Download Fundus photo showing bone spicules typical of Retinitis Fundus

Fundus photo showing bone spicules typical of Retinitis
Pigmentosa (black areas)
Fundus photo showing atrophy of the retina with
visible choroidal vessels (not usually visible)
What is Retinitis Pigmentosa?
Retinitis Pigmentosa is a group of genetic eye disorders that progressively causes atrophy of the
retina and typically affects both eyes. It is one of the most common forms of inherited retinal
degenerative conditions, and affects 1 in 3,700 people within the United States. Typically the
disease begins in childhood or early adulthood and the rate of progression varies between cases.
It affects the peripheral retina first (the outer retina) and progressively moves toward the central
retina. In some instances, retinitis pigmentosa progresses slowly and goes relatively unnoticed
(until in later stages of the disease), with atrophying of the retina occurring over a life-span. In
other cases, retinitis pigmentosa progresses quickly and can cause severe vision problems early
in life.
Mutations in over 50 genes have been shown to cause retinitis pigmentosa and there are three
main categories of the disease; autosomal dominant, autosomal recessive and x-linked. The main
difference between recessive genes and dominant genes is that in-order to develop the disease,
you need two copies (from both parents) of recessive genes, whereas you only need one copy of
a dominant gene (from either parent). X-linked genes are responsible for determining gender
(XX for females and XY for males). Most genes causing retinitis pigmentosa are autosomal
recessive. Autosomal dominant Retinitis Pigmentosa is the least pervasive of the three, where as
X-linked Retinitis Pigmentosa is the most pervasive.
Typically the first symptom of retinitis pigmentosa is night blindness. Patients with night
blindness have problems seeing or are clumsy in dimly lit rooms. This occurs because the
photoreceptor responsible for seeing in low-light settings (retinal rods) become damaged in
retinitis pigmentosa. Loss of peripheral vision occurs as the disease progresses and can cause
tunnel vision (a visual field of less than 10 degrees as measured by a Humphrey visual field test).
In the late stage of the disease, central vision can start to decrease, typically to 20/200 or below.
What are the risk factors?
Retinitis pigmentosa is a genetically inherited disease caused by either autosomal dominant,
autosomal recessive, or x-linked genes. Due to the lower number of autosomal dominant and xlinked genes that cause retinitis pigmentosa, most cases are autosomal recessive. Typically
neither parent has retinitis pigmentosa, and it is common that there are no cases of the disease
within several generations or in extended family members. However, it has been estimated that
around 1% of the population within the United States are carriers of retinitis pigmentosa causing
genes.
What are the Symptoms?
If the disease progress is slow, some patients may not notice any symptoms or may not realize
that there have been any changes in their vision. Common symptoms of retinitis pigmentosa
include:
1. Night Blindness
2. Loss of peripheral vision (tunnel vision)
3. Loss of central vision (in later stages)
Fluorescein Angiography showing staining of
the RPE as a result of hypertrophy and atrophy.
Fluorescein Angiography showing atrophic areas
moving towards the macula.
How can the doctor determine the extent of Retinitis Pigmentosa?
The doctor will perform a dilated exam using a slit lamp to determine the progress of the disease
and the affect it is having on the macula. Since Retinitis Pigmentosa primarily affects the outer
retina, the doctor will use an indirect ophthalmoscope to check the periphery. Several tests are
performed to help determine the progress and extent of the disease.
What tests are performed?
Testing is important because it helps the doctor to precisely document the extent of the retinitis
pigmentosa and how much atrophy is present, and measure changes that occur. The three types
of tests described below are performed in our clinic. The four tests described below are done in
our clinic
Optical Coherence Tomography (OCT) is a high definition image of the retina taken by a
scanning ophthalmoscope with a resolution of 5 microns. The doctor can use these images to
objectively determine the amount of atrophy within the retina and to detect changes that
occur between visits.
