Please use this identifier to cite or link to this item: https://doi.org/10.1007/s00439-014-1500-y
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dc.titleGenome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium
dc.contributor.authorLi Q.
dc.contributor.authorWojciechowski R.
dc.contributor.authorSimpson C.L.
dc.contributor.authorHysi P.G.
dc.contributor.authorVerhoeven V.J.M.
dc.contributor.authorIkram M.K.
dc.contributor.authorHöhn R.
dc.contributor.authorVitart V.
dc.contributor.authorHewitt A.W.
dc.contributor.authorOexle K.
dc.contributor.authorMäkelä K.-M.
dc.contributor.authorHo D.W.H.
dc.contributor.authorChew E.
dc.contributor.authorMihailov E.
dc.contributor.authorSmith G.D.
dc.contributor.authorBiino G.
dc.contributor.authorRudan I.
dc.contributor.authorSeppala I.
dc.contributor.authorKaprio J.
dc.contributor.authorCraig J.E.
dc.contributor.authorPolling J.R.
dc.contributor.authorMacGregor S.
dc.contributor.authorTideman J.-W.
dc.contributor.authorFondran J.R.
dc.contributor.authorWang J.J.
dc.contributor.authorLiao J.
dc.contributor.authorZhao J.H.
dc.contributor.authorXie J.
dc.contributor.authorBailey Wilson J.E.
dc.contributor.authorBurdon K.P.
dc.contributor.authorKhaw K.-T.
dc.contributor.authorYamashiro K.
dc.contributor.authorPirastu M.
dc.contributor.authorPortas L.
dc.contributor.authorFarrer L.
dc.contributor.authorRaffel L.J.
dc.contributor.authorChen L.J.
dc.contributor.authorXu L.
dc.contributor.authorDeangelis M.M.
dc.contributor.authorMorrison M.
dc.contributor.authorSchache M.
dc.contributor.authorCotch M.-F.
dc.contributor.authorMiyake M.
dc.contributor.authorFan Q.
dc.contributor.authorFossarello M.
dc.contributor.authorHe M.
dc.contributor.authorYoshimura N.
dc.contributor.authorWareham N.J.
dc.contributor.authorMizuki N.
dc.contributor.authorPfeiffer N.
dc.contributor.authorPolasek O.
dc.contributor.authorTam P.O.
dc.contributor.authorFoster P.J.
dc.contributor.authorChen P.
dc.contributor.authorCheng C.-Y.
dc.contributor.authorGharahkhani P.
dc.contributor.authorFogarty R.D.
dc.contributor.authorLuben R.N.
dc.contributor.authorIgo R.P.
dc.contributor.authorJr.
dc.contributor.authorKlein R.
dc.contributor.authorMohsen Hosseini S.
dc.contributor.authorJanmahasatian S.
dc.contributor.authorFeng S.
dc.contributor.authorPanda-Jonas S.
dc.contributor.authorSt Pourcain B.
dc.contributor.authorIyengar S.K.
dc.contributor.authorLass J.H.
dc.contributor.authorRantanen T.
dc.contributor.authorHaller T.
dc.contributor.authorNangia V.
dc.contributor.authorJhanji V.
dc.contributor.authorChen W.
dc.contributor.authorZhou X.
dc.contributor.authorGuo X.
dc.contributor.authorLi X.
dc.contributor.authorMcMahon G.
dc.contributor.authorVatavuk Z.
dc.contributor.authorThe CREAM consortium
dc.contributor.authorKemp J.P.
dc.contributor.authorNorthstone K.
dc.contributor.authorRahi J.S.
dc.contributor.authorCumberland P.M.
dc.contributor.authorMartin N.G.
dc.contributor.authorSanfilippo P.G.
dc.contributor.authorLu Y.
dc.contributor.authorWang Y.X.
dc.contributor.authorHayward C.
dc.contributor.authorPolašek O.
dc.contributor.authorCampbell H.
dc.contributor.authorBencic G.
dc.contributor.authorWright A.F.
dc.contributor.authorWedenoja J.
dc.contributor.authorZeller T.
dc.contributor.authorSchillert A.
dc.contributor.authorMirshahi A.
dc.contributor.authorLackner K.
dc.contributor.authorYip S.P.
dc.contributor.authorYap M.K.H.
dc.contributor.authorRied J.S.
dc.contributor.authorGieger C.
dc.contributor.authorMurgia F.
dc.contributor.authorWilson J.F.
dc.contributor.authorFleck B.
dc.contributor.authorYazar S.
dc.contributor.authorVingerling J.R.
dc.contributor.authorHofman A.
dc.contributor.authorUitterlinden A.
dc.contributor.authorRivadeneira F.
dc.contributor.authorAmin N.
dc.contributor.authorKarssen L.
dc.contributor.authorOostra B.A.
