Transcript Parkinson`s Disease

PARKINSON’S DISEASE
TOPICS TO BE DISCUSSED
1.
Definition
2.
Epidemiology
3.
Etiology
4.
Risk factor
5.
Types
6.
Signs and Symptoms
7.
Pathophysiology
8.
Staging
9.
Complications
10.
Diagnosis
11.
Pharmacotherapy
DEFINITION
Parkinson’s disease (PD) is a slow, progressive,
neurodegenerative disease of the extrapyramidal
motor system.
 Dopamine neurons in the substantia nigra are
primarily affected, and degeneration of these
neurons causes a disruption in the ability to
generate body movements.
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EPIDEMIOLOGY
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PD already the second most common neurodegenerative disease of
mid-to-late life in developed countries, will become increasingly
prevalent in developed countries in this century.
In India PD has a low prevalence except in the small Parsi
community.
In United States (US) and Western Europe.
Age
Incidence
60 – 69year
~1 in 200
70’s
~1 in 100
80’s
~1 in 35
An estimate of approximately 10million people worldwide are
living with Parkinson’s Disease.
PREVALENCE OF PARKINSON’S DISEASE
ETIOLOGY
1. Age – more than 60years.
2. Positive family history and Race.
3. Environmental Exposure: Herbicide and pesticide
exposure, metals ( manganese, iron) and steel alloy
industries.
4. Exposure to MPTP (1- methyl-4-phenyl-1,2,3,6
tetrahydropyridine), a potent neurotoxin.
5. Environmental factors such as rural living, drinking
well water.
6. Life experiences (trauma,emotional stress).
7. An INVERSE correlation between cigarette smoking
and caffeine intake in case-control studies.
RISK FACTOR
Age. Young adults rarely experience Parkinson's
disease. It ordinarily begins in middle or late life, and
the risk increases with age. People usually develop
the disease around age 60 or older.
 Heredity. Having a close relative with Parkinson's
disease increases the chances that you'll develop the
disease. However, your risks are still small unless
you have many relatives in your family with
Parkinson's disease.
 Sex. Men are more likely to develop Parkinson's
disease than are women.
 Exposure to toxins. Ongoing exposure to herbicides
and pesticides may put you at a slightly increased
risk of Parkinson's disease.

TYPES
1.
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2.
•
Primary or Idiopathic Parkinsonism
The cause of the disease is unknown.
Predominantly affecting the individuals over 60years of age.
Over the years the dopaminergic neurons degenerate due to
H2O2 and free radicals such as O2-(superoxide) and OONO(Peroxynitrite).
Secondary or Drug Induced Parkinsonism
There is no degeneration as seen in above case, but the
decrease ion dopamine is drug induced.
SIGNS AND SYMPTOMS
SIGNS AND SYMPTOMS (SSS)
1.
2.
3.
4.
5.
Increased muscular stimulation
leading to involuntary tremors
which occurs when the person
sits or even at rest(resting
tremors).
Typical pill rolling movement of
fingers and nodding of head
Bradykinesia- Difficulty and
slowness of movements.
Rigidity of muscles leading to
masked appearance of face.
Jerk
during
voluntary
movements.
6.
Aphonia- loss of voluntary control of
muscles of mouth and larynx leading to loss
of speech.
7. Posture and Gait:
- Gait is characterized by short
steps,with feet barely leaving the groung,
producing an audible shuffling noise.
- Stooping posture- forward flexed
posture
- Dystonia- Abnormal, sustained, painful
twisting
muscle
contractions,
often
affecting the foot and ankle.
8. Excessive secretion of salivary glands i.e
sialorrhoea and sebaceous glands
i.e seborrhoea
9. Absence of control over movements of eye.
10. Memory Disorder, loss of personal interest,
loss of reasoning and orientation.
PATHOPHYSIOLOGY
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The dopaminergic neuron from substantia nigra pars
compacta act on excitatory D1 receptors in the striatum and
causes excitation of the striatal neurons in the direct
pathway.
The excitation is neutralized when the dopaminergic neurons
from the substantia nigra pars compacta act on inhibitory D2
receptors in the stratum and cause the inhibition of the
striatal neurons in the indirect pathway.
In direct pathway, the globus pallidus medial is innervated
via inhibitory GABAergic neurons from the striatum.
Similarly, the neurotransmission from this region to the
thalamus is also carried out by inhibitory GABAergic
neurons.
