Sagol Brain Institute Tel Aviv, Wohl Institute for Advanced Imaging, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel; Sagol School of Neuroscience, Tel Aviv University, Tel Aviv, Israel; Departments of Comparative Medicine and Psychiatry, Yale University School of Medicine, New Haven, Connecticut; U.S. Department of Veterans Affairs National Center for Posttraumatic Stress Disorder, The Clinical Neurosciences Division, VA Connecticut Healthcare System, West Haven, Connecticut.
Sagol Brain Institute Tel Aviv, Wohl Institute for Advanced Imaging, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel; School of Psychological Sciences, Faculty of Social Sciences, Tel Aviv University, Tel Aviv, Israel.
Biol Psychiatry Cogn Neurosci Neuroimaging. 2022 Feb;7(2):150-161. doi: 10.1016/j.bpsc.2021.09.001. Epub 2021 Sep 15.
Processing negatively and positively valenced stimuli involves multiple brain regions including the amygdala and ventral striatum (VS). Posttraumatic stress disorder (PTSD) is often associated with hyperresponsivity to negatively valenced stimuli, yet recent evidence also points to deficient positive valence functioning. It is yet unclear what the relative contribution is of such opposing valence processing shortly after trauma to the development of chronic PTSD.
Neurobehavioral indicators of motivational positive versus negative valence sensitivities were longitudinally assessed in 171 adults (87 females, age = 34.19 ± 11.47 years) at 1, 6, and 14 months following trauma exposure (time point 1 [TP1], TP2, and TP3, respectively). Using a gambling functional magnetic resonance imaging paradigm, amygdala and VS functionality (activity and functional connectivity with the prefrontal cortex) in response to rewards versus punishments were assessed with relation to PTSD severity at different time points. The effect of valence processing was depicted behaviorally by the amount of risk taken to maximize reward.
PTSD severity at TP1 was associated with greater neural functionality in the amygdala (but not in the VS) toward punishments versus rewards, and with fewer risky choices. PTSD severity at TP3 was associated with decreased neural functionality in both the VS and the amygdala toward rewards versus punishments at TP1 (but not with risky behavior). Explainable machine learning revealed the primacy of VS-biased processing, over the amygdala, in predicting PTSD severity at TP3.
These results highlight the importance of biased neural responsivity to positive relative to negative motivational outcomes in PTSD development. Novel therapeutic strategies early after trauma may thus target both valence fronts.
处理正性和负性刺激涉及多个脑区,包括杏仁核和腹侧纹状体(VS)。创伤后应激障碍(PTSD)通常与对负性刺激的超反应性有关,但最近的证据也表明正性效价功能不足。创伤后不久,这种对立的效价处理对慢性 PTSD 的发展的相对贡献尚不清楚。
在创伤暴露后 1、6 和 14 个月(分别为时间点 1[TP1]、TP2 和 TP3),对 171 名成年人(87 名女性,年龄=34.19±11.47 岁)进行了纵向评估神经行为学指标,用于评估动机正性与负性效价敏感性。使用赌博功能磁共振成像范式,评估了奖赏与惩罚反应中杏仁核和 VS 的功能(活动和与前额叶皮层的功能连接)与不同时间点 PTSD 严重程度的关系。通过最大化奖励的风险承担量来描述效价处理的行为效应。
TP1 时的 PTSD 严重程度与惩罚相对于奖赏时杏仁核的神经功能增强有关,与冒险行为减少有关。TP3 时的 PTSD 严重程度与 TP1 时 VS 和杏仁核对奖赏的神经功能降低有关(但与冒险行为无关)。可解释的机器学习揭示了 VS 偏向处理相对于杏仁核在预测 TP3 时 PTSD 严重程度方面的首要作用。
这些结果强调了在 PTSD 发展过程中,对积极相对于消极动机结果的偏向神经反应的重要性。因此,创伤后早期的新治疗策略可能会同时针对这两个效价。