Pulmonary Disease and Exercise Tolerance in Boys With Fabry Disease

Fabry disease is due to an alteration in the genetic material (DNA) that causes a deficiency
of the alpha-galactosidase A enzyme. This enzyme aids in the breakdown and elimination of
certain types of fatty substances called glycolipids. These glycolipids are normally present
within the body in most cells. When alpha-galactosidase A is lacking, these glycolipids
build up in various tissues such as the eye, liver, kidney, skin, muscle, heart, and blood
vessels. The build up of glycolipid levels in these tissues, particularly
globotriaosylceramide (GL-3), is thought to cause the clinical symptoms that are associated
with Fabry disease. Fabry disease causes chronic kidney damage leading to a need for
dialysis or kidney transplantation, chronic heart damage leading to abnormal heart rhythms
and heart attacks and strokes at an early age, nervous system damage leading to chronic
pain, and a premature death. Because the gene for Fabry is on the X chromosome (men have
only one X chromosome while women have two), most patients with symptoms of Fabry are men
but many women have symptoms that may be as severe as men. There is currently a FDA approved
treatment available that treats many of the symptoms of Fabry, but it involves intravenous
infusions every other week and is very expensive.

When to start children on therapy is controversial because of its expense and inconvenience.
Children with significant pain or gastrointestinal problems are started on therapy
immediately, otherwise not until they are at least teenagers. Increasing evidence suggests
that even without overt symptoms, significant, irreversible damage may be occurring in
childhood. However, determining whether such damage is present or not requires biopsies.
There are no simple measures of disease severity.

Many Fabry children complain of exercise intolerance. In adults, the investigators have
found decreased lung function and ability to exercise on a treadmill. Whether or not lung
function and exercise capacity is abnormal in children is unknown. While lung function and
exercise tests are commonly part of routine evaluations for adults with Fabry, they are not
yet for children.

The objective of the proposed study is to more accurately define the lung and exercise
abnormalities in a group of 20 boys from 8-18 years of age with Fabry disease who have not
been treated with enzyme replacement therapy (Fabrazyme). This will be done by several
breathing tests and exercising on a treadmill. If the breathing tests are abnormal, then
testing would serve as an easy way to evaluate children and help decide when therapy should
be started and monitor the effectiveness of therapy.

Each person that consents to participate in the study will be required to commit to a single
study visit that will last approximately 4 hours at Cedars-Sinai Medical Center. The
participant will be expected to wear loose fit clothing and comfortable athletic footwear.

As part of the research, participants will be asked to participate in the following tests:

1. A pulmonary function test

2. Exercise test. Results will be forwarded to each participant's primary care physician.

All subjects must have previously been enrolled in the Fabry Registry and have the
recommended standard of care assessments in order to be eligible for this pilot study.

Inclusion Criteria:

- Fabry disease

- Male

- Between 8-18 years of age

- Enrolled in Fabry registry and have standard assessments

Exclusion Criteria:

- Enzyme replacement therapy or an experimental therapy

- Inability to perform the tests

- Other, serious medical conditions that would impact the tests