Résumé
Genome-wide association studies (GWASs) of follicular lymphoma (FL) have previously identified human leukocyte antigen (HLA) gene variants. To identify additional FL susceptibility loci, we conducted a large-scale two-stage GWAS in 4,523 case subjects and 13,344 control subjects of European ancestry. Five non-HLA loci were associated with FL risk: 11q23.3 (rs4938573, p = 5.79 × 10 -20) near CXCR5; 11q24.3 (rs4937362, p = 6.76 × 10 -11) near ETS1; 3q28 (rs6444305, p = 1.10 × 10 -10) in LPP; 18q21.33 (rs17749561, p = 8.28 × 10 -10) near BCL2; and 8q24.21 (rs13254990, p = 1.06 × 10 -8) near PVT1. In an analysis of the HLA region, we identified four linked HLA-DRβ1 multiallelic amino acids at positions 11, 13, 28, and 30 that were associated with FL risk (pomnibus = 4.20 × 10 -67 to 2.67 × 10 -70). Additional independent signals included rs17203612 in HLA class II (odds ratio [ORper-allele] = 1.44; p = 4.59 × 10 -16) and rs3130437 in HLA class I (ORper-allele = 1.23; p = 8.23 × 10 -9). Our findings further expand the number of loci associated with FL and provide evidence that multiple common variants outside the HLA region make a significant contribution to FL risk.
langue originale | Anglais |
---|---|
Pages (de - à) | 462-471 |
Nombre de pages | 10 |
journal | American Journal of Human Genetics |
Volume | 95 |
Numéro de publication | 4 |
Les DOIs | |
état | Publié - 1 janv. 2014 |
Modification externe | Oui |
Accès au document
Autres fichiers et liens
Contient cette citation
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver
}
Dans: American Journal of Human Genetics, Vol 95, Numéro 4, 01.01.2014, p. 462-471.
Résultats de recherche: Contribution à un journal › Article › Revue par des pairs
TY - JOUR
T1 - Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region
AU - Skibola, Christine F.
AU - Berndt, Sonja I.
AU - Vijai, Joseph
AU - Conde, Lucia
AU - Wang, Zhaoming
AU - Yeager, Meredith
AU - De Bakker, Paul I.W.
AU - Birmann, Brenda M.
AU - Vajdic, Claire M.
AU - Foo, Jia Nee
AU - Bracci, Paige M.
AU - Vermeulen, Roel C.H.
AU - Slager, Susan L.
AU - De Sanjose, Silvia
AU - Wang, Sophia S.
AU - Linet, Martha S.
AU - Salles, Gilles
AU - Lan, Qing
AU - Severi, Gianluca
AU - Hjalgrim, Henrik
AU - Lightfoot, Tracy
AU - Melbye, Mads
AU - Gu, Jian
AU - Ghesquières, Hervé
AU - Link, Brian K.
AU - Morton, Lindsay M.
AU - Holly, Elizabeth A.
AU - Smith, Alex
AU - Tinker, Lesley F.
AU - Teras, Lauren R.
AU - Kricker, Anne
AU - Becker, Nikolaus
AU - Purdue, Mark P.
AU - Spinelli, John J.
AU - Zhang, Yawei
AU - Giles, Graham G.
AU - Vineis, Paolo
AU - Monnereau, Alain
AU - Bertrand, Kimberly A.
AU - Albanes, Demetrius
AU - Zeleniuch-Jacquotte, Anne
AU - Gabbas, Attilio
AU - Chung, Charles C.
AU - Burdett, Laurie
AU - Hutchinson, Amy
AU - Lawrence, Charles
AU - Montalvan, Rebecca
AU - Liang, Liming
AU - Huang, Jinyan
AU - Ma, Baoshan
AU - Liu, Jianjun
AU - Adami, Hans Olov
AU - Glimelius, Bengt
AU - Ye, Yuanqing
AU - Nowakowski, Grzegorz S.
AU - Dogan, Ahmet
AU - Thompson, Carrie A.
AU - Habermann, Thomas M.
AU - Novak, Anne J.
AU - Liebow, Mark
AU - Witzig, Thomas E.
AU - Weiner, George J.
AU - Schenk, Maryjean
AU - Hartge, Patricia
AU - De Roos, Anneclaire J.
AU - Cozen, Wendy
AU - Zhi, Degui
AU - Akers, Nicholas K.
AU - Riby, Jacques
AU - Smith, Martyn T.
AU - Lacher, Mortimer
AU - Villano, Danylo J.
AU - Maria, Ann
AU - Roman, Eve
AU - Kane, Eleanor
AU - Jackson, Rebecca D.
