Age-related macular degeneration (AMD) represents the most common cause of blindness in patients over the age of 60. While both hereditary and environmental factors appear to play a role in the pathogenesis of the disease, no common genetic mutations have been identified. Based on laboratory evidence, one proposed hypothesis for this disease focuses on an altered injury response program of the retinal pigment epithelium and its interaction with altered macrophage response. To study this hypothesis, a clinical trial has been initiated - ?A Pilot Study Examining Gene Expression Patterns in Circulating Monocytes and Dermal Fibroblasts in Patients with Age-related Macular Degeneration?. This ongoing clinical trial is intended to test the hypothesis that patterns of gene expression involved in wound repair, cell injury and death as well as macrophage function are altered in the eyes of patients with AMD and these genetic alterations can be detected in peripheral sites other than the eye. Biopsied skin fibroblasts and circulating monocytes from patients with various forms of age-related macular degeneration are being obtained and gene expression patterns are being examined through various techniques including polymerase chain reaction, Northern blot analysis, differential display and microarray technology. The genetic expression patterns from AMD patients are being compared to age-matched control patients. The primary outcome of this study will be to determine if specific gene expression patterns can be identified which correlate with AMD.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Intramural Research (Z01)
Project #
1Z01EY000369-01
Application #
6507399
Study Section
(LI)
Project Start
Project End
Budget Start
Budget End
Support Year
1
Fiscal Year
2001
Total Cost
Indirect Cost
Name
U.S. National Eye Institute
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Hathout, Yetrib; Flippin, Jessica; Fan, Chenguang et al. (2005) Metabolic labeling of human primary retinal pigment epithelial cells for accurate comparative proteomics. J Proteome Res 4:620-7
Strunnikova, Nataly; Hilmer, Sara; Flippin, Jessica et al. (2005) Differences in gene expression profiles in dermal fibroblasts from control and patients with age-related macular degeneration elicited by oxidative injury. Free Radic Biol Med 39:781-96
Cousins, Scott W; Espinosa-Heidmann, Diego G; Csaky, Karl G (2004) Monocyte activation in patients with age-related macular degeneration: a biomarker of risk for choroidal neovascularization? Arch Ophthalmol 122:1013-8
Strunnikova, Nataly; Zhang, Connie; Teichberg, Diane et al. (2004) Survival of retinal pigment epithelium after exposure to prolonged oxidative injury: a detailed gene expression and cellular analysis. Invest Ophthalmol Vis Sci 45:3767-77