Understanding Genetic Risk for Aggression: Clues From the Brain’s Response to Social Exclusion

Background Although research indicates a relationship between the monoamine oxidase-A (MAOA) gene and aggression, the intervening neural and psychological mechanisms are unknown. Individuals with the low expression allele (MAOA-L) of a functional polymorphism in the MAOA gene might be prone to aggre...

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Veröffentlicht in:Biological psychiatry (1969) 2007-05, Vol.61 (9), p.1100-1108
Hauptverfasser: Eisenberger, Naomi I, Way, Baldwin M, Taylor, Shelley E, Welch, William T, Lieberman, Matthew D
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container_end_page 1108
container_issue 9
container_start_page 1100
container_title Biological psychiatry (1969)
container_volume 61
creator Eisenberger, Naomi I
Way, Baldwin M
Taylor, Shelley E
Welch, William T
Lieberman, Matthew D
description Background Although research indicates a relationship between the monoamine oxidase-A (MAOA) gene and aggression, the intervening neural and psychological mechanisms are unknown. Individuals with the low expression allele (MAOA-L) of a functional polymorphism in the MAOA gene might be prone to aggression because they are socially or emotionally hyposensitive and thus care less about harming others or because they are socially or emotionally hypersensitive and thus respond to negative social experiences with defensively aggressive behavior. Methods We investigated the relationships between the MAOA polymorphism, trait aggression, trait interpersonal hypersensitivity, and neural responses to social exclusion in 32 healthy men and women. Results The MAOA-L individuals (men and women) reported higher trait aggression than individuals with the high expression allele (MAOA-H). The MAOA-L individuals reported higher trait interpersonal hypersensitivity and showed greater dorsal anterior cingulate cortex (dACC) activity (associated with rejection-related distress) to social exclusion compared with MAOA-H individuals, consistent with a social hypersensitivity hypothesis. Moreover, the MAOA–aggression relationship was mediated by greater dACC reactivity to social exclusion, suggesting that MAOA might relate to aggression through socioemotional hypersensitivity. Conclusions These data suggest that the relationship between MAOA and aggression might be due to a heightened rather than a reduced sensitivity to negative socioemotional experiences like social rejection.
doi_str_mv 10.1016/j.biopsych.2006.08.007
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Individuals with the low expression allele (MAOA-L) of a functional polymorphism in the MAOA gene might be prone to aggression because they are socially or emotionally hyposensitive and thus care less about harming others or because they are socially or emotionally hypersensitive and thus respond to negative social experiences with defensively aggressive behavior. Methods We investigated the relationships between the MAOA polymorphism, trait aggression, trait interpersonal hypersensitivity, and neural responses to social exclusion in 32 healthy men and women. Results The MAOA-L individuals (men and women) reported higher trait aggression than individuals with the high expression allele (MAOA-H). The MAOA-L individuals reported higher trait interpersonal hypersensitivity and showed greater dorsal anterior cingulate cortex (dACC) activity (associated with rejection-related distress) to social exclusion compared with MAOA-H individuals, consistent with a social hypersensitivity hypothesis. Moreover, the MAOA–aggression relationship was mediated by greater dACC reactivity to social exclusion, suggesting that MAOA might relate to aggression through socioemotional hypersensitivity. Conclusions These data suggest that the relationship between MAOA and aggression might be due to a heightened rather than a reduced sensitivity to negative socioemotional experiences like social rejection.</description><identifier>ISSN: 0006-3223</identifier><identifier>EISSN: 1873-2402</identifier><identifier>DOI: 10.1016/j.biopsych.2006.08.007</identifier><identifier>PMID: 17137563</identifier><identifier>CODEN: BIPCBF</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adult ; Aggression ; Aggression - physiology ; Alleles ; Biological and medical sciences ; Brain Chemistry - genetics ; Cerebral Cortex - physiology ; Clinical Trials Data Monitoring Committees ; dorsal anterior cingulate cortex ; Emotions - physiology ; Female ; fMRI ; Genotype ; Humans ; Interpersonal Relations ; interpersonal sensitivity ; Magnetic Resonance Imaging ; Male ; MAOA gene ; MAOA-uVNTR ; Medical sciences ; neuroimaging ; Polymorphism, Genetic - genetics ; Psychiatry ; Psychological Tests ; Psychology. 