ALS - faculty at Chemeketa
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Transcript ALS - faculty at Chemeketa
ALS
Kate Crain
Amyotrophic Lateral Sclerosis
Lou Gehrig Disease
Charcot’s Syndrome
A brief history
Discovered in 1874 by French physician
J.M. Charcot.
Was thought to be caused by the same
virus as Polio.
Maybe its an environmental toxin
causing it?
An extremely high incidence observed in
Guam and trust territories of the Pacific
in the 1950’s.
What is ALS?
• Classified as a Motor Neuron Disorder.
• Progressive neurodegenerative disease
that effects nerve cells in the brain and
spinal cord.
• A-myo-trophic means no muscle
nourishment. Lateral identifies areas of
spinal cord where nerve cells that control
muscles are located. Sclerosis is
hardening or scarring.
Neuron is damaged and the signal to
the muscle is cut off causing
muscular atrophy.
Effects muscles innervated by the
cranial nerves and corticobulbar
tracts.
Involuntary muscles not effected.
Does not effect Heart, Brain, and
sexual organ function.
Three Classifications
Sporadic - Most common, occurring in
90 - 95% of cases.
Familial - When more than one case
occurs in a family, (Possibly genetic
dominant inheritance) 50% chance
offspring will inherit it in these families.
Guamanian - Isolated to those in Guam
and Japan.
Present research
Exact cause is still unknown.
Presently thought to be an
autoimmune disease, however…
Also thought to be the possible
result of excessive levels of
Glutamate in the brain.
What is Glutamate?
Glutamic Acid creates the taste
umami.
Found in muscles, brain, kidneys,
and liver for metabolism.
Non-essential Amino Acid.
Breaks down food and builds up
tissue.
Too much is found to be toxic.
Glutamate and ALS?
Elevated levels have been found in
the ICF of some ALS patients.
Experiments have found The
Glutamate Regulating Protein
missing or ineffective in Some
patients.
Exact link is still unknown.
Who is at risk?
Exact risk factors are still a mystery.
5,600 people are diagnosed each year.
As many as 30,000 Americans have ALS
at any given time.
60% of ALS patients are men.
93% of patients are white.
Most patients are between 40 - 70 years
old at diagnosis, average age is 55.
Life Expectancy
Most live 3 years after diagnosis.
Up to 10% live longer than 10
years.
In rare cases, the disorder will halt
or remit symptoms.
Diagnosing ALS
Hard to diagnose.
No exact test, must rule out
everything else.
Testing includes MRI, EMG, blood
and urine studies, spinal tap, muscle
and/or nerve biopsy.
Many diseases mimic ALS.
Signs and Symptoms
Weakness in hands
and feet
Fasciculations,
spastic, hyperactive
deep tendon reflexes
Clumsiness
Slurred speech
Dysphagia
Fatigue
Difficult
controlling facial
expressions and
tongue
Stiffness in
movements
Uncontrolled
laughter or crying
Cramps
Signs and Symptoms
Onset is so slight it may be
overlooked.
Muscle weakness is initial symptom
in 60% of patients.
Early Dysphagia is poor prognosis
due to complications with airway
and aspiration.
Treatment
Physical Therapy
Occupational therapy
Help with eating and drink may
become necessary
Respiratory support may become
necessary
BiPAP
Better living through
Chemistry?
Baclofen may help spasticity
Quinine or Phentyloin may help
cramps
Anticholenergics may help saliva
production
Pain management
Riluzole
Neuroprotective
Still not fully understood.
Inhibits Glutamate release, inactivation of
voltage-dependant Sodium Channels.
Not a cure, but helps in Bulbar-varient ALS.
Myotropin
In “Investigational New Drug”
status with FDA.
Recombinant Insulin-like growth
factor that seems to prevent neuron
loss and promote neuron
regeneration in animal studies.
Lou Gehrig
June 19, 1903 June 2, 1941
“Iron Horse”
1939 was his last
season with the
Yankees
Morrie Schwartz
Philosophy professor
at Brandeis
University
Interviewed by Ted
Koppel in a series on
“Nightline”
Subject of Tuesdays
With Morrie
Stephen Hawking
A Brief History
Of Time.
Black Holes and
Baby Universes.
The Universe in a
Nutshell.
Diagnosed at 21
Father of three
after diagnosis
ALS is not contagious
Thank you!