Mineralocorticoid Receptor Iso/Val (rs5522) Genotype Moderates the Association Between Previous Childhood Emotional Neglect and Amygdala Reactivity
Objective:The amygdala is especially reactive to threatening stimuli, and the degree of reactivity predicts individual differences in the expression of depression and anxiety. Emerging research suggests that emotional neglect during childhood as well as hypercortisolemia may lead to heightened threa...
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Veröffentlicht in: | The American journal of psychiatry 2012-05, Vol.169 (5), p.515-522 |
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description | Objective:The amygdala is especially reactive to threatening stimuli, and the degree of reactivity predicts individual differences in the expression of depression and anxiety. Emerging research suggests that emotional neglect during childhood as well as hypercortisolemia may lead to heightened threat-related amygdala reactivity. This raises the possibility that genetic variation affecting hypothalamic-pituitary-adrenal (HPA) axis function contributes to individual differences in amygdala reactivity, both independently and as a function of childhood emotional neglect.
Method:This study assessed whether the mineralocorticoid receptor iso/val polymorphism (rs5522), a functional genetic variant affecting HPA axis function, influenced threat-related amygdala reactivity in 279 individuals in late childhood and early adolescence. The study also explored the extent to which any effects of the genotype on amygdala reactivity were contingent upon previous childhood emotional neglect.
Results:Prior childhood emotional neglect and the val allele were associated with greater amygdala reactivity. Moreover, a significant genotype-by-emotional neglect interaction was observed whereby greater amygdala reactivity in val allele carriers was independent of previous childhood emotional neglect, while greater reactivity in iso homozygotes was revealed only in the context of a history of elevated emotional neglect. At relatively low levels of previous emotional neglect, val carriers had heightened amygdala reactivity relative to iso homozygotes.
Conclusions:These results suggest that relatively greater amygdala reactivity may represent a biological mechanism through which childhood adversity and functional genetic variation in HPA axis responsiveness to stress may mediate risk for psychopathology. |
doi_str_mv | 10.1176/appi.ajp.2011.11060855 |
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Method:This study assessed whether the mineralocorticoid receptor iso/val polymorphism (rs5522), a functional genetic variant affecting HPA axis function, influenced threat-related amygdala reactivity in 279 individuals in late childhood and early adolescence. The study also explored the extent to which any effects of the genotype on amygdala reactivity were contingent upon previous childhood emotional neglect.
Results:Prior childhood emotional neglect and the val allele were associated with greater amygdala reactivity. Moreover, a significant genotype-by-emotional neglect interaction was observed whereby greater amygdala reactivity in val allele carriers was independent of previous childhood emotional neglect, while greater reactivity in iso homozygotes was revealed only in the context of a history of elevated emotional neglect. At relatively low levels of previous emotional neglect, val carriers had heightened amygdala reactivity relative to iso homozygotes.
Conclusions:These results suggest that relatively greater amygdala reactivity may represent a biological mechanism through which childhood adversity and functional genetic variation in HPA axis responsiveness to stress may mediate risk for psychopathology.</description><identifier>ISSN: 0002-953X</identifier><identifier>EISSN: 1535-7228</identifier><identifier>DOI: 10.1176/appi.ajp.2011.11060855</identifier><identifier>PMID: 22407082</identifier><identifier>CODEN: AJPSAO</identifier><language>eng</language><publisher>Arlington, VA: American Psychiatric Publishing</publisher><subject>Adolescent ; Alleles ; Amygdala - physiopathology ; Biological and medical sciences ; Child ; Child & adolescent psychiatry ; Child abuse & neglect ; Child Abuse - psychology ; Female ; Functional Neuroimaging ; Genotype ; Genotype & phenotype ; Homozygote ; Humans ; Magnetic Resonance Imaging ; Male ; Medical sciences ; Mutation, Missense - genetics ; Mutation, Missense - physiology ; Neuropsychology ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology ; Psychopathology. Psychiatry ; Receptors, Mineralocorticoid - genetics ; Receptors, Mineralocorticoid - physiology ; Victimology</subject><ispartof>The American journal of psychiatry, 2012-05, Vol.169 (5), p.515-522</ispartof><rights>Copyright © American Psychiatric Association 2012</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © American Psychiatric Association</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a516t-a997698b0defa89abcf57d09c8d3d993b5a20a66229e42fb772188094eef85ac3</citedby><cites>FETCH-LOGICAL-a516t-a997698b0defa89abcf57d09c8d3d993b5a20a66229e42fb772188094eef85ac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://psychiatryonline.org/doi/epdf/10.1176/appi.ajp.2011.11060855$$EPDF$$P50$$Gappi$$H</linktopdf><linktohtml>$$Uhttps://psychiatryonline.org/doi/full/10.1176/appi.ajp.2011.11060855$$EHTML$$P50$$Gappi$$H</linktohtml><link.rule.ids>230,314,776,780,881,2842,21605,21606,21607,27901,27902,77763,77768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=25839882$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22407082$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bogdan, Ryan</creatorcontrib><creatorcontrib>Williamson, Douglas E.</creatorcontrib><creatorcontrib>Hariri, Ahmad R.</creatorcontrib><title>Mineralocorticoid Receptor Iso/Val (rs5522) Genotype Moderates the Association Between Previous Childhood Emotional Neglect and Amygdala Reactivity</title><title>The American journal of psychiatry</title><addtitle>Am J Psychiatry</addtitle><description>Objective:The amygdala is especially reactive to threatening stimuli, and the degree of reactivity predicts individual differences in the expression of depression and anxiety. Emerging research suggests that emotional neglect during childhood as well as hypercortisolemia may lead to heightened threat-related amygdala reactivity. This raises the possibility that genetic variation affecting hypothalamic-pituitary-adrenal (HPA) axis function contributes to individual differences in amygdala reactivity, both independently and as a function of childhood emotional neglect.
