Frontal subcortical executive dysfunction and minor hallucinations in Parkinson's disease are linked to sensitivity to somatomotor conflicts.

IF 5 3区 医学 Q2 NEUROSCIENCES
Jevita Potheegadoo, Léa F Duong Phan Thanh, Fosco Bernasconi, Nathalie H Meyer, Laurent Jenni, Marie E Maradan-Gachet, Cyrille Stucker, Herberto Dhanis, Sabina Catalano Chiuvé, Julien F Bally, Mayte Castro Jimenez, Vanessa Fleury, Judit Horvath, Benoît Wicki, Javier Pagonabarraga Mora, Paul Krack, Olaf Blanke
{"title":"Frontal subcortical executive dysfunction and minor hallucinations in Parkinson's disease are linked to sensitivity to somatomotor conflicts.","authors":"Jevita Potheegadoo, Léa F Duong Phan Thanh, Fosco Bernasconi, Nathalie H Meyer, Laurent Jenni, Marie E Maradan-Gachet, Cyrille Stucker, Herberto Dhanis, Sabina Catalano Chiuvé, Julien F Bally, Mayte Castro Jimenez, Vanessa Fleury, Judit Horvath, Benoît Wicki, Javier Pagonabarraga Mora, Paul Krack, Olaf Blanke","doi":"10.1177/1877718X261440703","DOIUrl":null,"url":null,"abstract":"<p><p>BackgroundMinor hallucinations (MH) affect 30-60% of patients with Parkinson's disease (PD), and are considered precursors to structured visual hallucinations and cognitive decline. While the link between structured visual hallucinations and dementia is well established, the neuropsychological correlates of MH in PD remain unclear; most studies finding no significant cognitive differences between patients with MH and those without any hallucinations.ObjectivesPresence hallucinations (PH) being among the most prevalent MH in PD, we used a robotic procedure delivering somatomotor conflicts inducing PH experimentally to investigate whether sensitivity to such robot-induced PH aids in detecting cognitive differences between patients with MH and without hallucinations.Methods31 PD patients with MH (PD-MH) and 37 without hallucinations (PD-nH) underwent neuropsychological assessment and the robotic procedure inducing PH. The sensitivity to report robot-induced PH was analyzed in relation to cognitive performance in neuropsychological tests.ResultsPD-MH patients reported more robot-induced PH than PD-nH patients, supporting previous findings. While both groups showed comparable performance in neuropsychological testing, we found a significant association between increased sensitivity to the PH-induction and poorer performance in frontal subcortical cognitive functions, in PD-MH patients, but not in PD-nH patients.ConclusionsThese findings demonstrate that sensitivity to robot-induced PH reveals a previously undetected link between MH and frontal subcortical cognitive deficits in PD, pointing to shared underlying mechanisms between executive dysfunction and somatomotor processes involved in MH. This approach offers a novel and clinically valuable means of identifying early cognitive vulnerability that assessments relying only on standard testing may overlook.</p>","PeriodicalId":16660,"journal":{"name":"Journal of Parkinson's disease","volume":" ","pages":"1877718X261440703"},"PeriodicalIF":5.0000,"publicationDate":"2026-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Parkinson's disease","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/1877718X261440703","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

BackgroundMinor hallucinations (MH) affect 30-60% of patients with Parkinson's disease (PD), and are considered precursors to structured visual hallucinations and cognitive decline. While the link between structured visual hallucinations and dementia is well established, the neuropsychological correlates of MH in PD remain unclear; most studies finding no significant cognitive differences between patients with MH and those without any hallucinations.ObjectivesPresence hallucinations (PH) being among the most prevalent MH in PD, we used a robotic procedure delivering somatomotor conflicts inducing PH experimentally to investigate whether sensitivity to such robot-induced PH aids in detecting cognitive differences between patients with MH and without hallucinations.Methods31 PD patients with MH (PD-MH) and 37 without hallucinations (PD-nH) underwent neuropsychological assessment and the robotic procedure inducing PH. The sensitivity to report robot-induced PH was analyzed in relation to cognitive performance in neuropsychological tests.ResultsPD-MH patients reported more robot-induced PH than PD-nH patients, supporting previous findings. While both groups showed comparable performance in neuropsychological testing, we found a significant association between increased sensitivity to the PH-induction and poorer performance in frontal subcortical cognitive functions, in PD-MH patients, but not in PD-nH patients.ConclusionsThese findings demonstrate that sensitivity to robot-induced PH reveals a previously undetected link between MH and frontal subcortical cognitive deficits in PD, pointing to shared underlying mechanisms between executive dysfunction and somatomotor processes involved in MH. This approach offers a novel and clinically valuable means of identifying early cognitive vulnerability that assessments relying only on standard testing may overlook.

帕金森病患者的额叶皮层下执行功能障碍和轻微幻觉与对躯体运动冲突的敏感性有关。
背景:轻微幻觉(MH)影响30-60%的帕金森病患者,被认为是结构性视幻觉和认知能力下降的前兆。虽然结构性视幻觉和痴呆之间的联系已经确立,但PD中MH的神经心理学相关性尚不清楚;大多数研究发现,MH患者和没有任何幻觉的患者在认知方面没有显著差异。存在幻觉(PH)是PD中最常见的MH之一,我们使用机器人程序传递躯体运动冲突诱导的PH,实验研究对这种机器人诱导的PH的敏感性是否有助于检测MH患者和无幻觉患者之间的认知差异。方法对31例伴有幻觉的PD患者(PD-MH)和37例无幻觉的PD- nh患者进行神经心理评估和机器人诱导PH的过程,分析机器人诱导PH报告的敏感性与神经心理测试中认知表现的关系。结果spd - mh患者比PD-nH患者报告更多机器人诱导的PH,支持先前的研究结果。虽然两组在神经心理学测试中表现相当,但我们发现PD-MH患者对ph诱导的敏感性增加与额叶皮层下认知功能的较差表现之间存在显著关联,而PD-nH患者则没有。这些研究结果表明,对机器人诱导的PH的敏感性揭示了以前未被发现的MH与PD患者额叶皮层下认知缺陷之间的联系,指出了MH中执行功能障碍和躯体运动过程之间的共同潜在机制。这种方法提供了一种新的、有临床价值的方法,可以识别早期认知脆弱性,而仅依靠标准测试的评估可能会忽视这种脆弱性。
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
CiteScore
8.40
自引率
5.80%
发文量
338
审稿时长
>12 weeks
期刊介绍: The Journal of Parkinson''s Disease (JPD) publishes original research in basic science, translational research and clinical medicine in Parkinson’s disease in cooperation with the Journal of Alzheimer''s Disease. It features a first class Editorial Board and provides rigorous peer review and rapid online publication.
×
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
小红书