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Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette Syndrome and Obsessive-Compulsive Disorder

Authors :
Yu, Dongmei
Mathews, Carol A.
Scharf, Jeremiah M.
Neale, Benjamin M.
Davis, Lea K.
Gamazon, Eric R.
Derks, Eske M.
Evans, Patrick
Edlund, Christopher K.
Crane, Jacquelyn
Fagerness, Jesen A.
Osiecki, Lisa
Gallagher, Patience
Gerber, Gloria
Haddad, Stephen
Illmann, Cornelia
McGrath, Lauren M.
Mayerfeld, Catherine
Arepalli, Sampath
Barlassina, Cristina
Barr, Cathy L.
Bellodi, Laura
Benarroch, Fortu
Berrió, Gabriel Bedoya
Bienvenu, O. Joseph
Black, Donald
Bloch, Michael H.
Brentani, Helena
Bruun, Ruth D.
Budman, Cathy L.
Camarena, Beatriz
Campbell, Desmond D.
Cappi, Carolina
Cardona Silgado, Julio C.
Cavallini, Maria C.
Chavira, Denise A.
Chouinard, Sylvain
Cook, Edwin H.
Cookson, M. R.
Coric, Vladimir
Cullen, Bernadette
Cusi, Daniele
Delorme, Richard
Denys, Damiaan
Dion, Yves
Eapen, Valsama
Egberts, Karin
Falkai, Peter
Fernandez, Thomas
Fournier, Eduardo
Garrido, Helena
Geller, Daniel
Gilbert, Donald
Girard, Simon L.
Grabe, Hans J.
Grados, Marco A.
Greenberg, Benjamin D.
Gross-Tsur, Varda
Grünblatt, Edna
Hardy, John
Heiman, Gary A.
Hemmings, Sian M.J.
Herrera, Luis D.
Hezel, Dianne M.
Hoekstra, Pieter J.
Jankovic, Joseph
Kennedy, James L.
King, Robert A.
Konkashbaev, Anuar I.
Kremeyer, Barbara
Kurlan, Roger
Lanzagorta, Nuria
Leboyer, Marion
Leckman, James F.
Lennertz, Leonhard
Liu, Chunyu
Lochner, Christine
Lowe, Thomas L.
Lupoli, Sara
Macciardi, Fabio
Maier, Wolfgang
Manunta, Paolo
Marconi, Maurizio
McCracken, James T.
Mesa Restrepo, Sandra C.
Moessner, Rainald
Moorjani, Priya
Morgan, Jubel
Muller, Heike
Murphy, Dennis L.
Naarden, Allan L.
Ochoa, William Cornejo
Ophoff, Roel A.
Pakstis, Andrew J.
Pato, Michele T.
Pato, Carlos N.
Piacentini, John
Pittenger, Christopher
Pollak, Yehuda
Rauch, Scott L.
Renner, Tobias
Reus, Victor I.
Richter, Margaret A.
Riddle, Mark A.
Robertson, Mary M.
Romero, Roxana
Rosário, Maria C.
Rosenberg, David
Ruhrmann, Stephan
Sabatti, Chiara
Salvi, Erika
Sampaio, Aline S.
Samuels, Jack
Sandor, Paul
Service, Susan K.
Sheppard, Brooke
Singer, Harvey S.
Smit, Jan H.
Stein, Dan J.
Strengman, Eric
Tischfield, Jay A.
Turiel, Maurizio
Valencia Duarte, Ana V.
Vallada, Homero
Veenstra-VanderWeele, Jeremy
Walitza, Susanne
Walkup, John
Wang, Ying
Weale, Mike
Weiss, Robert
Wendland, Jens R.
Westenberg, Herman G.M.
Yao, Yin
Hounie, Ana G.
Miguel, Euripedes C.
Nicolini, Humberto
Wagner, Michael
Ruiz-Linares, Andres
Cath, Danielle C.
McMahon, William
Posthuma, Danielle
Oostra, Ben A.
Nestadt, Gerald
Rouleau, Guy A.
Purcell, Shaun
Jenike, Michael A.
Heutink, Peter
Hanna, Gregory L.
Conti, David V.
Arnold, Paul D.
Freimer, Nelson
Stewart, S. Evelyn
Knowles, James A.
Cox, Nancy J.
Pauls, David L.
Publication Year :
2014

Abstract

Obsessive-compulsive disorder (OCD) and Tourette's syndrome are highly heritable neurodevelopmental disorders that are thought to share genetic risk factors. However, the identification of definitive susceptibility genes for these etiologically complex disorders remains elusive. The authors report a combined genome-wide association study (GWAS) of Tourette's syndrome and OCD.The authors conducted a GWAS in 2,723 cases (1,310 with OCD, 834 with Tourette's syndrome, 579 with OCD plus Tourette's syndrome/chronic tics), 5,667 ancestry-matched controls, and 290 OCD parent-child trios. GWAS summary statistics were examined for enrichment of functional variants associated with gene expression levels in brain regions. Polygenic score analyses were conducted to investigate the genetic architecture within and across the two disorders.Although no individual single-nucleotide polymorphisms (SNPs) achieved genome-wide significance, the GWAS signals were enriched for SNPs strongly associated with variations in brain gene expression levels (expression quantitative loci, or eQTLs), suggesting the presence of true functional variants that contribute to risk of these disorders. Polygenic score analyses identified a significant polygenic component for OCD (p=2×10(-4)), predicting 3.2% of the phenotypic variance in an independent data set. In contrast, Tourette's syndrome had a smaller, nonsignificant polygenic component, predicting only 0.6% of the phenotypic variance (p=0.06). No significant polygenic signal was detected across the two disorders, although the sample is likely underpowered to detect a modest shared signal. Furthermore, the OCD polygenic signal was significantly attenuated when cases with both OCD and co-occurring Tourette's syndrome/chronic tics were included in the analysis (p=0.01).Previous work has shown that Tourette's syndrome and OCD have some degree of shared genetic variation. However, the data from this study suggest that there are also distinct components to the genetic architectures of these two disorders. Furthermore, OCD with co-occurring Tourette's syndrome/chronic tics may have different underlying genetic susceptibility compared with OCD alone.

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.pmid..........18f199af2a20fca3b879e3e3d48957d8