dc.contributor.authorZhou X.
dc.contributor.authorTeo Y.-Y.
dc.contributor.authorTai E.S.
dc.contributor.authorVithana E.
dc.contributor.authorBarathi V.
dc.contributor.authorZheng Y.
dc.contributor.authorSiantar R.G.
dc.contributor.authorNeelam K.
dc.contributor.authorShin Y.
dc.contributor.authorLam J.
dc.contributor.authorYonova-Doing E.
dc.contributor.authorVenturini C.
dc.contributor.authorHosseini S.M.
dc.contributor.authorWong H.-S.
dc.contributor.authorLehtimäki T.
dc.contributor.authorKähönen M.
dc.contributor.authorRaitakari O.
dc.contributor.authorTimpson N.J.
dc.contributor.authorEvans D.M.
dc.contributor.authorKhor C.-C.
dc.contributor.authorAung T.
dc.contributor.authorYoung T.L.
dc.contributor.authorMitchell P.
dc.contributor.authorKlein B.
dc.contributor.authorvan Duijn C.M.
dc.contributor.authorMeitinger T.
dc.contributor.authorJonas J.B.
dc.contributor.authorBaird P.N.
dc.contributor.authorMackey D.A.
dc.contributor.authorWong T.Y.
dc.contributor.authorSaw S.-M.
dc.contributor.authorPärssinen O.
dc.contributor.authorStambolian D.
dc.contributor.authorHammond C.J.
dc.contributor.authorKlaver C.C.W.
dc.contributor.authorWilliams C.
dc.contributor.authorPaterson A.D.
dc.contributor.authorBailey-Wilson J.E.
dc.contributor.authorGuggenheim J.A.
dc.contributor.authorMeguro A.
dc.contributor.authorYoung A.L.
dc.contributor.authorVeluchamy A.B.
dc.contributor.authorMetspalu A.
dc.contributor.authorDöring A.
dc.contributor.authorKhawaja A.P.
dc.contributor.authorKlein B.E.
dc.contributor.authorPourcain B.S.
dc.contributor.authorDelcourt C.
dc.contributor.authorMaubaret C.
dc.contributor.authorPang C.P.
dc.date.accessioned2020-09-09T07:19:47Z
dc.date.available2020-09-09T07:19:47Z
dc.date.issued2015
dc.identifier.citationLi 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
dc.identifier.issn0340-6717
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/175292
dc.description.abstractTo 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).
dc.publisherSpringer
dc.sourceUnpaywall 20200831
dc.subjectneurexin
dc.subjectneurexin 1
dc.subjectunclassified drug
dc.subjectgenetic marker
dc.subjecthigh mobility group protein
dc.subjectnerve cell adhesion molecule
dc.subjectnerve protein
dc.subjectNRXN1 protein, human
dc.subjectTOX protein, human
dc.subjectadult
dc.subjectArticle
dc.subjectAsian
dc.subjectastigmatism
dc.subjectChinese
dc.subjectcontrolled study
dc.subjectEuropean
dc.subjectfemale
dc.subjectgene frequency
dc.subjectgene locus
dc.subjectgenetic association
dc.subjectgenetic risk
dc.subjectgenetic variability
dc.subjectgenotype
dc.subjecthuman
dc.subjectlogistic regression analysis
dc.subjectmajor clinical study
dc.subjectmale
dc.subjectmeta analysis (topic)
dc.subjectpriority journal
dc.subjectrefractive astigmatism
dc.subjectsingle nucleotide polymorphism
dc.subjectage
dc.subjectAsian continental ancestry group
dc.subjectastigmatism
dc.subjectCaucasian
dc.subjectcohort analysis
dc.subjectgenetic marker
dc.subjectgenetics
dc.subjectgenome-wide association study
dc.subjectmeta analysis
dc.subjectmiddle aged
dc.subjectpathology
dc.subjectAdult
dc.subjectAge Factors
dc.subjectAsian Continental Ancestry Group
dc.subjectAstigmatism
dc.subjectCell Adhesion Molecules, Neuronal
dc.subjectCohort Studies
dc.subjectEuropean Continental Ancestry Group
dc.subjectFemale
dc.subjectGenetic Markers
dc.subjectGenome-Wide Association Study
dc.subjectHigh Mobility Group Proteins
dc.subjectHumans
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectNerve Tissue Proteins
dc.typeArticle
dc.contributor.departmentOPHTHALMOLOGY
dc.contributor.departmentSAW SWEE HOCK SCHOOL OF PUBLIC HEALTH
dc.contributor.departmentMEDICINE
dc.description.doi10.1007/s00439-014-1500-y
dc.description.sourcetitleHuman Genetics
dc.description.volume134
dc.description.issue2
dc.description.page131-146
dc.published.statePublished
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