ID

45498

Beskrivning

Principal Investigator: Shannath Merbs, MD, PhD, The Wilmer Eye Institute, Johns Hopkins University, Baltimore, MD, USA MeSH: Glaucoma, Open-Angle https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000461 This is a case-control study of Primary Open Angle Glaucoma (POAG). POAG is a progressive optic neuropathy that eventually leads to blindness. More than 30 million people worldwide have Primary Open Angle Glaucoma (POAG), of which greater than 3 million are blind. Gene expression changes in the retina have been observed for POAG. Several recent studies, including the GLAUGEN (*Glau*coma *G*ene *En*vironment) initiative have used GWAS to identify correlative regions of the genome. Despite this, the genetic basis of Glaucoma is not well understood. Epigenetic variation may account for low heritability and environmental effects on human disease. Despite the significant advances being made in understanding the role of epigenetics in gene regulation in other fields, little is known about the relationship between DNA methylation patterns, retinal gene expression, and retinal disease. *The goal of this study is to identify differentially methylated regions in the peripheral blood of patients with POAG.* The case identification is as per the GLAUGEN description: Cases and controls were recruited from ophthalmology clinics and were examined by ophthalmologists. For cases the clinical exam included intraocular pressure measurements, optic nerve assessment and visual field evaluation. Controls had no family history of glaucoma, normal intraocular pressure and normal optic nerves. POAG and control samples come from Massachusetts Eye and Ear Infirmary (MEEI). These samples were collected and genotyped as part of the GLAUGEN study. From the MEEI, 50 patients were selected from POAG pedigrees, to include all the probands genotyped by CIDR and are currently undergoing exome sequencing, and to include additional genotyped probands who belong to pedigrees of sufficient size and structure that parent of origin effects could be evaluated. Additional individual-level phenotype and genotype data may be obtained through the authorized access portal of phs000308 (Geneva - Glaugen GWAS Study).

Länk

dbGap study = phs000461

Nyckelord

Versioner (2)

1. 2022-11-03 2022-11-03 - Dr. med. Lucy Kessler
2. 2022-12-13 2022-12-13 - Kristina Keller

Rättsinnehavare

Shannath Merbs, MD, PhD, The Wilmer Eye Institute, Johns Hopkins University, Baltimore, MD, USA

Uppladdad den

13 december 2022

DOI

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