Parkinson's Disease: New Treatments Slow Onslaught of Symptoms
by John Henkel
Joe Dulaney calls himself the Backward Man.
Although the tag is lighthearted, the awkward and dangerous dilemma he
often faces as his lower limbs simply lock in mid-stride is not. At these
moments, his body halts abruptly like a movie freeze-frame, and the only
way he can walk is to step backward.
"I've gotten to where I can move pretty fast in reverse,"
says Illinois resident Dulaney, 65, whose finessed footwork helps him cope
with one of many symptoms of Parkinson's disease.
Nationwide, as many as 1.5 million people suffer from Parkinson's,
according to the Parkinson's Disease Foundation. A chronic and progressive
disorder, Parkinson's strikes slightly more men than women and more whites
than blacks in the United States. Though the disease is found most often
in patients over 50, as many as 10 percent of patients--afflicted with the
so-called "young-onset" Parkinson's--are under 40. About 50,000
Americans are diagnosed with Parkinson's yearly, according to the National
Institute of Neurological Disorders and Stroke, which estimates that the
total cost of health care for Parkinson's patients will exceed $5.6
billion this year.
The Food and Drug Administration has approved nearly a dozen drugs for
treating Parkinson's, three of which have been put on the market just in
the past year. Also approved in 1997 was a device that is surgically
implanted in the brain to lessen the violent shaking experienced by some
Parkinson's patients. The 1996 discovery of a gene believed responsible
for a form of Parkinson's may result in future innovative treatments.
Despite the range of therapies available to ease the disease's
debilitating symptoms, however, treatments now on the market can neither
replace the faulty nerve cells that cause the disease nor stop Parkinson's
from progressing.
Numerous public figures have acknowledged their battle with
Parkinson's. Attorney General Janet Reno, evangelist Billy Graham, former
boxer Muhammad Ali, and former Alabama governor George Wallace all are
fighting the disease. Chinese leader Deng Xiaoping was in the late stages
of Parkinson's when he died last year at age 92.
Parkinson's also gained attention last year with passage of the Morris
K. Udall Parkinson's Research Act, which authorized $100 million for
Parkinson's research. At press time, the funds had not yet been
appropriated. Udall, who has Parkinson's, served in the House of
Representatives for 30 years.
What Is It?
Parkinson's disease is one of a larger group of neurological conditions
called motor system disorders. Historians have found evidence of the
disease as far back as 5000 B.C. It was first described as "the
shaking palsy" in 1817 by British doctor James Parkinson. Because of
Parkinson's early work in identifying symptoms, the disease came to bear
his name.
In the normal brain, some nerve cells produce the chemical dopamine,
which transmits signals within the brain to produce smooth movement of
muscles. In Parkinson's patients, 80 percent or more of these
dopamine-producing cells are damaged, dead, or otherwise degenerated. This
causes the nerve cells to fire wildly, leaving patients unable to control
their movements. Symptoms usually show up in one or more of four ways:
- tremor, or trembling in hands, arms, legs, jaw, and face
- rigidity, or stiffness of limbs and trunk
- bradykinesia, or slowness of movement
- postural instability or impaired balance and coordination.
Several structures of the brain are related to Parkinson's
disease. Basal ganglia affect normal movement and
walking; substantia nigra are types of basal ganglia that
produce the neurotransmitter dopamine, which sends messages that control
muscles. The globus pallidus is part of a larger
structure connected to the substantia nigra affecting movement, balance
and walking. The thalamus serves as a relay station for
brain impulses, and the cerebellum affects muscle
coordination.
Though full-blown Parkinson's can be crippling or disabling, experts
say early symptoms of the disease may be so subtle and gradual that
patients sometimes ignore them or attribute them to the effects of aging.
At first, patients may feel overly tired, "down in the dumps,"
or a little shaky. Their speech may become soft and they may become
irritable for no reason. Movements may be stiff, unsteady, or unusually
slow.
Joe Dulaney says he was in "perfect health" nine years ago
when his wife noticed that he had stopped swinging his right arm when he
walked. Soon, simple tasks such as brushing his teeth and combing his hair
became major ordeals. His right hand was always ice cold and he produced
small, jerky letters when he wrote.
