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Meditation experience is associated with differences in default mode network activity and connectivity

Judson A. Brewer, Patrick D. Worhunsky, Jeremy R. Gray, Yi-Yuan Tang, Jochen Weber, Hedy Kober

Proceedings of the National Academy of Sciences November 23, 2011 DOI: 10.1073/pnas.1112029108 via OpenAlex

Summary

AI-generated from the abstract

Experienced meditators show reduced activity in brain regions linked to self-referential thought and mind-wandering, particularly the medial prefrontal and posterior cingulate cortices, across different meditation types. They also exhibit stronger connections between areas involved in self-monitoring and cognitive control, such as the posterior cingulate, dorsal anterior cingulate, and dorsolateral prefrontal cortices, both at rest and during meditation. These neural patterns align with decreased mind-wandering, offering insight into how meditation may support present-moment awareness and well-being.

Study at a glance

Characteristics Observational cohort Peer reviewed
Population Experienced meditators and matched meditation-naive controls
Interventions Concentration Loving-Kindness Choiceless Awareness
Topics Default mode network Meditation
Keywords Posterior cingulate Precuneus Happiness
Citations 1,410
Key finding Experienced meditators showed deactivation of default-mode network nodes and stronger functional connectivity between self-monitoring and cognitive control regions, consistent with reduced mind-wandering.

Abstract

Many philosophical and contemplative traditions teach that "living in the moment" increases happiness. However, the default mode of humans appears to be that of mind-wandering, which correlates with unhappiness, and with activation in a network of brain areas associated with self-referential processing. We investigated brain activity in experienced meditators and matched meditation-naive controls as they performed several different meditations (Concentration, Loving-Kindness, Choiceless Awareness). We found that the main nodes of the default-mode network (medial prefrontal and posterior cingulate cortices) were relatively deactivated in experienced meditators across all meditation types. Furthermore, functional connectivity analysis revealed stronger coupling in experienced meditators between the posterior cingulate, dorsal anterior cingulate, and dorsolateral prefrontal cortices (regions previously implicated in self-monitoring and cognitive control), both at baseline and during meditation. Our findings demonstrate differences in the default-mode network that are consistent with decreased mind-wandering. As such, these provide a unique understanding of possible neural mechanisms of meditation.

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