U.S. panel recommends limiting use of highly sensitive C-reactive protein testing to patients with moderate or poorly defined cardiac risk
A panel of experts convened by the American
Heart Association and the Centers for Disease Control and Prevention
recommends limited use of highly sensitive C-reactive protein testing,
according to guidelines published in the January 28th issue of Circulation
Thomas A. Pearson, M.D., Ph.D., cochair of the writing group, said
there is “no need for highly sensitive C-reactive protein screening
of the entire adult population as a public-health measure.”
George A. Mensah, M.D., cochair of the writing
group, explained, “For clinicians and public health practitioners,
it is important to emphasize that although abnormal highly sensitive
C-reactive protein values identify high-risk persons, we have no
evidence that treatment strategies based on [protein] levels improve
survival or reduce cardiovascular complications.
“Although our statement identifies a subgroup
of patients who may benefit from [protein] testing, for most patients
the emphasis must remain on detection, treatment, and control of
the major risk factors, such as high blood pressure, high blood
cholesterol, cigarette smoking and diabetes,” added Mensah.
The writing group does not consider the new
test in the same category as cholesterol testing or blood pressure
screening. However, Pearson said the test might be useful when a
physician is undecided about a course of treatment for a patient
who is considered intermediate risk. For example, a person at intermediate
risk may be someone considered to have a 10 to 20 percent risk for
myocardial infarction in the next 10 years based on current health
status and history. “In those cases, a highly sensitive C-reactive
protein test might tip the scale to help a physician decide on moderate
or more intensive treatment,” he said.
Pearson explained that the writing group wanted
to address the concerns of physicians whose patients are requesting
protein testing, even though there has been very little clinical
evidence to support widespread testing. The joint panel reports
that the results of tests should be expressed as milligrams per
Liter (mg/L) with concentrations of less than 1.0 mg/L defined as
low risk, 1.0-3.0 mg/L as average risk, and concentrations higher
than 3.0 mg/L defined as high risk. People in the high-risk group
have about a 2-fold increase in relative risk for cardiovascular
disease compared with people in the low-risk group.
Pearson said the new recommendations are based
on currently available evidence and may change as new trial data
become available. At the present time, the panel states that protein
level can be an independent marker of risk and may be useful as
a tool for evaluating people with moderate risk. However, there
is insufficient evidence to use protein level to track the efficacy
of treatment.
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