A Genome-wide Association Study Identifies Risk Alleles in Plasminogen and P4HA2 Associated with Giant Cell Arteritis

被引:74
|
作者
David Carmona, F. [1 ,2 ,3 ]
Vaglio, Augusto [4 ]
Mackie, Sarah L. [5 ,6 ]
Hernandez-Rodriguez, Jose [7 ]
Monach, Paul A. [8 ]
Castaneda, Santos [9 ]
Solans, Roser [10 ]
Morado, Inmaculada C. [11 ]
Narvaez, Javier [12 ]
Ramentol-Sintas, Marc [10 ]
Pease, Colin T. [5 ,6 ]
Dasgupta, Bhaskar [13 ]
Watts, Richard [14 ]
Khalidi, Nader [15 ]
Langford, Carol A. [16 ]
Ytterberg, Steven [17 ]
Boiardi, Luigi [18 ]
Beretta, Lorenzo [19 ]
Govoni, Marcello [20 ]
Emmi, Giacomo [21 ]
Bonatti, Francesco [22 ]
Cimmino, Marco A. [23 ,24 ]
Witte, Torsten [25 ]
Neumann, Thomas [26 ]
Holle, Julia [27 ,28 ]
Schoenau, Verena [29 ]
Sailler, Laurent [30 ]
Papo, Thomas [31 ]
Haroche, Julien [32 ,33 ]
Mahr, Alfred [34 ]
Mouthon, Luc [35 ]
Molberg, Oyvind [36 ]
Diamantopoulos, Andreas P. [37 ]
Voskuyl, Alexandre [38 ]
Brouwer, Elisabeth [39 ]
Daikeler, Thomas [40 ]
Berger, Christoph T. [41 ,42 ]
Molloy, Eamonn S. [43 ]
O'Neill, Lorraine [43 ]
Blockmans, Daniel [44 ]
Lie, Benedicte A. [45 ,46 ]
Mclaren, Paul [47 ]
Vyse, Timothy J. [48 ,49 ,50 ]
Wijmenga, Cisca [51 ]
Allanore, Yannick [52 ]
Koeleman, Bobby P. C. [53 ]
Barrett, Jennifer H. [5 ,6 ]
Cid, Maria C. [7 ]
Salvarani, Carlo [18 ]
Merkel, Peter A. [54 ]
机构
[1] PTS Granada, CSIC, Inst Parasitol & Biomed Lopez Neyra, Granada 18016, Spain
[2] Univ Granada, Dept Genet, Granada 18016, Spain
[3] Univ Granada, Inst Biotecnol, Granada 18016, Spain
[4] Univ Hosp Parma, Unit Nephrol, I-43126 Parma, Italy
[5] Univ Leeds, Sch Med, Leeds LS7 4SA, W Yorkshire, England
[6] Leeds Teaching Hosp NHS Trust, NIHR Leeds Musculoskeletal Biomed Res Unit, Leeds LS7 4SA, W Yorkshire, England
[7] Univ Barcelona, Hosp Clin, Inst Invest Biomed August Pi & Sunyer IDIBAPS, Vasculitis Res Unit,Dept Autoimmune Dis, E-08036 Barcelona, Spain
[8] Boston Univ, Sect Rheumatol, Boston, MA 02118 USA
[9] Hosp Princesa, IIS IP, Dept Rheumatol, Madrid 28006, Spain
[10] Autonomous Univ Barcelona, Hosp Vall dHebron, Dept Internal Med, Autoimmune Syst Dis Unit, E-08035 Barcelona, Spain
[11] Hosp Clin San Carlos, Dept Rheumatol, Madrid 28040, Spain
[12] Hosp Univ Bellvitge IDIBELL, Dept Rheumatol, Barcelona 08907, Spain
[13] Southend Univ Hosp NHS Fdn Trust, Dept Rheumatol, Westcliff On Sea SS0 0RY, England
[14] Ipswich Hosp NHS Trust, Dept Rheumatol, Ipswich IP4 5PD, Suffolk, England
[15] McMaster Univ, Div Rheumatol, Hamilton, ON L8N 1Y2, Canada
[16] Cleveland Clin, Div Rheumatol, Cleveland, OH 44195 USA
[17] Mayo Clin, Div Rheumatol, Rochester, MN 55905 USA
[18] Azienda Osped Arcispedale Santa Maria Nuova, Ist Ricovero & Cura Carattere Sci, Dept Internal Med, Rheumatol Unit, I-42123 Reggio Emilia, Italy
[19] Fdn IRCCS Ca Granda Osped Maggiore Policlin, Referral Ctr System Autoimmune Dis, I-20122 Milan, Italy
[20] Univ Ferrara, Azienda Osped Univ S Anna, Dept Rheumatol, I-44121 Ferrara, Italy
[21] Univ Florence, Dept Expt & Clin Med, I-50134 Florence, Italy
[22] Univ Parma, Med Genet Unit, Dept Clin & Expt Med, I-43124 Parma, Italy
[23] Univ Genoa, Dept Internal Med, Res Lab, I-16132 Genoa, Italy
[24] Univ Genoa, Dept Internal Med, Acad Div Clin Rheumatol, I-16132 Genoa, Italy
[25] Hannover Med Sch, D-30625 Hannover, Germany
[26] Univ Hosp Jena, Innere Med Klin 3, D-07743 Jena, Germany
