Aberrant brain dynamics of large-scale functional networks across schizophrenia and mood disorder

IF 3.4 2区 医学 Q2 NEUROIMAGING
Takuya Ishida , Shinichi Yamada , Kasumi Yasuda , Shinya Uenishi , Atsushi Tamaki , Michiyo Tabata , Natsuko Ikeda , Shun Takahashi , Sohei Kimoto
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引用次数: 0

Abstract

Introduction

The dynamics of large-scale networks, which are known as distributed sets of functionally synchronized brain regions and include the visual network (VIN), somatomotor network (SMN), dorsal attention network (DAN), salience network (SAN), limbic network (LIN), frontoparietal network (FPN), and default mode network (DMN), play important roles in emotional and cognitive processes in humans. Although disruptions in these large-scale networks are considered critical for the pathophysiological mechanisms of psychiatric disorders, their role in psychiatric disorders remains unknown. We aimed to elucidate the aberrant dynamics across large-scale networks in patients with schizophrenia (SZ) and mood disorders.

Methods

We performed energy-landscape analysis to investigate the aberrant brain dynamics of seven large-scale networks across 50 healthy controls (HCs), 36 patients with SZ, and 42 patients with major depressive disorder (MDD) recruited at Wakayama Medical University. We identified major patterns of brain activity using energy-landscape analysis and estimated their duration, occurrence, and ease of transition.

Results

We identified four major brain activity patterns that were characterized by the activation patterns of the DMN and VIN (state 1, DMN (-) VIN (-); state 2, DMN (+) VIN (+); state 3, DMN (-) VIN (+); and state 4, DMN (+) VIN (-)). The duration of state 1 and the occurrence of states 1 and 2 were shorter in the SZ group than in HCs and the MDD group, and the duration of state 3 was longer in the SZ group. The ease of transition between states 3 and 4 was larger in the SZ group than in the HCs and the MDD group. The ease of transition from state 3 to state 4 was negatively associated with verbal fluency in patients with SZ. The current study showed that the brain dynamics was more disrupted in SZ than in MDD.

Conclusions

Energy-landscape analysis revealed aberrant brain dynamics across large-scale networks between SZ and MDD and their associations with cognitive abilities in SZ, which cannot be captured by conventional functional connectivity analyses. These results provide new insights into the pathophysiological mechanisms underlying SZ and mood disorders.

精神分裂症和心境障碍患者大脑大尺度功能网络动态变化异常
导言大尺度网络被称为功能同步脑区的分布式集合,包括视觉网络(VIN)、躯体运动网络(SMN)、背侧注意网络(DAN)、显著性网络(SAN)、边缘网络(LIN)、额顶网络(FPN)和默认模式网络(DMN)。虽然这些大规模网络的破坏被认为是精神疾病病理生理机制的关键,但它们在精神疾病中的作用仍然未知。我们对和歌山医科大学招募的 50 名健康对照(HCs)、36 名精神分裂症(SZ)患者和 42 名重度抑郁障碍(MDD)患者进行了能量景观分析,研究了七个大规模网络的异常大脑动态。我们利用能量景观分析确定了大脑活动的主要模式,并估计了它们的持续时间、发生率和转换难易程度。结果我们确定了四种主要的大脑活动模式,它们以 DMN 和 VIN 的激活模式为特征(状态 1,DMN (-) VIN (-);状态 2,DMN (+) VIN (+);状态 3,DMN (-) VIN (+);状态 4,DMN (+) VIN (-))。与 HCs 和 MDD 组相比,SZ 组的状态 1 持续时间以及状态 1 和 2 的出现时间更短,而 SZ 组的状态 3 持续时间更长。与 HCs 和 MDD 组相比,SZ 组在状态 3 和状态 4 之间的转换难度更大。SZ患者从状态3过渡到状态4的难易程度与言语流畅性呈负相关。结论能量景观分析揭示了SZ和MDD之间大规模网络的异常脑动力学及其与SZ认知能力的关联,而传统的功能连通性分析无法捕捉到这一点。这些结果为研究 SZ 和情绪障碍的病理生理机制提供了新的视角。
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来源期刊
Neuroimage-Clinical
Neuroimage-Clinical NEUROIMAGING-
CiteScore
7.50
自引率
4.80%
发文量
368
审稿时长
52 days
期刊介绍: NeuroImage: Clinical, a journal of diseases, disorders and syndromes involving the Nervous System, provides a vehicle for communicating important advances in the study of abnormal structure-function relationships of the human nervous system based on imaging. The focus of NeuroImage: Clinical is on defining changes to the brain associated with primary neurologic and psychiatric diseases and disorders of the nervous system as well as behavioral syndromes and developmental conditions. The main criterion for judging papers is the extent of scientific advancement in the understanding of the pathophysiologic mechanisms of diseases and disorders, in identification of functional models that link clinical signs and symptoms with brain function and in the creation of image based tools applicable to a broad range of clinical needs including diagnosis, monitoring and tracking of illness, predicting therapeutic response and development of new treatments. Papers dealing with structure and function in animal models will also be considered if they reveal mechanisms that can be readily translated to human conditions.
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