Center for Depression, Anxiety and Stress Research, McLean Hospital, Belmont, MA, USA; Department of Psychiatry, Harvard Medical School, MA, USA.
Cousins Center for Psychoneuroimmunology, University of California, Los Angeles, USA; Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, CA, USA.
J Affect Disord. 2015 Jul 15;180:104-11. doi: 10.1016/j.jad.2015.03.035. Epub 2015 Mar 28.
Major depressive disorder (MDD) is often precipitated by life stress and growing evidence suggests that stress-induced alterations in reward processing may contribute to such risk. However, no human imaging studies have examined how recent life stress exposure modulates the neural systems that underlie reward processing in depressed and healthy individuals.
In this proof-of-concept study, 12 MDD and 10 psychiatrically healthy individuals were interviewed using the Life Events and Difficulties Schedule (LEDS) to assess their perceived levels of recent acute and chronic life stress exposure. Additionally, each participant performed a monetary incentive delay task under baseline (no-stress) and stress (social-evaluative) conditions during functional MRI.
Across groups, medial prefrontal cortex (mPFC) activation to reward feedback was greater during acute stress versus no-stress conditions in individuals with greater perceived stressor severity. Under acute stress, depressed individuals showed a positive correlation between perceived stressor severity levels and reward-related mPFC activation (r=0.79, p=0.004), whereas no effect was found in healthy controls. Moreover, for depressed (but not healthy) individuals, the correlations between the stress (r=0.79) and no-stress (r=-0.48) conditions were significantly different. Finally, relative to controls, depressed participants showed significantly reduced mPFC gray matter, but functional findings remained robust while accounting for structural differences.
Small sample size, which warrants replication.
Depressed individuals experiencing greater recent life stress recruited the mPFC more under stress when processing rewards. Our results represent an initial step toward elucidating mechanisms underlying stress sensitization and recurrence in depression.
重度抑郁症(MDD)常由生活压力诱发,越来越多的证据表明,应激诱导的奖赏加工改变可能导致这种风险。然而,目前还没有人类影像学研究探讨近期生活压力暴露如何调节抑郁和健康个体的奖赏加工的神经机制。
在这项概念验证研究中,12 名 MDD 患者和 10 名精神健康个体接受了生活事件和困难量表(LEDS)访谈,以评估他们最近经历的急性和慢性生活压力暴露程度。此外,每位参与者在功能磁共振成像期间,在基线(无压力)和压力(社会评价)条件下进行了金钱激励延迟任务。
在整个组中,与基线(无压力)条件相比,在经历过更大的感知压力源严重程度的个体中,内侧前额叶皮质(mPFC)在急性压力下对奖赏反馈的激活更大。在急性压力下,抑郁个体表现出感知压力源严重程度与奖赏相关 mPFC 激活之间的正相关(r=0.79,p=0.004),而健康对照组则没有发现这种相关性。此外,对于抑郁(而非健康)个体,压力(r=0.79)和无压力(r=-0.48)条件之间的相关性存在显著差异。最后,与对照组相比,抑郁个体的 mPFC 灰质明显减少,但在考虑到结构差异时,功能发现仍然稳健。
样本量小,需要复制。
经历更大近期生活压力的抑郁个体在处理奖赏时,在压力下更多地招募 mPFC。我们的结果代表了阐明抑郁应激敏感化和复发机制的初步步骤。