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- Provides a diagnostic technique to determine if a subject is at risk for developing as well as monitoring the progression of dry type AMD in a subject
- Potential use in screening various compounds for their effectiveness in treating dry-type AMD
- Prospective application for diagnostic and treatment purposes
OVERVIEW
This Georgetown University novel diagnostic testing method identifies (measures) the expression and activity levels of various biomarkers including SI RT-1, AM PK, PARP2, PGC-1a, and AKT3 to determine whether the tested cells are at risk for developing dry age-related macular degeneration (AMD). The invention also screens target compounds in their effectiveness in treating dry AMD in a subject. Findings can then be used to treat dry AMD by administering a compound that reduces or induces the activity or expression of various proteins and enzymes.
BACKGROUND
Dry AMD is an eye disease that causes a decline in central vision through the degradation of the macula. It is very common in those over 50 and affects roughly 30-50 million people globally. The early pathobiology of dry AMD still has a lot unknown in addition to there being no known cure. There are also complications involved in delivering the drugs to the posterior portion of the eye. The invention addresses issues related to the diagnosis, treatment, and monitoring of dry AMD.
Benefit
Market Application
Publications
Published Patent Application No. US 2023/0417767 A1
Zhang M, Chu Y, Mowery J, Konkel B, Galli S, Theos AC, Golestaneh N. Pgc-1α repression and high-fat diet induce age-related macular degeneration-like phenotypes in mice. Dis Model Mech. 2018 Aug 16;11(9):dmm032698. doi: 10.1242/dmm.032698. PMID: 29925537; PMCID: PMC6176989.
Repressed SIRT1/PGC-1α pathway and mitochondrial disintegration in iPSC-derived RPE disease model of age-related macular degeneration. J Transl Med. 2016 Dec 20;14(1):344. doi: 10.1186/s12967-016-1101-8.
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