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Genetic correlations between intraocular pressure, blood pressure and primary open-angle glaucoma: a multi-cohort analysis

Authors :
Aschard, Hugues
Kang, Jae H
Iglesias, Adriana I
Hysi, Pirro
Cooke Bailey, Jessica N
Khawaja, Anthony P
Allingham, R Rand
Ashley-Koch, Allison
Lee, Richard K
Moroi, Sayoko E
Brilliant, Murray H
Wollstein, Gadi
Schuman, Joel S
Fingert, John H
Budenz, Donald L
Realini, Tony
Gaasterland, Terry
Scott, William K
Singh, Kuldev
Sit, Arthur J
Igo Jr, Robert P
Song, Yeunjoo E
Hark, Lisa
Ritch, Robert
Rhee, Douglas J
Gulati, Vikas
Haven, Shane
Vollrath, Douglas
Zack, Donald J
Medeiros, Felipe
Weinreb, Robert N
Cheng, Ching-Yu
Chasman, Daniel I
Christen, William G
Pericak-Vance, Margaret A
Liu, Yutao
Kraft, Peter
Richards, Julia E
Rosner, Bernard A
Hauser, Michael A
Klaver, Caroline C W
vanDuijn, Cornelia M
Haines, Jonathan
Wiggs, Janey L
Pasquale, Louis R
Source :
European Journal of Human Genetics: EJHG; November 2017, Vol. 25 Issue: 11 p1261-1267, 7p
Publication Year :
2017

Abstract

Primary open-angle glaucoma (POAG) is the most common chronic optic neuropathy worldwide. Epidemiological studies show a robust positive relation between intraocular pressure (IOP) and POAG and modest positive association between IOP and blood pressure (BP), while the relation between BP and POAG is controversial. The International Glaucoma Genetics Consortium (n=27 558), the International Consortium on Blood Pressure (n=69 395), and the National Eye Institute Glaucoma Human Genetics Collaboration Heritable Overall Operational Database (n=37 333), represent genome-wide data sets for IOP, BP traits and POAG, respectively. We formed genome-wide significant variant panels for IOP and diastolic BP and found a strong relation with POAG (odds ratio and 95% confidence interval: 1.18 (1.14–1.21), P=1.8 × 10−27) for the former trait but no association for the latter (P=0.93). Next, we used linkage disequilibrium (LD) score regression, to provide genome-wide estimates of correlation between traits without the need for additional phenotyping. We also compared our genome-wide estimate of heritability between IOP and BP to an estimate based solely on direct measures of these traits in the Erasmus Rucphen Family (ERF; n=2519) study using Sequential Oligogenic Linkage Analysis Routines (SOLAR). LD score regression revealed high genetic correlation between IOP and POAG (48.5%, P=2.1 × 10−5); however, genetic correlation between IOP and diastolic BP (P=0.86) and between diastolic BP and POAG (P=0.42) were negligible. Using SOLAR in the ERF study, we confirmed the minimal heritability between IOP and diastolic BP (P=0.63). Overall, IOP shares genetic basis with POAG, whereas BP has limited shared genetic correlation with IOP or POAG.

Details

Language :
English
ISSN :
10184813 and 14765438
Volume :
25
Issue :
11
Database :
Supplemental Index
Journal :
European Journal of Human Genetics: EJHG
Publication Type :
Periodical
Accession number :
ejs43436952
Full Text :
https://doi.org/10.1038/ejhg.2017.136