Dulaney's doctor diagnosed the problem as arthritis and prescribed
drugs to treat it. But symptoms worsened. Dulaney's voice dwindled to a
slight whisper. Leg cramps, dry mouth, severe constipation, itchy eyes,
and trouble turning over in bed tormented him. "My wrists were rigid
and my fingers were not flexible, so I couldn't even button my
shirt," he says. Still, another doctor seconded the arthritis
diagnosis and prescribed different drugs.
Finally fed up because his deteriorating condition prevented him from
doing simple tasks such as turning newspaper pages, putting money in his
wallet, and replacing a light bulb, Dulaney checked himself into a local
hospital, arriving in such a weakened state he couldn't walk.
Though a Parkinson's diagnosis rarely comes quickly, the three doctors
who examined Dulaney at the hospital agreed within minutes that his
classic symptoms indicated Parkinson's. The doctors gave him the
Parkinson's drug levodopa, marketed as Larodopa and in generic forms, and
the effect was nearly immediate.
"In one hour or so I was walking the halls. I took a shower by
myself and did one push-up to show off," says Dulaney. It was, for
the moment, as if the disease had somehow vanished. But Dulaney says he
soon became "fully aware" that because Parkinson's is
progressive, he could manage some symptoms with drugs, but the disease
wasn't about to go away.
Treating the Disease
The drug Dulaney took at the hospital, levodopa, is what doctors call
the "gold standard" of Parkinson's therapy, because it is often
the first-line treatment for the disease. Approved in 1970, levodopa helps
restore muscle control when it is converted to dopamine in the brain.
Why not give a patient dopamine directly? The reason is that dopamine
cannot get through the body's blood-brain barrier, which screens out
certain substances. But, although levodopa can pass through the barrier,
it changes to dopamine so quickly only a small amount actually makes it
into the brain. So to relieve symptoms, many patients need to take fairly
large doses, which can cause side effects such as nausea and dyskinesias
(involuntary movements).
To reduce these drawbacks, doctors often prescribe levodopa mixed with
carbidopa, a drug that is marketed as Sinemet or in generic versions.
About 80 percent of Parkinson's patients take this drug, according to drug
industry estimates. Carbidopa delays the conversion of levodopa to
dopamine until it reaches the brain, often lessening or even preventing
levodopa side effects. Carbidopa also decreases the amount of levodopa
needed. Because each Parkinson's patient reacts differently to treatment,
doctors and patients must work closely to find a tolerable balance between
the drug's benefits and side effects.
Though the levodopa-carbidopa combination can be so effective that some
patients forget for a while that they have Parkinson's, the drug is far
from perfect. Side effects aside, doses typically must be increased over
time, and the disease often manifests an "on-off" syndrome in
advanced patients in which the drug simply doesn't work for unpredictable
durations. Fortunately, alternatives are available.
Parkinson's experts are enthusiastic about the three new drugs FDA
approved in 1997: Mirapex (pramipexole dihydrochloride), Requip
(ropinirole hydrochloride), and Tasmar (tolcapone).
Enrico Fazzini, M.D., who runs a neurology clinic in New York City,
says the three new drugs are "really helping me to treat my
Parkinson's patients more effectively."
Mirapex and Requip, which mimic dopamine's role in the brain, allow
patients to regain some of their lost muscle control. Both are approved
for use alone or with levodopa drugs. In clinical trials, patients taking
Mirapex alone saw as much as a 30 percent improvement in symptoms.
Combining Mirapex with levodopa drugs allowed advanced patients to reduce
those doses by up to 25 percent. Requip trials showed similar benefits,
allowing patients to reduce levodopa doses by an average of 31 percent.
Tasmar is a new kind of drug called a COMT inhibitor. It also is
indicated for use with levodopa drugs. Researchers believe that Tasmar
blocks a key enzyme responsible for breaking down levodopa before it
reaches the brain. In trials, patients with a stable response to levodopa
drugs who took Tasmar experienced significant improvements in daily
activities such as talking, writing, walking, and dressing.
"Although we are still looking for a cure, COMT inhibitors
represent an entirely new class of therapy that will help many Parkinson's
patients attain better symptom control," says Emilio Alonso-Mendoza,
executive director of the National Parkinson Foundation.
Parkinson's drug therapy also can include:
- Parlodel (bromocriptine) and Permax (pergolide), which mimic
dopamine's role in the brain. They are sometimes given with levodopa
drugs to improve response.