Method:This study assessed whether the mineralocorticoid receptor iso/val polymorphism (rs5522), a functional genetic variant affecting HPA axis function, influenced threat-related amygdala reactivity in 279 individuals in late childhood and early adolescence. The study also explored the extent to which any effects of the genotype on amygdala reactivity were contingent upon previous childhood emotional neglect.
Results:Prior childhood emotional neglect and the val allele were associated with greater amygdala reactivity. Moreover, a significant genotype-by-emotional neglect interaction was observed whereby greater amygdala reactivity in val allele carriers was independent of previous childhood emotional neglect, while greater reactivity in iso homozygotes was revealed only in the context of a history of elevated emotional neglect. At relatively low levels of previous emotional neglect, val carriers had heightened amygdala reactivity relative to iso homozygotes.
Conclusions:These results suggest that relatively greater amygdala reactivity may represent a biological mechanism through which childhood adversity and functional genetic variation in HPA axis responsiveness to stress may mediate risk for psychopathology.</description><subject>Adolescent</subject><subject>Alleles</subject><subject>Amygdala - physiopathology</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child & adolescent psychiatry</subject><subject>Child abuse & neglect</subject><subject>Child Abuse - psychology</subject><subject>Female</subject><subject>Functional Neuroimaging</subject><subject>Genotype</subject><subject>Genotype & phenotype</subject><subject>Homozygote</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mutation, Missense - genetics</subject><subject>Mutation, Missense - physiology</subject><subject>Neuropsychology</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology</subject><subject>Psychopathology. Psychiatry</subject><subject>Receptors, Mineralocorticoid - genetics</subject><subject>Receptors, Mineralocorticoid - physiology</subject><subject>Victimology</subject><issn>0002-953X</issn><issn>1535-7228</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kd1uEzEQhVcIREPhFSpLCKlcJPV647V9gxSiUiq1gBAg7qyJPZs42qwX2wnKc_DCOD8thQuuLNvfnJk5pyjOSjoqS1FfQN-7ESz7EaNlmZ9oTSXnj4pBySs-FIzJx8WAUsqGilffT4pnMS7zlVaCPS1OGBtTQSUbFL9uXYcBWm98SM54Z8lnNNgnH8h19BffoCXnIXLO2GtyhZ1P2x7Jrbe5KGEkaYFkEqM3DpLzHXmL6SdiRz4F3Di_jmS6cK1deG_J5crvkCz4AectmkSgs2Sy2s4ttJDbgklu49L2efGkgTbii-N5Wnx9d_ll-n548_Hqejq5GQIv6zQEpUSt5IxabEAqmJmGC0uVkbaySlUzDoxCXTOmcMyamRCslJKqMWIjOZjqtHhz0O3XsxVag13KTug-uBWErfbg9N8_nVvoud_osaDZPJUFzo8Cwf9YY0x65aLBtoUO8-66pNlnpcaCZ_TlP-jSr0M2Y08xWlEpdoL1gTLBxxiwuR-mpHqXu97lrnPuepe7vss9F549XOW-7C7oDLw6AhANtE2Azrj4h-OyUnLPVQdu3-jBjP9t_xtRdMsY</recordid><startdate>20120501</startdate><enddate>20120501</enddate><creator>Bogdan, Ryan</creator><creator>Williamson, Douglas E.</creator><creator>Hariri, Ahmad R.</creator><general>American Psychiatric Publishing</general><general>American Psychiatric Association</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20120501</creationdate><title>Mineralocorticoid Receptor Iso/Val (rs5522) Genotype Moderates the Association Between Previous Childhood Emotional Neglect and Amygdala Reactivity</title><author>Bogdan, Ryan ; Williamson, Douglas E. ; Hariri, Ahmad R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a516t-a997698b0defa89abcf57d09c8d3d993b5a20a66229e42fb772188094eef85ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adolescent</topic><topic>Alleles</topic><topic>Amygdala - physiopathology</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child & adolescent psychiatry</topic><topic>Child abuse & neglect</topic><topic>Child Abuse - psychology</topic><topic>Female</topic><topic>Functional Neuroimaging</topic><topic>Genotype</topic><topic>Genotype & phenotype</topic><topic>Homozygote</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mutation, Missense - genetics</topic><topic>Mutation, Missense - physiology</topic><topic>Neuropsychology</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology</topic><topic>Psychopathology. Psychiatry</topic><topic>Receptors, Mineralocorticoid - genetics</topic><topic>Receptors, Mineralocorticoid - physiology</topic><topic>Victimology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bogdan, Ryan</creatorcontrib><creatorcontrib>Williamson, Douglas E.