Lecture 5: MS Flashcards

1
Q

Demyelination

A

disruption of myelin that coats neurons; makes the AP transmit slower

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2
Q

Multiple sclerosis definition

A

an idiopathic inflammatory demyelinating dz of CNS ; caused by an autoimmune attack on oligodendrocytes

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3
Q

Hallmark of MS

A

multiple scarred foci (plaques) with in the white matter of CNS and perivenular inflammation
-lesions primarily in white matter

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4
Q

MS Pathophysiology:

A

under inflammatory cndtns T cells, B cells, macrophages, granulocytes cross BBB and enter CNS; once inside target self antigens on oligodendrocytes, decreasing myelin production

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5
Q

Demographics of MS

A
  • age preference: 15-55
  • gender preference: females = 2:1
  • Genetics
  • Environment: born in northern states: 3x higher likelihood
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6
Q

Sx’s of MS: Episodic relapses

A
  • occur during different periods, but are short lived
  • progress over hrs to days
  • improve over days to weeks
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7
Q

Chronic Sx’s of MS

A

heat sensitivity; bowel/bladder/sexual dysfxn; fatigue; mood disorders; cognitive dysfxn; gait impairment

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8
Q

Most common Sx’s of MS

A

Limb sensory loss
Visual Loss: optic neuritis
Other: subacute weakness, diplopia, gait disturbance; balance probs; acute weakness

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9
Q

Transverse myelitis

A
  • sensory loss in one or both limbs
  • L’hermitte’s phenomenon: when flex neck have sharp shooting tingling down length of spinal cord
  • MS hug: feeling of tightness around chest
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10
Q

Optic neuritis

A
  • eye pain; decrease acuity

- optic disc edema

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11
Q

Dx of MS: 2 things must have

A

1) dissemination in space

2) dissemination in time

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12
Q

MS MRI

A
  • diagnostic test of choice

- T2/Flair: lesions are hyper intense; found periventricularly, juxtacortical, infratentorial or spinal cord

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13
Q

Dissemination in time

A

at least 2 lesions in locations typical for MS

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14
Q

Dissemination in space

A

either clinically or on
MRI: T2/Flair: hyperintense lesions with simultaneous enhancing lesions or see hyper intense lesions or enhancing lesions on F/U

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15
Q

Other diagnostic tools

A
  • LP

- Evoked Potentials

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16
Q

MS on LP

A
  • see oligoclonal bands in CSF: represents increased synthesis of ABs with limited # of responsible antigens in CSF
  • also see IgG in CSF
17
Q

MS Evoked Potentials

A

visual stimulation are presented and electrical impulse over primary visual cortex are recorded
-VEp will show increased latency suggesting signal thru optic nerve is slowed = optic neuritis

18
Q

Types of MS

A

1) Benign
2) Relapsing-Remitting
3) Primary progressive
4) Secondary progressive
5) Progressive Relapsing

19
Q

Relapsing-Remitting MS

A
  • multiple episodes of transient neuro dysfxn which may or may not completely resolve
  • But NO progressions btwn attacks = whatever disability had prior to attacks remains the same
20
Q

Primary Progressive

A

dz progresses relentlessly from onset

steady increase in disability w/out attacks

21
Q

Secondary Progressive

A

pts with relapsing remitting start to have progression btwn attacks; usually occurs after 17 yrs

22
Q

Progressive Relapsing

A

usually have relentless progression from onset but may have rare clinical relapses

23
Q

Clinically Isolate MS

A

First attack of MS

-2 common clinically isolated syndromes: optic neuritis and transverse myelitis

24
Q

Acute Relapse Tx of MS

A

IV methylprednisone

Plasma Exchange

25
Q

Dz Modifying Tx;s

A
  • Interferon Beta 1a: avonex, rabif
  • Interferon Beta 1b: Betaseron, extavia
  • Copaxone
  • *all have side effects
26
Q

Second line Agents

A

Mitoxantone

Natalizumab

27
Q

Oral Agents

A

Flingolimod
teriflunomide
dimethyl fumurate