AU - North, Kari E.
AU - Diver, W. Ryan
AU - Turner, Jenny
AU - Armstrong, Bruce K.
AU - Benavente, Yolanda
AU - Boffetta, Paolo
AU - Brennan, Paul
AU - Foretova, Lenka
AU - Maynadie, Marc
AU - Staines, Anthony
AU - McKay, James
AU - Brooks-Wilson, Angela R.
AU - Zheng, Tongzhang
AU - Holford, Theodore R.
AU - Chamosa, Saioa
AU - Kaaks, Rudolph
AU - Kelly, Rachel S.
AU - Ohlsson, Bodil
AU - Travis, Ruth C.
AU - Weiderpass, Elisabete
AU - Clavel, Jacqueline
AU - Giovannucci, Edward
AU - Kraft, Peter
AU - Virtamo, Jarmo
AU - Mazza, Patrizio
AU - Cocco, Pierluigi
AU - Ennas, Maria Grazia
AU - Chiu, Brian C.H.
AU - Fraumeni, Joseph F.
AU - Nieters, Alexandra
AU - Offit, Kenneth
AU - Wu, Xifeng
AU - Cerhan, James R.
AU - Smedby, Karin E.
AU - Chanock, Stephen J.
AU - Rothman, Nathaniel
N1 - Publisher Copyright: © 2014 by The American Society of Human Genetics. All rights reserved.
PY - 2014/1/1
Y1 - 2014/1/1
N2 - Genome-wide association studies (GWASs) of follicular lymphoma (FL) have previously identified human leukocyte antigen (HLA) gene variants. To identify additional FL susceptibility loci, we conducted a large-scale two-stage GWAS in 4,523 case subjects and 13,344 control subjects of European ancestry. Five non-HLA loci were associated with FL risk: 11q23.3 (rs4938573, p = 5.79 × 10 -20) near CXCR5; 11q24.3 (rs4937362, p = 6.76 × 10 -11) near ETS1; 3q28 (rs6444305, p = 1.10 × 10 -10) in LPP; 18q21.33 (rs17749561, p = 8.28 × 10 -10) near BCL2; and 8q24.21 (rs13254990, p = 1.06 × 10 -8) near PVT1. In an analysis of the HLA region, we identified four linked HLA-DRβ1 multiallelic amino acids at positions 11, 13, 28, and 30 that were associated with FL risk (pomnibus = 4.20 × 10 -67 to 2.67 × 10 -70). Additional independent signals included rs17203612 in HLA class II (odds ratio [ORper-allele] = 1.44; p = 4.59 × 10 -16) and rs3130437 in HLA class I (ORper-allele = 1.23; p = 8.23 × 10 -9). Our findings further expand the number of loci associated with FL and provide evidence that multiple common variants outside the HLA region make a significant contribution to FL risk.
AB - Genome-wide association studies (GWASs) of follicular lymphoma (FL) have previously identified human leukocyte antigen (HLA) gene variants. To identify additional FL susceptibility loci, we conducted a large-scale two-stage GWAS in 4,523 case subjects and 13,344 control subjects of European ancestry. Five non-HLA loci were associated with FL risk: 11q23.3 (rs4938573, p = 5.79 × 10 -20) near CXCR5; 11q24.3 (rs4937362, p = 6.76 × 10 -11) near ETS1; 3q28 (rs6444305, p = 1.10 × 10 -10) in LPP; 18q21.33 (rs17749561, p = 8.28 × 10 -10) near BCL2; and 8q24.21 (rs13254990, p = 1.06 × 10 -8) near PVT1. In an analysis of the HLA region, we identified four linked HLA-DRβ1 multiallelic amino acids at positions 11, 13, 28, and 30 that were associated with FL risk (pomnibus = 4.20 × 10 -67 to 2.67 × 10 -70). Additional independent signals included rs17203612 in HLA class II (odds ratio [ORper-allele] = 1.44; p = 4.59 × 10 -16) and rs3130437 in HLA class I (ORper-allele = 1.23; p = 8.23 × 10 -9). Our findings further expand the number of loci associated with FL and provide evidence that multiple common variants outside the HLA region make a significant contribution to FL risk.
UR - http://www.scopus.com/inward/record.url?scp=84921517901&partnerID=8YFLogxK
U2 - 10.1016/j.ajhg.2014.09.004
DO - 10.1016/j.ajhg.2014.09.004
M3 - Article
C2 - 25279986
AN - SCOPUS:84921517901
SN - 0002-9297
VL - 95
SP - 462
EP - 471
JO - American Journal of Human Genetics
JF - American Journal of Human Genetics
IS - 4
ER -