Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors

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Melin, Beatrice S. | Barnholtz-Sloan, Jill S. | Wrensch, Margaret R. | Johansen, Christoffer | Il'Yasova, Dora | Kinnersley, Ben | Ostrom, Quinn T. | Labreche, Karim | Chen, Yanwen | Armstrong, Georgina | Liu, Yanhong | Eckel-Passow, Jeanette E. | Decker, Paul A. | Labussiere, Marianne | Idbaih, Ahmed | Hoang-Xuan, Khe | Di Stefano, Anna-Luisa | Mokhtari, Karima | Delattre, Jean-Yves | Broderick, Peter | Galan Hercberg, Pilar | Gousias, Konstantinos | Schramm, Johannes | Schoemaker, Minouk J. | Fleming, Sarah J. | Herms, Stefan | Heilmann, Stefanie | Noethen, Markus M. | Wichmann, Heinz-Erich | Schreiber, Stefan | Swerdlow, Anthony | Lathrop, Mark | Simon, Matthias | Sanson, Marc | Andersson, Ulrika | Rajaraman, Preetha | Chanock, Stephen | Linet, Martha | Wang, Zhaoming | Yeager, Meredith | Wiencke, John K. | Hansen, Helen | Mccoy, Lucie | Rice, Terri | Kosel, Matthew L. | Sicotte, Hugues | Amos, Christopher I. | Bernstein, Jonine L. | Davis, Faith | Lachance, Dan | Lau, Ching | Merrell, Ryan T. | Shildkraut, Joellen | Ali-Osman, Francis | Sadetzki, Siegal | Scheurer, Michael | Shete, Sanjay | Lai, Rose K. | Claus, Elizabeth B. | Olson, Sara H. | Jenkins, Robert B. | Houlston, Richard S. | Bondy, Mélissa L.

Edité par CCSD ; Nature Publishing Group -

Genome-wide association studies (GWAS) have transformed our understanding of glioma susceptibility, but individual studies have had limited power to identify risk loci. We performed a meta-analysis of existing GWAS and two new GWAS, which totaled 12,496 cases and 18,190 controls. We identified five new loci for glioblastoma (GBM) at 1p31.3 (rs12752552; P = 2.04 x 10(-9), odds ratio (OR) = 1.22), 11q14.1 (rs11233250; P = 9.95 x 10(-10), OR = 1.24), 16p13.3 (rs2562152; P = 1.93 x 10-8, OR = 1.21), 16q12.1 (rs10852606; P = 1.29 x 10(-11), OR = 1.18) and 22q13.1 (rs2235573; P = 1.76 x 10(-10), OR = 1.15), as well as eight loci for non-GBM tumors at 1q32.1 (rs4252707; P = 3.34 x 10(-9), OR = 1.19), 1q44 (rs12076373; P = 2.63 x 10(-10), OR = 1.23), 2q33.3 (rs7572263; P = 2.18 x 10(-10), OR = 1.20), 3p14.1 (rs11706832; P = 7.66 x 10(-9), OR = 1.15), 10q24.33 (rs11598018; P = 3.39 x 10-8, OR = 1.14), 11q21 (rs7107785; P = 3.87 x 10(-10), OR = 1.16), 14q12 (rs10131032; P = 5.07 x 10(-11), OR = 1.33) and 16p13.3 (rs3751667; P = 2.61 x 10(-9), OR = 1.18). These data substantiate that genetic susceptibility to GBM and non-GBM tumors are highly distinct, which likely reflects different etiology.

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