Neuroscience of Ageing Flashcards
Which types of lesions are associated with Alzheimer’s disease
1/ Arteriovenous malformations and cerebral infarctions
2/ Senile plaques and neurofibrillary tangles
3/ Arteriovenous malformations and neurofibrillary tangles
4/ Senile plaques and cerebral infarction
2/ Senile plaques and neurofibrillary tangles
Associated with Alzheimer’s disease, senile plaques are formed by which protein?
1/ Tau protein
2/ Beta-amyloid protein
3/ Myelin oligodendrocyte glycoprotein
4/ Matrix extracellular phosphoglycoprotein
2/ Beta-amyloid protein
Associated with Alzheimer’s disease, neurofibrillary tangles are formed by which protein?
1/ Tau protein
2/ Beta-amyloid protein
3/ Myelin oligodendrocyte glycoprotein
4/ Matrix extracellular phosphoglycoprotein
1/ Tau protein
What happens to beta-amyloid protein during the onset of Alzheimer’s disease?
1/ It is over-regulated, leading to a lack of it
2/ It isn’t produced, leading to a lack of it
3/ It is under-regulated, leading to too much of it
4/ It is over produced, leading to too much of it
3/ It is under-regulated, leading to too much of it
It is normally broken down once released from a neuron. This regulatory process fails, leading to a build up. These form senile plaques.
What happens to tau protein during the onset of Alzheimer’s disease?
1/ It is over-regulated, leading to a lack of it
2/ It isn’t produced, leading to a lack of it
3/ It becomes defective
4/ It becomes too effective
3/ It becomes defective
Tau protein normally maintains the skeleton of a neuron (microtubules). Tau protein detaches from the skeleton in Alzheimer’s. This leads to be breakdown of the neuron skeleton, as well as the defective tau proteins joining to form filaments in the neuron. This leads to the death of the neuron (the dead neuron is the neurofibrillary tangle)
In Alzheimer’s disease, where do neurofibrillary tangles normally originate?
1/ Thalamus
2/ Hippocampus
3/ Basal ganglia
4/ The cortex
2/ Hippocampus
Essential to memory and learning. They then reach the whole brain, leading to global dysfunction
In Alzheimer’s disease, where to senile plaques normally originate?
1/ Thalamus
2/ Hippocampus
3/ Basal ganglia
4/ The cortex
4/ The cortex
Then the hippocampus, before spreading to the whole brain. Their progression does not correspond with the symptoms of the disease.
Which of the following is not a form of dementia
1/ Alzheimer's disease (AD) 2/ Vascular dementia (VD) 3/ Dementia with Lewy Bodies (DLB) 4/ Parkinson's disease 5/ Huntington's disease
5/ Huntington’s disease
Huntington’s disease is an inherited genetic condition that causes/can lead to dementia
Vascular dementia is caused by
1/ A stroke/strokes
2/ Microscopic build up of specific proteins
3/ A build up of senile plaques and neurofibrillary tangles
4/ An aggregate loss of dopamine due to a loss of cells in the substantia nigra
1/ A stroke/strokes
Alzheimer’s disease is caused by
1/ A stroke/strokes
2/ Microscopic build up of specific proteins
3/ A build up of senile plaques and neurofibrillary tangles
4/ An aggregate loss of dopamine due to a loss of cells in the substantia nigra
3/ A build up of senile plaques and neurofibrillary tangles
Dementia with Lewy Bodies is caused by
1/ A stroke/strokes
2/ Microscopic build up of specific proteins
3/ A build up of senile plaques and neurofibrillary tangles
4/ An aggregate loss of dopamine due to a loss of cells in the substantia nigra
2/ Microscopic build up of specific proteins
The protein is Lewy Bodies
Parkinson’s disease is caused by
1/ A stroke/strokes
2/ Microscopic build up of specific proteins
3/ A build up of senile plaques and neurofibrillary tangles
4/ An aggregate loss of dopamine due to a loss of cells in the substantia nigra
4/ An aggregate loss of dopamine due to a loss of cells in the substantia nigra
It has been estimated that some brain regions may lose up to 1% of their mass each year in healthy adults. This loss is
1/ Equally distributed
2/ Not equally distributed
3/ Exclusively located in the hippocampus
4/ Exclusively located in the cortex
2/ Not equally distributed
Grey matter in the brain…
