Lower-limb express visuomotor responses are spared in Parkinson’s disease during step initiation from a stable position

IF 3.6 3区 医学 Q1 CLINICAL NEUROLOGY
Lucas S. Billen , Jorik Nonnekes , Brian D. Corneil , Vivian Weerdesteyn
{"title":"Lower-limb express visuomotor responses are spared in Parkinson’s disease during step initiation from a stable position","authors":"Lucas S. Billen ,&nbsp;Jorik Nonnekes ,&nbsp;Brian D. Corneil ,&nbsp;Vivian Weerdesteyn","doi":"10.1016/j.clinph.2025.2110988","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>While motor impairments in Parkinson’s Disease are well-studied, less is known about how people with Parkinson’s Disease (PwPD) can nevertheless rapidly transform vision into action. These transformations can be studied by measuring express visuomotor responses (EVRs), which are stimulus-directed bursts of muscle activity thought to originate from the superior colliculus, reaching the periphery via the tecto-reticulospinal pathway.</div></div><div><h3>Methods</h3><div>We examined EVRs in the lower limbs during goal-directed step initiation in 20 PwPD and 20 healthy controls (HC). As lower-limb EVRs in the young have been shown to interact with postural control – which are often affected in PwPD − we manipulated postural demands by varying stance width and target location.</div></div><div><h3>Results</h3><div>Under low postural demand, both groups expressed consistent EVRs. EVR magnitudes were significantly higher in PwPD, yet decreased with greater disease severity. Under high postural demands, EVRs were suppressed and followed by strong anticipatory postural adjustments, which were smaller in PwPD compared to HC.</div></div><div><h3>Conclusions</h3><div>The circuit mediating EVRs may be upregulated in early PD to compensate for motor deficits experienced in daily life, but becomes progressively impaired as PD advances.</div></div><div><h3>Significance</h3><div>These findings provide novel insight into the neural underpinnings of rapid stepping in health and disease.</div></div>","PeriodicalId":10671,"journal":{"name":"Clinical Neurophysiology","volume":"179 ","pages":"Article 2110988"},"PeriodicalIF":3.6000,"publicationDate":"2025-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Neurophysiology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1388245725008405","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Objective

While motor impairments in Parkinson’s Disease are well-studied, less is known about how people with Parkinson’s Disease (PwPD) can nevertheless rapidly transform vision into action. These transformations can be studied by measuring express visuomotor responses (EVRs), which are stimulus-directed bursts of muscle activity thought to originate from the superior colliculus, reaching the periphery via the tecto-reticulospinal pathway.

Methods

We examined EVRs in the lower limbs during goal-directed step initiation in 20 PwPD and 20 healthy controls (HC). As lower-limb EVRs in the young have been shown to interact with postural control – which are often affected in PwPD − we manipulated postural demands by varying stance width and target location.

Results

Under low postural demand, both groups expressed consistent EVRs. EVR magnitudes were significantly higher in PwPD, yet decreased with greater disease severity. Under high postural demands, EVRs were suppressed and followed by strong anticipatory postural adjustments, which were smaller in PwPD compared to HC.

Conclusions

The circuit mediating EVRs may be upregulated in early PD to compensate for motor deficits experienced in daily life, but becomes progressively impaired as PD advances.

Significance

These findings provide novel insight into the neural underpinnings of rapid stepping in health and disease.
帕金森氏病在从稳定位置开始的步进过程中,下肢表达视觉运动反应得以保留
虽然帕金森病的运动损伤研究得很好,但人们对帕金森病(PwPD)患者如何将视力迅速转化为行动知之甚少。这些转变可以通过测量视觉运动表达反应(evr)来研究,evr是一种刺激导向的肌肉活动爆发,被认为起源于上丘,通过构造-网状脊髓通路到达外周。方法对20例PwPD患者和20例健康对照(HC)进行目标定向步启动过程中下肢evr的检测。由于年轻人的下肢evr已被证明与姿势控制相互作用-姿势控制在PwPD中经常受到影响-我们通过改变立场宽度和目标位置来操纵姿势需求。结果在低体位需求下,两组evr表达一致。PwPD患者EVR值显著升高,但随疾病严重程度的增加而降低。在高姿势要求下,evr被抑制,随后是强烈的预期姿势调整,PwPD的evr比HC小。结论在帕金森病早期,介导evr的神经回路可能被上调,以补偿日常生活中经历的运动缺陷,但随着帕金森病的进展,神经回路会逐渐受损。这些发现为健康和疾病快速发展的神经基础提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Clinical Neurophysiology
Clinical Neurophysiology 医学-临床神经学
CiteScore
8.70
自引率
6.40%
发文量
932
审稿时长
59 days
期刊介绍: As of January 1999, The journal Electroencephalography and Clinical Neurophysiology, and its two sections Electromyography and Motor Control and Evoked Potentials have amalgamated to become this journal - Clinical Neurophysiology. Clinical Neurophysiology is the official journal of the International Federation of Clinical Neurophysiology, the Brazilian Society of Clinical Neurophysiology, the Czech Society of Clinical Neurophysiology, the Italian Clinical Neurophysiology Society and the International Society of Intraoperative Neurophysiology.The journal is dedicated to fostering research and disseminating information on all aspects of both normal and abnormal functioning of the nervous system. The key aim of the publication is to disseminate scholarly reports on the pathophysiology underlying diseases of the central and peripheral nervous system of human patients. Clinical trials that use neurophysiological measures to document change are encouraged, as are manuscripts reporting data on integrated neuroimaging of central nervous function including, but not limited to, functional MRI, MEG, EEG, PET and other neuroimaging modalities.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信