The genetics of autoimmune diseases: a networked perspective

被引:111
作者
Baranzini, Sergio E. [1 ]
机构
[1] Univ Calif San Francisco, Dept Neurol, Sch Med, San Francisco, CA 94143 USA
关键词
GENOME-WIDE ASSOCIATION; SYSTEMIC-LUPUS-ERYTHEMATOSUS; IDENTIFIES SUSCEPTIBILITY VARIANTS; SINGLE NUCLEOTIDE POLYMORPHISMS; INFLAMMATORY-BOWEL-DISEASE; 7 COMMON DISEASES; MULTIPLE-SCLEROSIS; RHEUMATOID-ARTHRITIS; CROHNS-DISEASE; RISK LOCUS;
D O I
10.1016/j.coi.2009.09.014
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Modern tools for genetic analysis are producing a large impact on our understanding of autoimmunity. More than 30 genome-wide association studies (GWAS) have been published to date in several autoimmune diseases (AID) and hundreds of common variants have been identified that confer risk or protection. While statistical adjustments are essential to refine the list of potential associations with each disease, valuable information can be extracted by the systematic collection of moderately significant variants present in more than one trait. In this article, a compilation of all GWAS published to date in seven common AID is provided and a network-based analysis of shared susceptibility genes at different levels of significance is presented. While involvement of the MHC region in chromosome 6p21 is not in question for most AID, the complex genetic architecture of this locus poses a significant analytical challenge. On the other hand, by considering the contribution of non-MHC-related genes, similarities and differences among AID can be readily computed thus gaining insights into possible pathogenic mechanisms. Statistically significant excess sharing of non-MHC genes was found between type I diabetes (T1D) and all other AID studied, a result also seen for RA. A smaller but significant degree of sharing was observed for multiple sclerosis (MS), Celiac disease (CeD) and Crohn's disease (CD). The availability of GWAS data allows for a systematic analysis of similarities and differences among several AID. Using this class of approaches the unique genetic landscape for each autoimmune disease can start to be defined.
引用
收藏
页码:596 / 605
页数:10
相关论文
共 78 条
[1]   IL-23 and Autoimmunity: New Insights into the Pathogenesis of Inflammatory Bowel Disease [J].
Abraham, Clara ;
Cho, Judy H. .
ANNUAL REVIEW OF MEDICINE, 2009, 60 :97-110
[2]  
[Anonymous], 2010, Robbins and Cotran pathologic basis of disease, professional edition e-book
[3]   Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20 [J].
Bahlo, Melanie ;
Booth, David R. ;
Broadley, Simon A. ;
Brown, Matthew A. ;
Foote, Simon J. ;
Griffiths, Lyn R. ;
Kilpatrick, Trevor J. ;
Lechner-Scott, Jeanette ;
Moscato, Pablo ;
Perreau, Victoria M. ;
Rubio, Justin P. ;
Scott, Rodney J. ;
Stankovich, Jim ;
Stewart, Graeme J. ;
Taylor, Bruce V. ;
Wiley, James ;
Clarke, Glynnis ;
Cox, Mathew B. ;
Csurhes, Peter A. ;
Danoy, Patrick ;
Drysdale, Karen ;
Field, Judith ;
Foote, Simon J. ;
Greer, Judith M. ;
Guru, Preethi ;
Hadler, Johanna ;
McMorran, Brendan J. ;
Jensen, Cathy J. ;
Johnson, Laura J. ;
McCallum, Ruth ;
Merriman, Marilyn ;
Merriman, Tony ;
Pryce, Karen ;
Tajouri, Lotfi ;
Wilkins, Ella J. ;
Browning, Brian L. ;
Browning, Sharon R. ;
Perera, Devindri ;
Butzkueven, Helmut ;
Carroll, William M. ;
Chapman, Caron ;
Kermode, Allan G. ;
Marriott, Mark ;
Mason, Deborah ;
Heard, Robert N. ;
Pender, Michael P. ;
Slee, Mark ;
Tubridy, Niall ;
Willoughby, Ernest .
