Neurocomputational mechanisms underlying emotional awareness: Insights afforded by deep active inference and their potential clinical relevance

被引:59
作者
Smith, Ryan [1 ]
Lane, Richard D. [2 ]
Parr, Thomas [3 ]
Friston, Karl J. [3 ]
机构
[1] Laureate Inst Brain Res, 6655 S Yale Ave, Tulsa, OK 74136 USA
[2] Univ Arizona, Dept Psychiat, Tucson, AZ USA
[3] UCL, Inst Neurol, Wellcome Ctr Human Neuroimaging, London WC1N 3BG, England
关键词
Active inference; Emotional awareness; Somatic misattribution; Emotional working memory; Computational neuroscience; TORONTO-ALEXITHYMIA-SCALE; SITUATIONAL PANIC-ATTACKS; WORKING-MEMORY; FRONTOPARIETAL CONTROL; COGNITIVE-ABILITY; NEURAL BASIS; INTELLIGENCE; EXPERIENCE; NETWORKS; STRESS;
D O I
10.1016/j.neubiorev.2019.09.002
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Emotional awareness (EA) is recognized as clinically relevant to the vulnerability to, and maintenance of, psychiatric disorders. However, the neurocomputational processes that underwrite individual variations remain unclear. In this paper, we describe a deep (active) inference model that reproduces the cognitive-emotional processes and self-report behaviors associated with EA. We then present simulations to illustrate (seven) distinct mechanisms that (either alone or in combination) can produce phenomena - such as somatic misattribution, coarse-grained emotion conceptualization, and constrained reflective capacity - characteristic of low EA. Our simulations suggest that the clinical phenotype of impoverished EA can be reproduced by dissociable computational processes. The possibility that different processes are at work in different individuals suggests that they may benefit from distinct clinical interventions. As active inference makes particular predictions about the underlying neurobiology of such aberrant inference, we also discuss how this type of modelling could be used to design neuroimaging tasks to test predictions and identify which processes operate in different individuals - and provide a principled basis for personalized precision medicine.
引用
收藏
页码:473 / 491
页数:19
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