multiple sclerosis Flashcards
what is multiple sclerosis?
an autoimmune disease where the myelin sheath on myelinated fibers in the CNS are targeted
who are more likely to develop MS and when?
women are 2x more likely and the onset is typically 20-40 years
-caucasians more likely and COLDER regions (lol why)
myelinated fibers=
faster travel
unmyelinated= still normal
DEMYELINATED= not normal
etiology of MS?
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
viral trigger for MS?
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
pathology of MS?
- 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
most common locations of demylination
optic nerve, periventricular region, cerebellum, spinal cord, brain stem
manifestations of MS?
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
chronic exacerbation and remission in MS?
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
diagnosis of MS?
- 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
treatment of MS?
-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)
what drug is used for MS?
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)