Literature DB >> 27543885

Common variant in OXTR predicts growth in positive emotions from loving-kindness training.

Suzannah F Isgett1, Sara B Algoe1, Aaron J Boulton1, Baldwin M Way2, Barbara L Fredrickson3.   

Abstract

Ample research suggests that social connection reliably generates positive emotions. Oxytocin, a neuropeptide implicated in social cognition and behavior, is one biological mechanism that may influence an individual's capacity to extract positive emotions from social contexts. Because variation in certain genes may indicate underlying neurobiological differences, we tested whether several SNPs in two genes related to oxytocin signaling would show effects on positive emotions that were context-specific, depending on sociality. For six weeks, a sample of mid-life adults (N=122) participated in either socially-focused loving-kindness training or mindfulness training. During this timespan they reported their positive emotions daily. Five SNPs within OXTR and CD38 were assayed, and each was tested for its individual effect on daily emotions. The hypothesized three-way interaction between time, training type, and genetic variability emerged: Individuals homozygous for the G allele of OXTR rs1042778 experienced gains in daily positive emotions from loving-kindness training, whereas individuals with the T allele did not experience gains in positive emotions with either training. These findings are among the first to show how genetic differences in oxytocin signaling may influence an individual's capacity to experience positive emotions as a result of a socially-focused intervention.
Copyright © 2016 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Affective science; Genetics; Meditation; Oxytocin; Positive psychology; Vantage sensitivity

Mesh:

Substances:

Year:  2016        PMID: 27543885      PMCID: PMC5359600          DOI: 10.1016/j.psyneuen.2016.08.010

Source DB:  PubMed          Journal:  Psychoneuroendocrinology        ISSN: 0306-4530            Impact factor:   4.905


  47 in total

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