Glaucoma Often Occurs in Families
If you have glaucoma, there is a good chance that
someone else in your family may have it, too. For primary open-angle
glaucoma, the most common form of glaucoma, there is approximately a
one-in-five chance that a close relative also has glaucoma. For some
less common forms of glaucoma, such as Rieger’s syndrome and
glaucoma of childhood, the risk of brothers or sisters and children
developing the disease is close to 50%.

Figure 1: DNA (deoxyribonucleic acid) provides the
genetic message of the body. It has a special shape
called a “double helix,” due to its pair of twisted
strands of genetic material.
The heritable nature of glaucoma means that your
brothers, sisters, and children need to obtain regular eye
examinations, especially after age 40. If your glaucoma was first
detected at a young age, then your relatives should be examined at
an earlier age, too. They should be told to let their eye doctor
know that they have a close relative with glaucoma so that careful
attention can be directed at examination of the optic nerve.
Good News About Glaucoma
The good news about the heritable nature of
glaucoma is that it permits the use of powerful new scientific tools
of molecular genetics to study glaucoma. Molecular genetic studies
have made great strides in recent years in providing important
information about other inherited diseases such as cystic fibrosis,
Huntington’s disease, and retinitis pigmentosa. There is a good
reason to believe that they will provide important new information
about glaucoma, as well.
Since 1987, molecular genetic studies have been
directed at discovering new information about glaucoma. Progress has
been made in finding the region of DNA that is defective for some
forms of glaucoma, including Rieger’s syndrome, juvenile
open-angle glaucoma, iris hypoplasia, and aniridia. Even though
these are uncommon forms of glaucoma, they have features that make
them easier to study than primary open-angle glaucoma. Both Rieger’s
syndrome and aniridia are sometimes seen as part of a group of
abnormalities caused by rearrangements in a patient’s chromosomes.
These rearrangements can be seen under the microscope, and serve as
road maps leading scientists to the exact spot where the defective
gene lies. In the cases of juvenile open-angle glaucoma and iris
hypoplasia, the young age at which glaucoma develops and the 50%
risk of being affected leads to families in which many members have
glaucoma. This enables the genetic make-up of these affected
individuals to be determined.
Even though primary open-angle glaucoma is by far
the most common form of glaucoma in the United States, it is
difficult to study its genetic basis. Unlike the juvenile forms of
glaucoma, primary open-angle glaucoma strikes fairly late in life,
when the affected individual’s parents and some brothers and
sisters may no longer be living. The next generation may not yet be
old enough to show early evidence of the disease. Because of this,
single families large enough to study have not been identified.
Therefore, many smaller families will need to be pooled to find the
affected region.
Possible Benefits of Genetics Research in Glaucoma
How will this type of research help patients with
glaucoma? If scientists can find the defective gene or genes that
cause glaucoma, we should be able to identify the precise substances
responsible for causing it. This knowledge will allow us to better
understand the mechanisms that cause glaucoma.
This understanding might dramatically change the
way we treat glaucoma. In the distant future, it may be possible to
replace a glaucoma-causing gene and either prevent glaucoma or more
effectively treat it. A more immediate benefit would be the
development of treatment directed at replacing or altering
substances made by the defective genes. We might even envision a day
when a patient would take a specific medication to treat the
underlying cause of his or her glaucoma, rather than just lowering
eye pressure.
It may also be possible to develop blood tests
that can be used to screen for individuals at risk for glaucoma long
before eye pressure is increased, before the optic nerve is damaged,
and before the loss of visual field. In some families that have many
members with childhood glaucoma, we can already determine by a blood
test which children will develop glaucoma and which children will
not. The hope is that this type of testing may someday be available
for all forms of glaucoma.
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Dallas, TX 75231
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