额颞叶痴呆症患者的宏观功能网络组织受到破坏

IF 9.6 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
A. Bouzigues, V. Godefroy, V. Le Du, L. L. Russell, M. Houot, I. Le Ber, B. Batrancourt, R. Levy, J. D. Warren, J. D. Rohrer, D. S. Margulies, R. Migliaccio
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引用次数: 0

摘要

神经退行性痴呆症对高阶认知和行为功能影响深远。通过皮层梯度研究宏观功能网络可为了解神经退行性痴呆的过程和整体大脑功能提供有价值的见解。这种方法可以探索单模态-多模态分化以及大脑功能网络之间错综复杂的相互作用。我们将皮层梯度绘图应用于额叶痴呆(FTD)患者(行为-bvFTD、非流利和语义)和健康对照组的静息态功能磁共振成像数据。在健康对照组中,主梯度最大程度地区分了感觉运动网络和默认模式网络(DMN),次梯度区分了视觉网络和显著性网络(SN)。在所有 FTD 变体中,主梯度的单模态-多模态分化被破坏。然而,次梯度出现了广泛的破坏,影响了所有网络之间的相互作用,特别是在bvFTD中,而语义变体和非流利变体则在边缘和感觉运动网络中表现出更多的局灶性改变。此外,所有患者的视觉网络都出现了反应性和/或补偿性变化。重要的是,这些破坏超出了萎缩的分布范围,并与bvFTD患者的症状有关。总之,最佳的大脑功能需要网络以分离但协作的方式运行。在 FTD 患者中,我们的研究结果表明,网络之间的崩溃和分化丧失并不能完全用萎缩来解释。这些特定的皮层梯度指纹可作为一种功能特征,用于识别神经退行性疾病的早期变化或潜在的代偿过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Disruption of macroscale functional network organisation in patients with frontotemporal dementia

Disruption of macroscale functional network organisation in patients with frontotemporal dementia

Neurodegenerative dementias have a profound impact on higher-order cognitive and behavioural functions. Investigating macroscale functional networks through cortical gradients provides valuable insights into the neurodegenerative dementia process and overall brain function. This approach allows for the exploration of unimodal-multimodal differentiation and the intricate interplay between functional brain networks. We applied cortical gradients mapping to resting-state functional MRI data of patients with frontotemporal dementia (FTD) (behavioural-bvFTD, non-fluent and semantic) and healthy controls. In healthy controls, the principal gradient maximally distinguished sensorimotor from default-mode network (DMN) and the secondary gradient visual from salience network (SN). In all FTD variants, the principal gradient’s unimodal-multimodal differentiation was disrupted. The secondary gradient, however, showed widespread disruptions impacting the interactions among all networks specifically in bvFTD, while semantic and non-fluent variants exhibited more focal alterations in limbic and sensorimotor networks. Additionally, the visual network showed responsive and/or compensatory changes in all patients. Importantly, these disruptions extended beyond atrophy distribution and related to symptomatology in patients with bvFTD. In conclusion, optimal brain function requires networks to operate in a segregated yet collaborative manner. In FTD, our findings indicate a collapse and loss of differentiation between networks not solely explained by atrophy. These specific cortical gradients’ fingerprints could serve as a functional signature for identifying early changes in neurodegenerative diseases or potential compensatory processes.

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来源期刊
Molecular Psychiatry
Molecular Psychiatry 医学-精神病学
CiteScore
20.50
自引率
4.50%
发文量
459
审稿时长
4-8 weeks
期刊介绍: Molecular Psychiatry focuses on publishing research that aims to uncover the biological mechanisms behind psychiatric disorders and their treatment. The journal emphasizes studies that bridge pre-clinical and clinical research, covering cellular, molecular, integrative, clinical, imaging, and psychopharmacology levels.
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