Zusammenfassung der Ressource
APOE, Brain Reserve and Cognition
- Apolipoprotein E
- Gene located on chromosome 19
- involved in cholesterol
transportation
- affect likelihood of development of CVD?
- genotype determined by
combination of 3 alleles
- e2, e3 or e4
- e2/2 = lowest risk
- e2 provides protection
against dementia in old age
- e4/4 = highest risk
- 15% population prevalence of e4
- e4 carriers have
- smaller
hippocampi
- greater hippocampal
atrophy over time
- observed in demented
and healthy individuals
- greater and more diffuse activation of
hippocampal, prefrontal and parietal
brain areas in memory tasks
Anmerkungen:
- are e4 individuals less efficient
in processing information?
- Brain Reserve
Anmerkungen:
- stern (2002) good clear review
- buffers against pathological
progression of dementia
- individual differences in amount of
reserve an individual possesses
- passive
Anmerkungen:
- Stern (2002)
Stern et al (1999)
Tisserand et al (2001)
- neuroanatomical structures
deteriorate with age or disease
until a threshold is breached, at
which point cognitive impairment is
manifest
- threshold*
- active
- demographic or lifestyle factors contribute
to reserves against deleterious
consequences of ageing
- process tasks in more
efficient manner
- Katzman (1993) - education increases synaptic density
-> provides reserve against pathological progression
- brain is actively attempting to cope or
compensate for pathology
Anmerkungen:
- cognitive reserve
vs compensation
- the mind's resistance to damage of the brain
- i.e. deficits in cognition may not be apparent even though damage has taken place?
- hardware (brain reserve) vs software (cog reserve)
- Vitamin B12
- influence on brain reserve
- genetic predisposition to APOE + Vitamin B
= episodic memory deficits?
- differences observed in cognitive reserve
between e4 compared to non e4 due to vitB?
- ability to digest food efficiently decreases
with age - not digesting enough B12?
- low levels of B12 and folate associated with
lower episodic memory performance in old age
Anmerkungen:
- Calvaresi & Bryan (2001)
- Antagonistic Pleiotropy
- comes from evolutionary theory
- does a gene confer benefits in early life
but become a risk factor for disease in
later life?
- e.g. testosterone
- e4 associated with better cognitive performance in
childhood/ early adulthood but deficits in old age
- suggests a pleiotropic relationship between e4 and
cognition across lifespan
- NO evidence in support of this
- entorhinal cortex
Anmerkungen:
- e4 individuals have thinnest
- variation found in young people
- one of the first areas to exhibit and be
severely affected by neuropathology
associated with AD