January 6, 2005
Two Studies Suggest a Protein Has a Big Role in Heart
Disease
By GINA KOLATA 
 
educing the levels of a certain protein secreted by
the body may be as powerful a tool in slowing heart
disease and preventing heart attacks and
cardiac-related death as lowering cholesterol, two
teams of researchers are reporting today.

The studies, being published in The New England
Journal of Medicine, provide the strongest evidence
yet that the protein - known as CRP, for C-reactive
protein - plays a role in heart disease. 

The participants were patients with severe heart
disease who were taking high doses of statin drugs,
which reduce both cholesterol and CRP. Lower CRP
levels, the researchers found, were linked to a slower
progression of atherosclerosis and fewer heart attacks
and deaths. And this effect was independent of the
effect of lowering cholesterol.

"What we now have is hard clinical evidence that
reducing CRP is at least as important as lowering
cholesterol," said Dr. Paul Ridker of Brigham and
Women's Hospital in Boston, the lead author of one of
the studies. 

But other heart disease researchers cautioned that
more work was needed to prove that CRP directly causes
heart disease. And most agreed that because the new
studies involved only people with severe heart
disease, it remained unknown whether healthy people
would benefit from reducing their CRP levels.

Still, the study investigators said they suspected
that the results would be shown to apply more broadly.
If they are correct, a huge new market for the already
popular statins could be opened among people whose
cholesterol levels are normal but who have high levels
of CRP. Of people stricken by heart attacks, half have
normal cholesterol readings. 

Dr. Ridker's study addressed the question of whether
CRP levels independently predicted heart attacks and
deaths.

The second study, by Dr. Steven E. Nissen of the
Cleveland Clinic and his colleagues, asked whether CRP
independently predicted heart disease progression.

In both cases, the investigators concluded, the answer
was yes. (They, like most researchers in this field,
have received support from drug companies, and Dr.
Ridker is also an inventor of a test for CRP that his
institution licensed. He and his laboratory profit
from the use of the test.)

Some heart disease experts said the new studies
offered persuasive evidence that doctors should focus
on keeping CRP levels low in patients with severe
heart disease.

"This is missing-link evidence," said Dr. Sidney
Smith, a cardiologist at the University of North
Carolina who is a past president of the American Heart
Association and co-chairman of a committee of the
heart association and the American College of
Cardiology that sets treatment guidelines. 

Others, though, said CRP could instead be a marker for
something else being fought by statin drugs to reduce
heart disease risk.

"These are very important papers," said Dr. James I.
Cleeman, coordinator of the National Cholesterol
Education Program at the National Heart, Lung and
Blood Institute. "They are provocative. But we need to
recognize that the relationship between CRP and heart
disease is a developing story. This adds to the
evidence, but I'm not sure it settles the issue." 

CRP levels are low in healthy young people - usually
less than one milligram per liter of blood - but they
rise with age and with obesity, diabetes, smoking and
a sedentary life. If people lose weight, stop smoking,
exercise or take oral diabetes drugs, their CRP levels
fall. But a third of the population has levels greater
than three milligrams, and levels that high have been
associated with heart disease risk, Dr. Ridker said.

Even before the new findings, evidence had been
mounting that CRP and heart disease were somehow
linked. 

Scientists have developed hypotheses to explain why,
proposing that the protein could cause plaque to
develop in coronary arteries, lead plaque to burst
open or bring on the formation of blood clots that
then block arteries and cause heart attacks. Some drug
companies have started programs to develop drugs that
make a specific target of CRP and prevent its
synthesis.

But what the findings of those studies mean remains
uncertain. That CRP levels drop with exercise and
weight loss, for example, has led some experts to
argue that the protein is a marker of heart disease
risk, not a cause, just as gray hair is a marker
rather than a cause of aging.

CRP is made in the liver and also in the walls of
coronary arteries and possibly elsewhere in the body.
Its levels, which can be measured with a simple blood
test, often rise and remain high in patients who have
chronic inflammation from conditions like rheumatoid
arthritis, for example, or periodontal disease.
Patients with chronic inflammation also have an
increased risk of heart disease.

