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Genetic Studies of the Ocular Hypertension Treatments Study (OHTS) Participants



A Quantitative Traits Approach to Find Glaucoma Genes

Project Summary.  Eye doctors diagnose patients with glaucoma by taking measurements of key features of the eye that are quantitative or numerical.  Some of these quantitative features of glaucoma are eye pressure (measured in mm Hg), thickness of the cornea (measured in microns), the shape of the optic nerve (measured as the cup-to-disc ratio); and the extent of vision loss. The genes that control the magnitude of quantitative features of glaucoma likely contribute risk for developing disease. 


The primary goal of this project is identify the genes that control quantitative traits of glaucoma.

Jamie Tjaden-003 scrs

Subjects of the OHTS Genetics Study

Ocular Hypertension. Eyes are filled with fluid called aqueous humor that is under pressure. On average the pressure in the eye is around 15 mm Hg and eye pressure in most eyes falls within a limited range (between 9 and 21 mm Hg). When eye pressure is above this range, it is called ocular hypertension. Around 3% to 8% of Americans over the age of 40 have ocular hypertension.


Those with high pressure in their eyes (ocular hypertension) develop glaucoma more often than those with lower eye pressure.


Ocular Hypertension Treatment Study. The Ocular Hypertension Treatment Study (OHTS) is a large treatment trial that was sponsored by the National Eye Institute. Prior to this study, it was unclear if giving pressure-lowering medicines to individuals with ocular hypertension reduced their risk for later developing glaucoma.

The goal of the OHTS was to determine if treating individuals with ocular hypertension with pressure lowering medicines reduces their risk for developing glaucoma in the future. A total of 1637 subjects with ocular hypertension were enrolled in the OHTS. At the time of enrollment in the study none of the subjects had signs of glaucoma – they only had high eye pressure. Half of the subjects with ocular hypertension received pressure-lowering medicines, while the other half received a placebo. Both groups of subjects were followed over ten years to see if pressure-lowering medicines prevented some ocular hypertension subjects from getting glaucoma. At regular intervals members of the study received eye exams to see if they had developed glaucoma.


The major discovery of this treatment trial was that giving pressure-lowering medicines to those with ocular hypertension does in fact significantly reduces their risk for getting glaucoma.


More about the results of the OHTS is available at the OHTS center.


The Ocular Hypertension Treatment Study has been completed. However, 1,077 of the 1,636 subjects in this study contributed DNA samples for use in our studies of the genetics of glaucoma.



Quantitative Traits of Glaucoma

During the course of the Ocular Hypertension Treatment Study several quantitative features of glaucoma were measured on 1,636 study subjects. These quantitative traits include:


  • Eye pressure (measured in mm Hg)
  • Thickness of the cornea (measured in microns)
  • Optic nerve shape (measured as the cup-to-disc ratio)

Previous studies have shown that the magnitude of eye pressure, corneal thickness, and features of the optic nerve are determined to a large degree by the action of genes – genes that have not yet been identified.


Extremes of these quantitative features (such as high eye pressure, thin corneas, and large cup-to-disc ratio) are known to confer significant risk for glaucoma.


As a result, it is likely that the same genes that control the magnitude of these quantitative traits may also confer risk for developing glaucoma.


The goal of this project is find the genes that control these quantitative features of glaucoma.



Using Association Studies to Find Disease-Causing Genes

Association studies search for differences in the genomes between patients with a disease (i.e. with glaucoma) and normal control subjects (i.e. with no glaucoma). These differences help researchers map the location of disease-causing genes in the genome.


Association studies are effective in finding disease-causing genes when the disease can be traced to mutations that arose in a few common ancestors or founders. Those with disease today are descendants from common ancestors and are distant relatives.

 

 

This diagram does a good job of illustrating association studies.  The blue rectangle at the upper left corner represents the ancestor’s chromosome and the “X” represents a disease-causing mutation.  Descendents of this person that inherit the portion of the blue chromosome with the mutation also inherit the disease as shown on the right part of the diagram.

 

Descendents that inherit the piece of their ancestor’s chromosome (blue segments) that contain the ancestral mutation (represented by the X) also inherit neighboring marker alleles from their founder.  Consequently these marker alleles are more common in those with disease than in controls.

