multiple sclerosis Flashcards

1
Q

what is multiple sclerosis?

A

an autoimmune disease where the myelin sheath on myelinated fibers in the CNS are targeted

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2
Q

who are more likely to develop MS and when?

A

women are 2x more likely and the onset is typically 20-40 years
-caucasians more likely and COLDER regions (lol why)

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3
Q

myelinated fibers=

A

faster travel
unmyelinated= still normal
DEMYELINATED= not normal

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4
Q

etiology of MS?

A

it is unclear but there is STRONG familial tendency (15x more likely to develop)
-genetic susceptibility: MHC/HLA
hla= human leukocyte antigen
hla= gene complex that encodes for the MHC
gla on MHC 1 and 2
hla brings fragments of the virus to the surface of the cell so that the cell can be destroyed, the fragments are presented on MHC1
-viral trigger as well
-environmental factors
-complex trait etiology: multifactoral, polygenic

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5
Q

viral trigger for MS?

A

epstein barr virus—> much like in RF, the infection by EBV can bring on autoimmunity. An IR is triggered but once infection is cleared our defence cells continue to attack and kill self-antigens
in this case the brain

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6
Q

pathology of MS?

A
  • demyelinated fibers= slower, AP
  • antigens in myelin sheath are targeted by self antibodies
  • demyelination occurs in patches (irregular pattern)—> patches (plaques)
  • demyelination causes inflammation and damage, resulting in impaired impulse transmission and problems with conduction
  • oligodendrocyte necrosis (cells in CNS that produce myelin)
  • the location of demyelination varies
  • lymphocyte and macrophage infiltration: aka sclerotic patches
  • motor AND sensory neurons affected
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7
Q

most common locations of demylination

A

optic nerve, periventricular region, cerebellum, spinal cord, brain stem

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8
Q

manifestations of MS?

A

depends on stage of disease, location of plaques within brain and extent of demyelination

  • fatigue, visual impairment, paresthesia (abnormal sensations)
  • bowel and bladder dysfunction
  • decreased muscle strength
  • coordination and gait problems
  • chronic exacerbation and remission
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9
Q

chronic exacerbation and remission in MS?

A

very specific to this disease! periods of exacerbation: necrosis of oligodendrocytes and demyelination furthers
-in remission, presence of antibodies decrease and less t cell and macrophage infiltration, short lived usually

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10
Q

diagnosis of MS?

A
  • clinical presentation and history of exacerbations and remissions
  • MRI: identify areas of demyelination (plaques) their location and extent of damage
  • Labs: to exclude other causes of symptoms
  • CSF analysis: increased protein content, increased igG Ab d/t targeting self-antigens
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11
Q

treatment of MS?

A

-degenerative disease that often results in acute manifestations following a period of remission
-persistent relapses are treated w/ different drugs
-suppress immune response with steroids and to decrease inflammation
-steroids for relapse (+ interferon)
an interferon is a naturally occuring protein by IS, antiviral agent is not needed here, but the antinflam and immunoregulatory (suppress ab and t cells)

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12
Q

what drug is used for MS?

A

METHOTREXATE

  • this is preferred over interferons if possible
  • antifolate drug: side effect is inhibition of DNA replication, halting RBC and WBC production–> need folic supplement
  • typically give them the prescription, then rest of the week take folic acid
  • hepatotoxic (test liver fx)
  • CBC
  • symptoms (bowel and bladder dysfunction)
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