However, the nervous innervation from the thalamus to the
cortex is via the excitatory glutaminergic neurons which
results in voluntary movements
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In the indirect pathway,similar to the direct pathway,the
nervous innervation from the striatum to globus pallidum
lateral from these regions to subthalmic nucleus is through
inhibitory GABAergic neurons.But the transmission from the
subthalmic nucleus to globus pallidus medial is through
excitatory glutaminergic neurons.
The basic difference between two pathways is the type of
innervation to the two mentioned regions(globus pallidus
medials and substantia nigra par reticulus).
In direct pathway the innervation is inhibitory while in
indirect pathway it is excitatory in nature.
Hence any alterations in the innervation to the globus pallidus
medial and substantia nigra par reticulata ultimately affect
the neurotransmission to the cortex, which results in either
enhancement or suppression of voluntary movements.
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Physiologically,dopamine causes the activation of direct
pathway and inhibition of indirect pathway.
This results in excitation of cortex,leading to voluntary
movements.
In parkinsonism,where the dopamine gets depleted due to
destrution of dopaminergic neurons,the direct pathway get
suppressed while the indirect pathway get
overstimulated.This leads to decreased excitatory outflow
to the motor cortex resulting in the suppression of
voluntary movements
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Clinical features don’t emerge until >60-80% dopamine lost.
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Compensatory changes include hyperactivity in remaining
neurons (increased transmitter turnover), increase in
dopamine receptors; receptor supersensitivity.
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Other pigmented nuclei also affected (locus ceruleus and
raphe). Also cortex and other structures affected.
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Characteristic histological inclusion in affected neurons are
eosinophilic cytoplasmic inclusions in nigral cells called the
Lewy Bodies.
 Basal Ganglia
 Controls movement
 Dopamine
 Inhibitory
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neurotransmitter in the
basal ganglia
Acetylcholine
 Excitatory
neurotransmitter in the
basal ganglia
Without dopamine,
inhibitory influences are
lost and excitatory
mechanisms are
unopposed 
Neurons of basal ganglia
are over stimulated 
Excess muscle tone,
tremors & rigidity.
HOEHN AND YAHR STAGING OF PARKINSON'S
DISEASE
1.
Stage 1: Mild signs and symptoms on one side only, not
disabling but friends notice.
2.
Stage 2: Symptoms are bilateral, minimal disability, posture
and gait affected
3.
Stage 3: Significant slowing, dysfunction that is moderately
severe
4.
Stage 4: Severe symptoms, walking limited, rigidity,
bradykinesia, unable to live alone
5.
Stage 5: Cachectic, complete invalidism, unable to stand,
walk, require nursing care
COMPLICATIONS
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Thinking difficulties.
Depression and emotional changes..
Swallowing problems. .
Sleep problems and sleep disorders.
Bladder problems
Constipation
You may also experience:
 Blood pressure changes.
 Smell dysfunction.
 Fatigue
 Pain.
 Sexual dysfunction
DIAGNOSIS
1.
Neurological History
2.
Response to levodopa
3.
Imaging and Laboratory examination
4.
Physical Examination
DIAGNOSIS
There are no standard diagnostic tests for Parkinson’s.
1. Neurological History
 The doctor looks to see if your expression is animated.
 Your arms are observed for tremor, which is present either
when they are at rest, or extended.
 Is there stiffness in your limbs or neck?
 Can you rise from a chair easily?
 Do you walk normally or with short steps, and do your arms
swing symmetrically? The doctor will pull you backwards.
 How quickly are you able to regain your balance?
2. Response to levodopa
 A person’s good response to levodopa (which temporarily
restores dopamine action in the brain) may support the
diagnosis.
The main role of any additional testing is to exclude other diseases
that imitate Parkinson’s disease, such as stroke or hydrocephalus.
3. Imaging and Laboratory examination
a.
Blood test - usually to rule out any other condition, such as
abnormal thyroid hormone levels or liver damage.
b. MRI or CT scan - to check for signs of a stroke or brain tumor. If
there is/was no stroke or brain tumor, most MRI or CT scans of
people with Parkinson’s disease will appear normal.
c. PET (positron emission tomography) scan –
this imaging test may sometimes detect low
levels of dopamine in the brain.
4. Physical
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Examination:
Two of the four main symptoms must be present for a neurologist to consider a Parkinson’s
disease diagnosis, the patient must have two of
the four main symptoms.
They must be present over a specific period.
