University of Pittsburgh, Department of Psychiatry, United States of America.
University of Pittsburgh, Department of Psychiatry, United States of America.
J Affect Disord. 2023 Apr 14;327:128-136. doi: 10.1016/j.jad.2023.01.118. Epub 2023 Feb 3.
Adolescent depression is associated with both dysfunction in neural reward processing and peripheral inflammatory markers (PIMs), such as interleukin-6 (IL-6), C-reactive-protein (CRP), and tumor-necrosis factor alpha (TNFα). Few adolescent studies have examined neural-inflammatory marker associations and associated behavioral correlates, which would contribute to a better understanding of developmental processes linked to depression.
36 adolescents at high risk of depression completed an fMRI reward task (during anticipation and outcome), blood draw for PIMs (IL-6, CRP, and TNFα), and a behavioral task assessing motivation to expend effort. Analyses examined associations of task-dependent functional connectivity (FC; ventral striatum to frontal and default mode network brain regions), and if the interaction of PIMs and task-dependent FC predicted motivation to expend effort.
For anticipation contrast, TNFα was associated with increased task-dependent FC between the LVS and PCC/vmPFC. In moderation analyses, for anticipation contrasts, the combination of higher IL-6 and stronger FC (LVS-precuneus/PCC) was associated with lower motivation to expend effort, while for outcome contrasts, the combination of higher IL-6 and stronger FC (VS-precuneus/PCC) was associated with greater motivation to expend effort.
Our findings in adolescents during an important developmental time period suggest that PIMs are directly linked to greater FC between the VS and DMN brain regions during win anticipation, consistent with prior studies. Effects of PIMs on motivation to expend effort may vary the strength/type of neural reward processing (anticipation or outcome), which could guide better understanding how inflammatory markers and neural reward substrates contribute to development of depression in high-risk adolescents.
青少年抑郁症与神经奖励处理功能障碍和外周炎症标志物(PIMs)有关,如白细胞介素-6(IL-6)、C 反应蛋白(CRP)和肿瘤坏死因子 alpha(TNFα)。很少有青少年研究检查神经炎症标志物的关联及其相关的行为相关性,这将有助于更好地理解与抑郁症相关的发育过程。
36 名有抑郁高风险的青少年完成了 fMRI 奖励任务(在预期和结果期间)、抽取血液以测量 PIMs(IL-6、CRP 和 TNFα),并进行了一项评估努力意愿的行为任务。分析检查了任务相关功能连接(FC;腹侧纹状体到额叶和默认模式网络大脑区域)的关联,以及 PIMs 和任务相关 FC 的相互作用是否预测努力意愿。
对于预期对比,TNFα与 LVS 和 PCC/vmPFC 之间增加的任务相关 FC 相关。在调节分析中,对于预期对比,较高的 IL-6 和较强的 FC(LVS-楔前叶/PCC)的组合与较低的努力意愿相关,而对于结果对比,较高的 IL-6 和较强的 FC(VS-楔前叶/PCC)的组合与更大的努力意愿相关。
我们在青少年中的发现表明,在一个重要的发育时期,PIMs 直接与 VS 和 DMN 大脑区域之间更大的 FC 相关,这与之前的研究一致。PIMs 对努力意愿的影响可能因神经奖励处理(预期或结果)的强度/类型而异,这可以帮助更好地理解炎症标志物和神经奖励底物如何导致高风险青少年的抑郁发展。