Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
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Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants. / Wang, Anqi; Shen, Jiayi; Rodriguez, Alex A.; Saunders, Edward J.; Chen, Fei; Janivara, Rohini; Darst, Burcu F.; Sheng, Xin; Xu, Yili; Chou, Alisha J.; Benlloch, Sara; Dadaev, Tokhir; Brook, Mark N.; Plym, Anna; Sahimi, Ali; Hoffman, Thomas J.; Takahashi, Atushi; Matsuda, Koichi; Momozawa, Yukihide; Fujita, Masashi; Laisk, Triin; Figuerêdo, Jéssica; Muir, Kenneth; Ito, Shuji; Liu, Xiaoxi; Yamanashi, Yuji; Furukawa, Yoichi; Morisaki, Takayuki; Murakami, Yoshinori; Muto, Kaori; Nagai, Akiko; Obara, Wataru; Yamaji, Ken; Takahashi, Kazuhisa; Asai, Satoshi; Takahashi, Yasuo; Suzuki, Takao; Sinozaki, Nobuaki; Yamaguchi, Hiroki; Nordestgaard, Borge G.; Nielsen, Sune F.; Weischer, Maren; Bojesen, Stig E.; Røder, Andreas; Stroomberg, Hein V.; Sørensen, Karina Dalsgaard; Borre, Michael; Strom, Sara S.; Wang, Ying; Loos, Ruth J.F.; The Biobank Japan Project.
I: Nature Genetics, Bind 55, Nr. 12, 2023, s. 2065-2074.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
AU - Wang, Anqi
AU - Shen, Jiayi
AU - Rodriguez, Alex A.
AU - Saunders, Edward J.
AU - Chen, Fei
AU - Janivara, Rohini
AU - Darst, Burcu F.
AU - Sheng, Xin
AU - Xu, Yili
AU - Chou, Alisha J.
AU - Benlloch, Sara
AU - Dadaev, Tokhir
AU - Brook, Mark N.
AU - Plym, Anna
AU - Sahimi, Ali
AU - Hoffman, Thomas J.
AU - Takahashi, Atushi
AU - Matsuda, Koichi
AU - Momozawa, Yukihide
AU - Fujita, Masashi
AU - Laisk, Triin
AU - Figuerêdo, Jéssica
AU - Muir, Kenneth
AU - Ito, Shuji
AU - Liu, Xiaoxi
AU - Yamanashi, Yuji
AU - Furukawa, Yoichi
AU - Morisaki, Takayuki
AU - Murakami, Yoshinori
AU - Muto, Kaori
AU - Nagai, Akiko
AU - Obara, Wataru
AU - Yamaji, Ken
AU - Takahashi, Kazuhisa
AU - Asai, Satoshi
AU - Takahashi, Yasuo
AU - Suzuki, Takao
AU - Sinozaki, Nobuaki
AU - Yamaguchi, Hiroki
AU - Nordestgaard, Borge G.
AU - Nielsen, Sune F.
AU - Weischer, Maren
AU - Bojesen, Stig E.
AU - Røder, Andreas
AU - Stroomberg, Hein V.
AU - Sørensen, Karina Dalsgaard
AU - Borre, Michael
AU - Strom, Sara S.
AU - Wang, Ying
AU - Loos, Ruth J.F.
AU - The Biobank Japan Project
N1 - Publisher Copyright: © 2023, The Author(s), under exclusive licence to Springer Nature America, Inc.
PY - 2023
Y1 - 2023
N2 - The transferability and clinical value of genetic risk scores (GRSs) across populations remain limited due to an imbalance in genetic studies across ancestrally diverse populations. Here we conducted a multi-ancestry genome-wide association study of 156,319 prostate cancer cases and 788,443 controls of European, African, Asian and Hispanic men, reflecting a 57% increase in the number of non-European cases over previous prostate cancer genome-wide association studies. We identified 187 novel risk variants for prostate cancer, increasing the total number of risk variants to 451. An externally replicated multi-ancestry GRS was associated with risk that ranged from 1.8 (per standard deviation) in African ancestry men to 2.2 in European ancestry men. The GRS was associated with a greater risk of aggressive versus non-aggressive disease in men of African ancestry (P = 0.03). Our study presents novel prostate cancer susceptibility loci and a GRS with effective risk stratification across ancestry groups.
AB - The transferability and clinical value of genetic risk scores (GRSs) across populations remain limited due to an imbalance in genetic studies across ancestrally diverse populations. Here we conducted a multi-ancestry genome-wide association study of 156,319 prostate cancer cases and 788,443 controls of European, African, Asian and Hispanic men, reflecting a 57% increase in the number of non-European cases over previous prostate cancer genome-wide association studies. We identified 187 novel risk variants for prostate cancer, increasing the total number of risk variants to 451. An externally replicated multi-ancestry GRS was associated with risk that ranged from 1.8 (per standard deviation) in African ancestry men to 2.2 in European ancestry men. The GRS was associated with a greater risk of aggressive versus non-aggressive disease in men of African ancestry (P = 0.03). Our study presents novel prostate cancer susceptibility loci and a GRS with effective risk stratification across ancestry groups.
U2 - 10.1038/s41588-023-01534-4
DO - 10.1038/s41588-023-01534-4
M3 - Journal article
C2 - 37945903
AN - SCOPUS:85176259299
VL - 55
SP - 2065
EP - 2074
JO - Nature Genetics
JF - Nature Genetics
SN - 1061-4036
IS - 12
ER -
ID: 377987952