Threat-related amygdala functional connectivity is associated with 5-HTTLPR genotype and neuroticism
Author(s) -
M. Madsen,
Brenda Mc Mahon,
S. B. Andersen,
Hartwig R. Siebner,
Gitte M. Knudsen,
Patrick M. Fisher
Publication year - 2015
Publication title -
social cognitive and affective neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.229
H-Index - 103
eISSN - 1749-5024
pISSN - 1749-5016
DOI - 10.1093/scan/nsv098
Subject(s) - amygdala , neuroticism , precuneus , psychology , ventrolateral prefrontal cortex , 5 httlpr , functional magnetic resonance imaging , prefrontal cortex , posterior cingulate , orbitofrontal cortex , neuroscience , anterior cingulate cortex , ventromedial prefrontal cortex , default mode network , personality , genotype , cognition , biology , serotonin transporter , genetics , social psychology , gene
Communication between the amygdala and other brain regions critically regulates sensitivity to threat, which has been associated with risk for mood and affective disorders. The extent to which these neural pathways are genetically determined or correlate with risk-related personality measures is not fully understood. Using functional magnetic resonance imaging, we evaluated independent and interactive effects of the 5-HTTLPR genotype and neuroticism on amygdala functional connectivity during an emotional faces paradigm in 76 healthy individuals. Functional connectivity between left amygdala and medial prefrontal cortex (mPFC) and between both amygdalae and a cluster including posterior cingulate cortex, precuneus and visual cortex was significantly increased in 5-HTTLPR S' allele carriers relative to L(A)L(A) individuals. Neuroticism was negatively correlated with functional connectivity between right amygdala and mPFC and visual cortex, and between both amygdalae and left lateral orbitofrontal (lOFC) and ventrolateral prefrontal cortex (vlPFC). Notably, 5-HTTLPR moderated the association between neuroticism and functional connectivity between both amygdalae and left lOFC/vlPFC, such that S' carriers exhibited a more negative association relative to L(A)L(A) individuals. These findings provide novel evidence for both independent and interactive effects of 5-HTTLPR genotype and neuroticism on amygdala communication, which may mediate effects on risk for mood and affective disorders.
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