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Neurobiology of Learning and Memory
Prof. Anagnostaras
Lecture 10: Alzheimer’s Disease and
Cognitive Decline in Aging
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DementiaA syndrome characterized by a
decline in cognitive functions sufficient to cause impairment in
social and occupational performance
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Risk of Dementia is Risk of Dementia is Unrelenting with AgeUnrelenting with Age
0102030405060708090
100
Percent Impaired
65 to69
70 to74
75 to79
80 to84
85 to99
100 orolder
Age(years)
Percentage of Persons with Moderate to Severe Memory Impairment
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Causes of Dementia
8%5%
5%
7%
10%65%
Alzheimer's Disease (AD): 65%
AD & Vascular: 10%
Lewy body: 7%
AD and Lewy body: 5%
Vascular: 5%
Other: 8%
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Projected Numberof American’s with AD
5.9 6.88.7
11.8
14.3
4
0
4
8
12
16
2000 2010 2020 2030 2040 2050
Year
Millions
Evans, DA, et al. Milbank Quarterly 68:267-289; 1990.
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Prevalence of AD
95+ 53%
90 32%
85 19%
80 9%
AGE
AGE %
65 1
70 2
75 5
80 9
85 18
90 32
95+ 53Source: GAO, January 1998
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Alzheimer’s Disease Outline
Incidence: approx. 4 million Americans
Late onset: 65+ yrs (can occur earlier, but less than 10% of cases do - and in those cases caused by a specific gene mutation)
Women more likely to have it (b/c longer life span)
Can’t be diagnosed for certain until death
Currently linked to several genes (transgenic mouse models)
Terminal disease: live an avg. 8 yrs post-diagnosis
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The Implications of an Aging Society for AD Prevalence
• 40% of persons turning 65 in 2000 will survive to age 85
• 30-50% of persons reaching age 85 will have AD
Source: NEJM, 2000
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Overview• Progressive, degenerative brain disease
characterized by• Increasing memory loss• Other cognitive decline• changes in behavior, personality, judgment
and ADL’s (Activities of Daily Living)• Most common cause of dementia among
people aged 65 or over
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AD Characteristics
•beta amyloid (protein) plaques & neurofibrillary tangles form most prevalently in brain areas assoc. w/memory & cognitive function (entorhinal ctx, hippocampus, frontal ctx, parietal ctx)
•involves death of many cells, but esp. Ach-producing cells in the basal forebrain
•Symptoms: dementia, memory loss, confusion, language loss
•No cure; treat with Ach agonists (help w/early cognitive deficits)
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Ten Early Warning Symptoms
• Memory Loss That Affects Job Skills
• Difficulty Performing Familiar Tasks
• Problems with Language • Disorientation of Time and
Place • Poor or Impaired Judgment
• Problems with Abstract Thinking
• Misplacing Things • Changes in Mood or
Behavior • Changes in Personality • Loss of Initiative
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Severe Alzheimer’s Disease
The person cannot:• Communicate verbally• Understand words or instructions• Recognize self in the mirror or pictures• Recognize family members• Provide care for themselves
Usually die within 15 years(4th leading killer of adults)
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FAS Test
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Alzheimer’s Disease
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Alzheimer’s Disease (degeneration)
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www.ahaf.org/alzdis/about/ BrainAlzheimer.htm
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Alzheimer’s Disease (MRI)
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Alzheimer’s Disease (PET)
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brain scans of a healthyelderly person and apatient with Alzheimer’sdisease
Alzheimer
Normal
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Alzheimer’s Disease (cellular)
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Normal cortex cell
Alzheimer’s cell
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Alzheimer’s disease: plaques & tangles in memory areas
•affects entorhinal ctx (1), then hpc (2), frontal (3), parietal (3) lobes
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Alzheimer’s Disease (plaques & tangles)
Neurons withexternal plaques
Normal neuron
Neuron with internal neurofibrillary tangles(disrupted microtubules)
