Study
Sheds New Light On Pediatric Heart Conditions
Registry Points
To Genetics In Some Cases
A report from a data
registry on the sometimes-fatal childhood condition called pediatric
cardiomyopathy provides insights into this disease.
It also points the
way toward better diagnosis and perhaps even treatment, says
an expert who started the registry.
The report finds the
rare condition is more likely to strike boys than girls, and
is more common among African Americans and Hispanics than
Caucasians.
Cardiomyopathy consists
of a family of conditions that affect the heart muscle. About
1,000 children are born in the US each year with a form of cardiomyopathy.
Progress
in Treatment Is Lacking
While enormous strides
have been made in treating conditions caused by problems with
the heart's blood vessels, little progress has been made on
heart muscle problems. A transplant is the only hope for many
young cardiomyopathy patients.
"The time to transplantation
or death for children with cardiomyopathy has not improved during
the last 35 years," says a new report in the New England
Journal of Medicine.
That report provides
precise information about pediatric cardiomyopathy, such as
when it is diagnosed, its incidence in different ethnic groups,
and the percentage of the different kinds of cardiomyopathy.
The regions of the country covered in the report are New England
and the central southwest, which includes Texas, Oklahoma, and
Arkansas.
Those numbers alone
represent something new, says study author Dr. Steven E. Lipshultz,
who started the Pediatric Cardiomyopathy Registry when he was
at Boston Children's Hospital. He is now a professor of pediatrics
at the University of Rochester School of Medicine in New York.
"If you look at some
of the current textbooks in pediatric cardiology, you will find
they state that hypertrophic cardiomyopathy [in which the heart
muscle is abnormally thickened] is rare in adolescents," says
Dr. Lipshultz, after reflecting on new information from the
registry. "That is not true."
The registry says
42 percent of cases are hypertrophic, while 51 percent are dilated,
in which the heart muscle expands abnormally, with scattered
other causes accounting for the remainder.
Families May
Consider Screening
And while pediatric
cardiologists said in a survey the condition could be detected
at almost any age, the registry shows most cases being diagnosed
in the first year of life, Dr. Lipshultz says.
"That suggests that
many of the causes are genetic, while in adults many cases are
related to health habit issues," he says.
Other indicators that
genetics is important are striking differences in incidence
between the sexes and ethnic groups.
The incidence is 1.32
per 1,000 in boys compared to 0.92 per 1,000 in girls, in large
part because several genes for neuromuscular disease that can
also cause cardiomyopathy are more common in boys.
The condition is more
common in African-American children (1.4 cases per 1,000) and
in Hispanics (1.41 per 1,000) than in Caucasians (1.06 per 1,000).
The incidence was about 50 percent higher in the Southwest than
in New England, a finding that leaves the researchers puzzled.
The effect of genetics
can be important in early detection, Dr. Lipshultz says. It
is important to screen other family members when a case is diagnosed,
he says, to pick up cardiomyopathy that may be causing few or
no symptoms.
Second
Study Finds Similar Trends
What Lipshultz
also finds striking is that a study done in Australia, and reported
in the same issue of the journal, produces very similar numbers.
"These two studies,
done without knowledge of each other, have come up with almost
the same results," Dr. Lipshultz says.
That study, led by
Dr. Robert G. Weintraub of the Royal Children's Hospital in
Melbourne, covered all known cases diagnosed in children 10
and under between 1987 and 1996.
It found about the
same overall incidence, 1.24 per 1,000, the same concentration
of diagnoses in the first year of life and the same higher incidence
in a minority group, in this case Australian aborigines (2.47
per 1,000).
"It is remarkable"
the studies have similar results, but also fortunate, Dr. Weintraub
says. "We think that the two studies serve as external validation
to each other."
Dr. Weintraub is director
of the heart transplant program at Royal Children's Hospital,
which serves all of Australia. He says the study was undertaken
"to better gain an appreciation of how to plan heart transplantation
for those children who require it."
The study has helped
to give "a better appreciation of how these cases present and
behave, so we can make long-term predictions about which children
will require transplants," he says.
Always consult your
physician for more information.