[27] Klinikum Bad Bramstedt, Vasculitis Clin, D-24576 Bad Bramstedt, Germany
[28] Univ Hosp Schleswig Holstein, D-24576 Bad Bramstedt, Germany
[29] Univ Klinikum Erlangen, Dept Rheumatol & Immunol, D-91054 Erlangen, Germany
[30] Univ Toulouse, CHU Toulouse, INSERM, Serv Med Interne,Hop Purpan,UMR 1027, F-31059 Toulouse, France
[31] Univ Paris Diderot, Hop Bichat, Serv Med Interne, F-75018 Paris, France
[32] Hop La Pitie Salpetriere, AP HP, Dept Internal Med, F-75013 Paris, France
[33] Hop La Pitie Salpetriere, AP HP, French Reference Ctr Rare Autoimmune & Syst Dis, F-75013 Paris, France
[34] Univ Paris Diderot, Host St Louis, ECSTRA Team,UMR 1153, Sorbonne Paris Cite,Res Ctr,Dept Internal Med,Epi, F-75010 Paris, France
[35] Univ Paris 05, Cochin Hosp, AP HP, Natl Referral Ctr Rare Autoimmune & Syst Dis,Dept, F-75014 Paris, France
[36] Oslo Univ Hosp, Dept Rheumatol, N-0424 Oslo, Norway
[37] Hosp Southern Norway Trust, Dept Rheumatol, N-4604 Kristiansand, Norway
[38] Vrije Univ Amsterdam, Med Ctr, Amsterdam Rheumatol & Immunol Ctr, NL-1007 MB Amsterdam, Netherlands
[39] Univ Groningen, Univ Med Ctr Groningen, Dept Rheumatol & Clin Immunol, NL-9713 GZ Groningen, Netherlands
[40] Univ Hosp, Rheumatol Dept Internal Med, CH-4056 Basel, Switzerland
[41] Univ Hosp, Translat Immunol & Med Outpatient Clin, Dept Biomed, CH-4056 Basel, Switzerland
[42] Univ Hosp, Translat Immunol & Med Outpatient Clin, Dept Internal Med, CH-4056 Basel, Switzerland
[43] St Vincents Univ Hosp, Dublin Acad Med Ctr, Ctr Arthrit & Rheumat Dis, Dept Rheumatol, Dublin 4, Ireland
[44] Univ Hosp Gasthuisberg, Dept Gen Internal Med, B-3000 Leuven, Belgium
[45] Univ Oslo, Dept Med Genet, N-0450 Oslo, Norway
[46] Oslo Univ Hosp, N-0450 Oslo, Norway
[47] Swiss Inst Bioinformat, CH-1015 Lausanne, Switzerland
[48] Kings Coll London, Div Genet, London SE1 9RT, England
[49] Kings Coll London, Div Mol Med, London SE1 9RT, England
[50] Kings Coll London, Div Immunol Infect & Inflammatory Dis, London SE1 9RT, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
FUNCTIONAL VARIATION; DISEASE; PATHOGENESIS; VARIANTS; INSIGHTS; HYPOXIA; GENES; TOOL;
D O I
10.1016/j.ajhg.2016.11.013
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Giant cell arteritis (GCA) is the most common form of vasculitis in individuals older than SO years in Western countries. To shed light onto the genetic background influencing susceptibility for GCA, we performed a genome-wide association screening in a well-powered study cohort. After imputation, 1,844,133 genetic variants were analyzed in 2,134 case subjects and 9,125 unaffected individuals from ten independent populations of European ancestry. Our data confirmed HLA class II as the strongest associated region (independent signals: rs9268905, p = 1.94 x 10(-54), per-allele OR = 1.79; and rs9275592, p = 1.14 x 10(-4), OR = 2.08). Additionally, PLG and P4HA2 were identified as GCA risk genes at the genome-wide level of significance (rs4252134, p = 1.23 x 10(-10), OR = 1.28; and rs128738, p = 4.60 x 10(-9), OR = 1.32, respectively). Interestingly, we observed that the association peaks overlapped with different regulatory elements related to cell types and tissues involved in the pathophysiology of GCA. PLG and P4HA2 are involved in vascular remodelling and angiogenesis, suggesting a high relevance of these processes for the pathogenic mechanisms underlying this type of vasculitis.