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Microtubules are “Railroad” for nutrients, NT transport w/i neuron
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Alz Recent Research: Tangles
Tau = protein that keeps microtubules (“RR tracks”) aligned down length of neuron (tau = “RR ties”)
Pts with Alz have problematic tau --> curls & tangles microtubules (“RR tracks in jumble”)
Pin-1 (an enzyme), causes the bending of tau in AlzSO, block Pin-1 --> block problematic tau? Still researching…
Since neurons can’t get nutrients down length of axon…dies
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Alz Recent Research: Plaques
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Amyloid plaquesin human Alz(70 yrs old)
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Amyloid plaquesin transgenic mouse
http://www.newsandevents.utoronto.ca/bin1/001220a3.asp
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Study of Dementia in Swedish Twins – Concordance Rates
Monozygotic(%) Dizygotic(%)
Alzheimer’s disease 75 26All dementias 50 33
781 twins
aged 50 and over
surveyed every three years since 1970’s
Source: J Geront, 1997
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Genetics of Alzheimer's DiseaseGenetics of Alzheimer's DiseaseSeveral genetic Loci in Alzheimer's Disease:• Chromosome 21 (APP) : Early Onset FAD-6/50
amyloid precursor protein--> amyloid beta• Chromosome 1 (PS2) : Volga German FAD
presenilin2 (? -secretase activity)-risk factor• Chromosome 14 (PS1) : Early Onset FAD
presenilin1 (? -secretase activity)-40/44• Chromosome 19: Apo-E4 late onset risk factor
apolipoprotein E4+, E3–, E2 lethalE4- het = 3x, homo = 15x
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Expression profile of AD tangle and normal CA1 neurons (Ginsberg et al, 2000)
Relative expression intensities
Aspirated non-NFT (A) and NFT-bearing (B) CA1 neurons
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Expression of many genes affected in AD (Loring et al, 2001)
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Alz Recent Research: Plaques (cont’d)
•Plaque vaccine for AlzInject Alz (PDAPP) transgenic mice with beta-amyloid vaccine, can prevent plaques in young-aging mice AND can decrease plaques in mice that already have them
Amyloid plaquesin mouse hpc before vaccine
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Amyloid plaquesin mouse after
vaccine
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Schenk, D. et al, 1999,Nature 400 (July 8): 173.
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Schenk(2002)
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Amyloid-beta vaccine and Memory, Morgan et al., Nature, 2000
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Pharmacotherapy• There is no cure yet.• There are three drugs
that AD patient could take to slow the progression.
•They are: tacrine (Cognex), donepezil (Aricept), and rivostigmine (Exxelon).
These drugs are cholinesterase inhibitors
Several new drugs are Ach M1 receptor agonists.
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Normal Aging of the Brain
• Increase in time required to retrieve information
• Less able to register and retain new information
• Decrease in attention and concentration
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Normal Aging Versus Dementia
• Minimal memory impairment
• Little or no progression of impairment
• No functional consequences
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Mild Cognitive Impairment (MCI)
• Subjective memory complaints
• Objective memory impairments
• MMSE 24
• No/minor functional impairment
• No diagnosis of AD
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Annual Rates of Conversion fromMCI to Dementia Over 48 Months
100
0
88
12
76
24
64
36
52
48
0
20
40
60
80
100
MCI, %
0 12 24 36 48
Months
Alzheimer'sdisease
MCI
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Prevalence of Undetected, Mild Cognitive Impairment – Study Population
Mean age (yrs) 76Female (%) 58Education (yrs) 16Mean MMSE 28
N (%)Undetected dementia (n = 200) 22 (11)
Undetected MCI (n = 179) 17 (10)
Source: Hermann, Sager 2002
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Summary
Most cognitive impairments in aging due to dementia or pre-dementia
Most dementia is AD
Large heritable component
Large environmental component - e.g., diet
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Gene expression among mice of same strain, age, sex, housingGene expression among mice of same strain, age, sex, housing[6584 possible genes] (Lockhart & Barlow, 2001)[6584 possible genes] (Lockhart & Barlow, 2001)
Ignore this slide!!