The four main symptoms are:
 Tremor or shaking
 Bradykinesia - slowness of movement
 Rigidity (stiffness) of the arms, legs or trunk
 Postural instability - balance problems and
possible falls
MANAGEMENT
1.
2.
3.
Pharmacotherapy
Non-Pharmacotherapy
Surgery
ANTI-PARKINSONS DRUG
1.Dopaminergic drugs
a. Dopamine precursor
b. Peripheral Decarboxylase Inhibitors
c. Dopamine agonist
i). Ergot derivatives
ii). Non- ergot derivatives
d. MAO-B Inhibitors
e. Dopamine facilitator
f. COMT iInhibitors
2.Anticholinergic Drugs
a. Anti-cholinergics
b. Anti-histamines
1. Dopaminergic drugs
a. Dopamine preacursor
- Levodopa
b. Peripheral Decarboxylase Inhibitors
- Carbidopa
- Benserazide
c. Dopamine agonist
i). Ergot derivatives
- Bromocriptine
- Pergolide
- Lisuride
- Carbergolin
ii). Non- ergot derivatives
- Piribedil
- Ropinirole
- Pramipexole Apomorphine
- Rotigotine
d. MAO-B Inhibitors
- Seleginine
- Rasagiline
e. Dopamine facilitator
- Amantadine
f. COMT Inhibitors
- Entacapone
- Tolcapone
2.Anticholinergic Drugs
a. Anti-cholinergics
- Trihexyphenidyl
- Benztropine
- Procyclidine
- Biperiden
b. Anti-histamines
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- Diphenhydramine
- Orphenadrine
- Promethazine
LEVODOPA
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Well absorbed from gut, but > 90% is decarboxylated to
dopamine peripherally in GIT& blood vessels & only a small
proportion reaches the brain (dopamine does not readily cross
BBB). Therefore combined with peripheral decarboxylase
inhibitor that does not cross the blood-brain barrier along with
L-DOPA.
Peripheral decarboxylase inhibitors, carbidopa & benserazide,
are available as combination preparations with levodopa, as
Sinemet & Madopar, respectively.
CARBIDOPA
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Is a structural analogue of L-dopa.
Inhibits the conversion of L-dopa to dopamine in peripheral
tissue
Carbidopa is highly ionized at physiological pH and does
not cross the blood-brain barrier, so it does not inhibit the
formation of dopamine in CNS
It reduces GI and cardiovascular side effects of L-dopa and
enables about 75% reduction in dosage of L-dopa
L-dopa-carbidopa sustained release combination designed
to reduce “wearing off” effect
Drug
Dose
MOA
Dopaminergic
drugs
a. Dopamine
preacursor
I: 125
mg BD
M:
8 g/day
Levodopa increases
dopamine levels in the
brain leading to the
stimulation of
dopamine receptors.
Initial:
25mg
tab TD
Max: 8
tab/day
Inhibits the conversion
of L-dopa to dopamine
in peripheral tissue
1 mg
initially,
sed to
2.5
mg ,TD
up to 30
mg/day.
Bromocriptine is a
dopamine D2 and D3agonist which works by
activating postsynaptic
dopamine receptors
- Levodopa
b. Peripheral
Decarboxylase
Inhibitors
- Carbidopa
c. Dopamine
agonist
-Bromocriptine
Diagram
Drug
Dose
MOA
MAO-B
Inhibitors
10 mg/day
in single or
divided
doses
Selegiline increases
dopaminergic activity
by intervening with the
re-uptake of dopamine
at the synapse. It also
irreversibly inhibits the
MAO-B which is
involved in the
metabolism of
dopamine.
100
mg/day, up
to 100 mg
twice daily
Max: 400
mg/day.
Amantadine is a weak
dopamine agonist
possessing
antimuscarinic
properties. It alters
dopamine release and
re-uptake. It also
noncompetitively
antagonises N-methylD-aspartate.
- Seleginine
Dopamine
facilitator
- Amantadine
Diagram
Drug
COMT
Inhibitors
- Entacapone
Anticholinergics
- Bromocryptine
Dose
MOA
PO 200 mg w/
each
levodopa/dopa
decarboxylase
inhibitor
dose. Max:
200 mg
Entacapone is a
selective, reversible,
peripheral inhibitor of
COMT, an enzyme
involved in the
metabolism of dopamine
and levodopa.