引用
收藏
页码:64 / 74
页数:11
相关论文
共 50 条
  • [31] Genome-wide association study in Chinese cohort identifies one novel hypospadias risk associated locus at 12q13.13
    Chen, Zhongzhong
    Lin, Xiaoling
    Lei, Yunping
    Chen, Haitao
    Finnell, Richard H.
    Wang, Yaping
    Xu, Jianfeng
    Lu, Daru
    Xie, Hua
    Chen, Fang
    BMC MEDICAL GENOMICS, 2019, 12 (01)
  • [32] A replication study of genome-wide CNV association for hepatic biomarkers identifies nine genes associated with liver function
    Kim, Hyo-Young
    Byun, Mi-Jeong
    Kim, Heebal
    BMB REPORTS, 2011, 44 (09) : 578 - 583
  • [33] Genome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma
    Johnson, David C.
    Weinhold, Niels
    Mitchell, Jonathan S.
    Chen, Bowang
    Kaiser, Martin
    Begum, Dil B.
    Hillengass, Jens
    Bertsch, Uta
    Gregory, Walter A.
    Cairns, David
    Jackson, Graham H.
    Foersti, Asta
    Nickel, Jolanta
    Hoffmann, Per
    Noeethen, Markus M.
    Stephens, Owen W.
    Barlogie, Bart
    Davis, Faith E.
    Hemminki, Kari
    Goldschmidt, Hartmut
    Houlston, Richard S.
    Morgan, Gareth J.
    NATURE COMMUNICATIONS, 2016, 7
  • [34] A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12
    Fernandez-Rozadilla, Ceres
    Cazier, Jean-Baptiste
    Tomlinson, Ian P.
    Carvajal-Carmona, Luis G.
    Palles, Claire
    Lamas, Maria J.
    Baiget, Montserrat
    Lopez-Fernandez, Luis A.
    Brea-Fernandez, Alejandro
    Abuli, Anna
    Bujanda, Luis
    Clofent, Juan
    Gonzalez, Dolors
    Xicola, Rosa
    Andreu, Montserrat
    Bessa, Xavier
    Jover, Rodrigo
    Llor, Xavier
    Moreno, Victor
    Castells, Antoni
    Carracedo, Angel
    Castellvi-Bel, Sergi
    Ruiz-Ponte, Clara
    BMC GENOMICS, 2013, 14
  • [35] Large-Scale Genome-Wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer
    Lu, Yingchang
    Kweon, Sun-Seog
    Tanikawa, Chizu
    Jia, Wei-Hua
    Xiang, Yong-Bing
    Cai, Qiuyin
    Zeng, Chenjie
    Schmit, Stephanie L.
    Shin, Aesun
    Matsuo, Keitaro
    Jee, Sun Ha
    Kim, Dong-Hyun
    Kim, Jeongseon
    Wen, Wanqing
    Shi, Jiajun
    Guo, Xingyi
    Li, Bingshan
    Wang, Nan
    Zhang, Ben
    Li, Xinxiang
    Shin, Min-Ho
    Li, Hong-Lan
    Ren, Zefang
    Oh, Jae Hwan
    Oze, Isao
    Ahn, Yoon-Ok
    Jung, Keum Ji
    Conti, David V.
    Schumacher, Fredrick R.
    Rennert, Gad
    Jenkins, Mark A.
    Campbell, Peter T.
    Hoffmeister, Michael
    Casey, Graham
    Gruber, Stephen B.
