An international consortium of scientists dissects the shared genetic architecture of suicide attempts, psychiatric disorders, and non-psychiatric risk factors.
In the largest genetic study of suicide attempts to date, researchers have identified a region of the genome on chromosome 7 containing DNADNA, or deoxyribonucleic acid, is a molecule composed of two long strands of nucleotides that coil around each other to form a double helix. It is the hereditary material in humans and almost all other organisms that carries genetic instructions for development, functioning, growth, and reproduction. Nearly every cell in a person’s body has the same DNA. Most DNA is located in the cell nucleus (where it is called nuclear DNA), but a small amount of DNA can also be found in the mitochondria (where it is called mitochondrial DNA or mtDNA).”>DNA variations that increase the risk that a person will attempt suicide.
The study also found overlap in the genetic basis of suicide attempts and that of related psychiatric disorders, particularly major depression, and also with that of non-psychiatric risk factors such as smoking, risk-taking behavior, sleep disturbances, and poorer general health. The study results, published on November 30, 2021, in Biological Psychiatry, suggest that the genetic underpinnings of suicide attempts are partially shared and partially distinct from those of related psychiatric disorders.
Suicide is a worldwide public health problem, accounting for almost 800,000 deaths per year. Non-fatal suicide attempts are estimated to occur more than 20 times for every death by suicide and are a major source of disability, reduced quality of life, and social and economic burden. Suicidal thoughts and behaviors can be reduced with proper mental health support and treatment. Therefore, it is critical to gain insight into the underlying biological pathways involved in suicide attempts or suicidal thoughts, which could provide potential avenues to treatment and prevention strategies.
To help elucidate the underlying biology of suicide attempts, an international consortium of scientists from the International Suicide Genetics Consortium conducted a genome-wide association study. This method involves scanning the DNA of many people, looking for genetic markers that were more common in those who had made a suicide attempt. The team scanned more than 7.5 million common variations in the DNA sequence of nearly 550,000 people, almost 30,000 of whom had made a suicide attempt.
“In addition to identifying the risk location for suicide attempt on chromosome 7, we uncovered a strong overlap in the genetic basis of suicide attempt and that of psychiatric disorders, particularly major depression, as well as some overlap with the genetics of smoking, pain, risk-taking, sleep disturbances, and poorer general health,” said Niamh Mullins, PhD, Assistant Professor of Psychiatric Genomics at the Icahn School of Medicine at Mount Sinai, co-founder and co-chair of the consortium, and lead author of the paper. “This genetic overlap with non-psychiatric risk factors was largely unchanged by adjusting for psychiatric disorders, which suggests that a substantial component of the biological basis of suicide attempt is not simply a byproduct of comorbid psychiatric disease, but instead may be the result of shared biology with non-psychiatric risk factors.”
The association between genetic variations on chromosome 7 and risk of attempting suicide was also not mediated by comorbid psychiatric disorders, and was replicated through an independent analysis of more than 14,000 veterans who had made a suicide attempt from the Million Veterans Program, a national research program to learn how genes, lifestyle, and military exposures affect health and illness.
“This study is an exciting advancement of our understanding of how the genetics of suicide attempt relate to that of psychiatric and non-psychiatric risk factors,” said JooEun Kang, an MD-PhD student at Vanderbilt University Medical Center and co-lead author of this paper.
DNA variations in this region have previously been linked with insomnia, smoking, and risk-taking behavior, and although future work is needed to uncover the underlying biological mechanism, findings like these bring researchers a step closer to understanding the neurobiology of suicidality.
“The study findings also point to the importance of studying the potential direct causal paths between these risk factors and suicide attempt in patients with and without psychiatric illness,” added Douglas Ruderfer, PhD Associate Professor of Genetic Medicine, Psychiatry, and Biomedical Informatics at Vanderbilt University Medical Center, co-founder and co-chair of the consortium, and senior author of the paper.
The International Suicide Genetics Consortium includes more than 260 scientists in more than 20 countries who are dedicated to studying the genetic basis of suicidality. Their work provides the foundation for future larger studies to identify genetic risk factors for suicide attempts in other areas of the genome, as well as additional studies focused on suicidal thoughts. The ultimate goal of this research is to gain insight into the underlying biological pathways involved in suicidality, providing potential avenues to treatments and prevention strategies.