Initial: 1
mg/day in
divided
doses,
gradually
up to 6-10
mg/day
Trihexyphenidyl is a
tertiary amine
antimuscarinic, which
competitively inhibits
the effects of
acetylcholine at the
muscarinic receptors
of autonomic effector
sites
Diagram
Anticholinergics
ADRs
Indications
Benztropine (Cogentin),
trihexyphenidyl (Artane)
Dry mouth, dry eyes,
constipation,
hypotension, cognitive
impairment, urinary
retention
Useful for symptomatic
control of Parkinson’s
disease (benefits are
mild to moderate);
associated with more
adverse effects than
other drugs
Carbidopa/levodopa
Immediate- and
sustained-release
carbidopa/levodopa
(Sinemet)
Nausea, somnolence,
Levodopa is the most
dyskinesia, hypotension, effective medication and
hallucinations
remains the primary
treatment for
symptomatic
Parkinson’s disease; no
added benefit for motor
complications with
sustained-release
versus immediaterelease preparations
COMT inhibitors
Entacapone
(Comtan)
Diarrhea; exacerbates
Useful for managing motor
levodopa adverse effects; fluctuations (“wearing-off”
bright orange urine
effect) in patients taking
levodopa; levodopa dose may
Tolcapone (Tasmar) Diarrhea; exacerbates
levodopa adverse effects; need to be reduced if
dyskinesia appears
rare liver failure (liver
function monitoring
needed)
Dopamine agonists
Bromocriptine
(Parlodel)
Nausea, headache,
dizziness
Useful for early and advanced
disease
Pergolide (Permax)
Somnolence;
hallucinations; nausea;
edema; fibrosis of cardiac
valves, lung, and
retroperitoneum;
retroperitoneal and
pulmonary fibrosis
Useful for the initial treatment of
parkinsonism and as adjunct
therapy in patients taking
levodopa
MAO-B inhibitors
Selegiline (Eldepryl)
Nausea, insomnia, drug
interactions with other
MAO inhibitors/tyramine
Rasagaline (Azilect)
Weight loss, hypotension,
dry mouth, drug
interactions with other
MAO inhibitors/tyramine
Useful for symptomatic
control of Parkinson’s
disease (benefits are mild
to moderate) and as
adjuvant therapy for
patients with Parkinson’s
disease and motor
fluctuations
NMDA receptor inhibitor
Amantadine (Symmetrel)
Nausea, hypotension,
hallucinations, confusion,
edema
Useful for treating akinesia,
rigidity, tremor, dyskinesia
SURGERY
1.
Deep brain stimulation
2.
Pallidotomy
3.
Thalamotomy
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Deep brain stimulation
Affects movement by using electrical impulses to stimulate a
target area in the brain. The electrical impulses are generated
by wire electrodes surgically placed in the brain. Deep brain
stimulation may be used in addition to therapy with levodopa
or other drugs when drugs alone do not control symptoms
adequately.
It does not destroy brain tissue and has fewer risks than older,
more destructive surgical methods, such as pallidotomy and
thalamotomy.
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Pallidotomy involves the precise destruction of a
very small area in the deep part of the brain (the
globus pallidus) that causes symptoms.
Thalamotomy involves the precise destruction of
very small area in the deep part of the brain (the
thalamus) that causes symptoms.
NON- PHARMACOLOGICAL TREATMENT
Healthy eating
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Eat a nutritionally balanced diet that contains plenty of fruits,
vegetables and whole grains. Eating foods high in fiber and drinking
an adequate amount of fluids can help prevent constipation that is
common in Parkinson's disease.
A balanced diet also provides nutrients, such as omega-3 fatty acids,
that may be beneficial for people with Parkinson's disease.
Exercise
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Exercising may increase your muscle strength, flexibility and balance.
Exercise can also improve your well-being and reduce depression or
anxiety.
Try not to move too quickly.
Aim for your heel to strike the floor first when you're walking.
If you notice yourself shuffling, stop and check your posture.
It's best to stand up straight.
Look in front of you, not directly down, while walking.
Avoiding falls
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In the later stages of the disease, you may fall more easily.
The following suggestions may help:
Make a U-turn instead of pivoting your body over your feet.
Keep your center of gravity over your feet without leaning or
reaching.
Avoid carrying things while you walk.
Avoid walking backward.
Daily living activities

Daily living activities — such as dressing, eating, bathing and
writing — can be difficult for people with Parkinson's disease.
An occupational therapist can show you techniques that make
daily life easier
THANK YOU!!!