PD Flashcards

1
Q

Striatum Lentiform Nucleus

A

Striatum = caudate and putamen LN = GP and putamen

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2
Q

Communication of motor planning areas:

A

Cerebral cortex - thalamus - pedunculopontine nucleus - LMN

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3
Q

GABA, Glutamate, and Dopamine (I or E)

A

GABA - Glutamate + Dopamine -+

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4
Q

Percentage of dopaminergic neuro loss before sxs present:

A

60-80%

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5
Q

Epidemiology: Age, ethnicity, and sex

A

Age - peak onset is 60 Ethnicity - Caucasians > African Americans Sex - Males > females

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6
Q

Percentages of sporadic vs genetic PD

A

Sporadic - 90% Genetic - 10%

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7
Q

Etiology of sporadic PD

A

Oxidative stress Mitochondrial malfunction Inadequate neurotrophic factors Inflammatory glia

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8
Q

Occupations factors in PD

A

Pesticides, herbicides, heavy metals

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9
Q

Tobacco, coffee, alcohol factors in PD

A

Smoking - inverse Coffee - inverse Alcohol - possible inverse

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10
Q

Dietary factors in PD - Antioxidants, unsaturated fatty acids, dairy, dietary iron

A

A - may neutralize free radicles U - inverse Milk - positive Iron - possible positive, inconsistent

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11
Q

Causative genes for PD

A

Atypical presentation - young onset (<50), dystopia, early dementia

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12
Q

Susceptibility genes of PD

A

Complex interaction of environment and genetic factors

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13
Q

Cardinal signs

A

Tremor Rigidity Bradykinesia Poor posture

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14
Q

Tremor

A

Begins unilaterally, present in 70% of time

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15
Q

Rigidity

A

Initially affects proximal musculature and extends dismally

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16
Q

Aminesia/bradykinesia

A

A - loss of movement B - slowness of movement

17
Q

Dystopia

A

Repetitive movements and spasms - common in toes/foot

18
Q

Hypomima

A

Masked face

19
Q

Non-motor symptoms

A

Sleep disturbances Mood disorders (depression) Dysautonomia (OH) Constipation *Typically proceeds motor symptoms by years

20
Q

Dementia

A

Common in the later stages of PD

21
Q

Dementia with Lewy bodies

A
  • Progressive dementia with impairments in attention and executive function - Fluctuating cognition - Visual hallucinations
22
Q

Primary PD

A
  • 85% of all cases - Unilateral onset that professes slowly
23
Q

Subtypes of primary PD: Tremor and postural instability/gait disturbance

A

Tremor - Earlier age onset - Slower progression - More favorable prognosis Postural instability/gait - Severe cognitive dysfunction - Rapid progression - Poor prognosis

24
Q

Two variants of postural instability/gait disturbance PD

A

Postural instability with falling (PIF) Freezing of gait (FOG)

25
Q

Dx of PD

A
  • 2/4 symptoms present - Positive response to levodopa
26
Q

Vascular Parkinsonism

A
  • One or small strokes - LEs are more affected - Resting tremor not common
27
Q

Drug-induced Parkinsonism

A

-Caused my neuroleptic/anti-psychotic mess - Symmetrical presentation - Tardive/Orolingual dyskinesia - Ceasing meds can reverse sxs but can take up to 2 years

28
Q

Toxins - secondary Parkinsonism

A
  • Carbon monoxide - Heavy metals - Mercury
29
Q

Progressive supranuclear palsy

A
  • Postural instability and falls - Vertical gaze paresis - Difficulty controlling eyes (stare) - Median survival time: 5.3 years
30
Q

Multiple systems atrophy

A
  • Parkinsonism along with autonomic/cerebellum dysfunction - Median survival time: 8.5 years
31
Q

Corticobasalganglionic degeneration

A
  • Focal rigidity with limb apraxia - Alien hand syndrome - Median survival time: 6-8 years
32
Q

Median survival time of idiopathic PD

A

15.8 years with PNA being most common reason of death

33
Q

Negative prognostic factors

A
  • Younger age of onset - Early cognitive involvement - Lack of tremor at onset = PIGD
34
Q

Direct pathway

A
35
Q

Indirect pathway

A
36
Q

Modified Hoehn and YahrScale

A
37
Q

Unified Parkinson’s Disease Rating Scale

A