LC 2 - cognitive development and ageing Flashcards
1
Q
brain development over a lifetime
A
- Neurons are at max after birth
o Loss of neurons is not very great
o Neurons seem to shrink with age - Synapses decline steeply synaptic pruning
o Optimization of networks - Grey matter matures (increase of thickness) with age
o Primary cortices S1 and M1 ripen first (also V1 and auditory, etc)
o Cognitive regions ripen later - Connectivity changes with age (it decreases)
2
Q
cognitive functions
A
- Cognitive functions = Mental activity between sensory input & motor output
- Mediated by neocortical brain structures
- Neuropsychological definition:
o Intelligence
o Attention Learning and memory
o Problem solving / executive function
o Language ability
o Visuo-spatial ability Sensorimotor function (…)
o Memory (medial temporal lobe) - Important for daily functioning
- Unitary or compound?
o Cognition is not unitary but can be tested that way (MMSE)
3
Q
development of cognition
A
- Driven by brain plasticity interaction with environment is crucial
- Sequential timing of domain functions development
o Attentional control
o Information processing (basic)
o Cognitive flexibility
o Goal setting - Prefrontal cortex is essential for cognitive functions
- Pivotal role of attentional control (develops first)
4
Q
ageing patterns
A
- Word fluency is least affected by age
- Letter copying is more effected –> performance based outcomes (speed based)
- Control processes (processing new info) increase until maturity (mid-age) and decrease very hard at older age
o Seems linear but is slightly quadratic
o Variance in performance increases with age - Not all processes decline after maturity language can stay stable or even increase with older age
5
Q
brain plasticity over time
A
- The ability of the neuronal tissue to adapt to its environment
- Decreases vastly after infancy
- Gene expression and connectivity change with time –> deregulate
6
Q
ageing mechanisms
A
- Vascular ageing
- Oxidative stress
- Hormonal dysregulation
- Telomere attrition (not as important for brain since most cells do not divide except some stem cells – also found around the ventricles)
- Immunosenescence
7
Q
brain ageing
A
- Overall shrinkage (anterior / posterior gradient; grey > white matter)
- Loss in connectivity (white matter)
- Dopamine depletion
- Due to:
o (micro-) vascular changes (hypertension)
o changes in signalling pathways (e.g. insulin/IGF-1)
o oxidative stress
o recurrent / chronic inflammation
o stress-related corticoid levels
8
Q
overall health and cognition
A
- Brain depends on multiple organ systems for O2, glucose and nutrient supply
- Sensitive to metabolic disturbances
- Many diseases & pharmacological therapies have impact on brain function
- “Brain stressors”
o Hypertension
o CVDs
o Obstructive pulmonary disease (asthma)
o Renal failure
o Liver failure
o Cancer
o Thyroid dysfunction
o Endocrine disorders
9
Q
ageing, health and cognition
A
- Increase of variance in cognitive domains: ‘health-related vulnerability factors’?
- E.g., head trauma, vascular disease, life style, health
- Concept of ‘Brain reserve capacity’ (BRC)
o CNS redundancy overcapacity compensate for losses
o Proxy measures: e.g. brain size, cortical surface area - Age reduces BRC
- Lower BRC related to dementia risk
- LIBRA score measures the dementia risk as a function of lifestyle factors
- With age networks are reorganised to compensate for reduced BRC – often the other hemisphere will be used to complement the hemisphere that is used in young people
o This only works to a certain age, after 70 the compensation does not cover the pathological changes anymore
10
Q
vascular risk
A
- Vascular dysfunction (due to vascular risks like hypertension, diabetes, inactivity) leads to diffuse white matter lesions –> mild cognitive impairment –> (vascular) dementia
o More lesions –> higher dementia risk - Cognitive decline varies between the types of dementia
o AD= slow and constant decline
o Vascular= sudden changes that are irregular