Structure-function coupling as a correlate and potential biomarker of cognitive impairment in multiple sclerosis.

IF 3.1
Shanna D Kulik, Ilse M Nauta, Prejaas Tewarie, Ismail Koubiyr, Edwin van Dellen, Aurelie Ruet, Kim A Meijer, Brigit A de Jong, Cornelis J Stam, Arjan Hillebrand, Jeroen J G Geurts, Linda Douw, Menno M Schoonheim
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引用次数: 5

Abstract

Multiple sclerosis (MS) features extensive connectivity changes, but how structural and functional connectivity relate, and whether this relation could be a useful biomarker for cognitive impairment in MS is unclear. This study included 79 MS patients and 40 healthy controls (HCs). Patients were classified as cognitively impaired (CI) or cognitively preserved (CP). Structural connectivity was determined using diffusion MRI and functional connectivity using resting-state magnetoencephalography (MEG) data (theta, alpha1, and alpha2 bands). Structure-function coupling was assessed by correlating modalities, and further explored in frequency bands that significantly correlated with whole-brain structural connectivity. Functional correlates of short- and long-range structural connections (based on tract length) were then specifically assessed. Receiving operating curve analyses were performed on coupling values to identify biomarker potential. Only the theta band showed significant correlations between whole-brain structural and functional connectivity (rho = -0.26, p = 0.023, only in MS). Long-range structure-function coupling was stronger in CI patients compared to HCs (p = 0.005). Short-range coupling showed no group differences. Structure-function coupling was not a significant classifier of cognitive impairment for any tract length (short-range area under the curve (AUC) = 0.498, p = 0.976, long-range AUC = 0.611, p = 0.095). Long-range structure-function coupling was stronger in CI MS compared to HCs, but more research is needed to further explore this measure as biomarkers in MS.

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结构-功能耦合作为多发性硬化症认知障碍的相关和潜在生物标志物。
多发性硬化症(MS)具有广泛的连接改变,但结构和功能连接如何相关,以及这种关系是否可以作为MS认知障碍的有用生物标志物尚不清楚。本研究纳入79例MS患者和40例健康对照(hc)。患者分为认知受损(CI)和认知保留(CP)两组。结构连通性通过扩散MRI确定,功能连通性通过静息状态脑磁图(MEG)数据(theta, alpha1和alpha2波段)确定。通过相关模式评估结构-功能耦合,并在与全脑结构连通性显著相关的频带中进一步探索。然后专门评估了短期和长期结构连接的功能相关性(基于束长度)。对偶联值进行接收工作曲线分析,以确定生物标志物的潜力。只有theta波段显示全脑结构和功能连接之间存在显著相关性(rho = -0.26, p = 0.023,仅在MS中)。CI患者的远程结构-功能耦合比hcc患者更强(p = 0.005)。近程耦合无组间差异。结构-功能耦合在任何神经束长度(近距离曲线下面积(AUC) = 0.498, p = 0.976,远距离AUC = 0.611, p = 0.095)上都不是认知障碍的显著分类器。与hc相比,CI MS中的远程结构-功能耦合更强,但需要更多的研究来进一步探索这一指标在MS中的生物标志物作用。
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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