• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/14

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

14 Cards in this Set

  • Front
  • Back
Three requirements for dementia?
Persistent

Decline

Two or more areas of cognitive functioning
What are some different forms of generic dementia?
brain tumors

nutritional disorders (Korsakoff's syndrome)

prion diseases

vascular dementia (problems with supply of blood to the brain) - saw-tooth variability; 25% overlap with Alzheimer's disease

frontal temporal dementia - Pick's disease

Lewy body dementia - in conjunction with Parkinson's Disease

Alzheimer's Disease (50-70%)
Idiopathic disease
don't understand the underlying causes of a certain disease
Greatest risk factor for Alzheimer's Disease?
age (but AD is not a normal condition of aging)

65: 0.5% prevalence
85: 50% prevalence
Does AD shorten lifespan?
yes - survival average is 8-10 years after diagnosis; some patients live for 20 years

death typically occurs as a result of wasting, bladder or respiratory infections, accidents
Who has a higher prevalence of AD - women or men?
WOMEN

also, higher prevalence if the parent with AD was the mother instead of the father
Is AD genetic?
Yes - particularly in aggressive, early-onset dementia

tends to be familial rather than sporadic and the onset can occur in 40's or 50's. Perhaps an autosomal dominant pattern
Genes for early onset AD?
S182 gene, chromosome 14. 40 variations, accounts for about 80% of familial form of early-onset DAT - encodes for presinilin 1. Individuals with the S182 gene = larger amounts of beta-amyloid protein

STM2 gene (similar) - chromosome 1. 2 variations; accounts for most of the rest of the familial form of earl onset DAT - encodes for presinilin 2

Amyloid precursor protein (APP) leads to beta-amyloid protein. gene encoding for APP is on chromosome 21; 10 variations linked to AD; accounts for 2-3% of early-onset AD
Gene for late-onset AD?
apoE gene on chromosome 19

three alleles:

epsilon 2 (10%) - protective?
epsilon 3 (75%) - normal
epsilon 4 (15%) - associated with AD; apoE binds tau protein
apoE?
protein associated with late-onset AD; chromosome 19

apolipoprotein E is the main protein that transports cholesterol into the blood and is involved in fatty acid metabolism in brain and peripheral nervous system. The form of apoE protein formed by the epsilon 4 allele binds to tau protein.
How is AD diagnosed in living
mri scans and repeated neuropsychological testing can diagnose 80%
Two principal morphological changes used to diagnose AD post-mortem
neuritic plaques and neurofibrillary tangles

1. both are found in normal elderly persons but in much larger numbers in AD patients
2. both are abundant in areas such as the hippocampus, neocortex and damygdala --areas one would expect given the cognitive symptoms of AD
3. both are correlated with extent of dementia prior to the patient's death; better correlation for tangles than for plaques
neuritic plaques
extracellular masses consisting of a core of amyloid protein surrounded by what is probably neuritic debris and an outer margin of astrocytes
neurofibrillary tangles
masses of neurofibers occuring in the cytoplasm of neurons - often extending through the cell membrane to the outside of the cell; composed of paired helical filaments containing a lot of tau protein