    Gao, Jing
    Gao, Yu-Tang
    Pan, Zhi-Zhong
    Kamatani, Yoichiro
    Zeng, Yi-Xin
    Shu, Xiao-Ou
    Long, Jirong
    Matsuda, Koichi
    Zheng, Wei
    GASTROENTEROLOGY, 2019, 156 (05) : 1455 - 1466
  • [36] Genome-wide association study identifies genes associated with neuropathy in patients with head and neck cancer
    Reyes-Gibby, Cielito C.
    Wang, Jian
    Yeung, Sai-Ching J.
    Chaftari, Patrick
    Yu, Robert K.
    Hanna, Ehab Y.
    Shete, Sanjay
    SCIENTIFIC REPORTS, 2018, 8
  • [37] Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth
    Wang, Yunpeng
    Nudel, Ron
    Benros, Michael E.
    Skogstrand, Kristin
    Fishilevich, Simon
    Lancet, Doron
    Sun, Jiangming
    Hougaard, David M.
    Andreassen, Ole A.
    Mortensen, Preben Bo
    Buil, Alfonso
    Hansen, Thomas F.
    Thompson, Wesley K.
    Werge, Thomas
    PLOS GENETICS, 2020, 16 (11):
  • [38] Genome-wide association study identifies DRAM1 associated with Tourette syndrome in Taiwan
    Lin, Wei-De
    Liu, Ting-Yuan
    Chen, Yu-Chia
    Chou, I. -Ching
    Tsai, Fuu-Jen
    BIOMEDICAL JOURNAL, 2024, 47 (06)
  • [39] Genome-wide association study identifies three novel loci for type 2 diabetes
    Hara, Kazuo
    Fujita, Hayato
    Johnson, Todd A.
    Yamauchi, Toshimasa
    Yasuda, Kazuki
    Horikoshi, Momoko
    Peng, Chen
    Hu, Cheng
    Ma, Ronald C. W.
    Imamura, Minako
    Iwata, Minoru
    Tsunoda, Tatsuhiko
    Morizono, Takashi
    Shojima, Nobuhiro
    So, Wing Yee
    Leung, Ting Fan
    Kwan, Patrick
    Zhang, Rong
    Wang, Jie
    Yu, Weihui
    Maegawa, Hiroshi
    Hirose, Hiroshi
    Kaku, Kohei
    Ito, Chikako
    Watada, Hirotaka
    Tanaka, Yasushi
    Tobe, Kazuyuki
    Kashiwagi, Atsunori
    Kawamori, Ryuzo
    Jia, Weiping
    Chan, Juliana C. N.
    Teo, Yik Ying
    Shyong, Tai E.
    Kamatani, Naoyuki
    Kubo, Michiaki
    Maeda, Shiro
    Kadowaki, Takashi
    HUMAN MOLECULAR GENETICS, 2014, 23 (01) : 239 - 246
  • [40] Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer
    Amundadottir, Laufey
    Kraft, Peter
    Stolzenberg-Solomon, Rachael Z.
    Fuchs, Charles S.
    Petersen, Gloria M.
    Arslan, Alan A.
    Bueno-de-Mesquita, H. Bas
    Gross, Myron
    Helzlsouer, Kathy
    Jacobs, Eric J.
    LaCroix, Andrea
    Zheng, Wei
    Albanes, Demetrius
    Bamlet, William
    Berg, Christine D.
    Berrino, Franco
    Bingham, Sheila
    Buring, Julie E.
    Bracci, Paige M.
    Canzian, Federico
    Clavel-Chapelon, Francoise
    Clipp, Sandra
    Cotterchio, Michelle
    de Andrade, Mariza
    Duell, Eric J.
    Fox, John W., Jr.
    Gallinger, Steven
    Gaziano, J. Michael
    Giovannucci, Edward L.
    Goggins, Michael
    Gonzalez, Carlos A.
    Hallmans, Goran
    Hankinson, Susan E.
    Hassan, Manal
    Holly, Elizabeth A.
    Hunter, David J.
    Hutchinson, Amy
    Jackson, Rebecca
    Jacobs, Kevin B.
    Jenab, Mazda
    Kaaks, Rudolf
    Klein, Alison P.
    Kooperberg, Charles
    Kurtz, Robert C.
    Li, Donghui
    Lynch, Shannon M.
    Mandelson, Margaret
    McWilliams, Robert R.
    Mendelsohn, Julie B.
    Michaud, Dominique S.
    NATURE GENETICS, 2009, 41 (09) : 986 - U47