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DRD4-exonIII-VNTR moderates the effect of childhood adversities on emotional resilience in young-adults

dc.contributor.authorDas, Debjani
dc.contributor.authorCherbuin, Nicolas
dc.contributor.authorTan, Xiaoyun
dc.contributor.authorEasteal, Simon
dc.contributor.authorAnstey, Kaarin
dc.date.accessioned2015-10-27T01:24:37Z
dc.date.available2015-10-27T01:24:37Z
dc.date.issued2011-05-27
dc.date.updated2015-12-09T08:13:35Z
dc.description.abstractMost individuals successfully maintain psychological well-being even when exposed to trauma or adversity. Emotional resilience or the ability to thrive in the face of adversity is determined by complex interactions between genetic makeup, previous exposure to stress, personality, coping style, availability of social support, etc. Recent studies have demonstrated that childhood trauma diminishes resilience in adults and affects mental health. The Dopamine receptor D4 (DRD4) exon III variable number tandem repeat (VNTR) polymorphism was reported to moderate the impact of adverse childhood environment on behaviour, mood and other health-related outcomes. In this study we investigated whether DRD4-exIII-VNTR genotype moderates the effect of childhood adversities (CA) on resilience. In a representative population sample (n = 1148) aged 30-34 years, we observed an interactive effect of DRD4 genotype and CA (β = 0.132; p = 0.003) on resilience despite no main effect of the genotype when effects of age, gender and education were controlled for. The 7-repeat allele appears to protect against the adverse effect of CA since the decline in resilience associated with increased adversity was evident only in individuals without the 7-repeat allele. Resilience was also significantly associated with approach-/avoidance-related personality measures (behavioural inhibition/activation system; BIS/BAS) measures and an interactive effect of DRD4-exIII-VNTR genotype and CA on BAS was observed. Hence it is possible that approach-related personality traits could be mediating the effect of the DRD4 gene and childhood environment interaction on resilience such that when stressors are present, the 7-repeat allele influences the development of personality in a way that provides protection against adverse outcomes.
dc.description.sponsorshipThe study was supported by NHMRC of Australia Unit Grant No. 973302. DD is funded by NHMRC Capacity Building Grant No. 418020 in Population Health Research. NC is funded by NHMRC Research Fellowship No. 471501. KA is funded by NHMRC Research Fellowship No. 366756.en_AU
dc.format6 pages
dc.identifier.issn1932-6203en_AU
dc.identifier.urihttp://hdl.handle.net/1885/16115
dc.publisherPublic Library of Science
dc.relationhttp://purl.org/au-research/grants/nhmrc/973302
dc.relationhttp://purl.org/au-research/grants/nhmrc/418020
dc.relationhttp://purl.org/au-research/grants/nhmrc/471501
dc.relationhttp://purl.org/au-research/grants/nhmrc/366756
dc.rights© 2011 Das et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
dc.sourcePLoS ONE
dc.subjectadult
dc.subjectchild
dc.subjectdemography
dc.subjectexons
dc.subjectfemale
dc.subjecthumans
dc.subjectmale
dc.subjectmiddle aged
dc.subjectminisatellite repeats
dc.subjectpersonality
dc.subjectreceptors, dopamine d4
dc.subjectregression analysis
dc.subjectstress, psychological
dc.subjectyoung adult
dc.subjectresilience, psychological
dc.titleDRD4-exonIII-VNTR moderates the effect of childhood adversities on emotional resilience in young-adults
dc.typeJournal article
dcterms.dateAccepted2011-04-26
local.bibliographicCitation.issue5en_AU
local.bibliographicCitation.startpagee20177en_AU
local.contributor.affiliationDas, Debjani, College of Medicine, Biology and Environment, CMBE John Curtin School of Medical Research, Genome Sciences, The Australian National Universityen_AU
local.contributor.affiliationCherbuin, Nicolas, College of Medicine, Biology and Environment, CMBE Research School of Population Health, National Institute for Mental Health Research, The Australian National Universityen_AU
local.contributor.affiliationTan, Susan (Xiaoyun), College of Medicine, Biology and Environment, CMBE John Curtin School of Medical Research, Genome Sciences, The Australian National Universityen_AU
local.contributor.affiliationAnstey, Kaarin, College of Medicine, Biology and Environment, CMBE Research School of Population Health, National Institute for Mental Health Research, The Australian National Universityen_AU
local.contributor.affiliationEasteal, Simon, College of Medicine, Biology and Environment, CMBE John Curtin School of Medical Research, Genome Sciences, The Australian National Universityen_AU
local.contributor.authoruidu1817814en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor170100en_AU
local.identifier.absseo920502en_AU
local.identifier.ariespublicationu4020362xPUB205en_AU
local.identifier.citationvolume6en_AU
local.identifier.doi10.1371/journal.pone.0020177en_AU
local.identifier.essn1932-6203en_AU
local.identifier.scopusID2-s2.0-79957617207
local.identifier.thomsonID000291052500037
local.publisher.urlhttps://www.plos.org/en_AU
local.type.statusPublished Versionen_AU

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