Cholesterol-Lowering Statin Drug Clears
Clogged Arteries
Study Findings Explored by Lupus Experts
March 17, 2006 - A study
published in the Journal of the American
Medical Association has, for the first
time, shown that high doses of a
cholesterol-lowering “statin” drug can clear
the kind of sticky plaque and fatty deposits
in arteries that cause most heart attacks.
While there is no indication that any of
the more than 500 individuals involved in the
trial had systemic lupus erythematosus, the
findings are notable for people with this
chronic autoimmune disease because so many
have clogged arteries.
Already, many Americans—including
individuals with lupus—take “statin” drugs to
prevent or slow coronary artery disease, a
condition long viewed as relentlessly
progressive.
“The current study suggests that there is
potential for a more optimistic strategy,” the
JAMA study authors write, “in which
aggressive lipid-modulating strategies can
actually reverse the atherosclerotic disease
process.” If true, the statins may offer a
nonsurgical way to treat heart disease.
What does this study mean for people with
lupus?
The Lupus Research Institute asked two lupus
experts for their opinions.
“This is an exciting observation because it
indicates true potential for high doses of
statins to actually decrease atherosclerotic
areas in blood vessels, which should of course
lower the chances that a person will develop
heart attack,” said Bevra Hahn, M.D., Chief of
Rheumatology at the School of Medicine at the
University of California in Los Angeles.
“With regards to use in patients with
systemic lupus erythematosus (SLE), we must
remember that early data released in abstract
from the NIH-sponsored study of statins in
people with SLE showed that the side effects
of statins were considerably more common in
SLE patients than they are in the population
at large,” she said. Initial findings from the
two-year study of atorvastatin (Lipitor)
versus placebo for preventing lupus
atherosclerosis, published in the September
2005 abstract issue of Arthritis and
Rheumatism, point to more toxicity (liver
and muscle damage) from statins in people with
lupus than in the general population.
Dr. Hahn adds: “It may be that a good
strategy will be to identify SLE patients at
particularly high risk for atherosclerotic
heart attack and then use this new therapy. In
the meantime, we eagerly await the results of
the statin trial in SLE.”
Robert Eisenberg, M.D., Professor in the
Division of Rheumatology at the University of
Pennsylvania School of Medicine, said that
“based on the preliminary information I have
seen on this study, it appears that, if high
doses of statins lead to a more effective way
to prevent the cardiovascular consequences of
atherosclerosis, either primarily or
secondarily—such as in patients who have not
or have, respectively, experienced clinical
events—then clearly such an approach might
well be applicable to the SLE population by
helping to mitigate their greatly increased
risk of atherosclerotic cardiovascular
disease.”
He added: “It makes it all the more
important to define and validate additional
surrogate outcomes in the SLE population for
atherosclerotic cardiovascular disease, so
that novel therapeutic/preventative
approaches, such as high-intensity statins,
can be efficiently tested to see if they could
help SLE patients.”
The anti-inflammatory properties of statins
currently are being investigated for other
aspects of lupus as well, such as kidney
disease (nephritis) and overall inflammation.
This JAMA press release provides study
details:
Very High-Intensity Statin Therapy Shows
Promise
For Inducing Regression of Coronary
Atherosclerosis
CHICAGO, March 13, 2006— Patients
treated with very intensive statin therapy
lowered LDL-C levels on average by about 50
percent, increased HDL-C levels by 15 percent,
and showed regression of coronary
atherosclerosis, according to a study that
will appear in the April 5 issue of JAMA.
The study is being released early online to
coincide with its presentation at the American
College of Cardiology annual conference.
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