are used to treat AD?

A

Cholinesterase inhibitors (help memory) and Memantine (prevents premature cell death).

31
Q

Are cognitive exercises helpful in late-stage AD?

A

No, they are only useful in early stages.

32
Q

What is a major challenge for caregivers of AD patients?

A

Ensuring safety and managing behavioral changes.