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https://doi.org/10.1007/s00439-014-1500-y
Title: | 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 C.L. Hysi P.G. Verhoeven V.J.M. Ikram M.K. Höhn R. Vitart V. Hewitt A.W. Oexle K. Mäkelä K.-M. Ho D.W.H. Chew E. Mihailov E. Smith G.D. Biino G. Rudan I. Seppala I. Kaprio J. Craig J.E. Polling J.R. MacGregor S. Tideman J.-W. Fondran J.R. Wang J.J. Liao J. Zhao J.H. Xie J. Bailey Wilson J.E. Burdon K.P. Khaw K.-T. Yamashiro K. Pirastu M. Portas L. Farrer L. Raffel L.J. Chen L.J. Xu L. Deangelis M.M. Morrison M. Schache M. Cotch M.-F. Miyake M. Fan Q. Fossarello M. He M. Yoshimura N. Wareham N.J. Mizuki N. Pfeiffer N. Polasek O. Tam P.O. Foster P.J. Chen P. Cheng C.-Y. Gharahkhani P. Fogarty R.D. Luben R.N. Igo R.P. Jr. Klein R. Mohsen Hosseini S. Janmahasatian S. Feng S. Panda-Jonas S. St Pourcain B. Iyengar S.K. Lass J.H. Rantanen T. Haller T. Nangia V. Jhanji V. Chen W. Zhou X. Guo X. Li X. McMahon G. Vatavuk Z. The CREAM consortium Kemp J.P. Northstone K. Rahi J.S. Cumberland P.M. Martin N.G. Sanfilippo P.G. Lu Y. Wang Y.X. Hayward C. Polašek O. Campbell H. Bencic G. Wright A.F. Wedenoja J. Zeller T. Schillert A. Mirshahi A. Lackner K. Yip S.P. Yap M.K.H. Ried J.S. Gieger C. Murgia F. Wilson J.F. Fleck B. Yazar S. Vingerling J.R. Hofman A. Uitterlinden A. Rivadeneira F. Amin N. Karssen L. Oostra B.A. Zhou X. Teo Y.-Y. Tai E.S. Vithana E. Barathi V. Zheng Y. Siantar R.G. Neelam K. Shin Y. Lam J. Yonova-Doing E. Venturini C. Hosseini S.M. Wong H.-S. Lehtimäki T. Kähönen M. Raitakari O. Timpson N.J. Evans D.M. Khor C.-C. Aung T. Young T.L. Mitchell P. Klein B. van Duijn C.M. Meitinger T. Jonas J.B. Baird P.N. Mackey D.A. Wong T.Y. Saw S.-M. Pärssinen O. Stambolian D. Hammond C.J. Klaver C.C.W. Williams C. Paterson A.D. Bailey-Wilson J.E. Guggenheim J.A. Meguro A. Young A.L. Veluchamy A.B. Metspalu A. Döring A. Khawaja A.P. Klein B.E. Pourcain B.S. Delcourt C. Maubaret C. Pang C.P. |
Keywords: | neurexin neurexin 1 unclassified drug genetic marker high mobility group protein nerve cell adhesion molecule nerve protein NRXN1 protein, human TOX protein, human adult Article Asian astigmatism Chinese controlled study European female gene frequency gene locus genetic association genetic risk genetic variability genotype human logistic regression analysis major clinical study male meta analysis (topic) priority journal refractive astigmatism single nucleotide polymorphism age Asian continental ancestry group astigmatism Caucasian cohort analysis genetic marker genetics genome-wide association study meta analysis middle aged pathology Adult Age Factors Asian Continental Ancestry Group Astigmatism Cell Adhesion Molecules, Neuronal Cohort Studies European Continental Ancestry Group Female Genetic Markers Genome-Wide Association Study High Mobility Group Proteins Humans Male Middle Aged Nerve Tissue Proteins |
Issue Date: | 2015 | Publisher: | Springer | Citation: | Li Q., Wojciechowski R., Simpson C.L., Hysi P.G., Verhoeven V.J.M., Ikram M.K., Höhn R., Vitart V., Hewitt A.W., Oexle K., Mäkelä K.-M., Ho D.W.H., Chew E., Mihailov E., Smith G.D., Biino G., Rudan I., Seppala I., Kaprio J., Craig J.E., Polling J.R., MacGregor S., Tideman J.-W., Fondran J.R., Wang J.J., Liao J., Zhao J.H., Xie J., Bailey Wilson J.E., Burdon K.P., Khaw K.-T., Yamashiro K., Pirastu M., Portas L., Farrer L., Raffel L.J., Chen L.J., Xu L., Deangelis M.M., Morrison M., Schache M., Cotch M.-F., Miyake M., Fan Q., Fossarello M., He M., Yoshimura N., Wareham N.J., Mizuki N., Pfeiffer N., Polasek O., Tam P.O., Foster P.J., Chen P., Cheng C.-Y., Gharahkhani P., Fogarty R.D., Luben R.N., Igo R.P., Jr., Klein R., Mohsen Hosseini S., Janmahasatian S., Feng S., Panda-Jonas S., St Pourcain B., Iyengar S.K., Lass J.H., Rantanen T., Haller T., Nangia V., Jhanji V., Chen W., Zhou X., Guo X., Li X., McMahon G., Vatavuk Z., The CREAM consortium, Kemp J.P., Northstone K., Rahi J.S., Cumberland P.M., Martin N.G., Sanfilippo P.G., Lu Y., Wang Y.X., Hayward C., Polašek O., Campbell H., Bencic G., Wright A.F., Wedenoja J., Zeller T., Schillert A., Mirshahi A., Lackner K., Yip S.P., Yap M.K.H., Ried J.S., Gieger C., Murgia F., Wilson J.F., Fleck B., Yazar S., Vingerling J.R., Hofman A., Uitterlinden A., Rivadeneira F., Amin N., Karssen L., Oostra B.A., Zhou X., Teo Y.-Y., Tai E.S., Vithana E., Barathi V., Zheng Y., Siantar R.G., Neelam K., Shin Y., Lam J., Yonova-Doing E., Venturini C., Hosseini S.M., Wong H.-S., Lehtimäki T., Kähönen M., Raitakari O., Timpson N.J., Evans D.M., Khor C.-C., Aung T., Young T.L., Mitchell P., Klein B., van Duijn C.M., Meitinger T., Jonas J.B., Baird P.N., Mackey D.A., Wong T.Y., Saw S.-M., Pärssinen O., Stambolian D., Hammond C.J., Klaver C.C.W., Williams C., Paterson A.D., Bailey-Wilson J.E., Guggenheim J.A., Meguro A., Young A.L., Veluchamy A.B., Metspalu A., Döring A., Khawaja A.P., Klein B.E., Pourcain B.S., Delcourt C., Maubaret C., Pang C.P. (2015). Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium. Human Genetics 134 (2) : 131-146. ScholarBank@NUS Repository. https://doi.org/10.1007/s00439-014-1500-y | 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. © 2014, The Author(s). | Source Title: | Human Genetics | URI: | https://scholarbank.nus.edu.sg/handle/10635/175292 | ISSN: | 0340-6717 | DOI: | 10.1007/s00439-014-1500-y |
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