Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pgen.1000978
Title: A genome-wide association study of optic disc parameters
Authors: Ramdas W.D.
van Koolwijk L.M.E.
Ikram M.K. 
Jansonius N.M.
de Jong P.T.V.M.
Bergen A.A.B.
Isaacs A.
Amin N.
Aulchenko Y.S.
Wolfs R.C.W.
Hofman A.
Rivadeneira F.
Oostra B.A.
Uitterlinden A.G.
Hysi P.
Hammond C.J.
Lemij H.G.
Vingerling J.R.
Klaver C.C.W.
van Duijn C.M.
Keywords: binding protein
cell cycle protein 7
cyclin dependent kinase inhibitor 2B
protein Atoh7
transcription factor Six1
unclassified drug
article
chromosome 10q
chromosome 11q
chromosome 13q
chromosome 14q
chromosome 16q
chromosome 17q
chromosome 1p
chromosome 9p
gene locus
genetic association
genetic variability
human
myopia
Netherlands
open angle glaucoma
optic disk
optic disk cup
adolescent
adult
aged
female
genetic association
male
meta analysis
metabolism
middle aged
Adolescent
Adult
Aged
Aged, 80 and over
Female
Genetic Variation
Genome-Wide Association Study
Humans
Male
Middle Aged
Optic Disk
Young Adult
Issue Date: 2010
Citation: Ramdas W.D., van Koolwijk L.M.E., Ikram M.K., Jansonius N.M., de Jong P.T.V.M., Bergen A.A.B., Isaacs A., Amin N., Aulchenko Y.S., Wolfs R.C.W., Hofman A., Rivadeneira F., Oostra B.A., Uitterlinden A.G., Hysi P., Hammond C.J., Lemij H.G., Vingerling J.R., Klaver C.C.W., van Duijn C.M. (2010). A genome-wide association study of optic disc parameters. PLoS Genetics 6 (6) : 1-12. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pgen.1000978
Rights: Attribution 4.0 International
Abstract: The optic nerve head is involved in many ophthalmic disorders, including common diseases such as myopia and open-angle glaucoma. Two of the most important parameters are the size of the optic disc area and the vertical cup-disc ratio (VCDR). Both are highly heritable but genetically largely undetermined. We performed a meta-analysis of genome-wide association (GWA) data to identify genetic variants associated with optic disc area and VCDR. The gene discovery included 7,360 unrelated individuals from the population-based Rotterdam Study I and Rotterdam Study II cohorts. These cohorts revealed two genome-wide significant loci for optic disc area, rs1192415 on chromosome 1p22 (p =6.72*10 -19 ) within 117 kb of the CDC7 gene and rs1900004 on chromosome 10q21.3-q22.1 (p=2.67*10 -33 ) within 10 kb of the ATOH7 gene. They revealed two genome-wide significant loci for VCDR, rs1063192 on chromosome 9p21 (p =6.15*10 -11 ) in the CDKN2B gene and rs10483727 on chromosome 14q22.3-q23 (p=2.93*10 -10 ) within 40 kbp of the SIX1 gene. Findings were replicated in two independent Dutch cohorts (Rotterdam Study III and Erasmus Rucphen Family study; N=3,612), and the TwinsUK cohort (N=843). Meta-analysis with the replication cohorts confirmed the four loci and revealed a third locus at 16q12.1 associated with optic disc area, and four other loci at 11q13, 13q13, 17q23 (borderline significant), and 22q12.1 for VCDR. ATOH7 was also associated with VCDR independent of optic disc area. Three of the loci were marginally associated with open-angle glaucoma. The protein pathways in which the loci of optic disc area are involved overlap with those identified for VCDR, suggesting a common genetic origin. © 2010 Ramdas et al.
Source Title: PLoS Genetics
URI: https://scholarbank.nus.edu.sg/handle/10635/161663
ISSN: 15537390
DOI: 10.1371/journal.pgen.1000978
Rights: Attribution 4.0 International
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