Literature DB >> 24002674

Genome-wide association study and meta-analysis of intraocular pressure.

A Bilge Ozel1, Sayoko E Moroi, David M Reed, Melisa Nika, Caroline M Schmidt, Sara Akbari, Kathleen Scott, Frank Rozsa, Hemant Pawar, David C Musch, Paul R Lichter, Doug Gaasterland, Kari Branham, Jesse Gilbert, Sarah J Garnai, Wei Chen, Mohammad Othman, John Heckenlively, Anand Swaroop, Gonçalo Abecasis, David S Friedman, Don Zack, Allison Ashley-Koch, Megan Ulmer, Jae H Kang, Yutao Liu, Brian L Yaspan, Jonathan Haines, R Rand Allingham, Michael A Hauser, Louis Pasquale, Janey Wiggs, Julia E Richards, Jun Z Li.   

Abstract

Elevated intraocular pressure (IOP) is a major risk factor for glaucoma and is influenced by genetic and environmental factors. Recent genome-wide association studies (GWAS) reported associations with IOP at TMCO1 and GAS7, and with primary open-angle glaucoma (POAG) at CDKN2B-AS1, CAV1/CAV2, and SIX1/SIX6. To identify novel genetic variants and replicate the published findings, we performed GWAS and meta-analysis of IOP in >6,000 subjects of European ancestry collected in three datasets: the NEI Glaucoma Human genetics collaBORation, GLAUcoma Genes and ENvironment study, and a subset of the Age-related Macular Degeneration-Michigan, Mayo, AREDS and Pennsylvania study. While no signal achieved genome-wide significance in individual datasets, a meta-analysis identified significant associations with IOP at TMCO1 (rs7518099-G, p = 8.0 × 10(-8)). Focused analyses of five loci previously reported for IOP and/or POAG, i.e., TMCO1, CDKN2B-AS1, GAS7, CAV1/CAV2, and SIX1/SIX6, revealed associations with IOP that were largely consistent across our three datasets, and replicated the previously reported associations in both effect size and direction. These results confirm the involvement of common variants in multiple genomic regions in regulating IOP and/or glaucoma risk.

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Year:  2013        PMID: 24002674      PMCID: PMC3982323          DOI: 10.1007/s00439-013-1349-5

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


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