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Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses

Authors :
R. Rand Allingham
Julia E. Richards
William K. Scott
Janey L. Wiggs
Jessica N. Cooke Bailey
Robert Ritch
Michael A. Hauser
Arthur J. Sit
Joel S. Schuman
Jonathan L. Haines
Donald L. Budenz
Jae H. Kang
Margaret A. Pericak-Vance
Douglas E. Gaasterland
William G. Christen
Yutao Liu
Kang Zhang
Robert N. Weinreb
Donald J. Zack
Kuldev Singh
Felipe A. Medeiros
Terry Gaasterland
Gadi Wollstein
Douglas Vollrath
Louis R. Pasquale
Tony Realini
Richard K. Lee
Anthony P Khawaja
Murray H. Brilliant
S.E. Moroi
Paul R. Lichter
John H. Fingert
Peter Kraft
Source :
Investigative Ophthalmology & Visual Science, Khawaja, AP; Cooke Bailey, JN; Kang, JH; Rand Allingham, R; Hauser, MA; Brilliant, M; et al.(2016). Assessing the association of mitochondrial genetic variation with primary open-angle glaucoma using gene-set analyses. Investigative Ophthalmology and Visual Science, 57(11), 5046-5052. doi: 10.1167/iovs.16-20017. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/6tq4q4qp, Investigative ophthalmology & visual science, vol 57, iss 11
Publication Year :
2016
Publisher :
The Association for Research in Vision and Ophthalmology, 2016.

Abstract

© 2016, Association for Research in Vision and Ophthalmology Inc. All rights reserved. PURPOSE. Recent studies indicate that mitochondrial proteins may contribute to the pathogenesis of primary open-angle glaucoma (POAG). In this study, we examined the association between POAG and common variations in gene-encoding mitochondrial proteins. METHODS. We examined genetic data from 3430 POAG cases and 3108 controls derived from the combination of the GLAUGEN and NEIGHBOR studies. We constructed biological-system coherent mitochondrial nuclear-encoded protein gene-sets by intersecting the MitoCarta database with the Kyoto Encyclopedia of Genes and Genomes (KEGG) database. We examined the mitochondrial gene-sets for association with POAG and with normal-tension glaucoma (NTG) and high-tension glaucoma (HTG) subsets using Pathway Analysis by Randomization Incorporating Structure. RESULTS. We identified 22 KEGG pathways with significant mitochondrial protein-encoding gene enrichment, belonging to six general biological classes. Among the pathway classes, mitochondrial lipid metabolism was associated with POAG overall (P = 0.013) and with NTG (P = 0.0006), and mitochondrial carbohydrate metabolism was associated with NTG (P = 0.030). Examining the individual KEGG pathway mitochondrial gene-sets, fatty acid elongation and synthesis and degradation of ketone bodies, both lipid metabolism pathways, were significantly associated with POAG (P = 0.005 and P = 0.002, respectively) and NTG (P = 0.0004 and P < 0.0001, respectively). Butanoate metabolism, a carbohydrate metabolism pathway, was significantly associated with POAG (P = 0.004), NTG (P = 0.001), and HTG (P = 0.010). CONCLUSIONS. We present an effective approach for assessing the contributions of mitochondrial genetic variation to open-angle glaucoma. Our findings support a role for mitochondria in POAG pathogenesis and specifically point to lipid and carbohydrate metabolism pathways as being important.

Details

Language :
English
ISSN :
15525783 and 01460404
Volume :
57
Issue :
11
Database :
OpenAIRE
Journal :
Investigative Ophthalmology & Visual Science
Accession number :
edsair.doi.dedup.....27ad174fa9e24c4b05e595ebdff19f71
Full Text :
https://doi.org/10.1167/iovs.16-20017.