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Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

Authors :
Schumacher, Fredrick R
Al Olama, Ali Amin
Berndt, Sonja I
Benlloch, Sara
Ahmed, Mahbubl
Saunders, Edward J
Dadaev, Tokhir
Leongamornlert, Daniel
Anokian, Ezequiel
Cieza-Borrella, Clara
Goh, Chee
Brook, Mark N
Sheng, Xin
Fachal, Laura
Dennis, Joe
Tyrer, Jonathan
Muir, Kenneth
Lophatananon, Artitaya
Stevens, Victoria L
Gapstur, Susan M
Carter, Brian D
Tangen, Catherine M
Goodman, Phyllis J
Thompson, Ian M
Batra, Jyotsna
Chambers, Suzanne
Moya, Leire
Clements, Judith
Horvath, Lisa
Tilley, Wayne
Risbridger, Gail P
Gronberg, Henrik
Aly, Markus
Nordström, Tobias
Pharoah, Paul
Pashayan, Nora
Schleutker, Johanna
Tammela, Teuvo LJ
Sipeky, Csilla
Auvinen, Anssi
Albanes, Demetrius
Weinstein, Stephanie
Wolk, Alicja
Håkansson, Niclas
West, Catharine ML
Dunning, Alison M
Burnet, Neil
Mucci, Lorelei A
Giovannucci, Edward
Andriole, Gerald L
Cussenot, Olivier
Cancel-Tassin, Géraldine
Koutros, Stella
Beane Freeman, Laura E
Sorensen, Karina Dalsgaard
Orntoft, Torben Falck
Borre, Michael
Maehle, Lovise
Grindedal, Eli Marie
Neal, David E
Donovan, Jenny L
Hamdy, Freddie C
Martin, Richard M
Travis, Ruth C
Key, Tim J
Hamilton, Robert J
Fleshner, Neil E
Finelli, Antonio
Ingles, Sue Ann
Stern, Mariana C
Rosenstein, Barry S
Kerns, Sarah L
Ostrer, Harry
Lu, Yong-Jie
Zhang, Hong-Wei
Feng, Ninghan
Mao, Xueying
Guo, Xin
Wang, Guomin
Sun, Zan
Giles, Graham G
Southey, Melissa C
MacInnis, Robert J
FitzGerald, Liesel M
Kibel, Adam S
Drake, Bettina F
Vega, Ana
Gómez-Caamaño, Antonio
Szulkin, Robert
Eklund, Martin
Kogevinas, Manolis
Llorca, Javier
Castaño-Vinyals, Gemma
Penney, Kathryn L
Stampfer, Meir
Park, Jong Y
Sellers, Thomas A
Lin, Hui-Yi
Stanford, Janet L
Cybulski, Cezary
Source :
Nature genetics, vol 50, iss 7
Publication Year :
2018

Abstract

© 2018 The Author(s). Genome-wide association studies (GWAS) and fine-mapping efforts to date have identified more than 100 prostate cancer (PrCa)-susceptibility loci. We meta-analyzed genotype data from a custom high-density array of 46,939 PrCa cases and 27,910 controls of European ancestry with previously genotyped data of 32,255 PrCa cases and 33,202 controls of European ancestry. Our analysis identified 62 novel loci associated (P < 5.0 × 10-8) with PrCa and one locus significantly associated with early-onset PrCa (≤55 years). Our findings include missense variants rs1800057 (odds ratio (OR) = 1.16; P = 8.2 × 10-9; G>C, p.Pro1054Arg) in ATM and rs2066827 (OR = 1.06; P = 2.3 × 10-9; T>G, p.Val109Gly) in CDKN1B. The combination of all loci captured 28.4% of the PrCa familial relative risk, and a polygenic risk score conferred an elevated PrCa risk for men in the ninetieth to ninety-ninth percentiles (relative risk = 2.69; 95% confidence interval (CI): 2.55-2.82) and first percentile (relative risk = 5.71; 95% CI: 5.04-6.48) risk stratum compared with the population average. These findings improve risk prediction, enhance fine-mapping, and provide insight into the underlying biology of PrCa 1 .

Details

Database :
OpenAIRE
Journal :
Nature genetics, vol 50, iss 7
Accession number :
edsair.dedup.wf.001..ffc471389038129cafce11717f3e9d49