Corral-Frías N S, Nikolova Y S, Michalski L J, Baranger D A A, Hariri A R, Bogdan R
Department of Psychiatry,Washington University in St Louis,St Louis,MO,USA.
Laboratory of NeuroGenetics,Department of Psychology and Neuroscience,Duke University,Durham,NC,USA.
Psychol Med. 2015;45(12):2605-17. doi: 10.1017/S0033291715000525. Epub 2015 Apr 8.
Early life stress (ELS) is consistently associated with increased risk for subsequent psychopathology. Individual differences in neural response to reward may confer vulnerability to stress-related psychopathology. Using data from the ongoing Duke Neurogenetics Study, the present study examined whether reward-related ventral striatum (VS) reactivity moderates the relationship between retrospectively reported ELS and anhedonic symptomatology. We further assessed whether individual differences in reward-related VS reactivity were associated with other depressive symptoms and problematic alcohol use via stress-related anhedonic symptoms and substance use-associated coping.
Blood oxygen level-dependent functional magnetic resonance imaging (fMRI) was collected while participants (n = 906) completed a card-guessing task, which robustly elicits VS reactivity. ELS, anhedonic symptoms, other depressive symptoms, coping behavior, and alcohol use behavior were assessed with self-report questionnaires. Linear regressions were run to examine whether VS reactivity moderated the relationship between ELS and anhedonic symptoms. Structural equation models examined whether this moderation was indirectly associated with other depression symptoms and problematic alcohol use through its association with anhedonia.
Analyses of data from 820 participants passing quality control procedures revealed that the VS × ELS interaction was associated with anhedonic symptoms (p = 0.011). Moreover, structural equation models indirectly linked this interaction to non-anhedonic depression symptoms and problematic alcohol use through anhedonic symptoms and substance-related coping.
These findings suggest that reduced VS reactivity to reward is associated with increased risk for anhedonia in individuals exposed to ELS. Such stress-related anhedonia is further associated with other depressive symptoms and problematic alcohol use through substance-related coping.
早年生活应激(ELS)一直与后续精神病理学风险增加相关。对奖励的神经反应的个体差异可能使人易患与应激相关的精神病理学。利用正在进行的杜克神经遗传学研究的数据,本研究检验了与奖励相关的腹侧纹状体(VS)反应性是否会调节回顾性报告的ELS与快感缺失症状之间的关系。我们还进一步评估了与奖励相关的VS反应性的个体差异是否通过与应激相关的快感缺失症状和与物质使用相关的应对方式,与其他抑郁症状和酒精使用问题相关。
在参与者(n = 906)完成一项能强烈引发VS反应性的猜牌任务时,收集血氧水平依赖性功能磁共振成像(fMRI)数据。通过自我报告问卷评估ELS、快感缺失症状、其他抑郁症状、应对行为和酒精使用行为。进行线性回归以检验VS反应性是否调节了ELS与快感缺失症状之间的关系。结构方程模型检验了这种调节作用是否通过与快感缺失的关联,间接与其他抑郁症状和酒精使用问题相关。
对通过质量控制程序的820名参与者的数据进行分析发现,VS×ELS交互作用与快感缺失症状相关(p = 0.011)。此外,结构方程模型通过快感缺失症状和与物质相关的应对方式,将这种交互作用间接与非快感缺失性抑郁症状和酒精使用问题联系起来。
这些发现表明,暴露于ELS的个体中,VS对奖励的反应性降低与快感缺失风险增加相关。这种与应激相关的快感缺失通过与物质相关的应对方式,进一步与其他抑郁症状和酒精使用问题相关。