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IRIS
Objective: Suicidal behavior is heritable and is a major cause of death worldwide. Two large-scale genome-wide association studies (GWASs) recently discovered and cross-validated genome-wide significant (GWS) loci for suicide attempt (SA). The present study leveraged the genetic cohorts from both studies to conduct the largest GWAS meta-analysis of SA to date. Multi-ancestry and admixture-specific meta-analyses were conducted within groups of significant African, East Asian, and European ancestry admixtures. Methods: This study comprised 22 cohorts, including 43,871 SA cases and 915,025 ancestry-matched controls. Analytical methods across multi-ancestry and individual ancestry admixtures included inverse variance-weighted fixed-effects meta-analyses, followed by gene, gene-set, tissue-set, and drug-target enrichment, as well as summary-data-based Mendelian randomization with brain expression quantitative trait loci data, phenome-wide genetic correlation, and genetic causal proportion analyses. Results: Multi-ancestry and European ancestry admixture GWAS meta-analyses identified 12 risk loci at p values <5×10-8. These loci were mostly intergenic and implicated DRD2, SLC6A9, FURIN, NLGN1, SOX5, PDE4B, and CACNG2. The multi-ancestry SNP-based heritability estimate of SA was 5.7% on the liability scale (SE=0.003, p=5.7×10-80). Significant brain tissue gene expression and drug set enrichment were observed. There was shared genetic variation of SA with attention deficit hyperactivity disorder, smoking, and risk tolerance after conditioning SA on both major depressive disorder and posttraumatic stress disorder. Genetic causal proportion analyses implicated shared genetic risk for specific health factors. Conclusions: This multi-ancestry analysis of suicide attempt identified several loci contributing to risk and establishes significant shared genetic covariation with clinical phenotypes. These findings provide insight into genetic factors associated with suicide attempt across ancestry admixture populations, in veteran and civilian populations, and in attempt versus death.
GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors
Docherty, Anna R;Mullins, Niamh;Ashley-Koch, Allison E;Qin, Xuejun;Coleman, Jonathan R I;Shabalin, Andrey;Kang, JooEun;Murnyak, Balasz;Wendt, Frank;Adams, Mark;Campos, Adrian I;DiBlasi, Emily;Fullerton, Janice M;Kranzler, Henry R;Bakian, Amanda V;Monson, Eric T;Rentería, Miguel E;Walss-Bass, Consuelo;Andreassen, Ole A;Behera, Chittaranjan;Bulik, Cynthia M;Edenberg, Howard J;Kessler, Ronald C;Mann, J John;Nurnberger, John I;Pistis, Giorgio;Streit, Fabian;Ursano, Robert J;Polimanti, Renato;Dennis, Michelle;Garrett, Melanie;Hair, Lauren;Harvey, Philip;Hauser, Elizabeth R;Hauser, Michael A;Huffman, Jennifer;Jacobson, Daniel;Madduri, Ravi;McMahon, Benjamin;Oslin, David W;Trafton, Jodie;Awasthi, Swapnil;Berrettini, Wade H;Bohus, Martin;Chang, Xiao;Chen, Hsi-Chung;Chen, Wei J;Christensen, Erik D;Crow, Scott;Duriez, Philibert;Edwards, Alexis C;Fernández-Aranda, Fernando;Galfalvy, Hanga;Gandal, Michael;Gorwood, Philip;Guo, Yiran;Hafferty, Jonathan D;Hakonarson, Hakon;Halmi, Katherine A;Hishimoto, Akitoyo;Jain, Sonia;Jamain, Stéphane;Jiménez-Murcia, Susana;Johnson, Craig;Kaplan, Allan S;Kaye, Walter H;Keel, Pamela K;Kennedy, James