Columbia University, New York; New York State Psychiatric Institute, New York; Division of Clinical Developmental Neuroscience, Sackler Institute, New York.
Columbia University, New York; New York State Psychiatric Institute, New York.
J Am Acad Child Adolesc Psychiatry. 2022 Feb;61(2):308-320. doi: 10.1016/j.jaac.2021.04.014. Epub 2021 Jun 5.
Although depression and anxiety often have distinct etiologies, they frequently co-occur in adolescence. Recent initiatives have underscored the importance of developing new ways of classifying mental illness based on underlying neural dimensions that cut across traditional diagnostic boundaries. Accordingly, the aim of the study was to clarify reward-related neural circuitry that may characterize depressed-anxious youth.
The Boston Adolescent Neuroimaging of Depression and Anxiety Human Connectome Project tested group differences regarding subcortical volume and nucleus accumbens activation during an incentive processing task among 14- to 17-year-old adolescents presenting with a primary depressive and/or anxiety disorder (n = 129) or no lifetime history of mental disorders (n = 64). In addition, multimodal modeling examined predictors of depression and anxiety symptom change over a 6-month follow-up period.
Our findings highlighted considerable convergence. Relative to healthy youth, depressed-anxious adolescents exhibited reduced nucleus accumbens volume and activation following reward receipt. These findings remained when removing all medicated participants (∼59% of depressed-anxious youth). Subgroup analyses comparing anxious-only, depressed-anxious, and healthy youth also were largely consistent. Multimodal modeling showed that only structural alterations predicted depressive symptoms over time.
Multimodal findings highlight alterations within nucleus accumbens structure and function that characterize depressed-anxious adolescents. In the current hypothesis-driven analyses, however, only reduced nucleus accumbens volume predicted depressive symptoms over time. An important next step will be to clarify why structural alterations have an impact on reward-related processes and associated symptoms.
尽管抑郁和焦虑通常具有不同的病因,但它们在青少年中经常同时发生。最近的举措强调了根据跨越传统诊断界限的潜在神经维度来开发新的精神疾病分类方法的重要性。因此,本研究的目的是阐明可能特征化抑郁焦虑青少年的与奖励相关的神经回路。
波士顿青少年抑郁和焦虑人类连接组计划(Boston Adolescent Neuroimaging of Depression and Anxiety Human Connectome Project)在一项激励处理任务中测试了 14 至 17 岁青少年的亚皮质体积和伏隔核激活的组间差异,这些青少年患有原发性抑郁和/或焦虑障碍(n=129)或无终生精神障碍史(n=64)。此外,多模态建模检查了在 6 个月随访期间抑郁和焦虑症状变化的预测因素。
我们的发现强调了相当大的一致性。与健康青少年相比,抑郁焦虑青少年在获得奖励后表现出伏隔核体积和激活减少。当去除所有接受药物治疗的参与者(约 59%的抑郁焦虑青少年)时,这些发现仍然存在。比较仅焦虑、抑郁焦虑和健康青少年的亚组分析也基本一致。多模态建模表明,只有结构改变可以预测随时间推移的抑郁症状。
多模态研究结果突出了特征化抑郁焦虑青少年的伏隔核结构和功能改变。然而,在当前的假设驱动分析中,只有伏隔核体积减少随时间预测抑郁症状。下一步将是阐明为什么结构改变会对与奖励相关的过程和相关症状产生影响。