Fundus Photography is an image taken by a digital fundus camera to visually document the
retinitis pigmentosa
Fluorescein Angiography is a test that documents blood circulation in the retina using
fluorescein dye which luminesces under blue light. Fluorescein is injected into a vein in your
arm and digital fundus pictures are taken afterwards for 10 minutes. Fluorescein
Angiography is used to document the extent of atrophy within the retina and how blood
circulation has been affected by the disease progression.
Humphry Visual Field is a test that documents the amount of peripheral vision a person has,
and is performed individually for each eye. The eye not being tested is covered so that you
are unable to see with it. With the eye that is being tested, the technician will ask you to look
into the machine and fixate on a point in the center. During the test, you will push a button
each time you see a flashing light. It is important that the eye being tested remains fixated on
the point straight ahead through-out the test. If you move your eye around during the test, the
results will be inaccurate and the test will have to be repeated.
OCT image showing decreased retinal thickness
typical of RP patients. Note normal foveal thickness
Humphrey showing loss of peripheral
vision (tunnel vision)
What treatments are available for Retinitis Pigmentosa?
Currently there are no treatments for Retinitis Pigmentosa. The National Eye Institute
recommends that high doses of vitamin A (15,000 IU) be taken daily to help slow the
progression of Retinitis Pigmentosa. This recommendation is based on a large-scale trial that was
performed in 1993. A recent study published in the Archives of Ophthalmology reported that the
addition of Omega-3 (1,200mg per day) when just starting Vitamin A therapy helps to further
slow the progression of Retinitis Pigmentosa. The study also reported that in patients who had
been taking high doses of vitamin A for over 2 years, the addition of omega-3 only slowed the
decrease in visual field sensitivity. Another recent study, also published in the Archives of
Ophthalmology, reported that the addition of lutein to vitamin A therapy helped slow the
progression of visual loss within the midperiphery (beyond 30 degrees). More tests are needed to
verify the results of these two studies. Genetic testing and counseling can help determine which
type of retinitis pigmentosa you have and the implications it may have on your family.
Treatments in the future:
Retinal Chip: For the past 10 years, researchers have been working on a way of implanting a CMOS chip
(like that in a digital camera) in the back of the eye. With new breakthroughs in nanotechnology, progress
on the chip has accelerated quickly and a third generation chip (the Argus III) is almost ready to be tested.
While the first generation (the Argus I) chip only provided 16 pixels of resolution, the Argus III will
provide over 200 pixels of resolution. It is projected that when developed, the Argus V will provide near
1000 pixels of resolution, which is the number of pixels required for face recognition. Though great
strides are being made in retina chip technology, it will be several years before this treatment is available
to the public.
What is my follow up care?
Regular visits with us our recommended so that the progress of the disease can be closely
monitored. Here is a summary:
1. High doses of vitamin A (15,000 IU per day)
2. Addition on Omega-3 (1,200 mg per day)
3. Addition of Lutein (12 mg per day) if midperiphery vision is still present
4. Obtain genetic testing and counseling with us
References:
Berson EL, Rosner M, Sandberg MA, Weigel-DiFranco C, Brockhurst RJ, Hayes KC, Johnson
EJ, Anderson EJ, Johnson CA, Gaudio AR, Willett WC, Schaefer EJ. Clinical Trial of Lutein
in Patients With Retinitis Pigmentosa Receiving Vitamin A. Archives of Ophthalmology
2010;128(4):403-411
Berson EL, Rosner M, Sandberg MA, Weigel-DiFranco C, Moser A, Brockhurst RJ, Hayes KC,
Johnson EJ, Johnson CA, Anderson EJ, Gaudio AR, Willett WC, Schaefer EJ. Further
Evaluation of Docosahexaenoic Acid in Patients With Retinitis Pigmentosa Receiving
Vitamin A Treatment. Archives of Ophthalmology 2004;122:1306-1314
National Eye Institute (2008). Update on Vitamin A as a treatment for Retinitis Pigmentosa.
Accessed from http://www.nei.nih.gov/news/statements/pigmentosa.asp