Questions remain as to the protein's normal purpose in
the body. CRP was discovered about 70 years ago by
scientists who were trying to understand why some
strep bacteria caused disease and others did not. It
is so called because it was found in the third band,
which the scientists called Band C, in a gel used to
separate proteins.

Then, about half a century ago, doctors noticed that
after a heart attack, CRP flooded the patient's blood,
and for a while the protein was used to help diagnose
heart attacks.

Dr. Ridker's study involved 3,745 patients who had
been hospitalized with heart attacks or with severe
chest pain from the blocking of coronary arteries and
who were then followed for two and a half years. 

Dr. Ridker said that when the study, sponsored by
Bristol-Myers Squibb, was being planned several years
ago, the thought was that it would ask whether
moderate statin therapy - 40 milligrams a day with
Pravachol, a Bristol-Myers product - was as effective
in preventing heart attacks as more intense therapy:
80 milligrams a day of Lipitor, a statin made by
Pfizer Inc. 

"I said, 'This is a good study, but it can be better,'
" Dr. Ridker said. 

He proposed also asking about CRP. Would there be
fewer heart attacks and deaths among people in the
study with lower levels of the protein?

Dr. Ridker said he would have been happy to find a
benefit in lowering CPR levels that was only 10
percent or 20 percent that of lowering cholesterol,
adding, "We never dreamed we'd get a risk reduction as
large as the risk reduction from lowering LDL
cholesterol" - that is, the "bad" type of cholesterol.

Dr. Nissen's study, sponsored by Pfizer, examined
plaque in the coronary arteries of 502 patients with
heart disease, comparing intense statin therapy
against moderate and using the same doses of the same
drugs as in Dr. Ridker's research.

Intense therapy resulted in lower cholesterol levels
and slower growth of plaque, Dr. Nissen reported. But
he also suspected that something else was going on,
because some patients seemed to be doing much better
than others with the same cholesterol levels. 

Upon further analysis, Dr. Nissen found that levels of
CRP dropped independently of cholesterol and that
these reductions were independently associated with a
slowing of disease progression. In patients who
achieved low levels of both CRP and cholesterol, he
found, plaque in the coronary arteries actually
regressed.

"I'm looking right at the plaque, and when your CRP
level is reduced, you are stopping the disease," Dr.
Nissen said. "We are saying that CRP is a direct
participant in atherosclerosis." 

The next step, Dr. Ridker said, is to see if reducing
CRP levels can prevent heart attacks in healthy
people. His new study will enroll 15,000 people with
normal cholesterol levels but higher-than-average
levels of CRP, above two milligrams per liter of
blood. The participants will be randomly assigned to
take either 20 milligrams a day of a statin - Crestor,
made by AstraZeneca - or a placebo. 

Some experts say the latest findings make it clear
that doctors should monitor CRP levels in patients
with severe heart disease and do whatever it takes,
including giving high doses of the most powerful
statins, to get levels below two milligrams per liter
of blood.

"What these two papers are saying is that not only is
CRP a risk factor on its own, but we should be
aggressively treating it," said Dr. Valentin Fuster,
former president of the American Heart Association and
director of the cardiovascular institute at Mount
Sinai School of Medicine in New York.

But Dr. Daniel Rader, a heart disease researcher at
the University of Pennsylvania, said this might not be
so easy in patients already doing everything possible.


"You've already counseled them about lifestyle, you've
already given a statin, you're already targeting LDL
cholesterol to less than 70," a very low level that is
recommended by the current guidelines, he said. "So if
you find a high CRP, what do you do? Do you tell the
patient, 'Oh, this is bad. You're at high risk'?"

A difficult question, Dr. Ridker said, but one he
predicted would not arise very often. Most patients
with severe heart disease are not taking high doses of
statins, he said, so there is room for doctors to
experiment with higher doses and different drugs to
reduce CRP levels if necessary.

"There is a huge payoff" if doctors understand that
they need to test not just for cholesterol but also
for CRP, Dr. Ridker said, adding, "That alone will
save tens of thousands of lives right there."



The New York Times 


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