TY - JOUR
T1 - Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
AU - Verhoeven, Virginie J. M.
AU - Hysi, Pirro G.
AU - Wojciechowski, Robert
AU - Fan, Qiao
AU - Guggenheim, Jeremy A.
AU - Höhn, René
AU - Macgregor, Stuart
AU - Hewitt, Alex W.
AU - Nag, Abhishek
AU - Cheng, Ching-Yu
AU - Yonova-Doing, Ekaterina
AU - Zhou, Xin
AU - Ikram, M. Kamran
AU - Buitendijk, Gabriëlle H. S.
AU - McMahon, George
AU - Kemp, John P.
AU - Pourcain, Beate St
AU - Simpson, Claire L.
AU - Mäkelä, Kari-Matti
AU - Lehtimäki, Terho
AU - Kähönen, Mika
AU - Paterson, Andrew D.
AU - Hosseini, S. Mohsen
AU - Wong, Hoi Suen
AU - Xu, Liang
AU - Jonas, Jost B.
AU - Pärssinen, Olavi
AU - Wedenoja, Juho
AU - Yip, Shea Ping
AU - Ho, Daniel W. H.
AU - Pang, Chi Pui
AU - Chen, Li Jia
AU - Burdon, Kathryn P.
AU - Craig, Jamie E.
AU - Klein, Barbara E. K.
AU - Klein, Ronald
AU - Haller, Toomas
AU - Metspalu, Andres
AU - Khor, Chiea-Chuen
AU - Tai, E.-Shyong
AU - Aung, Tin
AU - Vithana, Eranga
AU - Tay, Wan-Ting
AU - Barathi, Veluchamy A.
AU - Chen, Peng
AU - Li, Ruoying
AU - Liao, Jiemin
AU - Zheng, Yingfeng
AU - Bergen, Arthur A. B.
AU - AUTHOR GROUP
AU - Chen, Wei
PY - 2013
Y1 - 2013
N2 - Refractive error is the most common eye disorder worldwide and is a prominent cause of blindness. Myopia affects over 30% of Western populations and up to 80% of Asians. The CREAM consortium conducted genome-wide meta-analyses, including 37,382 individuals from 27 studies of European ancestry and 8,376 from 5 Asian cohorts. We identified 16 new loci for refractive error in individuals of European ancestry, of which 8 were shared with Asians. Combined analysis identified 8 additional associated loci. The new loci include candidate genes with functions in neurotransmission (GRIA4), ion transport (KCNQ5), retinoic acid metabolism (RDH5), extracellular matrix remodeling (LAMA2 and BMP2) and eye development (SIX6 and PRSS56). We also confirmed previously reported associations with GJD2 and RASGRF1. Risk score analysis using associated SNPs showed a tenfold increased risk of myopia for individuals carrying the highest genetic load. Our results, based on a large meta-analysis across independent multiancestry studies, considerably advance understanding of the mechanisms involved in refractive error and myopia
AB - Refractive error is the most common eye disorder worldwide and is a prominent cause of blindness. Myopia affects over 30% of Western populations and up to 80% of Asians. The CREAM consortium conducted genome-wide meta-analyses, including 37,382 individuals from 27 studies of European ancestry and 8,376 from 5 Asian cohorts. We identified 16 new loci for refractive error in individuals of European ancestry, of which 8 were shared with Asians. Combined analysis identified 8 additional associated loci. The new loci include candidate genes with functions in neurotransmission (GRIA4), ion transport (KCNQ5), retinoic acid metabolism (RDH5), extracellular matrix remodeling (LAMA2 and BMP2) and eye development (SIX6 and PRSS56). We also confirmed previously reported associations with GJD2 and RASGRF1. Risk score analysis using associated SNPs showed a tenfold increased risk of myopia for individuals carrying the highest genetic load. Our results, based on a large meta-analysis across independent multiancestry studies, considerably advance understanding of the mechanisms involved in refractive error and myopia
U2 - https://doi.org/10.1038/ng.2554
DO - https://doi.org/10.1038/ng.2554
M3 - Article
C2 - 23396134
SN - 1061-4036
VL - 45
SP - 314
EP - 318
JO - Nature Genetics
JF - Nature Genetics
IS - 3
ER -