NATURE GENETICS, 2009, 41 (07) :824-U84
[4]   Pathway and network-based analysis of genome-wide association studies in multiple sclerosis [J].
Baranzini, Sergio E. ;
Galwey, Nicholas W. ;
Wang, Joanne ;
Khankhanian, Pouya ;
Lindberg, Raija ;
Pelletier, Daniel ;
Wu, Wen ;
Uitdehaag, Bernard M. J. ;
Kappos, Ludwig ;
Polman, Chris H. ;
Matthews, Paul M. ;
Hauser, Stephen L. ;
Gibson, Rachel A. ;
Oksenberg, Jorge R. ;
Barnes, Michael R. .
HUMAN MOLECULAR GENETICS, 2009, 18 (11) :2078-2090
[5]   Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis [J].
Baranzini, Sergio E. ;
Wang, Joanne ;
Gibson, Rachel A. ;
Galwey, Nicholas ;
Naegelin, Yvonne ;
Barkhof, Frederik ;
Radue, Ernst-Wilhelm ;
Lindberg, Raija L. P. ;
Uitdehaag, Bernard M. G. ;
Johnson, Michael R. ;
Angelakopoulou, Aspasia ;
Hall, Leslie ;
Richardson, Jill C. ;
Prinjha, Rab K. ;
Gass, Achim ;
Geurts, Jeroen J. G. ;
Kragt, Jolijn ;
Sombekke, Madeleine ;
Vrenken, Hugo ;
Qualley, Pamela ;
Lincoln, Robin R. ;
Gomez, Refujia ;
Caillier, Stacy J. ;
George, Michaela F. ;
Mousavi, Hourieh ;
Guerrero, Rosa ;
Okuda, Darin T. ;
Cree, Bruce A. C. ;
Green, Ari J. ;
Waubant, Emmanuelle ;
Goodin, Douglas S. ;
Pelletier, Daniel ;
Matthews, Paul M. ;
Hauser, Stephen L. ;
Kappos, Ludwig ;
Polman, Chris H. ;
Oksenberg, Jorge R. .
HUMAN MOLECULAR GENETICS, 2009, 18 (04) :767-778
[6]   Clustering of autoimmune diseases in families with a high-risk for multiple sclerosis: a descriptive study [J].
Barcellos, Lisa F. ;
Kamdar, Brinda B. ;
Ramsay, Patricia P. ;
DeLoa, Cori ;
Lincoln, Robin R. ;
Caillier, Stacy ;
Schmidt, Silke ;
Haines, Jonathan L. ;
Pericak-Vance, Margaret A. ;
Oksenberg, Jorge R. ;
Hauser, Stephen L. .
LANCET NEUROLOGY, 2006, 5 (11) :924-931
[7]   Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease [J].
Barrett, Jeffrey C. ;
Hansoul, Sarah ;
Nicolae, Dan L. ;
Cho, Judy H. ;
Duerr, Richard H. ;
Rioux, John D. ;
Brant, Steven R. ;
Silverberg, Mark S. ;
Taylor, Kent D. ;
Barmada, M. Michael ;
Bitton, Alain ;
Dassopoulos, Themistocles ;
Datta, Lisa Wu ;
Green, Todd ;
Griffiths, Anne M. ;
Kistner, Emily O. ;
Murtha, Michael T. ;
Regueiro, Miguel D. ;
Rotter, Jerome I. ;
Schumm, L. Philip ;
Steinhart, A. Hillary ;
Targan, Stephan R. ;
Xavier, Ramnik J. ;
Libioulle, Cecile ;
Sandor, Cynthia ;
Lathrop, Mark ;
Belaiche, Jacques ;
Dewit, Olivier ;
Gut, Ivo ;
Heath, Simon ;
Laukens, Debby ;
Mni, Myriam ;
Rutgeerts, Paul ;
Van Gossum, Andre ;
Zelenika, Diana ;
Franchimont, Denis ;
Hugot, Jean-Pierre ;
de Vos, Martine ;
Vermeire, Severine ;
Louis, Edouard ;
Cardon, Lon R. ;
Anderson, Carl A. ;
Drummond, Hazel ;
Nimmo, Elaine ;
Ahmad, Tariq ;
Prescott, Natalie J. ;
Onnie, Clive M. ;
Fisher, Sheila A. ;
Marchini, Jonathan ;
Ghori, Jilur .
