Our tears could one day tell us if we have glaucoma
Credit: Phil Jones, Senior Photographer, Augusta University
AUGUSTA, Ga. (June 10, 2019) – Contrary to what many of us think, high pressure inside the eye does not define glaucoma and investigators want to know if the proteins circulating in the fluid of our eyes might.
While some patients do have classic high pressure inside the eye, the reality is others with glaucoma don’t, says Dr. Ashok Sharma, proteomics and bioinformatics expert in the Center for Biotechnology and Genomic Medicine and Department of Population Health Sciences at the Medical College of Georgia at Augusta University.
Since glaucoma, a leading cause of blindness worldwide, also has no clear, early symptoms, by the time patients realize they have a problem they can have significant optic nerve damage and vision loss, says Dr. Lane Ulrich, ophthalmologist in the MCG Department of Ophthalmology and James and Jean Culver Vision Discovery Institute at AU, and a study co-investigator.
Now MCG investigators are working to associate the protein profile present in the eye’s fluid with the obvious structural damage to the eye glaucoma causes. Their goals are to find a better way to diagnose the common eye problem, monitor its progress and maybe find new treatment targets. If they do, your tears may one day provide the fluid needed to perform such tests.
Sharma is principal investigator on a $1.5 million grant from the National Institutes of Health that is enabling examination over the next four years of the fluid of 200 patients with glaucoma and 400 with cataracts serving as controls.
They are comparing the protein profile in the millionth of a liter of fluid, or aqueous humor, found in the eye – and removed as part of surgery – with clinical data, like images of a misshapen optic nerve, and other demographic and health data like age and race, to begin to write a proteomic signature for glaucoma.
They also are creating a database of the proteins and related clinical and scientific info they find that other scientists can access for their own studies. Eventually, the database may be expanded to include data from other labs, Sharma says.
“Probably half the people who have glaucoma do not have intraocular pressures above average,” says Dr. Kathryn Bollinger, ophthalmologist, glaucoma specialist and retinal cell biologist in the MCG Department of Ophthalmology and the Culver Vision Discovery Institute, and a study co-investigator.
Conversely, some with what is considered high pressure don’t have the potentially blinding condition. While the bottom line is damage to the neurons in the eye, the level of intraocular pressure that causes damage varies in different people, she says.
“That is part of the reason why these studies are so important, because we don’t have a clear diagnostic indication for glaucoma based simply on intraocular pressure,” Bollinger says.
“After we find a patient actually has glaucoma, we would like to classify them as adequately controlled and therefore stable rather than progressing,” adds Ulrich. “So we are looking for a good way to not only identify these patients but also to monitor them better.”
While exactly where ocular proteins come from and what they do is largely a mystery, it is clear they are part of the microenvironment of glaucoma that should provide good clues about what is occurring at the molecular level, Sharma says.
“The aqueous humor has a lot of molecular information because it is in contact with tissues in the eye and there are proteins coming in and out, and all those molecules might be related to function,” Sharma says.
Previous technologies to look at these and other proteins required the entire fluid volume to look at just one or two proteins rather than the large number current technologies enable. Sharma developed the systems that are enabling all the information gathered to be analyzed, stored and integrated.
Their preliminary studies of the eye fluid of 66 patients – about half of whom either had or were suspected to have glaucoma – found 807 unique proteins, 43 of which were significantly altered in patients with glaucoma.
Ophthalmologists routinely check eye pressure as a part of the eye exam, really at any age but more often as people age, says Ulrich. But they also look in the back of the eye at the optic nerve, which connects the eye to the brain, for these classic shape changes that indicate it’s under too much pressure, he says. When they see changes, they get images to further confirm and study those changes.
“I usually tell patients it’s sort of like a volcano, it’s got a crater and then there is an edge of the volcano. In glaucoma, the crater gets bigger and bigger and bigger,” Ulrich says.
Like people themselves, some individuals’ nerves can handle pressure better than others and you can’t tell who they are by looking.
“We see patients all the time who have vision loss due to glaucoma that, if recognized earlier, could have been prevented,” Bollinger says. “That is the idea here, to identify a signature that indicates early on that particular person either is predisposed to developing glaucoma or they are not.”
“This kind of study will allow us to really pinpoint people and to target our treatment toward people who need it,” she says.
Glaucoma typically first affects peripheral vision; advanced disease causes total vision loss and is a leading cause of irreversible blindness worldwide. Treatments include eye drops that reduce pressure by reducing the production or increasing the outflow of aqueous humor. Surgery can also improve outflow.
While glaucoma is a risk for everyone, especially as we age, it is a higher risk for blacks over age 40 and people with a family history. Associated risks include hypertension, diabetes, tobacco use and long-term use of corticosteroids.
During cataract and glaucoma surgery, the tiny amount of aqueous humor is removed, typically discarded and temporarily replaced with a clear viscoelastic gel until the natural biofluid can build back up.
Other co-investigators on the study, all from MCG, include Dr. Sylvia Smith, chair of the Department of Cellular Biology and Anatomy; Dr. Shruti Sharma, vascular and endothelial biologist; Dr. Wenbo Zhi, biochemical engineer; and Dr. Yutao Liu, vision scientist and human geneticist.
Collaborators also include MCG ophthalmologists Drs. David Bogorad and Amy Estes. Sharma is also director of the Graduate Program in Genomic Medicine in the MCG Center for Biotechnology and Genomic Medicine and a member of the Culver Vision Discovery Institute.