- Eldepryl (selegiline hydrochloride), also called deprenyl and
available in generic versions, which can enhance and prolong levodopa
response by delaying the breakdown of naturally occurring and
levodopa-formed dopamine, allowing accumulation in surviving nerve
cells.
A Brain "Pacemaker"
FDA approved an important tool for controlling Parkinson's tremors last
August. The Activa Tremor Control Therapy consists of a wire surgically
implanted deep within the brain and connected to a pulse generator,
similar to a cardiac pacemaker, implanted near the collarbone. Whenever a
tremor begins, patients can activate the device by passing a hand-held
magnet over the generator.
The system delivers a mild electrical stimulation that blocks the
dysfunctional brain signals that cause tremor. Effects are often dramatic.
"Before the implant, patients can't raise a glass of water or a
spoonful of food to their mouths without spilling it or striking
themselves in the face," says William Koller, M.D., neurology
chairman at Kansas University Medical Center. "Within hours, these
same patients are sipping tea from a cup and eating peas with a fork, with
no signs of their disability."
Surgery Options
A brain operation shown to be helpful for many Parkinson's patients,
especially those in late stages of the disease, is called pallidotomy.
Doctors are not sure why the procedure works, but an October 1997 report
in the New England Journal of Medicine stated that half of the patients in
a pallidotomy study at Toronto Hospital, who before the surgery needed
help in eating, dressing, and personal hygiene, were able to resume these
activities independently. The study cautioned, however, that some of the
surgery's effects diminished after two years and that the long-term
effectiveness of the procedure still is unknown.
In pallidotomy, a surgeon makes a tiny hole in the skull and uses a
tiny electric probe to destroy a small portion of the globus pallidus,
which experts believe is overactive in Parkinson's patients. Before
operating, the surgeon has "mapped" the patient's brain with
imaging techniques such as magnetic resonance and knows precisely where
the probe should go. The patient is kept awake, but under sedation, so the
surgeon can note responses to stimuli. Though both sides of the brain have
a globus pallidus, pallidotomies typically are performed on one side at a
time. After the patient has recuperated, a second procedure is done if
needed.
For Tom Riess, who has undergone the procedure four times over the last
six years, the surgery helped reduce his Parkinson's symptoms, especially
the violent shaking, "which was literally killing me," he says.
"Unfortunately, it left me with severely impaired speech, which is a
fairly common consequence," says the 51-year-old Californian, a
Parkinson's patient for 17 years. "Still, the tradeoff is
worthwhile."
Thalamotomy, a surgical procedure that destroys a specific group of
cells in the thalamus, the brain's communications center, is aimed at the
5 to 10 percent of Parkinson's patients with disabling tremor in the hand
or arm. It reduces or eliminates tremor in as many as 90 percent of
patients.
On the Horizon
A number of potential Parkinson's treatments in research laboratories
now show much promise. They include:
- Neurotrophic proteins--These appear to protect nerve cells from the
premature death that prompts Parkinson's. One hurdle is getting the
proteins past the blood-brain barrier.
- Neuroprotective agents--Researchers are examining naturally
occurring enzymes that appear to deactivate "free radicals,"
chemicals some scientists think may be linked to the damage done to
nerve cells in Parkinson's and other neurological disorders.
- Neural tissue transplants--Researchers are studying ways to implant
neural tissues from fetal pigs into the brain to restore the
degenerate area. In a clinical trial conducted in part at Boston
University School of Medicine, three patients out of 12 implanted with
the pig tissues showed significant reduction in symptoms.
- Genetic engineering--Scientists are modifying the genetic code of
individual cells to create dopamine-producing cells from other cells,
such as those from the skin.
Experts say some of these new treatments are still far off. Others say
they are hopeful that with bolstered research efforts, such as those
earmarked in last year's Udall Act, innovative new therapies will be
available in the near future.
"I'm optimistic," says Perry Cohen, 52, a Washington, D.C.,
Parkinson's activist and patient for two years. "I think we are on
the verge of an important development. I'm confident that I won't have to
go through the agony I've seen others go through."
John Henkel is a staff writer for FDA Consumer. This article originally appeared in the FDA Consumer magazine, published by the U.S. Food and Drug Administration, in the July-August 1998 issue.
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