NATURE GENETICS, 2008, 40 (08) :955-962
[8]   The expanding genetic overlap between multiple sclerosis and type I diabetes [J].
Booth, David R. ;
Heard, Robert N. ;
Stewart, Graeme J. ;
Goris, An ;
Dobosi, Rita ;
Dubois, Benedicte ;
Lorentzen, Aslaug R. ;
Celius, Elisabeth G. ;
Harbo, Hanne F. ;
Spurkland, Anne ;
Olsson, Tomas ;
Kockum, Ingrid ;
Link, Jenny ;
Hillert, Jan ;
Ban, Maria ;
Baker, Amie ;
Sawcer, Stephen ;
Compston, Alastair ;
Mihalova, Tania ;
Strange, Richard ;
Hawkins, Clive ;
Ingram, Gillian ;
Robertson, Neil P. ;
De Jager, Philip L. ;
Hafler, David A. ;
Barcellos, Lisa F. ;
Ivinson, Adrian J. ;
Pericak-Vance, Margaret ;
Oksenberg, Jorge R. ;
Hauser, Stephen L. ;
McCauley, Jacob L. ;
Sexton, David ;
Haines, Jonathan .
GENES AND IMMUNITY, 2009, 10 (01) :11-14
[9]   Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls [J].
Burton, Paul R. ;
Clayton, David G. ;
Cardon, Lon R. ;
Craddock, Nick ;
Deloukas, Panos ;
Duncanson, Audrey ;
Kwiatkowski, Dominic P. ;
McCarthy, Mark I. ;
Ouwehand, Willem H. ;
Samani, Nilesh J. ;
Todd, John A. ;
Donnelly, Peter ;
Barrett, Jeffrey C. ;
Davison, Dan ;
Easton, Doug ;
Evans, David ;
Leung, Hin-Tak ;
Marchini, Jonathan L. ;
Morris, Andrew P. ;
Spencer, Chris C. A. ;
Tobin, Martin D. ;
Attwood, Antony P. ;
Boorman, James P. ;
Cant, Barbara ;
Everson, Ursula ;
Hussey, Judith M. ;
Jolley, Jennifer D. ;
Knight, Alexandra S. ;
Koch, Kerstin ;
Meech, Elizabeth ;
Nutland, Sarah ;
Prowse, Christopher V. ;
Stevens, Helen E. ;
Taylor, Niall C. ;
Walters, Graham R. ;
Walker, Neil M. ;
Watkins, Nicholas A. ;
Winzer, Thilo ;
Jones, Richard W. ;
McArdle, Wendy L. ;
Ring, Susan M. ;
Strachan, David P. ;
Pembrey, Marcus ;
Breen, Gerome ;
St Clair, David ;
Caesar, Sian ;
Gordon-Smith, Katherine ;
Jones, Lisa ;
Fraser, Christine ;
Green, Elain K. .
NATURE, 2007, 447 (7145) :661-678
[10]   Identification of ZNF313/RNF114 as a novel psoriasis susceptibility gene [J].
Capon, Francesca ;
Bijlmakers, Marie-Jose ;
Wolf, Natalie ;
Quaranta, Maria ;
Huffmeier, Ulrike ;
Allen, Michael ;
Timms, Kirsten ;
Abkevich, Victor ;
Gutin, Alexander ;
Smith, Rhodri ;
Warren, Richard B. ;
Young, Helen S. ;
Worthington, Jane ;
Burden, A. David ;
Griffiths, Christopher E. M. ;
Hayday, Adrian ;
Nestle, Frank O. ;
Reis, Andre ;
Lanchbury, Jerry ;
Barker, Jonathan N. ;
Trembath, Richard C. .
HUMAN MOLECULAR GENETICS, 2008, 17 (13) :1938-1945