What is Glaucoma?

Take Home Points

Most likely, you were told you had or might have glaucoma at a routine exam of your eyes and had no idea that anything might be wrong. Most common types of glaucoma give no indication that they’re there (the medical term for this is that the disease is asymptomatic). There are two main types of glaucoma: open angle and angle closure glaucoma. Half of the people in the developed world with these types of glaucoma don’t know they have the disease, while in the developing world most cases are unfortunately undiagnosed and untreated. This is partly because some people don’t go for eye exams. It is also because not all eye doctors recognize glaucoma when they examine the eye.

When you look at something, the light enters your eyes and a description of what you see is transmitted to your brain. Your eye has several major parts that assist in this job. Each of the parts is made up of cells, the building blocks of your body. These cells have different specialized jobs; some hold your body together like bricks and mortar, while others send messages to each other like a cell phone sending through towers to another cell phone. Cells called retinal ganglion cells are particularly important because it is these cells that are damaged in glaucoma. When light comes into the eye, the light is received first in cells called rods and cones. These cells (also called photoreceptors, because they receive the light) send information about what you are seeing to a second layer of cells, and finally layer 2 cells link up to layer 3 cells, where the ganglion cells are.

Ganglion cells are the cells that die in glaucoma. Once they die, they are not replaced by new cells. This is not true in your skin or even on the front surface of the eye, the cornea, both of which make new cells all the time. But ganglion cells, like other nerve cells in the brain do not make new cells by duplicating themselves. There is a good reason why not. New nerve cells would possibly mess up the complicated circuits already there. We must think how complex the eye and the brain are. There are 1 trillion nerve cells in the human brain and each has about 100 connections or synapses to other nerve cells (100 trillion, or 100,000,000,000,000 for those who like zeroes). In addition, ganglion cells in the retina are surrounded by supporting neurons called amacrine cells and other supporting cells called glia. In the eye there are 3 kinds of glia: astroglia, because they are shaped like pointy stars; microglia because they are small; and Müller cells because Dr. Müller got them named for himself. From the time the retina begins to develop in the womb until around the time of birth, nerve cells are turning into the various types that will be present in the adult (about 10 kinds in the retina). And, up until the age of 6 years of age, the eye’s nerve cells are still forming their final permanent connections to other nerve cells in the eye and to partner cells in the brain. Some eye nerve cells connect to other nerve cells at both ends, picking up information from a previous layer and passing it along to the next layer. The ganglion cells that die in glaucoma are that kind of double-ended neuron.

Even more amazing, ganglion cells pick up all the information from the other nerve cells in the retina and carry it out of the eye on their one fiber through the optic nerve head (Figure 1) to the next way-station in the brain (the lateral geniculate). From there, there is another relay to the back of the brain where more complex visual processes go on. The ganglion cell’s fiber is amazingly long. If the cell body in the retina were the size of a basketball, the fiber would be as long as a football field (the actual fiber is about 2 inches long). On its way, this fiber has to pass through the wall of the eye to get into the brain. The optic nerve head, where the fiber leaves the eye is the ganglion cell’s Achilles heel, a spot where the stress of the eye wall and the need for good blood supply in a tight spot can kink it and disrupt its communication (see section How did you get glaucoma?). We have known for a long time that the normal flow of chemicals within the ganglion cell fiber is blocked in glaucoma just where fibers leave the eye. This is how the ganglion cell is injured and dies.

Eye and optic nerve anatomy
Eye and optic nerve anatomy
Figure 1: Eye and optic nerve anatomy. The drawing shows the main parts of the eye: cornea, iris, lens, trabecular meshwork, ciliary body, aqueous humor, choroid, sclera, retina, and optic nerve head. The photograph is the optic nerve head, a round area with blood vessels radiating out from it.

So, once a large number of ganglion cells die from glaucoma, the patient’s peripheral vision is affected seriously. How many have to die to really cause vision loss? Glaucoma Center of Excellence research shows that it takes the loss of about 30% of the ganglion cells to reach the point where the doctor’s tests (visual field tests) show that the patient’s vision is definitely abnormal.

