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Health Briefs
June
7 , 2002
by Robert A. Wascher, M.D., F.A.C.S.
NEW CORONARY ARTERY STENT REDUCES RISK
OF RESTENOSIS
In the past, people with clinically significant narrowing of their main
coronary arteries all required open heart surgery and coronary bypass
grafting to restore blood flow to the heart. More recently, however, coronary
artery stents (expandable mesh tubes that resembles those paper "Chinese
handcuffs" you played with when you were a kid) have made it possible
for many patients to avoid going under the surgeon's knife. These diminutive
vascular conduits are threaded-up through an artery in the leg or arm,
and are then passed through the area of blockage in the affected coronary
artery. These internal bypass devices have a very high rate of success
in restoring coronary artery blood flow but, in 25 to 40 percent of cases,
the body responds to the device by gradually narrowing the stented artery
again. A number of approaches have been taken to reduce the incidence
of restenosis in stented arteries. In this week's New England Journal
of Medicine is a study that looked at rapamycin-impregnated stents as
a novel way of reducing the restenosis rate. Rapamycin is often used as
an anti-rejection medication in transplant patients, as the drug inhibits
certain immune cells from dividing and attacking the transplanted organs.
The researchers coated coronary artery
stents with rapamycin, and then randomized 238 patients to receive either
a rapamycin-coated stent or a non-coated stent. The patients were then
followed for at least one year after stenting. The patients who had the
rapamycin-coated stents implanted were found to have significantly less
restenosis than patients receiving the conventional stents. After being
observed for 12 months, fully 27 percent of the patients with conventional
stents developed at least a 50 percent reduction in the diameter of the
stented artery, while none of the patients with the rapamycin-coated stents
experienced a comparable degree of reduction in arterial diameter. Most
importantly, 29 percent of the standard-stent group experienced a heart
attack, death, or the need for emergent bypass during the 12 month follow-up
period, while only 6 percent of the rapamycin-coated stent group experienced
any of these severe complications of coronary artery restenosis. This
study convincingly demonstrated a dramatic reduction in the most common
complication associated with coronary artery stents, and along with other
similarly successful interventions, further advances the state of the
art of non-surgical coronary artery disease treatment.
POSSIBLE CAUSE OF PARKINSON'S DISEASE
IDENTIFIED
Parkinson's Disease (PD), which affects about 1.5 million Americans, is
a neurological syndrome that causes tremors, difficulties in starting
and stopping movements, a peculiar stiffness of the body, depression and,
in some cases, dementia. The area in the brain that is affected by the
disease is known as the substantia nigra, and is thought to be an important
relay system for nerve cell impulses involved in movement. For reasons
that have eluded scientists since it was first described in 1817 by the
British physician James Parkinson, dopamine-secreting neurons in this
area of the brain die off, causing the symptoms of PD. However, a new
study, just reported in Nature Medicine, has identified at least one possible
cause of Parkinson's Disease. A brain protein called alpha-synuclein is
known to be elevated in the substantia nigra of most patients with PD.
In this study, the scientists added alpha-synuclein to healthy substantia
nigra neurons growing in a culture dish, and observed that this protein
actually appeared to convert the dopamine secreted by substantia nigra
neurons into a toxic compound which then, in turn, killed the neurons.
Ironically, alpha-synuclein appears to have a protective effect on neurons
that do not secrete dopamine in other parts of the brain. Most spontaneous
cases PD have long been suspected to arise from exposure to unknown environmental
toxins. It is, therefore, especially intriguing that this Nature Medicine
study concluded that alpha-synuclein converts dopamine into a neurotoxin
by way of oxygen free radicals, which are byproducts of normal metabolism,
and the metabolism of numerous drugs and toxins as well. If alpha-synuclein
does in fact cause or mediate the onset of PD, this knowledge could serve
as a critical starting point for the development of drugs that target
this protein, or the free radicals that also appear to be involved. PD
might then be prevented in many cases or, at least, more effectively treated
than is possible at the present time.
BRIEFLY...
Bioflavanoids are in the news a great deal these days. Antioxidant flavanoids
contained in tea and other natural sources are thought to have a variety
of beneficial effects, including the elimination of potentially harmful
free radicals that have been linked to an increased risk of heart disease
and some cancers. The journal Cancer Research is reporting that silibinin,
a flavanoid found in the milk thistle plant, is capable of significantly
inhibiting the growth of human prostate cancer cells implanted in mice.
Silibinin reduced tumor volume in these mice by 53 to 64 percent, and
appeared to have virtually no observable toxicity. Human studies using
this compound are currently being planned.
A Duke University team has studied pregnancy
and birth rates among unmarried teenagers in Texas. They found that conception
rates dipped during the summer months, and then dramatically increased
again when school started in the fall. Their conclusion, not surprisingly,
was that most teens meet their sexual partners at school....
When breast cancers spread, their favorite
target is the skeletal system. Traditionally, a nuclear medicine bone
scan is utilized to evaluate breast cancer patients for possible spread
of their cancer to their bones. The nuclear medicine bone scan has been
around for decades, and is very sensitive to any disruption of the bone
caused by inflammation, injury or tumors. Unfortunately, arthritis, relatively
minor injuries and infections can all cause a positive bone scan result,
making this test rather nonspecific as a cancer detection tool. PET scans,
on the other hand, are both very sensitive and very specific for tumors.
In the Journal of Cancer Research & Clinical Oncology, a new study has
compared the two types of scans, and has found PET to be as sensitive
as bone scans in detecting metastatic breast cancer lesions in the bone.
However, unlike bone scans, PET was also found to be highly specific for
metastatic bone tumors. In another words, bone scans picked up even subtle
abnormalities in the skeleton, irrespective of whether cancer metastases
were present or not. An abnormal PET scan, however, was far more likely
to represent a true metastasis of breast cancer to the bone than an abnormal
nuclear medicine bone scan.
Dr. Robert A. Wascher
Dr. Robert A. Wascher is
a senior research fellow in molecular & surgical oncology at the John Wayne
Cancer Institute in Santa Monica, CA
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