情绪和奖赏期间的纹状体反应与接近-回避冲突行为有关,在患有焦虑症或抑郁症的成年人身上会发生改变。

IF 4.1 2区 医学 Q2 NEUROSCIENCES
Timothy J McDermott, Hannah Berg, James Touthang, Elisabeth Akeman, Mallory J Cannon, Jessica Santiago, Kelly T Cosgrove, Ashley N Clausen, Namik Kirlic, Ryan Smith, Michelle G Craske, James L Abelson, Martin P Paulus, Robin L Aupperle
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引用次数: 0

摘要

背景:我们以前曾报道过健康成年人在使用接近-回避冲突(AAC)决策任务时,在功能磁共振成像(fMRI)中奖励、显著性和执行控制区域的激活情况。进一步研究焦虑症和抑郁症与 AAC 过程中神经反应差异的关系,可为了解和治疗焦虑症和抑郁症提供参考。我们测试了焦虑症或抑郁症患者在 AAC 过程中神经激活发生改变的假设:我们使用线性混合效应模型对 118 名寻求治疗的焦虑症或抑郁症成人和 58 名健康成人进行了比较,以研究 AAC 决策过程中神经激活(fMRI)的群体水平差异。相关分析检验了行为和神经测量之间的关系:结果:焦虑或抑郁的成年人在对情感刺激做出反应时,纹状体的参与度更高(p = 0.008,d = 0.31),而与价值无关;在奖励反馈时,纹状体的参与度较弱(p = 0.046,d = -0.27),而与是否存在金钱奖励无关。在决策过程中,无论是否存在冲突,他们的杏仁核活动也会减弱(p = 0.023,d = -0.32)。在各组中,冲突决策期间的接近行为与情感刺激期间的纹状体激活呈反向相关(p < 0.001,r = -0.28),与奖励反馈期间的纹状体激活呈正向相关(p < 0.001,r = 0.27):局限性:我们的跨诊断方法无法对特定焦虑症进行比较,我们的横断面方法也无法进行因果推断:焦虑和抑郁与对 AAC 神经反应的改变有关。研究结果与纹状体在行动选择和奖赏反应中的作用一致,并指出纹状体反应性是未来的治疗目标。焦虑症或抑郁症患者杏仁核活动的减弱可能是抑制情感显著性和保持接近的一种补偿反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Striatal reactivity during emotion and reward relates to approach-avoidance conflict behaviour and is altered in adults with anxiety or depression.

Striatal reactivity during emotion and reward relates to approach-avoidance conflict behaviour and is altered in adults with anxiety or depression.

Striatal reactivity during emotion and reward relates to approach-avoidance conflict behaviour and is altered in adults with anxiety or depression.

Striatal reactivity during emotion and reward relates to approach-avoidance conflict behaviour and is altered in adults with anxiety or depression.

Background: We have previously reported activation in reward, salience and executive control regions during functional MRI (fMRI) using an approach-avoidance conflict (AAC) decision-making task with healthy adults. Further investigations into how anxiety and depressive disorders relate to differences in neural responses during AAC can inform their understanding and treatment. We tested the hypothesis that people with anxiety or depression have altered neural activation during AAC.

Methods: We compared 118 treatment-seeking adults with anxiety or depression and 58 healthy adults using linear mixed-effects models to examine group-level differences in neural activation (fMRI) during AAC decision-making. Correlational analyses examined relationships between behavioural and neural measures.

Results: Adults with anxiety or depression had greater striatal engagement when reacting to affective stimuli (p = 0.008, d = 0.31) regardless of valence, and weaker striatal engagement during reward feedback (p = 0.046, d = -0.27) regardless of the presence of monetary reward. They also had blunted amygdala activity during decision-making (p = 0.023, d = -0.32) regardless of the presence of conflict. Across groups, approach behaviour during conflict decision-making was inversely correlated with striatal activation during affective stimuli (p < 0.001, r = -0.28) and positively related to striatal activation during reward feedback (p < 0.001, r = 0.27).

Limitations: Our transdiagnostic approach did not allow for comparisons between specific anxiety disorders, and our cross-sectional approach did not allow for causal inference.

Conclusion: Anxiety and depression were associated with altered neural responses to AAC. Findings were consistent with the role of the striatum in action selection and reward responsivity, and they point toward striatal reactivity as a future treatment target. Blunting of amygdala activity in anxiety or depression may indicate a compensatory response to inhibit affective salience and maintain approach.

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来源期刊
CiteScore
6.80
自引率
2.30%
发文量
51
审稿时长
2 months
期刊介绍: The Journal of Psychiatry & Neuroscience publishes papers at the intersection of psychiatry and neuroscience that advance our understanding of the neural mechanisms involved in the etiology and treatment of psychiatric disorders. This includes studies on patients with psychiatric disorders, healthy humans, and experimental animals as well as studies in vitro. Original research articles, including clinical trials with a mechanistic component, and review papers will be considered.
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