What
Is Cardiomyopathy?
Cardiomyopathy is
any disease of the heart muscle in which the heart loses its
ability to pump blood effectively.
In some instances,
heart rhythm is disturbed, leading to irregular heartbeats,
or arrhythmias. There may be multiple causes of cardiomyopathy,
including viral infections. Sometimes, the exact cause of the
muscle disease is never found.
Cardiomyopathy differs
from many of the other disorders of the heart in several ways,
including the following:
-
Cardiomyopathy can, and often
does, occur in the young.
-
The condition is fairly uncommon,
affecting only about 50,000 Americans (adults and children).
-
Cardiomyopathy is a leading
cause for heart transplantation.
-
The condition tends to be
progressive and sometimes worsens fairly quickly.
-
It may be associated with
diseases involving other organs, as well as the heart.
Always consult your
physician for more information.
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June 2003
Study
Sheds New Light on Pediatric Heart Conditions
Progress
in Treatment Is Lacking
Families
May Consider Screening
Second
Study Finds Similar Trends
What
Is Cardiomyopathy?
What
Types of Cardiomyopathy Commonly Affect Children?
Online
Resources
What
Types of Cardiomyopathy Commonly Affect Children?
dilated (congestive)
cardiomyopathy
This is the most common
form of cardiomyopathy. The heart muscle is enlarged and stretched
(dilated), causing the heart to become weak and pump inefficiently.
Other problems that
may occur with dilated cardiomyopathy include the following:
-
irregular heart rhythms
-
risk of blood clots
-
congestive heart failure
Various infections
(including viral) which lead to an inflammation of the heart
muscle (myocarditis) can cause this type of cardiomyopathy.
Contact with toxins
or very powerful therapeutic drugs, such as certain types of
chemotherapy given to fight cancer, have been known to cause
dilated cardiomyopathy.
Heredity can also
be a factor. Twenty percent of people with dilated cardiomyopathy
have a parent or sibling with the disease.
In many cases, a specific
cause for this type of the disease is never identified.
Because the heart
muscle is weak and unable to pump enough blood to meet the body's
demands, the body tries to preserve blood flow to essential
organs such as the brain and kidneys by reducing blood flow
to other areas of the body, such as the skin and muscles.
The following are
the most common symptoms of dilated cardiomyopathy. However,
each child may experience symptoms differently.
Symptoms may include:
-
pale or ashen skin color
-
cool, sweaty skin
-
rapid heart rate
-
rapid breathing rate
-
shortness of breath
-
fatigue
-
irritability
-
chest pain
-
poor appetite
-
slow growth
hypertrophic cardiomyopathy (Also known as hypertrophic
obstructive cardiomyopathy, HOCM; asymmetric septal hypertrophy,
ASH; or idiopathic hypertrophic subaortic stenosis, IHSS.)
In this type of cardiomyopathy,
the muscle mass of the left ventricle of the heart is larger
than normal, or the wall between the two ventricles (septum)
becomes enlarged.
These abnormalities
obstruct the blood flow from the left ventricle.
The thickened muscle or septal wall can also affect one of the
leaflets of the mitral valve, which separates the left atrium
and the left ventricle. The valve leaflet becomes leaky, allowing
blood to move backwards from the left ventricle into the left
atrium, instead of forward to the body.
Hypertrophic cardiomyopathy
is often hereditary. One-half of children with the disease have
a parent or sibling with varying degrees of left ventricular
muscle or ventricular wall enlargement, although relatives may
or may not have symptoms.
Children with hypertrophic
cardiomyopathy may have symptoms that increase with exertion
or symptoms may be unpredictable.
Symptoms may include
shortness of breath on exertion; dizziness; fainting; chest
pain; or abnormal heart rhythms. However, each child may experience
symptoms differently.
Consult your child's physician for more information regarding
the specific outlook for your child.
Online
Resources
(Our Organization
is not responsible for the content of Internet sites.)
American
Academy of Pediatrics
American
Heart Association
Centers
for Disease Control and Prevention (CDC)
National
Heart, Lung, and Blood Institute (NHLBI)
National
Institutes of Health (NIH)
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