Generalizability of established prostate cancer risk variants in men of African ancestry

Genome‐wide association studies have identified more than 80 risk variants for prostate cancer, mainly in European or Asian populations. The generalizability of these variants in other racial/ethnic populations needs to be understood before the loci can be used widely in risk modeling. In our study,...

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Veröffentlicht in:International journal of cancer 2015-03, Vol.136 (5), p.1210-1217
Hauptverfasser: Han, Ying, Signorello, Lisa B., Strom, Sara S., Kittles, Rick A., Rybicki, Benjamin A., Stanford, Janet L., Goodman, Phyllis J., Berndt, Sonja I., Carpten, John, Casey, Graham, Chu, Lisa, Conti, David V., Rand, Kristin A., Diver, W. Ryan, Hennis, Anselm J.M., John, Esther M., Kibel, Adam S., Klein, Eric A., Kolb, Suzanne, Le Marchand, Loic, Leske, M. Cristina, Murphy, Adam B., Neslund‐Dudas, Christine, Park, Jong Y., Pettaway, Curtis, Rebbeck, Timothy R., Gapstur, Susan M., Zheng, S. Lilly, Wu, Suh‐Yuh, Witte, John S., Xu, Jianfeng, Isaacs, William, Ingles, Sue A., Hsing, Ann, Easton, Douglas F., Eeles, Rosalind A., Schumacher, Fredrick R., Chanock, Stephen, Nemesure, Barbara, Blot, William J., Stram, Daniel O., Henderson, Brian E., Haiman, Christopher A.
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Sprache:eng
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Zusammenfassung:Genome‐wide association studies have identified more than 80 risk variants for prostate cancer, mainly in European or Asian populations. The generalizability of these variants in other racial/ethnic populations needs to be understood before the loci can be used widely in risk modeling. In our study, we examined 82 previously reported risk variants in 4,853 prostate cancer cases and 4,678 controls of African ancestry. We performed association testing for each variant using logistic regression adjusted for age, study and global ancestry. Of the 82 known risk variants, 68 (83%) had effects that were directionally consistent in their association with prostate cancer risk and 30 (37%) were significantly associated with risk at p 
ISSN:0020-7136
1097-0215
DOI:10.1002/ijc.29066