Test 2 Flashcards
1- What types of cells in the brain are affected in patients with MS? Does MS affect the central or peripheral nervous system?
Oligodendroglial cells
CNS
White matter disease- inflammation of white matter which degrades/ breaks down/ destroys it, forming plaque, causing a loss of myelin, slowing down the brain
2- What affect does heat or pregnancy have on patients with MS?
Heat- (Uhthoff’s symptoms)- worsens MS symptoms
Pregnancy- lessens symptoms or puts into remission
3- Compare the basic differences between the different courses of MS (e.g. relapse remitting, secondary progression, etc).
Relapsing- remitting MS- 25%, unpredictable relapses during which new symptoms appear or existing symptoms become more severe. Can last for days or months, there is partial or total recovery. Disease may be inactive for months or years. Common among younger people. 1 in 4 people have relapse symptoms
Benign MS- 20%, person has one or two attacks with complete recovery. Associated with less severe symptoms at onset and minimal disability. Does NOT come back
Secondary Progressive MS- most common form 40%, initial pattern may be relapsing- remitting, however this is development of progressive disability later in the course of the disease, symptoms do not go away
Primary Progressive MS- 15%, characterized by slow onset and steadily worsening symptoms. Accumulation of deficits and disability. Least common
4- Review effects of genetics and environmental factors on an individual’s chances of developing MS (e.g. temperate climates, race, gender, etc.).
Age of onset- 70% diagnosed between 20-40 years, less common but possible above 60, children are very rare
Race- whites are twice as likely at risk than others, Native Alaskan, Africa, and Scandinavians are extremely low
Gender- females are 2-3 times greater
Environmental- north of equator is 5x at higher risk, if grown up in this area until 16 you are at elevated risk
Genetics- identical twins- 30%, fraternal twins- 4%, 20x (2%) increase risk if immediate family has it
5- What are some hypothesized causes of MS?
Auto-immune disease (killer t-cells may attack myelin) and genetics
6- What symptoms are associated with MS?
Varies from patient to patient
Vision disturbances, *muscle weakness or stiffness, *coordination problems, spasticity, paresthesia, impairment of pain temperature touch sense, pain, ataxia, tremor, speech disturbances, bladder/ bowel dysfunction, depression, cognitive abnormalities, **fatigue/ malaise (feeling unweel)
Attention/concentration, short term memory, information processing, executive function, perception, speech
7- Review frequencies of dementia and cognitive impairment in MS and ALS.
MS- 40-65% have some level of cognitive impairment
ALS- many individuals develop dementia
8- Review the basic symptoms of ALS (e.g. fasciculations, dysphagia, muscle weakness, respiratory failure).
Onset is either in the limbs (75%) or bulbar (throat)
Called Lou Gehris’s Disease
Affects pre-central gyrus (motor movement)
Gray matter neuron disease
Weakness (atrophy), cramping, stiffness and tightness (spasticity), twitches (fasciculation), dysarthia (problems producing speech), chewing and dysphagia (problems eating and swallowing), breathing, hyperreflexia (gag reflex)
9- What is the difference between familial ALS and sporadic ALS?
Familial ALS- inherited, rarer, 5-10%, can inherit SOD1 enzyme
Sporadic ALS- 90-95%, no family history,
If one parent has SOD1 enzyme, 50% chance it can be passed to the child
10- What is the difference between bulbar onset ALS and limb onset ALS?
Limb onset ALS- 75%, symptoms begin in arms or legs
Bulbar onset ALS- symptoms begin with speech or swallowing
Symptoms are a result of muscle weakness and atrophy, they worsen and spread
11- Which neurons in the body are affected by ALS? (Hint: think upper motor vs. lower motor).
Grey matter disease
Upper motor neurons- affects precentral gyrus (controls execution of motor movement, betz cells lost)
Lower motor neurons- ventral horn of the spinal cord (afferent signals that tell body to move)
12- What is an aneurysm, which neuroimaging technique may by useful in making a diagnosis in a living patient, and what treatments are available?
Aneurysm- weak spot on a blood vessel, usually congenital (born with it), ballooning out of a blood vessel, when it breaks is what causes the hemorrhagic stroke, you want to stabilize it, do not do anything to raise blood pressure
Neuroimaging techniques- CT, MRI, **cerebral angiography
Treatments- aneurysm clip, coiling
13- Review the basic differences between embolic and thrombotic strokes.
Thrombotic- stationary clot
Thrombus- buildup of atherosclerosis
Atherosclerosis- happens inside of blood vessels, fatty or plaque buildup, things like high cholesterol, main one*
Stenosis- narrowing of blood vessel
Platelets- they stick together to help stop bleeding
Arteriosclerosis- hardening of arteries, something you see in diabetes or smokers
Embolic- blood clot in motion
Embolus- blockage causing piece of material
Plaque- made up of fat, cholesterol, calcium, and other substances found in the blood
Atrial fibrillation- contraction of the heart that is rapid and irregular, Afib
14- Why is it important to treat a stroke patient with drugs as quickly as possible?
To restore blood flow to the brain to prevent sever and permanent damage as well as possible deaths
Medications thin the blood and dissolve the clot for ischemic strokes
15- What are transient ischemic attacks?
TIAs- mini strokes, not hemorrhagic in nature typically, usually in older people, usually produce isolated symptoms (tingling, dizziness, smell), symptoms resolve, but can add up and cause larger issues, increases risk for major stroke (20-35%), 50,000 diagnosed each year,
Anterior- motor coordination, muscle weakness, problems speaking
Posterior- double vision, dizziness, neglect
*major warning sign because of the fact that they can add up, should be put on blood thinners