Laureate Institute for Brain Research, 6655 South Yale Avenue, Tulsa, OK 74136, USA.
Laureate Institute for Brain Research, 6655 South Yale Avenue, Tulsa, OK 74136, USA; University of Tulsa, 800 South Tucker Drive, Tulsa, OK 74104, USA.
J Affect Disord. 2024 Dec 1;366:98-105. doi: 10.1016/j.jad.2024.08.143. Epub 2024 Aug 24.
Dysregulation of fear processing through altered sensitivity to threat is thought to contribute to the development of anxiety disorders and major depressive disorder (MDD). However, fewer studies have examined fear processing in MDD than in anxiety disorders. The current study used propensity matching to examine the hypothesis that comorbid MDD and anxiety (AnxMDD) shows greater neural correlates of fear processing than MDD, suggesting that the co-occurrence of AnxMDD is exemplified by exaggerated defense related processes.
195 individuals with MDD (N = 65) or AnxMDD (N = 130) were recruited from the community and completed multi-level assessments, including a Pavlovian fear learning task during functional imaging. Visual images paired with threat (conditioned stimuli: CS+) were compared to stimuli not paired with threat (CS-).
MDD and AnxMDD showed significantly different patterns of activation for CS+ vs CS- in the dorsal anterior insula/inferior frontal gyrus (partial eta squared; ηp = 0.02), dorsolateral prefrontal cortex (ηp = 0.01) and dorsal anterior/mid cingulate cortex (ηp = 0.01). These differences were driven by greater activation to the CS+ in AnxMDD versus MDD.
Limitations include the cross-sectional design, a scream US rather than shock and half the number of MDD as AnxMDD participants.
AnxMDD showed a pattern of increased activation in regions identified with fear processing. Effects were consistently driven by threat, further suggesting fear signaling as the emergent target process. Differences emerged in regions associated with salience processing, attentional orienting/conflict, self-relevant processing and executive functioning in comorbid anxiety and depression, thereby highlighting potential treatment targets for this prevalent and treatment resistant group.
通过改变对威胁的敏感性来调节恐惧处理,被认为是导致焦虑症和重度抑郁症(MDD)发展的原因。然而,与焦虑症相比,研究MDD 中恐惧处理的研究较少。本研究使用倾向匹配来检验以下假设:共病 MDD 和焦虑症(AnxMDD)表现出更大的恐惧处理神经相关性,表明 AnxMDD 的共同发生是以夸张的防御相关过程为特征。
从社区招募了 195 名 MDD(N=65)或 AnxMDD(N=130)患者,他们完成了多层次评估,包括功能成像期间的 Pavlovian 恐惧学习任务。与威胁配对的视觉图像(条件刺激:CS+)与未与威胁配对的刺激(CS-)进行比较。
MDD 和 AnxMDD 在背侧前岛叶/额下回(部分 eta 平方;ηp=0.02)、背外侧前额叶皮层(ηp=0.01)和背侧前/中扣带皮层(ηp=0.01)中,CS+与 CS-的激活模式存在显著差异。这些差异是由 AnxMDD 中 CS+的激活高于 MDD 引起的。
局限性包括横断面设计、尖叫 US 而非冲击以及 MDD 参与者数量为 AnxMDD 参与者的一半。
AnxMDD 在与恐惧处理相关的区域显示出增加的激活模式。这些影响始终由威胁驱动,进一步表明恐惧信号作为新兴的目标过程。在共病焦虑和抑郁中,突显处理、注意力定向/冲突、自我相关处理和执行功能相关的区域出现差异,从而突出了针对这一普遍存在且治疗抵抗的人群的潜在治疗靶点。