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Individuals with the low expression allele (MAOA-L) of a functional polymorphism in the MAOA gene might be prone to aggression because they are socially or emotionally hyposensitive and thus care less about harming others or because they are socially or emotionally hypersensitive and thus respond to negative social experiences with defensively aggressive behavior. Methods We investigated the relationships between the MAOA polymorphism, trait aggression, trait interpersonal hypersensitivity, and neural responses to social exclusion in 32 healthy men and women. Results The MAOA-L individuals (men and women) reported higher trait aggression than individuals with the high expression allele (MAOA-H). The MAOA-L individuals reported higher trait interpersonal hypersensitivity and showed greater dorsal anterior cingulate cortex (dACC) activity (associated with rejection-related distress) to social exclusion compared with MAOA-H individuals, consistent with a social hypersensitivity hypothesis. Moreover, the MAOA–aggression relationship was mediated by greater dACC reactivity to social exclusion, suggesting that MAOA might relate to aggression through socioemotional hypersensitivity. Conclusions These data suggest that the relationship between MAOA and aggression might be due to a heightened rather than a reduced sensitivity to negative socioemotional experiences like social rejection.</description><subject>Adult</subject><subject>Aggression</subject><subject>Aggression - physiology</subject><subject>Alleles</subject><subject>Biological and medical sciences</subject><subject>Brain Chemistry - genetics</subject><subject>Cerebral Cortex - physiology</subject><subject>Clinical Trials Data Monitoring Committees</subject><subject>dorsal anterior cingulate cortex</subject><subject>Emotions - physiology</subject><subject>Female</subject><subject>fMRI</subject><subject>Genotype</subject><subject>Humans</subject><subject>Interpersonal Relations</subject><subject>interpersonal sensitivity</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>MAOA gene</subject><subject>MAOA-uVNTR</subject><subject>Medical sciences</subject><subject>neuroimaging</subject><subject>Polymorphism, Genetic - genetics</subject><subject>Psychiatry</subject><subject>Psychological Tests</subject><subject>Psychology. 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Psychiatry</topic><topic>Risk</topic><topic>Social Environment</topic><topic>social exclusion</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Eisenberger, Naomi I</creatorcontrib><creatorcontrib>Way, Baldwin M</creatorcontrib><creatorcontrib>Taylor, Shelley E</creatorcontrib><creatorcontrib>Welch, William T</creatorcontrib><creatorcontrib>Lieberman, Matthew D</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biological psychiatry (1969)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Eisenberger, Naomi I</au><au>Way, Baldwin M</au><au>Taylor, Shelley E</au><au>Welch, William T</au><au>Lieberman, Matthew D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Understanding Genetic Risk for Aggression: Clues From the Brain’s Response to Social Exclusion</atitle><jtitle>Biological psychiatry (1969)</jtitle><addtitle>Biol Psychiatry</addtitle><date>2007-05-01</date><risdate>2007</risdate><volume>61</volume><issue>9</issue><spage>1100</spage><epage>1108</epage><pages>1100-1108</pages><issn>0006-3223</issn><eissn>1873-2402</eissn><coden>BIPCBF</coden><abstract>Background Although research indicates a relationship between the monoamine oxidase-A (MAOA) gene and aggression, the intervening neural and psychological mechanisms are unknown. Individuals with the low expression allele (MAOA-L) of a functional polymorphism in the MAOA gene might be prone to aggression because they are socially or emotionally hyposensitive and thus care less about harming others or because they are socially or emotionally hypersensitive and thus respond to negative social experiences with defensively aggressive behavior. Methods We investigated the relationships between the MAOA polymorphism, trait aggression, trait interpersonal hypersensitivity, and neural responses to social exclusion in 32 healthy men and women. Results The MAOA-L individuals (men and women) reported higher trait aggression than individuals with the high expression allele (MAOA-H). The MAOA-L individuals reported higher trait interpersonal hypersensitivity and showed greater dorsal anterior cingulate cortex (dACC) activity (associated with rejection-related distress) to social exclusion compared with MAOA-H individuals, consistent with a social hypersensitivity hypothesis. Moreover, the MAOA–aggression relationship was mediated by greater dACC reactivity to social exclusion, suggesting that MAOA might relate to aggression through socioemotional hypersensitivity. Conclusions These data suggest that the relationship between MAOA and aggression might be due to a heightened rather than a reduced sensitivity to negative socioemotional experiences like social rejection.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>17137563</pmid><doi>10.1016/j.biopsych.2006.08.007</doi><tpages>9</tpages></addata></record>
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subjects Adult
Aggression
Aggression - physiology
Alleles
Biological and medical sciences
Brain Chemistry - genetics
Cerebral Cortex - physiology
Clinical Trials Data Monitoring Committees
dorsal anterior cingulate cortex
Emotions - physiology
Female
fMRI
Genotype
Humans
Interpersonal Relations
interpersonal sensitivity
Magnetic Resonance Imaging
Male
MAOA gene
MAOA-uVNTR
Medical sciences
neuroimaging
Polymorphism, Genetic - genetics
Psychiatry
Psychological Tests
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Risk
Social Environment
social exclusion
title Understanding Genetic Risk for Aggression: Clues From the Brain’s Response to Social Exclusion
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