TY - CHAP
T1 - Genetics and epigenetics of human aggression
AU - Odintsova, Veronika V
AU - Hagenbeek, Fiona A
AU - van der Laan, Camiel M
AU - van de Weijer, Steve
AU - Boomsma, Dorret I
N1 - Copyright © 2023 Elsevier B.V. All rights reserved.
PY - 2023
Y1 - 2023
N2 - There is substantial variation between humans in aggressive behavior, with its biological etiology and molecular genetic basis mostly unknown. This review chapter offers an overview of genomic and omics studies revealing the genetic contribution to aggression and first insights into associations with epigenetic and other omics (e.g., metabolomics) profiles. We allowed for a broad phenotype definition including studies on "aggression," "aggressive behavior," or "aggression-related traits," "antisocial behavior," "conduct disorder," and "oppositional defiant disorder." Heritability estimates based on family and twin studies in children and adults of this broadly defined phenotype of aggression are around 50%, with relatively small fluctuations around this estimate. Next, we review the genome-wide association studies (GWAS) which search for associations with alleles and also allow for gene-based tests and epigenome-wide association studies (EWAS) which seek to identify associations with differently methylated regions across the genome. Both GWAS and EWAS allow for construction of Polygenic and DNA methylation scores at an individual level. Currently, these predict a small percentage of variance in aggression. We expect that increases in sample size will lead to additional discoveries in GWAS and EWAS, and that multiomics approaches will lead to a more comprehensive understanding of the molecular underpinnings of aggression.
AB - There is substantial variation between humans in aggressive behavior, with its biological etiology and molecular genetic basis mostly unknown. This review chapter offers an overview of genomic and omics studies revealing the genetic contribution to aggression and first insights into associations with epigenetic and other omics (e.g., metabolomics) profiles. We allowed for a broad phenotype definition including studies on "aggression," "aggressive behavior," or "aggression-related traits," "antisocial behavior," "conduct disorder," and "oppositional defiant disorder." Heritability estimates based on family and twin studies in children and adults of this broadly defined phenotype of aggression are around 50%, with relatively small fluctuations around this estimate. Next, we review the genome-wide association studies (GWAS) which search for associations with alleles and also allow for gene-based tests and epigenome-wide association studies (EWAS) which seek to identify associations with differently methylated regions across the genome. Both GWAS and EWAS allow for construction of Polygenic and DNA methylation scores at an individual level. Currently, these predict a small percentage of variance in aggression. We expect that increases in sample size will lead to additional discoveries in GWAS and EWAS, and that multiomics approaches will lead to a more comprehensive understanding of the molecular underpinnings of aggression.
KW - Adult
KW - Child
KW - Humans
KW - Genome-Wide Association Study
KW - Epigenesis, Genetic/genetics
KW - Aggression
KW - DNA Methylation/genetics
KW - Genomics
UR - https://www.scopus.com/pages/publications/85168727844
UR - https://www.scopus.com/pages/publications/85168727844#tab=citedBy
U2 - 10.1016/B978-0-12-821375-9.00005-0
DO - 10.1016/B978-0-12-821375-9.00005-0
M3 - Chapter
C2 - 37633706
SN - 9780128213759
T3 - Handbook of Clinical Neurology
SP - 13
EP - 44
BT - Brain and Crime
A2 - Swaab, Hanna
A2 - Meynen, Gerben
PB - Elsevier / ScienceDirect
ER -