Depression Raises Risk of Death for Heart Attack
Victims for Years After Attack
Only about 25 to 30% of these patients receive
antidepressant drugs, treatment
By Jim Dryden
March 3, 2008 -- Depressed heart attack patients
have a higher risk for sudden death in the months following a heart
attack. Now a team led by researchers from Washington University School
of Medicine in St. Louis has found that the risk continues for many
years.
"There's a two- to four-fold increase in a person's
risk of dying following a heart attack if they also happen to be
depressed," says Robert. M. Carney, Ph.D., lead author of the new study
and professor of psychiatry at Washington University.
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"Previously we
thought the impact of depression was strongest for the first three to
six months following a heart attack and then gradually dropped off
within a couple of years. Instead, we found that the effect lasts for at
least five years."
Carney, with colleagues from Duke University
Medical Center, Harvard University, Yale University, the National Heart,
Lung and Blood Institute (NIH) and the Mayo Clinic, followed more than
750 heart attack patients for five years. The findings will appear in an
upcoming issue of the Journal of Affective Disorders and are currently
available online.
Patients followed in the study had participated in
the NIH-funded project Enhancing Recovery in Coronary Heart Disease
Patients (ENRICHD). A little less than half were diagnosed with
depression.
In the five years following a heart attack, 106
patients died. Of those, 62 had been diagnosed with depression, while 44
had not. In gauging the effects of depression, the investigators also
considered other risks including age, smoking, hypertension, gender and
diabetes.
Some of those factors, like younger age and female
gender, lower mortality risk. Smoking and diabetes tend to raise the
risk of dying. Carney says his team used statistical methods to evaluate
the ways in which the various factors influenced mortality risk. Then
they removed the influence of all other factors from the risk equation
in order to consider the statistical impact of depression itself.
"We found that after adjusting for those risk
factors, depression continues to play a statistically significant role,"
he says.
One possible explanation for depression's lingering
influence on mortality is its recurring nature. Because the disorder can
come and go over many years, it also may continue to increase the risk
of death for many years.
"People typically are depressed for a while, then
they'll either get better with treatment or it may subside on its own,"
Carney says.
"But depression can always recur, and we think that
because it is a recurring problem, whatever depression is doing to
mortality risk after a heart attack, it continues doing for quite a long
time."
Past studies have differed over how much depression
affects survival following a heart attack. But Carney believes these new
findings are more reliable because all of the patients in this study
were personally interviewed to determine their depression status,
whereas other studies have relied on self-reporting.
"In our experience, self-reporting tends to
overestimate the risk because it's often not possible to evaluate the
causes of various symptoms on self-report questionnaires," he explains.
"Say somebody reports having sleeping problems
that would go into the depression column as a symptom. But it's possible
they are sleeping poorly because of a bad back or because they have to
get up and go to the bathroom frequently during the night. During an
interview, we can determine whether an individual symptom is related to
depression or can be explained in some other way."
Carney's team also found that any clinically
relevant depression increases the risk of death in heart attack
patients. The risk was elevated both for patients with major depression,
which requires the presence of five or more symptoms, and minor
depression, which requires between two and four symptoms for diagnosis.
Major depression was associated with higher risk,
but minor depression also was associated with a significant increase in
mortality risk.
Even with mounting evidence of a link between
depression and death in heart attack patients, only about 25 to 30
percent of these patients receive antidepressant drugs or other
depression treatments.
That doesn't surprise Carney. His team reported in
2003 in the Journal of the American Medical Association that providing
treatment for depression seemed to have little effect on whether
patients survived or had a second heart attack. This could be because
the treatments don't work for all patients, Carney says, and he suggests
if current depression treatments could be improved, survival rates might
increase, too.
To this end, his team is studying whether omega-3
fatty acids the fatty acids found in fish oil might improve
antidepressant therapies in heart patients. They're giving an
antidepressant drug and a special formulation of omega-3 to some heart
patients and comparing them to depressed heart patients who receive an
antidepressant but no omega-3.
"We have not been satisfied with the effectiveness
of standard antidepressants at alleviating depression in this population
of patients," Carney says. "We're studying omega-3, because there's
preliminary evidence that the fatty acids also might make depression
therapies more effective, both in treating depression and in improving
heart health."
The new study is enrolling people with depression
who have suffered a heart attack at least three months previously. After
being evaluated for depression, patients will take an antidepressant and
be randomly assigned to take a capsule containing either omega-3 or corn
oil for 12 weeks. Carney's team evaluates both mood and heart function
during the course of the study.
All medication, supplements, medical and
psychiatric evaluations are provided free of charge. For more
information about the study, call Cathi at (314) 286-1517 or Carol at
(314) 286-1315.
Editors Notes:
Carney RM, Freedland KE, Steinmeyer B, Blumenthal
JA, Berkman LF, Watkins LL, Czajkowski SM, Burg MM, Jaffe AS. Depression
and five-year survival following acute myocardial infarction: a
prospective study. Journal of Affective Disorders, 2008.
doi:10.1016/j.jad.2007.12.005
This study was supported by grants from the
National Heart, Lung, and Blood Institute (NHLBI) of the National
Institutes of Health, and from the Lewis and Jean Sachs Charitable Lead
Trust, St. Louis, MO
This ENRICHD study was supported by contracts from
the National Heart, Lung, and Blood Institute (NHLBI) of the National
Institutes of Health. Pfizer Inc. provided setraline (Zoloft) for that
study.
Washington University School of Medicine's 2,100
employed and volunteer faculty physicians also are the medical staff of
Barnes-Jewish and St. Louis Children's Hospitals. The School of Medicine
is one of the leading medical research, teaching, and patient care
institutions in the nation, currently ranked fourth in the nation by
U.S. News & World Report. Through its affiliations with Barnes-Jewish
and St. Louis Children's Hospitals, the School of Medicine is linked to
BJC HealthCare.