DNA methylation of OXTR is associated with parasympathetic nervous system activity and amygdala morphology

Oxytocin has anxiolytic properties whose mechanisms of action are still being identified. DNA methylation in the promoter region of the oxytocin receptor gene (OXTR), an epigenetic modification that putatively reflects a downtuning of the oxytocin system, has previously been implicated in the regula...

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Bibliographic Details
Main Authors: Connelly, J.J (Author), Goldbeck, L. (Author), Lancaster, K. (Author), Morris, J.P (Author), Puglia, M.H (Author)
Format: Article
Language:English
Published: Oxford University Press 2018
Subjects:
Online Access:View Fulltext in Publisher
LEADER 02913nam a2200625Ia 4500
001 10.1093-scan-nsy086
008 220706s2018 CNT 000 0 und d
020 |a 17495016 (ISSN) 
245 1 0 |a DNA methylation of OXTR is associated with parasympathetic nervous system activity and amygdala morphology 
260 0 |b Oxford University Press  |c 2018 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1093/scan/nsy086 
520 3 |a Oxytocin has anxiolytic properties whose mechanisms of action are still being identified. DNA methylation in the promoter region of the oxytocin receptor gene (OXTR), an epigenetic modification that putatively reflects a downtuning of the oxytocin system, has previously been implicated in the regulation of fear-related responses through the amygdala. In this study, we attempted to characterize the relationship between methylation of OXTR and anxiogenesis using two distinct endophenotypes: autonomic nervous system activity and subcortical brain structure. In 79 participants, we found that increased OXTR methylation is associated with attenuated resting parasympathetic tone, measured using high-frequency heart rate variability. Further, we found that this relationship is mediated by brain morphology, such that OXTR methylation is associated with increased gray matter of the central amygdala which is, in turn, associated with decreased parasympathetic tone. These results further our understanding of epigenetic regulation of the human oxytocin system and its role in anxiogenesis. © The Author(s) 2018. 
650 0 4 |a amygdala 
650 0 4 |a Amygdala 
650 0 4 |a anatomy and histology 
650 0 4 |a anxiety 
650 0 4 |a Anxiety 
650 0 4 |a body mass 
650 0 4 |a Body Mass Index 
650 0 4 |a cholinergic system 
650 0 4 |a DNA methylation 
650 0 4 |a DNA Methylation 
650 0 4 |a Epigenesis, Genetic 
650 0 4 |a female 
650 0 4 |a Female 
650 0 4 |a genetic epigenesis 
650 0 4 |a genetics 
650 0 4 |a gray matter 
650 0 4 |a Gray Matter 
650 0 4 |a heart rate 
650 0 4 |a Heart Rate 
650 0 4 |a human 
650 0 4 |a Humans 
650 0 4 |a Magnetic Resonance Imaging 
650 0 4 |a male 
650 0 4 |a Male 
650 0 4 |a neuroimaging 
650 0 4 |a Neuroimaging 
650 0 4 |a Neuroimaging epigenetics 
650 0 4 |a nuclear magnetic resonance imaging 
650 0 4 |a OXTR methylation 
650 0 4 |a OXTR protein, human 
650 0 4 |a oxytocin receptor 
650 0 4 |a Parasympathetic nervous system 
650 0 4 |a Parasympathetic Nervous System 
650 0 4 |a physiology 
650 0 4 |a Receptors, Oxytocin 
650 0 4 |a young adult 
650 0 4 |a Young Adult 
700 1 |a Connelly, J.J.  |e author 
700 1 |a Goldbeck, L.  |e author 
700 1 |a Lancaster, K.  |e author 
700 1 |a Morris, J.P.  |e author 
700 1 |a Puglia, M.H.  |e author 
773 |t Social Cognitive and Affective Neuroscience