</creatorcontrib><creatorcontrib>Hariri, Ahmad R.</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>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The American journal of psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bogdan, Ryan</au><au>Williamson, Douglas E.</au><au>Hariri, Ahmad R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mineralocorticoid Receptor Iso/Val (rs5522) Genotype Moderates the Association Between Previous Childhood Emotional Neglect and Amygdala Reactivity</atitle><jtitle>The American journal of psychiatry</jtitle><addtitle>Am J Psychiatry</addtitle><date>2012-05-01</date><risdate>2012</risdate><volume>169</volume><issue>5</issue><spage>515</spage><epage>522</epage><pages>515-522</pages><issn>0002-953X</issn><eissn>1535-7228</eissn><coden>AJPSAO</coden><abstract>Objective:The amygdala is especially reactive to threatening stimuli, and the degree of reactivity predicts individual differences in the expression of depression and anxiety. Emerging research suggests that emotional neglect during childhood as well as hypercortisolemia may lead to heightened threat-related amygdala reactivity. This raises the possibility that genetic variation affecting hypothalamic-pituitary-adrenal (HPA) axis function contributes to individual differences in amygdala reactivity, both independently and as a function of childhood emotional neglect.
Method:This study assessed whether the mineralocorticoid receptor iso/val polymorphism (rs5522), a functional genetic variant affecting HPA axis function, influenced threat-related amygdala reactivity in 279 individuals in late childhood and early adolescence. The study also explored the extent to which any effects of the genotype on amygdala reactivity were contingent upon previous childhood emotional neglect.
Results:Prior childhood emotional neglect and the val allele were associated with greater amygdala reactivity. Moreover, a significant genotype-by-emotional neglect interaction was observed whereby greater amygdala reactivity in val allele carriers was independent of previous childhood emotional neglect, while greater reactivity in iso homozygotes was revealed only in the context of a history of elevated emotional neglect. At relatively low levels of previous emotional neglect, val carriers had heightened amygdala reactivity relative to iso homozygotes.
Conclusions:These results suggest that relatively greater amygdala reactivity may represent a biological mechanism through which childhood adversity and functional genetic variation in HPA axis responsiveness to stress may mediate risk for psychopathology.</abstract><cop>Arlington, VA</cop><pub>American Psychiatric Publishing</pub><pmid>22407082</pmid><doi>10.1176/appi.ajp.2011.11060855</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Alleles Amygdala - physiopathology Biological and medical sciences Child Child & adolescent psychiatry Child abuse & neglect Child Abuse - psychology Female Functional Neuroimaging Genotype Genotype & phenotype Homozygote Humans Magnetic Resonance Imaging Male Medical sciences Mutation, Missense - genetics Mutation, Missense - physiology Neuropsychology Psychology. Psychoanalysis. Psychiatry Psychopathology Psychopathology. Psychiatry Receptors, Mineralocorticoid - genetics Receptors, Mineralocorticoid - physiology Victimology |
title | Mineralocorticoid Receptor Iso/Val (rs5522) Genotype Moderates the Association Between Previous Childhood Emotional Neglect and Amygdala Reactivity |
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