L;Kim, Minsoo;Klump, Kelly L;Levey, Daniel F;Li, Dong;Liao, Shih-Cheng;Lieb, Klaus;Lilenfeld, Lisa;Marshall, Christian R;Mitchell, James E;Okazaki, Satoshi;Otsuka, Ikuo;Pinto, Dalila;Powers, Abigail;Ramoz, Nicolas;Ripke, Stephan;Roepke, Stefan;Rozanov, Vsevolod;Scherer, Stephen W;Schmahl, Christian;Sokolowski, Marcus;Starnawska, Anna;Strober, Michael;Su, Mei-Hsin;Thornton, Laura M;Treasure, Janet;Ware, Erin B;Watson, Hunna J;Witt, Stephanie H;Woodside, D Blake;Yilmaz, Zeynep;Zillich, Lea;Adolfsson, Rolf;Agartz, Ingrid;Alda, Martin;Alfredsson, Lars;Appadurai, Vivek;Artigas, María Soler;Van der Auwera, Sandra;Azevedo, M Helena;Bass, Nicholas;Bau, Claiton H D;Baune, Bernhard T;Bellivier, Frank;Berger, Klaus;Biernacka, Joanna M;Bigdeli, Tim B;Binder, Elisabeth B;Boehnke, Michael;Boks, Marco P;Braff, David L;Bryant, Richard;Budde, Monika;Byrne, Enda M;Cahn, Wiepke;Castelao, Enrique;Cervilla, Jorge A;Chaumette, Boris;Corvin, Aiden;Craddock, Nicholas;Djurovic, Srdjan;Foo, Jerome C;Forstner, Andreas J;Frye, Mark;Gatt, Justine M;Giegling, Ina;Grabe, Hans J;Green, Melissa J;Grevet, Eugenio H;Grigoroiu-Serbanescu, Maria;Gutierrez, Blanca;Guzman-Parra, Jose;Hamshere, Marian L;Hartmann, Annette M;Hauser, Joanna;Heilmann-Heimbach, Stefanie;Hoffmann, Per;Ising, Marcus;Jones, Ian;Jones, Lisa A;Jonsson, Lina;Kahn, René S;Kelsoe, John R;Kendler, Kenneth S;Kloiber, Stefan;Koenen, Karestan C;Kogevinas, Manolis;Krebs, Marie-Odile;Landén, Mikael;Leboyer, Marion;Lee, Phil H;Levinson, Douglas F;Liao, Calwing;Lissowska, Jolanta;Mayoral, Fermin;McElroy, Susan L;McGrath, Patrick;McGuffin, Peter;McQuillin, Andrew;Mehta, Divya;Melle, Ingrid;Mitchell, Philip B;Molina, Esther;Morken, Gunnar;Nievergelt, Caroline;Nöthen, Markus M;O'Donovan, Michael C;Ophoff, Roel A;Owen, Michael J;Pato, Carlos;Pato, Michele T;Penninx, Brenda W J H;Potash, James B;Power, Robert A;Preisig, Martin;Quested, Digby;Ramos-Quiroga, Josep Antoni;Reif, Andreas;Ribasés, Marta;Richarte, Vanesa;Rietschel, Marcella;Rivera, Margarita;Roberts, Andrea;Roberts, Gloria;Rouleau, Guy A;Rovaris, Diego L;Sanders, Alan R;Schofield, Peter R;Schulze, Thomas G;Scott, Laura J;Serretti, Alessandro;Shi, Jianxin;Sirignano, Lea;Sklar, Pamela;Smeland, Olav B;Smoller, Jordan W;Sonuga-Barke, Edmund J S;Trzaskowski, Maciej;Tsuang, Ming T;Turecki, Gustavo;Vilar-Ribó, Laura;Vincent, John B;Völzke, Henry;Walters, James T R;Weickert, Cynthia Shannon;Weickert, Thomas W;Weissman, Myrna M;Williams, Leanne M;Wray, Naomi R;Zai, Clement C;Agerbo, Esben;Børglum, Anders D;Breen, Gerome;Demontis, Ditte;Erlangsen, Annette;Gelernter, Joel;Glatt, Stephen J;Hougaard, David M;Hwu, Hai-Gwo;Kuo, Po-Hsiu;Lewis, Cathryn M;Li, Qingqin S;Liu, Chih-Min;Martin, Nicholas G;McIntosh, Andrew M;Medland, Sarah E;Mors, Ole;Nordentoft, Merete;Olsen, Catherine M;Porteous, David;Smith, Daniel J;Stahl, Eli A;Stein, Murray B;Wasserman, Danuta;Werge, Thomas;Whiteman, David C;Willour, Virginia;Coon, Hilary;Beckham, Jean C;Kimbrel, Nathan A;Ruderfer, Douglas M
2023-01-01
Abstract
