Original Article

Molecular Psychiatry (2015) 20, 786–792; doi:10.1038/mp.2014.130; published online 28 October 2014

Genetic background of extreme violent behavior

J Tiihonen1,2,3,19, M-R Rautiainen3,19, H M Ollila3,4, E Repo-Tiihonen2, M Virkkunen5,6, A Palotie7,8,9,10,11, O Pietiläinen3, K Kristiansson3, M Joukamaa12, H Lauerma3,13,14, J Saarela15, S Tyni16, H Vartiainen16, J Paananen17, D Goldman18 and T Paunio3,5,6

  1. 1Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden
  2. 2Department of Forensic Psychiatry, University of Eastern Finland, Niuvanniemi Hospital, Kuopio, Finland
  3. 3National Institute for Health and Welfare, Helsinki, Finland
  4. 4Stanford University Center for Sleep Sciences, Palo Alto, CA, USA
  5. 5Department of Psychiatry, University of Helsinki, Institute of Clinical Medicine, Helsinki, Finland
  6. 6Department of Psychiatry, Helsinki University Central Hospital, Helsinki, Finland
  7. 7Wellcome Trust Sanger Institute, Hinxton, Cambridgeshire, England
  8. 8Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA
  9. 9Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA
  10. 10Institute for Molecular Medicine Finland, University of Helsinki, Helsinki, Finland
  11. 11Psychiatric & Neurodevelopmental Genetics Unit, Department of Psychiatry, Massachusetts General Hospital, Boston, MA, USA
  12. 12Social Psychiatry Unit, School of Health Sciences, University of Tampere, Finland
  13. 13Psychiatric Hospital for Prisoners, Turku, Finland
  14. 14University of Turku, Turku, Finland
  15. 15Finnish Genome Center, Helsinki, Finland
  16. 16The Criminal Sanctions Agency, Helsinki, Finland
  17. 17University of Eastern Finland, Bioinformatics Center, Kuopio, Finland
  18. 18Laboratory of Neurogenetics, National Institute on Alcohol Abuse and Alcoholism, Rockville, MD, USA

Correspondence: Professor J Tiihonen, Karolinska Institutet, Department of Clinical Neuroscience, Byggnad R5, Stockholm, S-171 76, Sweden; Professor T Paunio, National Institute for Health and Welfare, PO Box 30, FI-00271, Finland. E-mail: jari.tiihonen@ki.se or tiina.paunio@thl.fi

19These authors contributed equaliy to this work.

Received 26 June 2014; Revised 25 August 2014; Accepted 28 August 2014
Advance online publication 28 October 2014

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Abstract

In developed countries, the majority of all violent crime is committed by a small group of antisocial recidivistic offenders, but no genes have been shown to contribute to recidivistic violent offending or severe violent behavior, such as homicide. Our results, from two independent cohorts of Finnish prisoners, revealed that a monoamine oxidase A (MAOA) low-activity genotype (contributing to low dopamine turnover rate) as well as the CDH13 gene (coding for neuronal membrane adhesion protein) are associated with extremely violent behavior (at least 10 committed homicides, attempted homicides or batteries). No substantial signal was observed for either MAOA or CDH13 among non-violent offenders, indicating that findings were specific for violent offending, and not largely attributable to substance abuse or antisocial personality disorder. These results indicate both low monoamine metabolism and neuronal membrane dysfunction as plausible factors in the etiology of extreme criminal violent behavior, and imply that at least about 5–10% of all severe violent crime in Finland is attributable to the aforementioned MAOA and CDH13 genotypes.