Colic Lejla, Sankar Anjali, Goldman Danielle A, Kim Jihoon A, Blumberg Hilary P
Department of Psychiatry and Psychotherapy, Jena University Hospital, Jena, Germany.
German Center for Mental Health, partner site Halle-Jena-Magdeburg, Jena, Germany.
Mol Psychiatry. 2025 Mar;30(3):1089-1101. doi: 10.1038/s41380-024-02758-4. Epub 2024 Sep 27.
Neurodevelopmental mechanisms are increasingly implicated in bipolar disorder (BD), highlighting the importance of their study in young persons. Neuroimaging studies have demonstrated a central role for frontotemporal corticolimbic brain systems that subserve processing and regulation of emotions, and processing of reward in adults with BD. As adolescence and young adulthood (AYA) is a time when fully syndromal BD often emerges, and when these brain systems undergo dynamic maturational changes, the AYA epoch is implicated as a critical period in the neurodevelopment of BD. Functional magnetic resonance imaging (fMRI) studies can be especially informative in identifying the functional neuroanatomy in adolescents and young adults with BD (BD) and at high risk for BD (HR-BD) that is related to acute mood states and trait vulnerability to the disorder. The identification of early emerging brain differences, trait- and state-based, can contribute to the elucidation of the developmental neuropathophysiology of BD, and to the generation of treatment and prevention targets. In this critical review, fMRI studies of BD and HR-BD are discussed, and a preliminary neurodevelopmental model is presented based on a convergence of literature that suggests early emerging dysfunction in subcortical (e.g., amygdalar, striatal, thalamic) and caudal and ventral cortical regions, especially ventral prefrontal cortex (vPFC) and insula, and connections among them, persisting as trait-related features. More rostral and dorsal cortical alterations, and bilaterality progress later, with lateralization, and direction of functional imaging findings differing by mood state. Altered functioning of these brain regions, and regions they are strongly connected to, are implicated in the range of symptoms seen in BD, such as the insula in interoception, precentral gyrus in motor changes, and prefrontal cortex in cognition. Current limitations, and outlook on the future use of neuroimaging evidence to inform interventions and prevent the onset of mood episodes in BD, are outlined.
神经发育机制越来越多地与双相情感障碍(BD)相关,凸显了在年轻人中研究它们的重要性。神经影像学研究表明,额颞叶皮质边缘脑系统在BD成年患者的情绪处理与调节以及奖赏处理中发挥着核心作用。由于青少年和青年期(AYA)是完全综合征性BD常出现的时期,且这些脑系统会经历动态成熟变化,因此AYA时期被认为是BD神经发育的关键时期。功能磁共振成像(fMRI)研究在识别BD青少年和青年患者(BD)以及BD高风险患者(HR - BD)中与急性情绪状态和疾病特质易感性相关的功能性神经解剖结构方面可能特别有意义。识别基于特质和状态的早期出现的脑差异,有助于阐明BD的发育性神经病理生理学,并有助于生成治疗和预防靶点。在这篇批判性综述中,讨论了BD和HR - BD的fMRI研究,并基于文献综述提出了一个初步的神经发育模型,该模型表明皮质下(如杏仁核、纹状体、丘脑)以及尾侧和腹侧皮质区域,特别是腹侧前额叶皮质(vPFC)和脑岛,以及它们之间的连接存在早期出现的功能障碍,并作为与特质相关的特征持续存在。更靠前和背侧的皮质改变以及双侧性变化出现较晚,伴有功能成像结果的偏侧化,且其方向因情绪状态而异。这些脑区以及与它们紧密相连的脑区功能改变,与BD中出现的一系列症状有关,例如脑岛与内感受、中央前回与运动变化、前额叶皮质与认知有关。概述了当前的局限性以及未来利用神经影像学证据为干预措施提供信息并预防BD情绪发作的前景。