High-resolution analysis of DNA copy number alterations in patients with primary open-angle glaucoma

Khaled K. Abu-Amero, Ali Hellani, Patrick Bender, George L. Spaeth, Jonathan Myers, L. Jay Katz, Marlene Moster, Thomas M. Bosley

Research output: Contribution to journalArticle

Abstract

Purpose: To determine whether patients with isolated primary open-angle glaucoma (POAG) have evidence of chromosomal copy number alterations. Methods: Twenty-seven Caucasian and African-American POAG patients and 12 ethnically matched controls were carefully screened for possible glaucoma and tested for chromosomal copy number alterations using high resolution array comparative genomic hybridization. Results: No POAG patient had evidence of chromosomal copy number alterations when compared to normal ethnically matched controls. Additionally, there was no evidence of somatic mosaicism in any tested POAG patient. Conclusions: Chromosomal deletions and/or duplications were not detected in POAG patients as compared to controls. Other chromosomal imbalances such as translocations, inversions, and some ploidies cannot be detected by current array comparative genomic hybridization technology, and other nuclear genetic, mitochondrial abnormalities, or epigenetic factors cannot be excluded as a possible contributing factor to POAG pathogenesis.

Original languageEnglish (US)
Pages (from-to)1594-1598
Number of pages5
JournalMolecular vision
Volume15
StatePublished - Aug 15 2009

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ASJC Scopus subject areas

  • Ophthalmology

Cite this

Abu-Amero, K. K., Hellani, A., Bender, P., Spaeth, G. L., Myers, J., Katz, L. J., Moster, M., & Bosley, T. M. (2009). High-resolution analysis of DNA copy number alterations in patients with primary open-angle glaucoma. Molecular vision, 15, 1594-1598.