past present in dementia, 2013

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    From Past to Present

    The Historical note andDementia Burden

    Surat Tanprawate*, MD, MSc(Lond.), FRCP(T)Chiang Mai University

    *Certificate in History of Medicine, Birkbeck University, London

    *Wellcome Medical History Library2013 Lecture for Dementia Better Care, Chiang Mai, Thailand

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    Man fools himself.He prays for a long life,yet he fears an old age.

    Chinese Proverb

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    Longevity

    Shigechiyo Izumi, Japan

    29th June 186521st February

    1986 Age: 120 years 237 days

    Sarah Knauss, America

    24th September 1880

    30th December1999 Age: 119 years 97 days

    Maria Esther Heredia de Capovilla,

    Ecuador

    14th September 1889

    27th August2006 Age: 116 years 347 days

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    Human Life Expectancy At Birth

    Adapted from: Hayflick L. How and Why We Age. 1994

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    Life Expectancy at Age 65

    1965.5 years

    2005.20 years

    Worldwide over 1/2 of all humans whohave ever lived to age 65 are alive today!

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    Senile

    The world is rapidly becoming geriatric

    Latin root, sen in senile meanspertaining to old age, not demented!

    Gerontology is the study of aging Geriatrics is the medical care of the aged

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    Prevalence of dementia in 6 WHO world regions(based on data extracted from Global prevalence of dementia: a Delphi consensus study)

    Ferri et al. Lancet 2005; 366: 21117)

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    (b) Causes of dementia in patients > 70 years or older(a) Causes of dementia in patients < 70 years old.

    A Canadian cohort study of cognitive impairment and related dementias (ACCORD)Neuroepidemiology2003; 22: 26574).

    Cause of Dementia

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    Dementia booming of the

    aging baby boomers

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    Historical noteThe past make the future

    The Historical Note The discovery of Alzheimers disease

    The plaque, the tangle and Amyloid cascade Genetic breakthrough

    The diagnosis, and treatment

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    A 100 year journey fromdiscovery to treatment

    Auguste D (1906)

    Alois Alzheimer

    German psychiatrist

    Auguste D hand writing

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    A 100 year journey fromdiscovery to treatment

    In November 1906, at a Germanpsychiatrists meeting,Alois Alzheimerpresented the pathological findings on abrain of a 56 y.o. woman who died aftera progressive dementia

    Auguste D (1906)

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    Bielschowsky-stained tissue

    sections

    Bielschowsky-stained amyloid plaques from Auguste D

    Bielschowsky-stained neurofibrillarytangles from Auguste D

    Drawing of neurofibrillary tangle byAlois Alzheimer

    Alois Alzheimer: ThePsychiatrist with theMicroscope

    Auguste D

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    Johann F (1911): The secondcase from Alois AlzheimerReport

    Bielschowsky-stained tissue sections from Johann F.

    Cerebral cortex Bielschowsky-stainedamyloid plaques

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    Ultrastructural studiesof AD pathology

    a neurofibrillary tangle contains masses

    of fibers with a periodic structure

    paired helical filamentsearly 1960s

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    Amyloid cascade hypothesis

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    The history-continue

    1983:Coyle et al: Acetylcholine deficit inthe cortex

    1995: the first gene abnormalities infamilial Alzheimer disease are identified(Presenilin 1 & 2)

    Individual with trisomy 21 (Downs syndrome) exhibit high

    prevalence rates of AD neuropathology.

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    Mild, Moderate & Severe stages

    Mild Moderate Severe

    Memory loss

    Language

    problems

    Mood swings

    Personality

    changes

    Diminished

    judgment

    Behavioral, personality

    changes

    Unable to learn/recall

    new information

    Long-term memory affected

    Wandering, agitation,

    aggression, confusion

    Require assistance w/ADL

    Gait, incontinence,

    motor disturbances

    Bedridden

    Unable to perform ADL

    Placement in

    long-term care

    needed

    Dementia/Alzheimers

    Stage

    Symptoms

    Volicer L. Clin Geriatr Med. 2001;17:377-391.

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    William Utermohlen -self portraits

    WU a patient with AD at the DRC - was aware of decline in his painting skills

    Progressive decline in cognitive functions

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    Neuroimaging methods

    (a) Computed tomography (CT)

    (b) magnetic resonance (MR)

    (c) positron emission tomography(PET)

    (d) single photon emission CT

    (SPECT)

    (e) functional MRI (fMRI).

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