Glaucoma creeps up on us without notice because of several features. First, it involves the slow loss of retinal ganglion cells (Figure 2). Because these cells carry the visual messages through which we see, losing them causes our vision loss. But ganglion cells die so gradually in most persons with glaucoma that we don’t notice the loss. We begin life with around one million ganglion cells and barring major eye disease, 75% of them last until we are 90 years old. Glaucoma speeds up the rate at which they die. Each ganglion cell has its own location in the eye to receive light signals over a tiny area that is up to one millimeter wide. As the tiny fibers of each ganglion cell leave the eye, they are vulnerable to being injured at their exit point, the optic nerve head.

Retinal ganglion cell
Figure 2: Retinal ganglion cell. A photograph of a retinal ganglion cell, with its central cell body from which branches spread out to receive messages from other nerve cells. The axon fiber that carries its message out of the eye to the brain leaves the picture at the right. When this fiber passes out of the eye at the optic nerve head, it is injured in glaucoma, causing the ganglion cell to die.

The second reason glaucoma is a silent disease is that the ganglion cells most likely to die are those that provide us with our side vision. Only late in the disease does it attack our center vision, where we have our 20/20 reading ability. We don’t rely as much on our side vision as we do the center vision. When we are reading or watching TV or surfing the net, our attention is focused on the object in front of us, not things off to one side. This means that the vision loss from glaucoma is not noticeable in its early stages. You can get a feeling for where the initial damage happens by looking at Figure 3. Close your left eye and hold this book (or computer) at a normal reading distance of about 14 inches. Look at the right page with your right eye, where the words are in bold print. The typical place for early glaucoma damage to cause you not to see is on the left page, where some of the print has been removed as an illustration. Since we normally pay most attention to directly where we’re reading, most of us would not notice anything wrong if this part of the vision were missing.

Early vision loss
Figure 3: Early vision loss. An example of the zone in which early glaucoma vision loss happens. Follow instructions in text for how to view this drawing.

Another reason that glaucoma’s damage is not noticed early on is that it typically affects only one eye at first. The other eye is still fully functional. Both eyes get similar information about the world, and the brain converts the two separate signals into a single picture. With both eyes open, as we view the world, any object is seen by both eyes and its image is sent to the brain by both. If the brain gets the image from either eye, we see it and we think nothing is missing. In fact, loss of the image from one eye does cause a loss of the ability to see things in three dimensions. This ability helps us to tell how far away from us something is in space and is called stereoscopic vision. So, we can lose a lot of vision from one eye, but if the other eye is unaffected by glaucoma, we don’t notice. Clinical research from our Wilmer Institute Center for Glaucoma Excellence shows that the typical person with glaucoma loses twice as much vision in the worse-affected eye compared to the better eye, but if left untreated, eventually both eyes become abnormal and this really decreases our ability to enjoy life.

Fourth, we’re pretty adaptable creatures, and we alter our behavior to take account of the damage, even without knowing it. When investigators evaluate how much glaucoma damage it takes to affect patient’s daily activities, they find that damage has to be pretty bad before it is recognized as a problem. Yet, when the actual functional capability is measured, in such things as reading, walking, and driving, it is clear that persons with significant glaucoma damage read more slowly, walk more carefully, bump into things more, and give up driving sooner than others.

One fundamental fact is that vision lost from glaucoma does not come back and no present treatment can restore it. Some parts of your body, such as your skin, can recover from damage because those organs can build new cells to replace damaged cells. This is not true for nerve cells in the brain or the eye. The ganglion cells that are damaged in glaucoma cannot be fixed or replaced once they are damaged. The layer of nerve tissue in the eye that contains the ganglion cells (the retina) is a very complicated network of 10 types of cells. Ganglion cells are the only ones to die from glaucoma, but their loss causes rearrangements in the retina and up in the brain’s relay centers to which they go. To put back function, we will need to insert new nerve cells in their place, to reconnect the new cells to the cells that are still there, and to make those connections work with the existing connections in the way that they did originally. While our laboratory, along with others, has taken the first steps in this process, it is a long way to go to successfully restore vision in a human eye (see section Can glaucoma be cured?).

