重度抑郁症白质功能性连接体梯度功能障碍。

IF 2.9
Psychoradiology Pub Date : 2025-04-28 eCollection Date: 2025-01-01 DOI:10.1093/psyrad/kkaf008
Baoxin Yu, Xiaoyi Sun, Mingrui Xia
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引用次数: 0

摘要

背景:重性抑郁障碍(MDD)是一种以脑白质(WM)紊乱为主的常见精神障碍。虽然许多研究都集中在WM结构上,但对MDD中WM的功能失调组织仍然知之甚少。方法:使用来自48名MDD患者和68名健康对照(HC)的静息状态功能磁共振成像数据,我们表征了参与者的WM功能连接组梯度,并确定了MDD的整体和区域变化。此外,我们检验了梯度特性与抑郁症状严重程度之间的关系。最后进行外部验证和敏感性分析,以确保结果的可靠性。结果:两组WM连接组的主要梯度从大、上纵束延伸到钩侧束(UF)和丘脑前辐射(ATR),均表现为由浅到深的模式。与HC相比,MDD患者的梯度范围更窄,空间变异更小,表明WM层次收缩。在神经束特异性水平上,MDD患者在小钳子、左侧ATR和UF以及双侧扣带回和扣带回海马中表现出较低的梯度评分,而在大钳子、双侧下纵束和上纵束中表现出较高的梯度评分。WM束梯度模式解释了37.2%的临床严重程度差异,其中额枕下束、扣带海马、ATR、UF和皮质脊髓束的贡献最大。结论:这些发现突出了MDD中WM功能连接组梯度的改变及其与临床严重程度的关联,为该疾病的神经生物学机制和症状评估的潜在生物标志物提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
White matter functional connectome gradient dysfunction in major depressive disorder.

Background: Major depressive disorder (MDD) is a prevalent psychiatric disorder with disruptions in brain white matter (WM). While much research has focused on WM structure, the dysfunctional organization of WM in MDD remains poorly understood.

Methods: Using resting-state functional magnetic resonance imaging data from 48 MDD patients and 68 healthy controls (HC), we characterized the WM functional connectome gradients across participants and identified both global and regional alterations in MDD. Furthermore, we examined the relationship between gradient properties and depressive symptom severity. External validation and sensitivity analyses were finally conducted to ensure the reliability of results.

Results: The principal WM connectome gradient extended from the forceps major and superior longitudinal fasciculus to the uncinate fasciculus (UF) and anterior thalamic radiation (ATR), exhibiting a superficial-to-deep pattern in both groups. Compared to HC, MDD patients displayed a narrower gradient range and lower spatial variation, indicating a contracted WM hierarchy. At the tract-specific level, MDD patients exhibited lower gradient scores in the forceps minor, left ATR and UF, and bilateral cingulate gyrus and cingulum hippocampus, but higher gradient scores in the forceps major, bilateral inferior longitudinal fasciculus and superior longitudinal fasciculus. WM tract gradient patterns explained 37.2% of the variance in clinical severity, with the strongest contributions from the inferior fronto-occipital fasciculus, cingulum hippocampus, ATR, UF, and corticospinal tract.

Conclusions: These findings highlight altered WM functional connectome gradient in MDD and their association with clinical severity, offering novel insights into the neurobiological mechanisms of the disorder and potential biomarkers for symptom evaluation.

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