A prefrontal thalamocortical readout for conflict-related executive dysfunction in schizophrenia.

IF 11.7 1区 医学 Q1 CELL BIOLOGY
Anna S Huang, Ralf D Wimmer, Norman H Lam, Bin A Wang, Sahil Suresh, Maxwell J Roeske, Burkhard Pleger, Michael M Halassa, Neil D Woodward
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引用次数: 0

Abstract

Executive dysfunction is a prominent feature of schizophrenia and may drive core symptoms. Dorsolateral prefrontal cortex (dlPFC) deficits have been linked to schizophrenia executive dysfunction, but mechanistic details critical for treatment development remain unclear. Here, capitalizing on recent animal circuit studies, we develop a task predicted to engage human dlPFC and its interactions with the mediodorsal thalamus (MD). We find that individuals with schizophrenia exhibit selective performance deficits when attention is guided by conflicting cues. Task performance correlates with lateralized MD-dlPFC functional connectivity, identifying a neural readout that predicts susceptibility to conflict during working memory in a larger independent schizophrenia cohort. In healthy subjects performing a probabilistic reversal task, this MD-dlPFC network predicts switching behavior. Overall, our three independent experiments introduce putative biomarkers for executive function in schizophrenia and highlight animal circuit studies as inspiration for the development of clinically relevant readouts.

精神分裂症患者冲突相关执行功能障碍的前额丘脑皮层读数。
执行功能障碍是精神分裂症的一个突出特征,并可能导致核心症状。背外侧前额叶皮层(dlPFC)缺陷与精神分裂症的执行功能障碍有关,但对治疗发展至关重要的机制细节仍不清楚。在此,我们利用最近的动物回路研究,开发了一项任务,该任务预计会调动人类前额叶皮层(dlPFC)及其与丘脑内侧(MD)的相互作用。我们发现精神分裂症患者在注意力受冲突线索引导时会表现出选择性表现缺陷。任务表现与侧向 MD-dlPFC 功能连通性相关,从而在更大的独立精神分裂症队列中确定了预测工作记忆中易受冲突影响的神经读数。在执行概率反转任务的健康受试者中,这种 MD-dlPFC 网络可预测切换行为。总之,我们的三项独立实验引入了精神分裂症执行功能的潜在生物标志物,并强调了动物回路研究对开发临床相关读数的启发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cell Reports Medicine
Cell Reports Medicine Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
CiteScore
15.00
自引率
1.40%
发文量
231
审稿时长
40 days
期刊介绍: Cell Reports Medicine is an esteemed open-access journal by Cell Press that publishes groundbreaking research in translational and clinical biomedical sciences, influencing human health and medicine. Our journal ensures wide visibility and accessibility, reaching scientists and clinicians across various medical disciplines. We publish original research that spans from intriguing human biology concepts to all aspects of clinical work. We encourage submissions that introduce innovative ideas, forging new paths in clinical research and practice. We also welcome studies that provide vital information, enhancing our understanding of current standards of care in diagnosis, treatment, and prognosis. This encompasses translational studies, clinical trials (including long-term follow-ups), genomics, biomarker discovery, and technological advancements that contribute to diagnostics, treatment, and healthcare. Additionally, studies based on vertebrate model organisms are within the scope of the journal, as long as they directly relate to human health and disease.
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