Parkinson`s Disease (PD) and Treatment
Download
Report
Transcript Parkinson`s Disease (PD) and Treatment
Jieun Park
Chem-5398
Outline
Overview
Diagnosis
Treatment
Physical Therapy
Drug Therapy
Surgery
New Research
2
Overview
Second most common human
neurodegenerative disorder.
Prevalence of 1 out 272 in U.S.
Increases to 4 to 5% for ages 85 and over.
Degeneration of dopaminergic neurons in
the substantia nigra.
Dopamine
3
Overview cont’d
Symptoms caused by insufficient dopamine.
3 main symptoms:
Tremors
Rigidity
Slowed motion (Bradykinesia)
Other symptoms include:
Dementia, sleep disturbances, depression, etc.
4
Overview cont’d
Common cause of chronic progressive
parkinsonism.
Exact causes still yet unknown.
Gene mutation
Toxins
Trauma
5
Diagnosis
No definitive tests for PD. PET scans
can aid to determine levels of dopamine.
Difficult to diagnose, many symptoms
shared with other disorders.
Medical history and neurological tests
are conducted to diagnose.
Usually, if two of the cardinal symptoms are
present.
6
Treatment – Parkinson’s Disease
No cure for PD.
Treatment can be divided into two stages.
Early and Later stages
Early stage
Onset of symptoms, treated with physical therapy and
medications (Levodopa, dopamine agonists, etc)
Later stage
Usually after having received 5+ years of levodopa
treatment.
“Wearing-off” and “On/Off” effect develops, other
medication in conjunction levodopa is commenced.
MAO-B and COMT inhibitors.
7
Treatment – Physical Therapy
Regular exercise
Recommended throughout the life of disorder.
Helps maintain and improve mobility and strength.
Physical exercise aids in rigidity relief, muscle
strength and flexibility, balance, etc.
Caution is advised to avoid sudden movements or
strenuous activities – fall could result in serious
injury.
8
Treatment – Drug Therapy
Levodopa (L-DOPA)
Preferred medication to control major symptoms.
Usually administered at the early onset of disorder.
Drug is well tolerated and side affects are limited.
Levodopa
Dopamine
9
Drug Therapy – L-DOPA
L-DOPA is converted to Dopamine by
enzyme DOPA decarboxylase (DDC).
10
Drug Therapy – L-DOPA
Used with Carbidopa, which blocks the early
conversion of L-DOPA into dopamine.
Carbidopa
11
Drug Therapy – L-DOPA
12
Drug Therapy – L-DOPA
Side effects include
Psychiatric symptoms; linked to depression
Nausea and vomiting
Prolonged use can cause “wearing-off” effect.
Leads to other motor complications, such as
dyskinesia.
Still the preferred treatment for symptoms.
Drug brand name: Sinemet ®
13
Drug Therapy – L-DOPA
L-DOPA can cross blood-brain barrier, when
dopamine cannot. This led to the idea of
using L-DOPA as treatment for PD.
First used in the 1960’s, with daily increase
dosage program.
L-DOPA used in combination with Carbidopa
in 1967.
Increases potency of L-DOPA up to 4-fold.
14
Treatment – Drug Therapy
Dopamine Agonists
Acts directly on the dopamine receptors.
Initially was used with L-DOPA.
Today, sometimes prescribed before L-
DOPA, to delay “wearing-off” effect and
other motor complications brought on by
prolonged use of L-DOPA.
Pramipexole
Dopamine
15
Drug Therapy - DOPA agonists
Triggers dopamine receptors in place of
depleted dopamine neurotransmitters.
http://www.youtube.com/watch?v=dTdW8q9hukw&feature=related
16
Drug Therapy – DOPA agonists
Adverse side effects
Nausea, dizziness, hallucinations
Sleep attacks, hypotension
Permax ® (pergolide) pulled after direct link
to fibrosis of cardiac valves that can lead to
death. Unavailable in U.S. since 2007.
17
Treatment – Drug Therapy
Monoamine Oxidase B (MAOB) Inhibitors
Delays or reduces breakdown of dopamine by
MAO-B.
Used as monotherapy or in conjunction with
L-DOPA, it can reduce the dosage of L-DOPA by
15%.
Selegeline
18
Drug therapy – MAO-B Inhibitors
MAO-B is an enzyme that metabolizes
dopamine.
From the breakdown of dopamine,
hydrogen peroxide is produced, which the
oxidative stress can damage
dopaminergic neurons in the substantia
nigra. (Possibly neuroprotective)
MAO-B inhibitor delays or reduces the
metabolism of dopamine.
19
20
Drug therapy – MAO-B Inhibitors
Side effects of L-DOPA may be
enhanced by selegeline.
Nausea and dizziness.
21
Treatment – Drug Therapy
Catechol O-Methyl Transferase (COMT)
Inhibitors
Inactivates and degrades neurotransmitters,
such as dopamine.
Mainly used in combination with L-DOPA, it
increases the half-life of L-DOPA.
Delays “wearing-off” effect of L-DOPA and
other motor complications such as dyskinesia
Tolcapone(Tasmar ®)
22
Drug therapy – COMT Inhibitors
COMT catalyses methylation of L-DOPA.
Addition of COMT inhibitor along with LDOPA and carbidopa prolongs the half-life
of L-DOPA and increases the amount in
the CNS.
This increases “on” time for L-DOPA.
Tasmar ® are hepatotoxic.
Diarrhea and sleep disturbances
23
Treatment – Drug Therapy
Amantadine
Antiviral agent.
Known to aid in reducing dyskinesia.
Anticholinergics
Improve tremors and stiffness
Cause impairment and constipation
24
Treatment - Surgery
Before commerciality of levodopa, surgical
treatment were preferred.
Early surgeries were successful with
tremors, but failed to relieve other symptoms.
“Means of last resort” due to high risk of
potential complications.
Recent advances in neurosurgical
procedures allow for better treatment.
25
Surgery
Deep Brain Stimulation
Brain pacemaker, sends electrical impulses to
brain to stimulate the subthalamic nucleus.
Improves motor functions and reduce motor
complications.
Complications include: brain
hemorrhage, seizures, death.
26
New Researches
Nicotine
Intake of nicotine has shown to slow the
degeneration of neurons.
Acts similar to levodopa.
Melatonin
Serotonin derivative that helps insomnia.
Also shown to cause a reduction in
production of neurodegenerative radicals.
27
Assigned Reading
Jankovic, Joseph; Aguilar, L. Giselle. Current
approaches to the treatment of Parkinson's
disease. Neuropsychiatric Disease and
Treatment (2008), 4(4), 743-757.
28
Homework Problems
1.
2.
3.
Which medicinal treatment is generally
started for younger patients with mild
symptoms in early-stage treatment?
Levodopa is used with which drug and why?
Describe “wearing-off” and “on-off” effect.
29
References
Davie, C. A. “A review of Parkinson’s disease”, British
Medical Bulletin, 86 (2008): 109-127
Munchau, A., Bhatia, K P. “Pharmacological treatment
of Parkinson’s disease”, Postgrad Med J, 76
(2000): 602-610
Rao, Shobha A., Hoffman, Laura A., Shakil, Amer.
“Parkinson’s Disease: Diagnosis and Treatment.”,
American Family Physician, 74 (2006): 2046-2054
Singh, N., Pillay, V., Choonara, Y. E. “Advances in the
treatment of Parkinson’s disease”, Progress in
Neurobiology, 81 (2007): 29-44
Images from Wikipedia, Google
30