Grogans Shannon E, DeYoung Kathryn A, Hur Juyoen, Anderson Allegra S, Islam Samiha, Kim Hyung Cho, Wedlock Jazmine, Craig Logan E, Tillman Rachael M, Das Sanjana, Kuhn Manuel, Conway Christopher C, Fox Andrew F, Smith Jason F, Shackman Alexander J
Department of Psychology, University of Maryland.
Department of Psychology, Yonsei University, Seoul, Republic of Korea.
bioRxiv. 2025 Jun 12:2025.06.11.659182. doi: 10.1101/2025.06.11.659182.
Anxiety, depression, and related internalizing illnesses are a leading burden on global public health, and often emerge during times of stress. Yet the underlying neurobiology has remained enigmatic, hindering treatment development.
Here we used a combination of tools-including a well-established threat-anticipation fMRI paradigm and longitudinal assessments of internalizing symptoms and negative life events (NLEs)-to identify the neural systems associated with future internalizing illness in a risk-enriched sample of 224 emerging adults followed for 2.5 years. We performed parallel analyses in an overlapping sample of 209 participants who completed a popular threat-related faces paradigm.
Here we show that heightened reactivity to uncertain-threat anticipation in the bed nucleus of the stria terminalis and the periaqueductal gray is associated with a worsening longitudinal course of broadband internalizing symptoms among individuals with low levels of NLE exposure. These associations were specific to uncertain threat and generally remained significant when controlling for concurrent measures of threat-elicited distress or psychophysiological arousal, highlighting the added value of the neuroimaging measures. Symptom trajectories were unrelated to amygdala and frontocortical reactivity to anticipated threat. Contrary to past research, amygdala reactivity to threat-related faces was unrelated to future symptoms.
These observations provide a novel neurobiological framework for conceptualizing transdiagnostic internalizing risk and lay the groundwork for mechanistic and therapeutics research. A racially diverse, risk-enriched sample and pre-registered, best-practices approach enhance confidence in the robustness and translational relevance of these results.
焦虑、抑郁及相关内化性疾病是全球公共卫生的主要负担,且常在压力时期出现。然而,其潜在的神经生物学机制一直不明,阻碍了治疗方法的开发。
在此,我们运用了多种工具,包括成熟的威胁预期功能磁共振成像范式以及对内化症状和负面生活事件(NLEs)的纵向评估,以在224名处于风险增加状态的新兴成年人样本中识别与未来内化性疾病相关的神经系统,该样本随访了2.5年。我们在209名完成了一种常见的与威胁相关的面部范式的参与者的重叠样本中进行了平行分析。
我们发现,终纹床核和导水管周围灰质对不确定威胁预期的反应性增强,与低水平NLE暴露个体的宽带内化症状纵向病程恶化相关。这些关联特定于不确定威胁,并且在控制威胁引发的痛苦或心理生理唤醒的同时测量时通常仍具有显著性,突出了神经影像学测量的附加价值。症状轨迹与杏仁核和前额叶皮质对预期威胁的反应性无关。与过去的研究相反,杏仁核对威胁相关面部的反应性与未来症状无关。
这些观察结果为概念化跨诊断内化风险提供了一个新的神经生物学框架,并为机制和治疗研究奠定了基础。一个种族多样、风险增加的样本以及预先注册的最佳实践方法增强了对这些结果的稳健性和转化相关性的信心。