ALS Flashcards

1
Q

definition of ALS

A

–rare, progressive neuro disorder characterized by the loss of motor neurons

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2
Q

survival for ALS patients

A

–death usually occurs around 3 years after diagnosis
–fatal due to respiratory failure

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3
Q

etiology of ALS

A

unknown

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4
Q

risk factors for ALS

A

–age: 40-70
–male
–genetics
–smoking

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5
Q

patho of ALS

A

–motor neurons in the brainstem and spinal cord gradually degenerate
–axonal degeneration, demyelination, and sclerosis/scarring occurs
–electrical and chemical messages from the brain do not reach the muscles

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6
Q

what is the end result of ALS patho?

A

dead neurons

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7
Q

what could cause ALS?

A

excitotoxicity hypothesis

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8
Q

excitotoxicity hypothesis

A

excessive levels of glutamate initiates a cascade of events that lead to neuron death

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9
Q

glutamate

A

excitatory neurotransmitter

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10
Q

why do we think excitotoxicity hypothesis plays a role?

A

–elevated glutamate levels in the CSF
–antiglutaminergic drug improves survival

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11
Q

symptoms of ALS

A

–weakness of upper extremities
–dysarthria, dysphagia, drooling
–cognitive and behavioral changes
–constipation
–sleep problems
–breathing

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12
Q

what occurs with upper extremity weakness in ALS?

A

–muscle wasting
–spasticity
spinal form of ALS

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13
Q

classification of riluzole

A

glutamate inhibitor

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14
Q

therapeutic indication for riluzole

A

only drug approved for ALS

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15
Q

MOA of riluzole

A

–glutamate agonist
–reduces damage to motor neurons

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16
Q

side effects of riluzole

A

–dizziness
–GI upset
–hepatotoxicity

17
Q

does riluzole increase life expectancy?

A

yes (by 3-6 months)