Hemispheric divergence of interoceptive processing across psychiatric disorders.

IF 6.4 1区 生物学 Q1 BIOLOGY eLife Pub Date : 2024-11-13 DOI:10.7554/eLife.92820
Emily M Adamic, Adam R Teed, Jason Avery, Feliberto de la Cruz, Sahib Khalsa
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Abstract

Interactions between top-down attention and bottom-up visceral inputs are assumed to produce conscious perceptions of interoceptive states, and while each process has been independently associated with aberrant interoceptive symptomatology in psychiatric disorders, the neural substrates of this interface are unknown. We conducted a preregistered functional neuroimaging study of 46 individuals with anxiety, depression, and/or eating disorders (ADE) and 46 propensity-matched healthy comparisons (HC), comparing their neural activity across two interoceptive tasks differentially recruiting top-down or bottom-up processing within the same scan session. During an interoceptive attention task, top-down attention was voluntarily directed towards cardiorespiratory or visual signals. In contrast, during an interoceptive perturbation task, intravenous infusions of isoproterenol (a peripherally-acting beta-adrenergic receptor agonist) were administered in a double-blinded and placebo-controlled fashion to drive bottom-up cardiorespiratory sensations. Across both tasks, neural activation converged upon the insular cortex, localizing within the granular and ventral dysgranular subregions bilaterally. However, contrasting hemispheric differences emerged, with the ADE group exhibiting (relative to HCs) an asymmetric pattern of overlap in the left insula, with increased or decreased proportions of co-activated voxels within the left or right dysgranular insula, respectively. The ADE group also showed less agranular anterior insula activation during periods of bodily uncertainty (i.e. when anticipating possible isoproterenol-induced changes that never arrived). Finally, post-task changes in insula functional connectivity were associated with anxiety and depression severity. These findings confirm the dysgranular mid-insula as a key cortical interface where attention and prediction meet real-time bodily inputs, especially during heightened awareness of interoceptive states. Furthermore, the dysgranular mid-insula may indeed be a 'locus of disruption' for psychiatric disorders.

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不同精神障碍患者的内感知处理存在半球差异。
自上而下的注意力和自下而上的内脏输入之间的相互作用被认为会产生有意识的内感知状态感知,虽然每个过程都与精神疾病的异常内感知症状有独立的关联,但这种界面的神经基底尚不清楚。我们对 46 名焦虑症、抑郁症和/或进食障碍患者(ADE)和 46 名倾向匹配的健康对比者(HC)进行了一项预先登记的功能神经影像学研究,比较了他们在同一扫描过程中,在两个不同的自上而下或自下而上处理的互感任务中的神经活动。在感知间注意任务中,自上而下的注意力会自愿指向心肺或视觉信号。与此相反,在感知间干扰任务中,以双盲和安慰剂对照的方式静脉注射异丙肾上腺素(一种外周作用的β肾上腺素能受体激动剂),以驱动自下而上的心肺感觉。在这两项任务中,神经激活都集中在岛叶皮层,定位在双侧颗粒和腹侧颗粒下区。然而,ADE 组出现了截然不同的半球差异,(相对于 HCs)左侧岛叶出现了不对称的重叠模式,左侧或右侧粒状下丘脑岛叶内共同激活的体素比例分别增加或减少。在身体不确定时期(即预期异丙肾上腺素可能诱发的变化从未发生时),ADE 组的前脑岛粒细胞激活也较少。最后,任务后脑岛功能连接的变化与焦虑和抑郁的严重程度有关。这些研究结果证实,脑岛中半部是大脑皮层的一个关键界面,在这里,注意力和预测与实时身体输入相交汇,尤其是在增强对感知间状态的意识时。此外,大脑中半球下部可能确实是精神疾病的 "干扰点"。
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来源期刊
eLife
eLife BIOLOGY-
CiteScore
12.90
自引率
3.90%
发文量
3122
审稿时长
17 weeks
期刊介绍: eLife is a distinguished, not-for-profit, peer-reviewed open access scientific journal that specializes in the fields of biomedical and life sciences. eLife is known for its selective publication process, which includes a variety of article types such as: Research Articles: Detailed reports of original research findings. Short Reports: Concise presentations of significant findings that do not warrant a full-length research article. Tools and Resources: Descriptions of new tools, technologies, or resources that facilitate scientific research. Research Advances: Brief reports on significant scientific advancements that have immediate implications for the field. Scientific Correspondence: Short communications that comment on or provide additional information related to published articles. Review Articles: Comprehensive overviews of a specific topic or field within the life sciences.
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