Decrease in walking ability with increased functional connectivity between multiple brain areas in Parkinson's disease: a functional near-infrared spectroscopy study.

IF 4.1 2区 医学 Q2 GERIATRICS & GERONTOLOGY
Frontiers in Aging Neuroscience Pub Date : 2024-10-30 eCollection Date: 2024-01-01 DOI:10.3389/fnagi.2024.1454598
Jin Wang, Jiewei Lu, Yue Wang, Zhilin Shu, Yuanyuan Cheng, Xinyuan Zhang, Yang Yu, Jianda Han, Zhizhong Zhu, Ningbo Yu, Jialing Wu
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引用次数: 0

Abstract

Introduction: Gait disturbances significantly impact the mobility and quality of life of individuals with Parkinson's disease (PD). This study aims to delve into the cortical mechanisms underlying gait disorders in PD, specifically focusing on the prefrontal cortex (PFC), premotor cortex (PMC), and primary somatosensory cortex (PSC).

Objective: To compare the functional connectivity of the PFC, PMC, and PSC regions during walking between individuals with PD and healthy controls.

Methods: The study included 30 individuals with PD (mean age 62.40 ± 7.16 years) and 22 healthy older adults (mean age 60.95 ± 6.34 years). All participants were requested to walk back and forth at a comfortable pace for 30 s over a 10-meter course three times. A mobile functional near-infrared spectroscopy (fNIRS) system was employed to evaluate the oxyhemoglobin concentration change (∆HbO2). To assess the interactions between the PFC, PMC, and PSC, the connectivity strength between different fNIRS channels was computed.

Results: Individuals with PD in the off-state exhibited significantly decreased walking speed and shorter stride length compared to the healthy controls. For six brain regions including the left (L) and right (R) PFC, PMC, and PSC, no significant differences in functional connectivity within each region were found between the PD and control groups. However, when it comes to the functional connectivity between every two regions, the PD group exhibited stronger functional connectivity than the control group in the LPFC-LPMC, LPFC-RPMC, LPFC-LPSC, RPFC-LPMC, RPFC-LPSC, LPMC-LPSC, LPMC-RPSC, and RPMC-RPSC. Positive correlations were found between gait performance (speed and stride length) and functional connectivity within the RPMC as well as between the RPMC and the RPSC.

Conclusion: Individuals with PD exhibit notable gait disturbances and increased functional connectivity in brain regions responsible for sensorimotor integration and motor function in their off-state. Strengthening the functional connectivity within the RPMC and between the RPMC and the RPSC could be a potential target for future treatments of gait impairments in PD.

帕金森病患者行走能力下降,但多个脑区之间的功能连接性增强:一项功能性近红外光谱研究。
导言:步态障碍严重影响帕金森病(PD)患者的活动能力和生活质量。本研究旨在深入研究帕金森病步态障碍的皮质机制,特别关注前额叶皮质(PFC)、运动前皮质(PMC)和初级体感皮质(PSC):比较帕金森氏症患者和健康对照组在行走过程中前额皮质、运动前皮质和初级躯体感觉皮质区域的功能连接性:研究对象包括 30 名帕金森病患者(平均年龄 62.40 ± 7.16 岁)和 22 名健康老年人(平均年龄 60.95 ± 6.34 岁)。所有参与者都被要求以舒适的步伐在 10 米长的路线上来回行走 30 秒,共三次。采用移动式功能性近红外光谱(fNIRS)系统评估氧合血红蛋白浓度变化(ΔHbO2)。为了评估前脑功能分区、后脑功能分区和前脑功能分区之间的相互作用,计算了不同 fNIRS 通道之间的连接强度:结果:与健康对照组相比,处于关闭状态的帕金森病患者的步行速度明显下降,步幅也更短。在包括左(L)和右(R)PFC、PMC 和 PSC 在内的六个脑区,帕金森病组和对照组在每个脑区内的功能连通性没有发现显著差异。然而,就每两个区域之间的功能连接性而言,帕金森病组在 LPFC-LPMC、LPFC-RPMC、LPFC-LPSC、RPFC-LPMC、RPFC-LPSC、LPMC-LPSC、LPMC-RPSC 和 RPMC-RPSC 的功能连接性强于对照组。研究发现,步态表现(速度和步幅)与RPMC内部以及RPMC与RPSC之间的功能连接呈正相关:结论:帕金森病患者表现出明显的步态障碍,在非运动状态下,负责感觉运动整合和运动功能的大脑区域的功能连接性增加。加强 RPMC 内部以及 RPMC 与 RPSC 之间的功能连接可能是未来治疗步态障碍的潜在目标。
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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来源期刊
Frontiers in Aging Neuroscience
Frontiers in Aging Neuroscience GERIATRICS & GERONTOLOGY-NEUROSCIENCES
CiteScore
6.30
自引率
8.30%
发文量
1426
期刊介绍: Frontiers in Aging Neuroscience is a leading journal in its field, publishing rigorously peer-reviewed research that advances our understanding of the mechanisms of Central Nervous System aging and age-related neural diseases. Specialty Chief Editor Thomas Wisniewski at the New York University School of Medicine is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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