Lowering Cholesterol
Early in Life Protects Against Heart Disease Later
New research from UT Southwestern Medical Center indicates that
lowering “bad” blood cholesterol earlier in life,
even by a modest amount, confers substantial protection from
coronary heart disease.
The new findings, appearing in the March 23 issue of The New
England Journal of Medicine, found that people with genetic variations
affording them lower low-density lipoprotein (LDL) cholesterol
in their blood from birth were significantly less likely to develop
coronary heart disease later in life than those without the variations.
These variations exist in a recently discovered gene called PCSK9.
Based on 15 years of data tracking more than 12,000 multiethnic
subjects ranging in age from 45 to 64, the researchers found
that people who had cholesterol-lowering genetic variations that
lowered their LDL level by about 40 milligrams per deciliter
were eight times less likely to develop coronary heart disease
than those without the mutations. Those with genetic profiles
lowering their LDL by about 20 mg/dl from average had a twofold
reduction in heart disease.
“These data indicate that a moderate, life-long reduction
in LDL cholesterol is associated with substantial reduction in
the incidence of coronary events, even in populations with a
high prevalence of other cardiovascular risk factors,” said
Dr. Helen Hobbs, the study’s senior author, director of
the Eugene McDermott Center for Human Growth and Development
and an investigator in the Howard Hughes Medical Institute at
UT Southwestern. She also directs the Donald W. Reynolds Cardiovascular
Clinical Research Center at UT Southwestern. Dr. Hobbs coauthored
the study with Dr. Jonathan Cohen, professor of internal medicine
and researchers from the UT Health Science Center in Houston
and the University of Mississippi Medical Center in Jackson.
Dr. Scott Grundy, director of the Center for Human Nutrition
at UT Southwestern, served as chairman of the National Cholesterol
Education Program’s Expert Panel on Detection, Evaluation
and Treatment of High Blood Cholesterol in Adults, which in 2001
set guidelines for the clinical use of cholesterol-lowering medications
to reduce the risk of cardiovascular disease. “This study
demonstrates the great importance of high blood cholesterol in
causing coronary heart disease,” said Dr. Grundy.
“It also shows the benefit of maintaining a low cholesterol
level throughout life. The foundation for keeping low blood cholesterol
is a reduced intake of saturated fats and cholesterol and maintaining
a desirable body weight. But in some people it may be necessary
to add drugs to reduce cholesterol levels. Fortunately, newer
cholesterol-lowering drugs have been developed that are both
effective and safe for most people.
Previous research has established that people with a high level
of LDL cholesterol in their blood are at greater risk of developing
coronary heart disease. The present study further documents that
life-long reductions in LDL cholesterol can actually help prevent
heart disease.
Previous findings by Dr. Hobbs and colleagues at UT Southwestern
had identified specific mutations in the gene called PCSK9 that
are associated with lower LDL cholesterol levels in people who
have the mutations. Those genetic studies were based on data
gathered from the UT Southwestern-directed Dallas Heart Study,
a groundbreaking multiyear investigation of cardiovascular disease
involving 6,000 Dallas County residents.
The new findings are based on data obtained from subjects drawn
from the Atherosclerosis Risk in Communities Study (ARIC), which
tracked the health of participants from four communities in Mississippi,
Minnesota, North Carolina and Maryland for 15 years, beginning
in 1987. UT Southwestern’s collaborators at the UT Health
Science Center in Houston analyzed blood samples from those participants
to determine who carried the cholesterol-lowering genetic variations.
The researchers then tracked the subjects’15-year health
history and found the association between lower long-term LDL
levels and lower risk of heart disease.
The PCSK9 gene produces an enzyme that normally controls the
number of LDL receptors lining the surface of liver cells. These
LDL receptors latch on to LDL and remove it from the blood. Dr.
Hobbs and co-workers previously found that genetic mutations
that inactivate PCSK9 result in lower levels of the PCSK9 enzyme,
leading to higher levels of LDL receptors. By increasing the
amount of “bad” cholesterol the liver cells can remove
from the blood, LDL levels are lower in the blood of people with
the mutations.
High levels of PCSK9 tend to raise the blood concentrations
of LDL. Currently statins are the standard class of drugs prescribed
to lower LDL in patients. However, statin treatment may increase
the production of the PCSK9 enzyme, Dr. Hobbs said, which in
turn may limit the effectiveness of these drugs. Developing new
therapies that inhibit PCSK9 activity not only should lower LDL
levels, but in addition, might enhance the effectiveness of statins,
she said. |