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. |