 

The goal of an association study is to scan the genome for regions in which patients have different marker allele frequencies than controls (the blue segment indicated with arrow at the bottom of the diagram).  These regions may contain an ancestral disease-causing mutation.



Association study of participants in the OHTS

The goal of this project is find the genes that control these quantitative features of glaucoma.  Rather than search for genes that directly cause glaucoma, we are using an association study to identify the genes that cause extremes of features of glaucoma listed below:


  • Eye pressure (measured in mm Hg)
  • Thickness of the cornea (measured in microns)
  • Optic nerve shape (measured as the cup-to-disc ratio)

Measures of these features have been collected from participants in the OHTS.


DNA samples from 1,077 participants in the OHTS are currently being tested for 1,200,000 genetic markers evenly distributed across the entire genome.


We will compare the magnitudes of each quantitative trait with genetic markers.  The goal of this study is to map the location of the genes that control the magnitude of eye pressure, corneal thickness, and optic nerve shape.  These genes may also be important risk factors for developing glaucoma. 



RESEARCH TEAM

John Fingert, M.D., Ph.D.
Principal Investigator
University of Iowa
Michael Kass, M.D.
Co-Investigator
Washington University
       
Todd Scheetz, Ph.D.
Co-Investigator
University of Iowa
Mae Gordon, Ph.D.
Co-Investigator
Washington University
       
Jian Huan, Ph.D.
Co-Investigator
University of Iowa
Michael G. Anderson
Co-Investigator
       
Kai Wang, Ph.D.
Co-Investigator
University of Iowa
   


Funding Support for the Association Study of Participants of the OHTS

Funding support for the genetic studies of the Ocular Hypertension Treatment Study participants has been awarded by the National Eye Institute (R01EY018825).



Our Research

  • Ocular Hypertension Treatment Study
    Ocular Hypertension Treatment Study
  • Pigment Dispersion Syndrome
    Pigment Dispersion Syndrome
  • Normal Tension Glaucoma
    Normal Tension Glaucoma
  • Cavitary Optic Disc Anomalies
    Cavitary Optic Disc Anomalies
  • Patient Responses to Glaucoma Medicines (Pharmacogenomics)
    Patient Responses to Glaucoma Medicines (Pharmacogenomics)
  • Animal Models of Eye Disease
    Animal Models of Eye Disease
  • Exfoliation Syndrome

Genetic Studies of the Ocular Hypertension Treatments Study (OHTS) Participants

OHTS-icon

Project Summary. Eye doctors diagnose patients with glaucoma by taking measurements of key features of the eye that are quantitative or numerical. Some of these quantitative features of glaucoma are eye pressure (measured in mm Hg), thickness of the cornea (measured in microns), the shape of the optic nerve (measured as the cup-to-disc ratio); and the extent of vision loss. The genes that control the magnitude of quantitative features of glaucoma likely contribute risk for developing disease.


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Genetic Studies of Pigment Dispersion Syndrome

pigmentary

Pigment dispersion syndrome is an eye condition in which the pigment from the iris is released within the eye and leads to elevated intraocular pressure and glaucoma in some patients.  Pigment dispersion syndrome may afflict as many as 2.5%.  Those with pigment dispersion syndrome are at high risk for developing a related form of glaucoma, pigmentary glaucoma.

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Genetic Studies of Normal Tension Glaucoma

normal-tensionProject Summary.  Glaucoma often runs in families.  In rare cases, a large number of family members have normal tension glaucoma that is passed down from generation to generation in an obvious pattern.  We have enrolled several such families with normal tension glaucoma into our research program. 

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Genetic Studies of Cavitary Optic Disc Anomalies (CODA)

CODA1Cavitary optic disc anomalies (CODA) is a congenital disease in which the optic nerve is deeply excavated at birth much like cupping that occurs in severe cases of glaucoma.

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Genetic Studies of Patient Responses to Glaucoma Medicines (Pharmacogenomics)

pharmacogenomicsMore information on this research coming soon....

Genetic Studies of Animal Models of Eye Disease

mouseMore information about this research coming soon.....

Exfoliation Syndrome

Exfoliation syndrome is a common condition in which a flaky white material is deposited in many tissues of the eye (the lens, the cornea, and the drainage structures) and throughout the body. Exfoliation syndrome is an important cause of glaucoma as up to half of those with exfoliation syndrome eventually develop a secondary glaucoma (exfoliation glaucoma).

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