Mild Cognitive Impairment & Subjective Cognitive Decline Flashcards

1
Q

Difference between SCD and MCI

A
  • SCD: The patient thinks there are changes but we can’t see changes on the tests
  • MCI: There is a subjective measure for it on a test, but it’s still liveable
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2
Q

Continuum of decline

A
  • The progression through the stages of cognitive decline and dementia
  • It is not necessarily linear
  • Not guarantee of progression to dementia
  • Can be reversed before stage 3
  • 10% convert from MCI to dementia annually
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3
Q

Stage 1 of the continuum of decline

A
  • No objective or subjective evidence for cognitive decline or impairment
  • No behavioural symptoms
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4
Q

Stage 2 of the continuum of decline

A
  • Subjective or/and subtle objective cognitive decline
  • Does not meet criteria for impairment
  • Mild, recent onset behavioural symptoms could co-occur or be the predominant symptom
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5
Q

Stage 3 of the continuum of decline

A
  • Objective cognitive decline to the level of impairment and mild functional impairment possible, but independence preserved
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6
Q

Stage 4 of the continuum of decline

A
  • Mild dementia
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7
Q

Stage 5 of the continuum of decline

A
  • Moderate dementia
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8
Q

Stage 6 of the continuum of decline

A
  • Severe dementia
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9
Q

Preclinical dementia

A
  • Subjective cognitive decline
  • Perceived deficits in cognition
  • No objective deficits in cognition
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10
Q

Aging to Mild Cognitive Impairment

A
  • Declines that are more severe then what is expected for their age and education is considered mild cognitive impairment
  • Changes in memory
  • Changes in language
  • Changes in visuospatial function
  • Changes in attention or executive functioning
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11
Q

Aging to MCI to Dementia

A
  • Declines that are more severe then what is expected for their age and education is considered mild cognitive impairment
  • Once the declines begin to impede on daily functioning the individual is diagnosed as having dementia
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12
Q

What is MCI

A
  • A condition in which someone experiences cognitive declines beyond what is expected in normal aging
  • These declines are severe enough to be noticed by the person and loved ones
  • The declines do not affect their ability to carry out everyday activities
  • May or may not progress to develop dementia
  • Can be reverted back but they have a higher chance of developing AD or dementia
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13
Q

MCI risk factors

A
  • Lower education
  • APOE e4 status: allele that is a marker for AD/Dementia
  • Increased age
  • Family history of AD or dementia
  • Conditions associated with cardiovascular disease
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14
Q

MCI Misdiagnosed

A
  • Sometimes MCI can be treated because it’s associated with some underlying condition
  • Depression
  • Metabolic causes
  • Infection causes
  • Sleep disorders
  • Neurological disorders
  • Perceived stress
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15
Q

Cognitive Problems

A
  • Changes in memory
  • Changes in language
  • Changes in visuospatial function
  • Changes in attention/executive function
  • Typically we use a cut off of 1.5SD below age and education matched means to show problems
  • MoCA and other tests are what we use to evaluate this
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16
Q

MCI Subtypes

A
  • Cognitive tests will determine which subtype of MCI a person has
  • Single domain: One cognitive domain impaired
  • Multiple domain: Multiple cognitive domains impaired
  • Amnestic MCI: Memory is mainly affected
  • Non-amnestic MCI: Other cognitive functions are affected
17
Q

MCI Outcomes by subtype

A
  • Amnestic MCI: AD, Vascular dementia
  • Non-amnestic MCI: FTD, Lewy body dementia, Parkinson’s disease dementia
18
Q

Brain changes in MCI

A
  • Atrophy: Typically see people with MCI having less brain volume compared to normal
  • Amyloid buildup: Increases in amyloid deposits throughout the brain
  • Tau buildup: Increases in tau, particularly in temporal lobe structure
19
Q

Progression of MCI to Dementia

A
  • 10 to 15% of individuals with MCI develop dementia each year
  • 1/3 of people with MCI develop dementia within 5 years
20
Q

Factors that increase risk of development from MCI to Dementia

A
  • Older age
  • APOE e4 status
  • Hippocampal atrophy on structural MRI
  • Vascular abnormalities
  • Biomarker positivity: Tau and amyloid
21
Q

Reducing progression from MCI to Dementia

A
  • Treating underlying conditions
  • Stopping medications that may be causing cognitive decline
  • Non pharmalogic interventions include:
  • Regular physical exercise
  • A diet in low fat and rich in fruits and vegetables
  • Omega 3 fatty acids
  • Keeping your brain active
  • Being social
22
Q

Subjective Cognitive Decline (SCD)

A
  • An indicator of declining cognitive function
  • Pre clinical dementia
  • Self perceived decline in memory and/or other cognitive abilities relative to the previous level of performance, but there is an absence of objective neuropsychological deficits
  • Increases likelihood of having biomarker abnormalities consistent with dementia pathology
  • Increases risk for future pathological cognitive decline and dementia
23
Q

Brain changes in SCD

A
  • Atrophy: typically see people with SCD have less brain volume compared to non-SCD older adults increase complaints means more decline in the left and right hippocampi
  • Amyloid buildup: Increases in amyloid deposits throughout the brain
  • Tau buildup: Increases in tau, particularly in the enthorhinal region
24
Q

Conversion from SCD to MCI/Dementia

A
  • Twice as likely to develop dementia than those with SCD
  • Features that increase likelihood of preclinical AD
  • Subject decline in memory rather than in other domains of cognition
  • Age at onset of SCD is over 60
  • Concerns associated with SCD
  • Feeling of performing worse than others of the same age group
  • Confirmation of cognitive decline by an informant
  • Presence of the APOE e4 genotype
  • Biomarker evidence for AD (defines preclinical AD)
25
Q

Sex differences in dementia

A
  • There are more females diagnosed
  • Females exhibit more pathology
  • Females show more decline in cognition associated with the same amount of brain changes as males
  • Females are more likely to have a faster progression than males
26
Q

Race differences in dementia

A
  • Black older adults are twice as likely to develop dementia than white adults
  • Racial differences exist in prevalence of risk factors
  • Some studies suggest black older adults have a faster progression and shorter survival time after diagnosis than white older adults