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情绪调节受损:双相情感障碍及未患病亲属中重新评价和分心的神经关联

Impaired regulation of emotion: neural correlates of reappraisal and distraction in bipolar disorder and unaffected relatives.

作者信息

Kanske P, Schönfelder S, Forneck J, Wessa M

机构信息

Department of Social Neuroscience, Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.

Department of Clinical Psychology and Neuropsychology, Johannes Gutenberg University, Mainz, Germany.

出版信息

Transl Psychiatry. 2015 Jan 20;5(1):e497. doi: 10.1038/tp.2014.137.

Abstract

Deficient emotion regulation has been proposed as a crucial pathological mechanism in bipolar disorder (BD). We therefore investigated emotion regulation impairments in BD, the related neural underpinnings and their etiological relevance for the disorder. Twenty-two euthymic patients with bipolar-I disorder and 17 unaffected first-degree relatives of BD-I patients, as well as two groups of healthy gender-, age- and education-matched controls (N=22/17, respectively) were included. Participants underwent functional magnetic resonance imaging while applying two different emotion regulation techniques, reappraisal and distraction, when presented with emotional images. BD patients and relatives showed impaired downregulation of amygdala activity during reappraisal, but not during distraction, when compared with controls. This deficit was correlated with the habitual use of reappraisal. The negative connectivity of amygdala and orbitofrontal cortex (OFC) observed during reappraisal in controls was reversed in BD patients and relatives. There were no significant differences between BD patients and relatives. As being observed in BD patients and unaffected relatives, deficits in emotion regulation through reappraisal may represent heritable neurobiological abnormalities underlying BD. The neural mechanisms include impaired control of amygdala reactivity to emotional stimuli and dysfunctional connectivity of the amygdala to regulatory control regions in the OFC. These are, thus, important aspects of the neurobiological basis of increased vulnerability for BD.

摘要

情绪调节缺陷已被认为是双相情感障碍(BD)的关键病理机制。因此,我们研究了双相情感障碍患者的情绪调节障碍、相关神经基础及其与该疾病病因的相关性。研究纳入了22名处于缓解期的双相I型障碍患者、17名双相I型障碍患者未受影响的一级亲属,以及两组在性别、年龄和教育程度上相匹配的健康对照者(每组分别为22名/17名)。参与者在观看情绪性图像时,应用重新评价和分心这两种不同的情绪调节技术时接受功能磁共振成像检查。与对照组相比,双相情感障碍患者及其亲属在重新评价过程中杏仁核活动的下调受损,但在分心过程中未受损。这种缺陷与重新评价的习惯性使用相关联。在对照组重新评价过程中观察到的杏仁核与眶额皮质(OFC)的负性连接在双相情感障碍患者及其亲属中发生了逆转。双相情感障碍患者与其亲属之间没有显著差异。正如在双相情感障碍患者及其未受影响的亲属中所观察到的那样,通过重新评价进行情绪调节的缺陷可能代表双相情感障碍潜在的可遗传神经生物学异常。神经机制包括对杏仁核对情绪刺激反应性的控制受损以及杏仁核与眶额皮质调节控制区域的连接功能障碍。因此,这些是双相情感障碍易感性增加的神经生物学基础的重要方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38df/4312831/6f19153f08e4/tp2014137f1.jpg

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