One final important fact is that all of the forms of glaucoma are related to some degree to the pressure inside the eye. The eye is something like a camera, with lenses at the front (called the cornea and the lens) and the film or the digital receiving surface at the back (the retina; Figure 1). For clear vision, we need the image placed on the retina and not moving, since if it is not stable, it would seem blurred. The eye is filled with fluid which must be kept within a narrow range of pressure, like the air pressure inside of a bicycle tire. The fluid inside the eye is not the fluid we make when our eyes tear (or when we cry). Tears come from glands outside the eye and are not directly related to glaucoma. Like a bicycle tire, the eye must have the correct pressure inside to work properly. The balance between fluid flowing in and out of the eye maintains a higher pressure inside the eye than outside. This pressure difference produces stress in the eye wall (the sclera), keeping it tense and stable so that the retina’s image is clear.

The normal eye pressure is about 15 millimeters of mercury. This is enough pressure to make the images stable on the retina by keeping the wall of the eye firm. The wall of the eye is made of 3 layers: the white outer layer or sclera, the middle layer containing blood vessels (the choroid), and the retina with its nerves. Pressure is maintained by having fluid come into the eye at one location (the ciliary body) and leave through the main outflow zone (the trabecular meshwork). The continuous flow of this fluid (the aqueous humor) also nourishes the structures inside the eye that have no blood supply of their own.

Whether the eye pressure is a bit lower or higher, there is always some physical tension (called stress by engineers) in the sclera. The higher the pressure, the more is the stress. Because the fibers of ganglion cells must go through the sclera at the optic nerve head to go up to the brain, they are damaged by this stress (Figure 4).

Retinal ganglion cells and the optic nerve head
Figure 4: Retinal ganglion cells and the optic nerve head. Drawing at the left shows 2 ganglion cells (shaped like spiders) in the retina and their fiber passing to the nerve head. In the nerve head, the fibers are injured by stress (arrows) applied to them or to their supporting tissues, which causes kinking of fibers. At the right, the support structure of the nerve head is seen from inside the eye. Ganglion cell fibers pass out of the eye through the many small holes. Stress in the eye wall pulls on this structure and damages the fibers (which were removed to make this picture).

Ganglion cells are damaged by prolonged eye wall stress and this is the cause of damage to your vision in glaucoma. This means that the higher the pressure, the greater the chance for glaucoma. However, not everyone's eyes react to pressure in the same way. The fibers in some people's eyes can tolerate greater amounts of pressure than others. If my eye has a thinner wall than yours, or is bigger in diameter, it will have more stress from the same amount of pressure (Figure 5).

Eye size and glaucoma
Figure 5: Eye size and glaucoma. Drawings show small eye with thicker eye wall (above) and larger eye with thinner wall (below). There is stress in the eye wall from eye pressure in both eyes (arrows), but the stress is greater (bigger arrows) in the big, thin-walled eye. Near-sighted (myopic) eyes are therefore more likely to get open angle glaucoma.

So, glaucoma can happen at any pressure, as long as the effects of stress are sufficient to kill ganglion cells. In fact, half of those with the most common type of glaucoma, called open angle glaucoma, always have a normal level of eye pressure. In their eyes, the stress of normal pressure (combined with other features) is enough to kill ganglion cells. Therefore, it is not necessarily “elevated” pressure that is the enemy in glaucoma (see section Low tension glaucoma doesn’t exist and you don’t have a brain tumor). All present treatment for glaucoma is designed to reduce the damaging level of pressure found in the untreated person, lowering it to a safer level that will allow no further damage (see section What is the target pressure?)

Experts say that the official start of glaucoma is when one of the eyes has suffered actual structural and functional damage. This damage shows up as specific abnormalities on standard examination tests (see section What tests are needed to diagnose glaucoma?). Before this point, there are many persons who are suspected to have glaucoma but have not met the official damage criteria, and they are called glaucoma suspects. In the offices of many eye doctors, these strict definitions are not used and some doctors use the term glaucoma more broadly to mean anyone whom they intend to treat with eye drops.

The next sections describe the various types of glaucoma and how they differ.

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