Seda Sacu, Magda Dubois, Frank H Hezemans, Pascal-M Aggensteiner, Maximilian Monninger, Daniel Brandeis, Tobias Banaschewski, Tobias U Hauser, Nathalie E Holz
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Psychopathology measures were collected at the time of functional magnetic resonance imaging investigation and during the COVID-19 pandemic. We applied a principal component analysis to capture common variations across 7 adversity measures. The resulting adversity factors (factor 1: postnatal psychosocial adversities and prenatal maternal smoking; factor 2: prenatal maternal stress and obstetric adversity; factor 3: lower maternal stimulation) were linked with psychopathology and neural responses in the core reward network using multiple regression analysis.</p><p><strong>Results: </strong>We found that the adversity dimension primarily informed by lower maternal stimulation was linked to lower expected value representation in the right putamen, right nucleus accumbens, and anterior cingulate cortex. 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引用次数: 0
摘要
背景:早期的不良经历被认为会影响奖赏学习和决策的基本过程。然而,在逆境背景下调查这些回路的计算神经影像学研究并不多,而且仅限于在青少年样本中进行的研究,因此长期影响尚未得到探讨:利用一项纵向出生队列研究的数据(n=156,87 名女性),我们调查了逆境与奖赏学习计算标记(即预期值 (EV)、预测错误)之间的关联。所有参与者在33岁时都完成了一项基于fMRI的被动回避任务。我们在进行 fMRI 研究时和 COVID-19 大流行期间收集了心理病理学测量数据。我们采用主成分分析来捕捉七种逆境测量的共同变异。通过多元回归分析,我们将得出的逆境因子(因子-1:产后社会心理逆境和产前母亲吸烟;因子-2:产前母亲压力和产科逆境;因子-3:较低的母亲刺激)与精神病理学和核心奖赏网络的神经反应联系起来:结果:我们发现,主要由较低的母体刺激引起的逆境维度与右侧丘脑、右侧伏隔核(NAcc)和前扣带回皮层中较低的 EV 表征有关。在COVID-19大流行期间,右侧NAcc中的EV编码进一步介导了这一逆境维度与精神病理学之间的关系,并预测了较高的孤僻症状:我们的研究结果表明,在照顾者环境中的早期逆境经历可能会对奖赏相关脑区的奖赏学习产生长期的破坏性影响,而奖赏学习可能与次优决策相关,从而可能增加发展为精神病理学的脆弱性。
Early-Life Adversities Are Associated With Lower Expected Value Signaling in the Adult Brain.
Background: Early adverse experiences are assumed to affect fundamental processes of reward learning and decision making. However, computational neuroimaging studies investigating these circuits in the context of adversity are sparse and limited to studies conducted in adolescent samples, leaving the long-term effects unexplored.
Methods: Using data from a longitudinal birth cohort study (n = 156; 87 female), we investigated associations between adversities and computational markers of reward learning (i.e., expected value, prediction errors). At age 33 years, all participants completed a functional magnetic resonance imaging-based passive avoidance task. Psychopathology measures were collected at the time of functional magnetic resonance imaging investigation and during the COVID-19 pandemic. We applied a principal component analysis to capture common variations across 7 adversity measures. The resulting adversity factors (factor 1: postnatal psychosocial adversities and prenatal maternal smoking; factor 2: prenatal maternal stress and obstetric adversity; factor 3: lower maternal stimulation) were linked with psychopathology and neural responses in the core reward network using multiple regression analysis.
Results: We found that the adversity dimension primarily informed by lower maternal stimulation was linked to lower expected value representation in the right putamen, right nucleus accumbens, and anterior cingulate cortex. Expected value encoding in the right nucleus accumbens further mediated the relationship between this adversity dimension and psychopathology and predicted higher withdrawn symptoms during the COVID-19 pandemic.
Conclusions: Our results suggested that early adverse experiences in caregiver context might have a long-term disruptive effect on reward learning in reward-related brain regions, which can be associated with suboptimal decision making and thereby may increase the vulnerability of developing psychopathology.
期刊介绍:
Biological Psychiatry is an official journal of the Society of Biological Psychiatry and was established in 1969. It is the first journal in the Biological Psychiatry family, which also includes Biological Psychiatry: Cognitive Neuroscience and Neuroimaging and Biological Psychiatry: Global Open Science. The Society's main goal is to promote excellence in scientific research and education in the fields related to the nature, causes, mechanisms, and treatments of disorders pertaining to thought, emotion, and behavior. To fulfill this mission, Biological Psychiatry publishes peer-reviewed, rapid-publication articles that present new findings from original basic, translational, and clinical mechanistic research, ultimately advancing our understanding of psychiatric disorders and their treatment. The journal also encourages the submission of reviews and commentaries on current research and topics of interest.