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Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium.

Authors :
Li Q
Wojciechowski R
Simpson CL
Hysi PG
Verhoeven VJ
Ikram MK
Höhn R
Vitart V
Hewitt AW
Oexle K
Mäkelä KM
MacGregor S
Pirastu M
Fan Q
Cheng CY
St Pourcain B
McMahon G
Kemp JP
Northstone K
Rahi JS
Cumberland PM
Martin NG
Sanfilippo PG
Lu Y
Wang YX
Hayward C
Polašek O
Campbell H
Bencic G
Wright AF
Wedenoja J
Zeller T
Schillert A
Mirshahi A
Lackner K
Yip SP
Yap MK
Ried JS
Gieger C
Murgia F
Wilson JF
Fleck B
Yazar S
Vingerling JR
Hofman A
Uitterlinden A
Rivadeneira F
Amin N
Karssen L
Oostra BA
Zhou X
Teo YY
Tai ES
Vithana E
Barathi V
Zheng Y
Siantar RG
Neelam K
Shin Y
Lam J
Yonova-Doing E
Venturini C
Hosseini SM
Wong HS
Lehtimäki T
Kähönen M
Raitakari O
Timpson NJ
Evans DM
Khor CC
Aung T
Young TL
Mitchell P
Klein B
van Duijn CM
Meitinger T
Jonas JB
Baird PN
Mackey DA
Wong TY
Saw SM
Pärssinen O
Stambolian D
Hammond CJ
Klaver CC
Williams C
Paterson AD
Bailey-Wilson JE
Guggenheim JA
Source :
Human genetics [Hum Genet] 2015 Feb; Vol. 134 (2), pp. 131-46. Date of Electronic Publication: 2014 Nov 04.
Publication Year :
2015

Abstract

To identify genetic variants associated with refractive astigmatism in the general population, meta-analyses of genome-wide association studies were performed for: White Europeans aged at least 25 years (20 cohorts, N = 31,968); Asian subjects aged at least 25 years (7 cohorts, N = 9,295); White Europeans aged <25 years (4 cohorts, N = 5,640); and all independent individuals from the above three samples combined with a sample of Chinese subjects aged <25 years (N = 45,931). Participants were classified as cases with refractive astigmatism if the average cylinder power in their two eyes was at least 1.00 diopter and as controls otherwise. Genome-wide association analysis was carried out for each cohort separately using logistic regression. Meta-analysis was conducted using a fixed effects model. In the older European group the most strongly associated marker was downstream of the neurexin-1 (NRXN1) gene (rs1401327, P = 3.92E-8). No other region reached genome-wide significance, and association signals were lower for the younger European group and Asian group. In the meta-analysis of all cohorts, no marker reached genome-wide significance: The most strongly associated regions were, NRXN1 (rs1401327, P = 2.93E-07), TOX (rs7823467, P = 3.47E-07) and LINC00340 (rs12212674, P = 1.49E-06). For 34 markers identified in prior GWAS for spherical equivalent refractive error, the beta coefficients for genotype versus spherical equivalent, and genotype versus refractive astigmatism, were highly correlated (r = -0.59, P = 2.10E-04). This work revealed no consistent or strong genetic signals for refractive astigmatism; however, the TOX gene region previously identified in GWAS for spherical equivalent refractive error was the second most strongly associated region. Analysis of additional markers provided evidence supporting widespread genetic co-susceptibility for spherical and astigmatic refractive errors.

Details

Language :
English
ISSN :
1432-1203
Volume :
134
Issue :
2
Database :
MEDLINE
Journal :
Human genetics
Publication Type :
Academic Journal
Accession number :
25367360
Full Text :
https://doi.org/10.1007/s00439-014-1500-y