1. Dayna Ryan, PT, DPT Winter 2012

2.  Primarily known as a disease of CNS myelin (demyelination)  Recent evidence shows early involvement of CNS axons as well Lesions numerous in cerebrum, brainstem, cerebellum, SC, optic nerve and chiasm

3. Bright spots are areas of plaques http://www.nationalmssociety.org

4.  Autoimmune  Infectious agent, viral or bacterial  Environment has an effect with higher incidence in the Northern U.S.  migration south before age 15 decreases the risk  may be related to decreased vitamin D generation in more wintery climates  Genetic link makes people more susceptible to the disease  Recent evidence (2010): increased risk of developing MS after Epstein-Barr Virus infection

5. Dysregulation of Immune response Inflammation of CNS Degeneration Mylin of CNS

6. 1. Peripheral activation of T cells 2. Adhesion to endothelial cell wall 3. Chemo-attraction 4. Invasion through blood-brain barrier 5. Reactivation in CNS – can damage myelin and axons

8.  Possible link with Vitamin D and amount of sunlight exposure at different latitudes  Possible link with infectious diseases From: http://www.mult-sclerosis.org/ms_world.html

9.  Motor:  Spasticity  Weakness  Coordination (cerebellar)  Sensory  Paresthesias  Numbness  Visual (optic neuritis) Scotoma (blind spot) Diplopia  Nystagmus  Cognitive changes  Depression  Fatigue  Often most disabling condition  Sleep disorders  Autonomic  Pulmonary dysfunction

10.  Brainstem S/S  Gaze palsies  Nystagmus (if CN VIII involved)  Dysarthria  Vertigo  Cerebellar S/S  Hypotonia  Dysarthria  Ataxia  Decreased coordination  Trunk weakness  Postural and movement disorders

11.  Cerebral S/S  Optic neuritis – plaques commonly occur on CN II May cause unilateral vision loss, often with pain in the eye Scotoma = blind spots Blurred vision or diplopia  can become blind Abnormal visual fields  Depression  Progressive cognitive dysfunction Memory loss Loss of higher order functioning

12.  Before the advent of MRI, diagnosis would not occur until several instances of MS occurred over a period of years.  Some patients reported a time lag of up to 15 years from the onset of symptoms to the time of diagnosis.  As late as 1998, the average time from onset of symptoms to time of diagnosis was approximately 4 years (Ebers GC & Sadovnick AD 1998).

13.  Patient history  MRI  Increased levels of immunoglobulin G (IgG) in the cerebrospinal fluid  The diagnosis of MS is only given to patients who either have persistent symptoms of MS with MRI evidence of MS plaques or to patients who have repeated exacerbations with MRI evidence of MS plaques.  Kurtzke Expanded Disability Status Scale

17.  Diagnosis of CIS given to patients who present with first incident of neurologic symptoms that last at least 24 hours and are caused by inflammation/demyelination in one or more areas of the CNS  People with CIS who have brain lesions on MRI are at high risk of having a 2nd neurologic episode and being diagnosed with MS  Risk of being diagnosed with MS is lower for if no MRI evidence of neurologic lesions.

18. Relapsing-Remitting  Clearly defined flare-ups (relapses) or episodes of acute worsening of neurologic function  These are followed by partial or complete recovery periods (remissions) between attacks that are free of disease progression  Most common form of MS at time of initial diagnosis (Approximately 85% at onset)

19. Secondary Progressive  Initial period of relapsing- remitting disease followed by a steady worsening disease course with or without occasional flare- ups, minor remissions (recoveries) or plateaus  If left untreated, 50% of people with relapsing- remitting MS develop this form of the disease within 10 years of initial diagnosis

20. Pre-Clinical Relapsing- Remitting Secondary Progressive Exacerbation Nerve Cell Loss Relapsing – Remitting MS Progression

21. Primary Progressive  Nearly continuous worsening of disease from the onset, with no distinct relapses or remissions  Many variations in rate of progression over time, occasional plateaus, and temporary minor improvements  Relatively rare - Approximately 10% at onset

22. Progressive Relapsing  Steadily worsening disease from the onset  Also have clear acute flare- ups (relapses), with or without recovery  In contrast to relapsing- remitting MS, the periods between relapses are characterized by continuing disease progression  Relatively rare – approximately 5% at onset

23.  Average time spent in each EDSS level Below is a graph showing the average time a person spends in each EDSS level. http://www.mult-sclerosis.org/expandeddisabilitystatusscale.html

24.  Avonex (Interferon beta 1-a)  weekly intermuscular injections  Betaseron (Interferon beta 1-b)  subcutaneous injection every other day  Rebif (Interferon beta 1-a)  Subcutaneous injections 3x/week  Common side effects:  Flu-like symptoms (headache, fatigue, muscle aches, fever)  Depression/anxiety  Liver problems  Blood problems  Thyroid problems  Allergic problems  Seizures (Avonex)

25.  Copaxone (glutimer acetate)  Daily subcutaneous injections  Novantrone (mitroxantrone)  Intervenous injections every 3 months for max of 2-3 years  Tysabri (natalizumab)  Intervenous infusion every 4 weeks

26.  Spasticity  Baclofen  Bladder problems  Cholinergics  Depression  Anti-depressants  Fatigue  Anti-depressants  Heat sensitivity  Fans  Good hydration  Cooling vests

27.  Acupuncture  Bee venom therapy  Marijuana  Yoga  Tai Chi  Reiki  Polarity therapy  Mushrooms  Herbs  Frequently used  Need to ask about these when taking history

28.  Course is highly variable across patients  Life span modestly reduced on average  Mean of one exacerbation per year (more frequent earlier in disease)  Exacerbations commonly occur following viral infections  Approximately 2/3 of patients with MS develop a progressive phase with residual disabilities  In 50% of cases, cause of death is attributable to MS (pneumonia, pulmonary embolism, bacterial sepsis from UTI or decubiti)

29.  Better prognosis with:  Acute onset  Female gender  Younger age of onset  Higher degree of remission after 1 st attack  Initial presentation limited to eyes or sensory symptoms  Initial attack limited to one area of the CNS  Worse prognosis with:  Onset after age 35  Early cerebellar or lower brainstem symptoms  Primary progressive course occurs  More lesions in initial MRI

30.  National Multiple Sclerosis Society http://www.nationalmssociety.org/index.aspx http://www.nationalmssociety.org/index.aspx  Multiple Sclerosis Association of America http://www.msassociation.org/  Multiple Sclerosis Foundation http://www.msfocus.org/