If you are in crisis, please call the National Suicide Prevention 24-hour Lifeline at 1-800-273-TALK (8255), or contact the Crisis Text Line by texting TALK to 741741, or visit their website at: http://suicidepreventionlifeline.org.
Reference: “Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors” by Niamh Mullins, JooEun Kang, Adrian I. Campos, Jonathan R.I. Coleman, Alexis C. Edwards, Hanga Galfalvy, Daniel F. Levey, Adriana Lori, Andrey Shabalin, Anna Starnawska, Mei-Hsin Su, Hunna J. Watson, Mark Adams, Swapnil Awasthi, Michael Gandal, Jonathan D. Hafferty, Akitoyo Hishimoto, Minsoo Kim, Satoshi Okazaki, Ikuo Otsuka, Stephan Ripke, Erin B. Ware, Andrew W. Bergen, Wade H. Berrettini, Martin Bohus, Harry Brandt, Xiao Chang, Wei J. Chen, Hsi-Chung Chen, Steven Crawford, Scott Crow, Emily DiBlasi, Philibert Duriez, Fernando Fernández-Aranda, Manfred M. Fichter, Steven Gallinger, Stephen J. Glatt, Philip Gorwood, Yiran Guo, Hakon Hakonarson, Katherine A. Halmi, Hai-Gwo Hwu, Sonia Jain, Stéphane Jamain, Susana Jiménez-Murcia, Craig Johnson, Allan S. Kaplan, Walter H. Kaye, Pamela K. Keel, James L. Kennedy, Kelly L. Klump, Dong Li, Shih-Cheng Liao, Klaus Lieb, Lisa Lilenfeld, Chih-Min Liu, Pierre J. Magistretti, Christian R. Marshall, James E. Mitchell, Eric T. Monson, Richard M. Myers, Dalila Pinto, Abigail Powers, Nicolas Ramoz, Stefan Roepke, Vsevolod Rozanov, Stephen W. Scherer, Christian Schmahl, Marcus Sokolowski, Michael Strober, Laura M. Thornton, Janet Treasure, Ming T. Tsuang, Stephanie H. Witt, D. Blake Woodside, Zeynep Yilmaz, Lea Zillich, Rolf Adolfsson, Ingrid Agartz, Tracy M. Air, Martin Alda, Lars Alfredsson, Ole A. Andreassen, Adebayo Anjorin, Vivek Appadurai, María Soler Artigas, Sandra Van der Auwera, M. Helena Azevedo, Nicholas Bass, Claiton H.D. Bau, Bernhard T. Baune, Frank Bellivier, Klaus Berger, Joanna M. Biernacka, Tim B. Bigdeli, Elisabeth B. Binder, Michael Boehnke, Marco P. Boks, Rosa Bosch, David L. Braff, Richard Bryant, Monika Budde, Enda M. Byrne, Wiepke Cahn, Miguel Casas, Enrique Castelao, Jorge A. Cervilla, Boris Chaumette, Sven Cichon, Aiden Corvin, Nicholas Craddock, David Craig, Franziska Degenhardt, Srdjan Djurovic, Howard J. Edenberg, Ayman H. Fanous, Jerome C. Foo, Andreas J. Forstner … Henry R. Kranzler, Qingqin S. Li, Nicholas G. Martin, Andrew M. McIntosh, Ole Mors, Merete Nordentoft, Catherine M. Olsen, David Porteous, Robert J. Ursano, Danuta Wasserman, Thomas Werge, David C. Whiteman, Cynthia M. Bulik, Hilary Coon, Ditte Demontis, Anna R. Docherty, Po-Hsiu Kuo, Cathryn M. Lewis, J. John Mann, Miguel E. Rentería, Daniel J. Smith, Eli A. Stahl, Murray B. Stein, Fabian Streit, Virginia Willour and Douglas M. Ruderfer, 9 September 2021, Biological Psychiatry.