Objective: Suicidal behavior is heritable and is a major cause of death worldwide. Two large-scale genome-wide association studies (GWASs) recently discovered and cross-validated genome-wide significant (GWS) loci for suicide attempt (SA). The present study leveraged the genetic cohorts from both studies to conduct the largest GWAS meta-analysis of SA to date. Multi-ancestry and admixture-specific meta-analyses were conducted within groups of significant African, East Asian, and European ancestry admixtures. Methods: This study comprised 22 cohorts, including 43,871 SA cases and 915,025 ancestry-matched controls. Analytical methods across multi-ancestry and individual ancestry admixtures included inverse variance-weighted fixed-effects meta-analyses, followed by gene, gene-set, tissue-set, and drug-target enrichment, as well as summary-data-based Mendelian randomization with brain expression quantitative trait loci data, phenome-wide genetic correlation, and genetic causal proportion analyses. Results: Multi-ancestry and European ancestry admixture GWAS meta-analyses identified 12 risk loci at p values <5×10-8. These loci were mostly intergenic and implicated DRD2, SLC6A9, FURIN, NLGN1, SOX5, PDE4B, and CACNG2. The multi-ancestry SNP-based heritability estimate of SA was 5.7% on the liability scale (SE=0.003, p=5.7×10-80). Significant brain tissue gene expression and drug set enrichment were observed. There was shared genetic variation of SA with attention deficit hyperactivity disorder, smoking, and risk tolerance after conditioning SA on both major depressive disorder and posttraumatic stress disorder. Genetic causal proportion analyses implicated shared genetic risk for specific health factors. Conclusions: This multi-ancestry analysis of suicide attempt identified several loci contributing to risk and establishes significant shared genetic covariation with clinical phenotypes. These findings provide insight into genetic factors associated with suicide attempt across ancestry admixture populations, in veteran and civilian populations, and in attempt versus death.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11387/165129
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simulazione ASN
Il report seguente simula gli indicatori relativi alla propria produzione scientifica in relazione alle soglie ASN 2023-2025 del proprio SC/SSD. Si ricorda che il superamento dei valori soglia (almeno 2 su 3) è requisito necessario ma non sufficiente al conseguimento dell'abilitazione. La simulazione si basa sui dati IRIS e sugli indicatori bibliometrici alla data indicata e non tiene conto di eventuali periodi di congedo obbligatorio, che in sede di domanda ASN danno diritto a incrementi percentuali dei valori. La simulazione può differire dall'esito di un’eventuale domanda ASN sia per errori di catalogazione e/o dati mancanti in IRIS, sia per la variabilità dei dati bibliometrici nel tempo. Si consideri che Anvur calcola i valori degli indicatori all'ultima data utile per la presentazione delle domande.
La presente simulazione è stata realizzata sulla base delle specifiche raccolte sul tavolo ER del Focus Group IRIS coordinato dall’Università di Modena e Reggio Emilia e delle regole riportate nel DM 589/2018 e allegata Tabella A. Cineca, l’Università di Modena e Reggio Emilia e il Focus Group IRIS non si assumono alcuna responsabilità in merito all’uso che il diretto interessato o terzi faranno della simulazione. Si specifica inoltre che la simulazione contiene calcoli effettuati con dati e algoritmi di pubblico dominio e deve quindi essere considerata come un mero ausilio al calcolo svolgibile manualmente o con strumenti equivalenti.