1/ Grows during adolescence and then plateaus in the third decade of life, decreasing thereafter
2/ Increases until the age of 10, followed by a gradual decrease until about 70
3/ Increases until the age of 5, followed by a gradual decrease until about 70
4/ Grows during adolescence and then plateaus in the fifth decade of life, decreasing thereafter
3/ Increases until the age of 5, followed by a gradual decrease until about 70
White matter in the brain…
1/ Grows during adolescence and then plateaus in the third decade of life, decreasing thereafter
2/ Increases until the age of 10, followed by a gradual decrease until about 70
3/ Increases until the age of 5, followed by a gradual decrease until about 70
4/ Grows during adolescence and then plateaus in the fifth decade of life, decreasing thereafter
1/ Grows during adolescence and then plateaus in the third decade of life, decreasing thereafter
White matter is made up of…
1/ White neurons
2/ Axons insulated by myelin
3/ Dendrites insulated by calcium
4/ The corpus callosum
2/ Axons insulated by myelin
Decline in white matter is associated with a decline in
1/ Motor control
2/ Emotional stability
3/ Processing speed
4/ Long term memory capacity
3/ Processing speed
This is a threshold phenomenon, rather than linear
Which ability is surprisingly well preserved in normal ageing?
1/ Spatial orientation
2/ Numerical abilities
3/ Attentional processes
4/ Language abilities
4/ Language abilities
The preservation of language abilities in an ageing brain can be explained by
1/ Neuro-functional reorganisation
2/ Neuro-lateral reproduction
3/ Neuro-structural specific preservation
4/ Aggregate increase in PFC volume
1/ Neuro-functional reorganisation
Such as additional frontal recruitment in older adults (when compared to younger ones) when performing verbal cued-recall tasks (Osorio et al, 2009)
Who is responsible for the Cognitive Reserve hypothesis?
1/ Roberto Cabeza
2/ Yaakov Stern
3/ Patricia Reuter-Lorenz and Denise Park
4/ Davis et al. (including Cabeza)
5/ Patricia Reuter-Lorenz and Cindy Lustig
2/ Yaakov Stern
Possibly due to factors like educational and occupational attainment, a person’s ability to withstand neurological decline for longer without expressing clinical symptoms is known as
1/ Compensation-Related Utilisation of Neural Circuits Hypothesis (CRUNCH)
2/ Scaffolding Theory of Ageing and Cognition (STAC)
3/ Cognitive Reserve Hypothesis
4/ Hemispheric Asymmetry Reduction in OLDer adults (HAROLD)
5/ The Posterior-Anterior Shift in Ageing (PASA)
3/ Cognitive Reserve Hypothesis
Studies have found that people who show greater cognitive reserves…
1/ Never show clinical symptoms of cognitive decline
2/ Show clinical symptoms of cognitive decline later, and the experience a slower decline
3/ Show clinical symptoms of cognitive decline later, and the experience a faster decline
4/ Show clinical symptoms of cognitive decline earlier, and the experience a slower decline
3/ Show clinical symptoms of cognitive decline later, and the experience a faster decline
Cognitive Reserve can be subdivided into 2 categories; Cognitive reserve and brain reserve. Cognitive reserve is characterised by
1/ Differences in cortical volume
2/ Differences in the outcome of tasks on a cognitive test
3/ Differences in the brain structure that may increase tolerance to pathology
4/ Differences between individuals in how tasks are performed that might enable some people to be more resilient to brain changes than others
4/ Differences between individuals in how tasks are performed that might enable some people to be more resilient to brain changes than others
Cognitive Reserve can be subdivided into 2 categories; Cognitive reserve and brain reserve. Brain reserve is characterised by
1/ Differences in cortical volume
2/ Differences in the outcome of tasks on a cognitive test
3/ Differences in the brain structure that may increase tolerance to pathology
4/ Differences between individuals in how tasks are performed that might enable some people to be more resilient to brain changes than others
3/ Differences in the brain structure that may increase tolerance to pathology