The effect of sample size on polygenic hazard models for prostate cancer.
The effect of sample size on polygenic hazard models for prostate cancer.
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DOI:
10.1038/s41431-020-0664-2
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发表时间:
2020-10
期刊:
影响因子:
--
通讯作者:
PRACTICAL Consortium
中科院分区:
文献类型:
--
作者:
Karunamuni RA;Huynh-Le MP;Fan CC;Eeles RA;Easton DF;Kote-Jarai Z;Amin Al Olama A;Benlloch Garcia S;Muir K;Gronberg H;Wiklund F;Aly M;Schleutker J;Sipeky C;Tammela TLJ;Nordestgaard BG;Key TJ;Travis RC;Neal DE;Donovan JL;Hamdy FC;Pharoah P;Pashayan N;Khaw KT;Thibodeau SN;McDonnell SK;Schaid DJ;Maier C;Vogel W;Luedeke M;Herkommer K;Kibel AS;Cybulski C;Wokolorczyk D;Kluzniak W;Cannon-Albright L;Brenner H;Schöttker B;Holleczek B;Park JY;Sellers TA;Lin HY;Slavov C;Kaneva R;Mitev V;Batra J;Clements JA;Spurdle A;Australian Prostate Cancer BioResource (APCB);Teixeira MR;Paulo P;Maia S;Pandha H;Michael A;Mills IG;Andreassen OA;Dale AM;Seibert TM;PRACTICAL Consortium
We determined the effect of sample size on performance of polygenic hazard score (PHS) models in prostate cancer. Age and genotypes were obtained for 40,861 men from the PRACTICAL consortium. The dataset included 201,590 SNPs per subject, and was split into training and testing sets. Established-SNP models considered 65 SNPs that had been previously associated with prostate cancer. Discovery-SNP models used stepwise selection to identify new SNPs. The performance of each PHS model was calculated for random sizes of the training set. The performance of a representative Established-SNP model was estimated for random sizes of the testing set. Mean HR98/50 (hazard ratio of top 2% to average in test set) of the Established-SNP model increased from 1.73 [95% CI: 1.69–1.77] to 2.41 [2.40–2.43] when the number of training samples was increased from 1 thousand to 30 thousand. Corresponding HR98/50 of the Discovery-SNP model increased from 1.05 [0.93–1.18] to 2.19 [2.16–2.23]. HR98/50 of a representative Established-SNP model using testing set sample sizes of 0.6 thousand and 6 thousand observations were 1.78 [1.70–1.85] and 1.73 [1.71–1.76], respectively. We estimate that a study population of 20 thousand men is required to develop Discovery-SNP PHS models while 10 thousand men should be sufficient for Established-SNP models.
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影响因子:
1.3
作者:
Therneau, TM;Li, HZ
通讯作者:
Li, HZ
DOI:
10.1002/pros.23037
发表时间:
2015-09
期刊:
The Prostate
影响因子:
--
作者:
Szulkin R;Whitington T;Eklund M;Aly M;Eeles RA;Easton D;Kote-Jarai ZS;Amin Al Olama A;Benlloch S;Muir K;Giles GG;Southey MC;Fitzgerald LM;Henderson BE;Schumacher F;Haiman CA;Schleutker J;Wahlfors T;Tammela TL;Nordestgaard BG;Key TJ;Travis RC;Neal DE;Donovan JL;Hamdy FC;Pharoah P;Pashayan N;Khaw KT;Stanford JL;Thibodeau SN;McDonnell SK;Schaid DJ;Maier C;Vogel W;Luedeke M;Herkommer K;Kibel AS;Cybulski C;Lubiński J;Kluźniak W;Cannon-Albright L;Brenner H;Butterbach K;Stegmaier C;Park JY;Sellers T;Lin HY;Slavov C;Kaneva R;Mitev V;Batra J;Clements JA;Australian Prostate Cancer BioResource;Spurdle A;Teixeira MR;Paulo P;Maia S;Pandha H;Michael A;Kierzek A;Practical Consortium;Gronberg H;Wiklund F
