| Literature DB >> 28853718 |
Hugues Aschard1, Jae H Kang2, Adriana I Iglesias3, Pirro Hysi4, Jessica N Cooke Bailey5,6, Anthony P Khawaja7, R Rand Allingham8, Allison Ashley-Koch9, Richard K Lee10, Sayoko E Moroi11, Murray H Brilliant12, Gadi Wollstein13, Joel S Schuman13, John H Fingert14, Donald L Budenz15, Tony Realini16, Terry Gaasterland17, William K Scott18, Kuldev Singh19, Arthur J Sit20, Robert P Igo5, Yeunjoo E Song5,6, Lisa Hark21, Robert Ritch22, Douglas J Rhee23, Vikas Gulati24, Shane Haven24, Douglas Vollrath25, Donald J Zack26, Felipe Medeiros27, Robert N Weinreb27, Ching-Yu Cheng28,29,30, Daniel I Chasman31, William G Christen31, Margaret A Pericak-Vance18, Yutao Liu32, Peter Kraft1,33, Julia E Richards11, Bernard A Rosner1,2, Michael A Hauser8,9, Caroline C W Klaver3,34, Cornelia M vanDuijn3, Jonathan Haines5,6, Janey L Wiggs35, Louis R Pasquale2,35.
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.Entities:
Mesh:
Year: 2017 PMID: 28853718 PMCID: PMC5643970 DOI: 10.1038/ejhg.2017.136
Source DB: PubMed Journal: Eur J Hum Genet ISSN: 1018-4813 Impact factor: 5.351