通讯作者:
Wiklund F
影响因子:
30.8
作者:
Eeles, Rosalind A.;Al Olama, Ali Amin;Benlloch, Sara;Saunders, Edward J.;Leongamornlert, Daniel A.;Tymrakiewicz, Malgorzata;Ghoussaini, Maya;Luccarini, Craig;Dennis, Joe;Jugurnauth-Little, Sarah;Dadaev, Tokhir;Neal, David E.;Hamdy, Freddie C.;Donovan, Jenny L.;Muir, Ken;Giles, Graham G.;Severi, Gianluca;Wiklund, Fredrik;Gronberg, Henrik;Haiman, Christopher A.;Schumacher, Fredrick;Henderson, Brian E.;Le Marchand, Loic;Lindstrom, Sara;Kraft, Peter;Hunter, David J.;Gapstur, Susan;Chanock, Stephen J.;Berndt, Sonja I.;Albanes, Demetrius;Andriole, Gerald;Schleutker, Johanna;Weischer, Maren;Canzian, Federico;Riboli, Elio;Key, Tim J.;Travis, Ruth C.;Campa, Daniele;Ingles, Sue A.;John, Esther M.;Hayes, Richard B.;Pharoah, Paul D. P.;Pashayan, Nora;Khaw, Kay-Tee;Stanford, Janet L.;Ostrander, Elaine A.;Signorello, Lisa B.;Thibodeau, Stephen N.;Schaid, Dan;Maier, Christiane;Vogel, Walther;Kibel, Adam S.;Cybulski, Cezary;Lubhiski, Jan;Cannon-Albright, Lisa;Brenner, Hermann;Park, Jong Y.;Kaneva, Radka;Batra, Jyotsna;Spurdle, Amanda B.;Clements, Judith A.;Teixeira, Manuel R.;Dicks, Ed;Lee, Andrew;Dunning, Alison M.;Baynes, Caroline;Conroy, Don;Maranian, Melanie J.;Ahmed, Shahana;Govindasami, Koveela;Guy, Michelle;Wilkinson, Rosemary A.;Sawyer, Emma J.;Morgan, Angela;Dearnaley, David P.;Horwich, Alan;Huddart, Robert A.;Khoo, Vincent S.;Parker, Christopher C.;Van As, Nicholas J.;Woodhouse, Christopher J.;Thompson, Alan;Dudderidge, Tim;Ogden, Chris;Cooper, Colin S.;Lophatananon, Artitaya;Cox, Angela;Southey, Melissa C.;Hopper, John L.;English, Dallas R.;Aly, Markus;Adolfsson, Jan;Xu, Jiangfeng;Zheng, Siqun L.;Yeager, Meredith;Kaaks, Rudolf;Diver, W. Ryan;Gaudet, Mia M.;Stern, Mariana C.;Corral, Roman;Joshi, Amit D.;Shahabi, Ahva;Wahlfors, Tiina;Tammela, Teuvo L. J.;Auvinen, Anssi;Virtamo, Jarmo;Klarskov, Peter;Nordestgaard, Borge G.;Roder, M. Andreas;Nielsen, Sune F.;Bojesen, Stig E.;Siddiq, Afshan;FitzGerald, Liesel M.;Kolb, Suzanne;Kwon, Erika M.;Karyadi, Danielle M.;Blot, William J.;Zheng, Wei;Cai, Qiuyin;McDonnell, Shannon K.;Rinckleb, Antje E.;Drake, Bettina;Colditz, Graham;Wokolorczyk, Dominika;Stephenson, Robert A.;Teerlink, Craig;Muller, Heiko;Rothenbacher, Dietrich;Sellers, Thomas A.;Lin, Hui-Yi;Slavov, Chavdar;Mitev, Vanio;Lose, Felicity;Srinivasan, Srilakshmi;Maia, Sofia;Paulo, Paula;Lange, Ethan;Cooney, Kathleen A.;Antoniou, Antonis C.;Vincent, Daniel;Bacot, Francois;Tessier, Daniel C.;Kote-Jarai, Zsofia;Easton, Douglas F.
通讯作者:
Easton, Douglas F.
影响因子:
23.4
作者:
Aly, Markus;Wiklund, Fredrik;Xu, Jianfeng;Isaacs, William B.;Eklund, Martin;D'Amato, Mauro;Adolfsson, Jan;Gronberg, Henrik
通讯作者:
Gronberg, Henrik
影响因子:
2.1
作者:
Machiela, Mitchell J.;Chen, Chia-Yen;Chen, Constance;Chanock, Stephen J.;Hunter, David J.;Kraft, Peter
通讯作者:
Kraft, Peter